Patent Application
20220396597
The present disclosure generally relates to N-methyl-d-aspartate receptors (NMDAR) and/or potentiating γ-aminobutyric acid receptors (GABAAR) agents and uses thereof are described. Uses of these agents include methods of treating or preventing various psychiatric diseases, disorders, or conditions and methods of treating or preventing alcohol use disorder in a subject in need thereof.
Neuroactive steroids are a class of compounds that are emerging as potentially efficacious for treating neuropsychiatric disorders. Neuroactive steroids and ketamine are two classes of compounds that possess rapid antidepressant action and may be useful when conventional antidepressants fail (Abdallah et al., 2018; Duman et al., 2019; Gunduz-Bruce et al., 2019; Kanes et al., 2017; Meltzer-Brody et al., 2018; Meltzer-Brody and Kanes, 2020; Zanos and Gould, 2018). Neurosteroids and synthetic neuroactive steroids in clinical development primarily act as positive allosteric modulators (PAMS) of GABAA receptors (GABAARs). These compounds prolong IPSCs and augment tonic current at GABAARs (Belelli et al., 2020). In contrast, ketamine is an NMDAR antagonist (MacDonald et al., 1987). Although the relevance of GABAAR potentiation and NMDAR antagonism to therapeutic, anti-depressant benefit are still under active investigation, compounds with dual actions at GABAARs and NMDA receptors could be particularly effective antidepressants. In addition, drugs with dual actions at both of these receptor classes, such as acamprosate, are of interest in alcohol use disorder (Kufahl et al., 2014). Thus, combined GABAAR PAM and NMDAR negative allosteric modulator (NAM) effects may have high clinical applicability.
Brexanolone is a formulation of allopregnanolone, an endogenous neurosteroid, and is FDA approved for treatment of postpartum depression. Allopregnanolone is representative of neurosteroids and their analogues that are 3α-hydroxy neurosteroids. This 3α-hydroxyl group appears to be requisite for strong GABAAR PAM action (Covey et al., 2001). However, 3α-hydroxysteroids are typically ineffective at NMDARs.
Sulfated neurosteroids, such as pregnenolone sulfate and pregnanolone sulfate, modulate both GABAARs and NMDARs. These steroids can be either NMDAR PAMs or NAMs, depending on NMDAR subunit composition and neurosteroid structure (Horak et al., 2006; Korinek et al., 2011; Malayev et al., 2002; Park-Chung et al., 1997). Although the mechanisms of NMDAR modulation have not been fully elucidated, inhibition by some sulfated neurosteroids, including pregnanolone sulfate, is dependent on channel activation (Petrovic et al., 2005). The actions of sulfated neurosteroids on NMDARs are typically not very potent compared with GABAAR actions of either 3α-hydroxy neurosteroids or sulfated neurosteroids. Further, sulfated steroids inhibit, rather than augment, GABAAR function. The structural requirements for this inhibition are quite diverse: the enantiomer of pregnenolone sulfate is an effective NAM (Nilsson et al., 1998); the position of the negatively charged group can vary with little impact on inhibition (Mennerick et al., 2001; Schubring et al., 2012); and a wide variety of negatively charged amphiphiles inhibit GABAAR function by a similar mechanism (Chisari et al., 2010).
Further, there is large unmet clinical need for medications to treat alcohol use disorder (AUD), which takes a very high personal and public health toll in the United States and worldwide. Medications remain underdeveloped. Only three drugs are FDA approved to treat AUD: disulfiram (Antabuse), acamprosate (Campral), and naltrexone (Revia, Vivitrol). Disulfiram works by inhibiting acetaldehyde dehydrogenase, causing nausea in patients who drink, and it outperforms placebo only when the study is open label rather than blinded, suggesting that psychological threat may provide most of the benefit. Acamprosate is modestly efficacious in patients and is the only drug of the three that mainly works by reducing craving in abstinent patients. It appears somewhat more effective in patients than naltrexone, based on meta-analysis of aggregated abstinence measures. However, the efficacy of acamprosate has been called into question. Therefore, there remains a critical need for medications to treat alcohol use disorder (AUD).
Aspects of the present invention are directed to various compounds that are useful as NMDAR inhibiting and/or GABAAR potentiating agents. These compounds include those of formula (I) and pharmaceutically acceptable salts thereof:
wherein:
R1 is hydrogen, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R2 is hydrogen, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, C1 to C6 haloalkyl, —CH2O—RA, or —CH2O(C═O)—RB;
R3 is hydrogen, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 haloalkyl, —CH2O—RA, or —CH2O(C═O)—RB;
each RA is independently C1 to C6 alkyl or C1 to C6 haloalkyl;
each RB is independently hydrogen, C1 to C6 alkyl, or C1 to C6 haloalkyl;
R4 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R5 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R6 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R7 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
X is hydroxy, OSO3H, OSO3−NH4+, SO3H, SO2H, COOH, NH(CH2)m—Y, H2PO4, HPO3R8, C(R9)2COOH, C(R9)2—Y, or other negatively charged group at physiological pH;
Y is OSO3H, SO3H, SO2H, COOH, H2PO4, HPO3R8, or other negatively charged group at physiological pH;
each R8 is independently hydrogen, C1 to C6 alkyl or C1 to C6 haloalkyl;
each R9 is independently hydrogen, C1 to C6 alkyl, C1 to C6 haloalkyl, or halo;
m is an integer from 1 to 6; and
n is an integer from 1 to 8.
In some embodiments, the compound of formula (I) has NMDA receptor inhibitory activity and/or GABAA receptor potentiation activity.
Aspects of the present disclosure also provide for a method of inhibiting N-methyl-d-aspartate receptors (NMDAR) and/or potentiating γ-aminobutyric acid receptors (GABAAR). In some embodiments, the method comprises administering to a subject a composition comprising an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.
In some embodiments, the subject has or is suspected of having a psychiatric disease, disorder, or condition. As such, various methods are for treating or preventing a psychiatric disease, disorder, or condition in a subject in need thereof. For example, the psychiatric disease, disorder, or condition is a depression related disease, major depressive disorder, or anxiety.
Further aspects relate to methods of treating or preventing alcohol use disorder in a subject in need thereof comprising administering to the subject a composition comprising an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof. In some embodiments, the compound has the following structure:
or pharmaceutically acceptable salt thereof.
Other objects and features will be in part apparent and in part pointed out hereinafter.
Those of skill in the art will understand that the drawings, described below, are for illustrative purposes only. The drawings are not intended to limit the scope of the present teachings in any way.
The present disclosure is based, at least in part, on the discovery of compounds exhibiting steroid modulating activity with actions at both NMDA and GABAA receptors. As shown herein, various compounds of formula (I) (e.g., MQ-221) exhibit action relative to other similar (sulfated, 3β hydroxyl) compounds is the unique effect of GABA, rather than NMDA, potentiation.
Surprisingly, it has been discovered that a sulfated, 3β-hydroxy neurosteroid analogue, MQ-221, inhibits NMDAR function but also potentiates GABAAR function, thereby exhibiting an unusual but potentially clinically desirable constellation of effects. Although prolonged channel activation yielded the expected inhibition of GABAAR function, IPSCs showed net potentiation under physiological conditions. Potentiation of GABAAR function was distinct from the mechanism governing potentiation by anesthetic neurosteroids (Hosie et al., 2007). Inhibition of NMDAR function showed weaker channel activation dependence than pregnanolone sulfate (3α5βPS). MQ-221 was unique among four stereoisomers explored in the constellation of actions at GABAA and NMDARs. Taken together, MQ-221 and like analogs represent a new class of compounds with unique psychoactive effects that is beneficial for treating a variety of neuropsychiatric disorders.
The FDA approval of ketamine, an antagonist of N-methyl-D-aspartate (NMDA) receptors, and brexanolone, a neurosteroid that potentiates GABAA receptor function, has unveiled two separate inroads for treating depression-related illness. Compounds with both actions may represent a new generation of antidepressant drugs, and this invention discloses a compound with this unusual constellation of actions. It has unusual potentiating actions at GABAARs and negatively modulates NMDARs. At both NMDARs and GABAARs, it acted in the low μM range, making it unusual among steroidal NMDAR modulators, which typically require >30 μM for effectiveness.
The disclosed compositions and analogs thereof can be anew treatment for major depressive disorder.
Up to one third of patients suffering from depressive disorders are not aided by current medication. The FDA approval of ketamine, an antagonist of N-methyl-D-aspartate (NMDA) receptors, and brexanolone, a neurosteroid that potentiates GABAA receptor function, has unveiled two complementary inroads for the development of treatments for depression-related disorders. Compounds with both actions may represent a new generation of antidepressant drugs. Sulfated steroids have been of some interest as therapeutic agents in other contexts. Although some sulfated neurosteroids negatively modulate NMDARs, all known sulfated steroids antagonize GABAAR function, an action that is likely counterproductive in the search for antidepressant drugs. Here, the compounds described herein, e.g., MQ-221, which bears structural similarity to sulfated neurosteroids was characterized. However, MQ-221 has unexpected potentiating actions at GABAARs and negatively modulates NMDARS. At both NMDARs and GABAARs, MQ-221 acted in the low μM range, making it unique among steroidal NMDAR modulators, which typically require >30 μM for effectiveness. Activity at GABAARs was biphasic with inhibition increasing with both GABA and MQ-221 concentration, but potentiation dominated the actions of 1 μM MQ-221 on inhibitory synaptic currents. At NMDARs, inhibition by MQ-221 was independent of membrane potential and NMDA concentration. Unlike ketamine and the well-studied sulfated steroid pregnanolone sulfate (3α5βS), MQ-221 acted on closed NMDA channels, although it exhibited some activation dependence, as assessed by comparing drug pre-application with agonist co-application protocols. Three stereoisomers of MQ-221 were also examined and found that none of them had the actions of MQ-221.
The compounds described herein can be useful in treating psychiatric diseases, disorders, and conditions, such as neuropathological conditions.
Such psychiatric diseases, disorders, and conditions can be a depression-related illness, such as major depressive disorder. As such, the compounds described herein can be an anti-depressant drug.
Such psychiatric diseases, disorders, and conditions can be anxiety. As such, the compositions described herein can be an anti-anxiety drug.
Other psychiatric diseases, disorders, and conditions can be a disorder associated with NMDR or GABAAR, such as sleep disorders, epilepsy, or schizophrenia.
The compounds described herein can also be used to treat or prevent alcohol use disorder in a subject in need thereof.
As noted, there is large unmet clinical need for novel medications to treat alcohol use disorder (AUD), which takes a very high personal and public health toll in the United States and worldwide. Medications remain underdeveloped. Acamprosate may be the most useful treatment, although it shows weak clinical and pharmacodynamic efficacy. Based on the acamprosate targets of GABAA receptors (GABAARs) and NMDA receptors (NMDARs), the unique neurosteroid analogues described herein, e.g., MQ-221, acts more potently at the dual targets of GABAARs and NMDARs. Without being bound by theory, the enhanced potency and efficacy of MQ-221-like compounds over acamprosate provides a superior medication to existing drug treatments of AUD. Accordingly, the disclosed compositions and analogs thereof can be a new treatment for AUD.
Accordingly, one preferred method of treating or preventing alcohol use disorder in a subject in need thereof comprises administering to the subject a composition comprising an effective amount of a compound of the following structure:
or pharmaceutically acceptable salt thereof.
NMDA Receptor Inhibiting/GABAA Receptor Potentiating Agents
Compositions as described herein are N-methyl-d-aspartate (NMDA) receptor negative allosteric modulators, negative allosteric modulators (NAM), and/or inhibitors of the NMDA receptor. They are closely related and similar to NMDA receptor antagonists. The N-methyl-d-aspartate receptor (NMDAR) family has many critical roles in CNS function and in various neuropathological and psychiatric conditions.
Compositions as described herein are GABAA receptor positive allosteric modulators (or GABAA receptor potentiators). GABAA receptor positive allosteric modulators are positive allosteric modulator (PAM) molecules that increase the activity of the GABAA receptor protein in the vertebrate central nervous system. GABA is a major inhibitory neurotransmitter in the central nervous system. Upon binding, it triggers the GABAA receptor to open its chloride channel to allow chloride ions into the neuron, making the cell hyperpolarized and less likely to fire. GABAA PAMs increase the effect of GABA by making the channel open more frequently or for longer periods. However, they have no effect if GABA or another agonist is not present.
Unlike GABAA receptor agonists, GABAA PAMs do not bind at the same active site as the γ-aminobutyric acid (GABA) neurotransmitter molecule. Instead, they affect the receptor by binding at a different site on the protein. This is called allosteric modulation.
Chemical agents as described herein have a unique effect on GABA potentiation and the compounds can exhibit strong activity in the 1 μM range rather than >30 μM (one order of magnitude smaller dose).
An NMDA receptor inhibiting/GABAA receptor potentiating agent can be either an NMDA receptor inhibiting agent or a GABAA receptor potentiating agent or both.
Examples of NMDA receptor inhibiting/GABAA receptor potentiating agents are described herein and include compounds of formula (I) and pharmaceutically acceptable salts thereof:
wherein:
R1 is hydrogen, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R2 is hydrogen, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, C1 to C6 haloalkyl, —CH2O—RA, or —CH2O(C═O)—RB;
R3 is hydrogen, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 haloalkyl, —CH2O—RA, or —CH2O(C═O)—RB;
each RA is independently C1 to C6 alkyl or C1 to C6 haloalkyl;
each RB is independently hydrogen, C1 to C6 alkyl, or C1 to C6 haloalkyl;
R4 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R5 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R6 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
R7 is hydrogen, hydroxy, C1 to C6 alkyl, C1 to C6 alkenyl, C1 to C6 alkynyl, C1 to C6 alkoxy, or C1 to C6 haloalkyl;
X is hydroxy, OSO3H, OSO3−NH4+, SO3H, SO2H, COOH, NH(CH2)m—Y, H2PO4, HPO3R8, C(R9)2COOH, C(R9)2—Y, or other negatively charged group at physiological pH;
Y is OSO3H, SO3H, SO2H, COOH, H2PO4, HPO3R8, or other negatively charged group at physiological pH;
each R8 is independently hydrogen, C1 to C6 alkyl or C1 to C6 haloalkyl;
each R9 is independently hydrogen, C1 to C6 alkyl, C1 to C6 haloalkyl, or halo;
m is an integer from 1 to 6; and
n is an integer from 1 to 8.
Pharmaceutically acceptable salts thereof include various salts, without limitation, as described herein. Preferred salts include amine salts, lithium salts, sodium salts, potassium salts, and mixtures thereof.
In various compounds of formula (I), the bond at the 4,5 position is a single bond. Alternatively, in some compounds, the bond at the 4,5 position is a double bond.
In various compounds of formula (I), the bond at the 5,6 position is a single bond. Alternatively, in some compounds, the bond at the 5,6 position is a double bond.
In various compounds of formula (I), R1 is hydrogen, C1 to C4 alkyl, or C1 to C4 haloalkyl; R4 is hydrogen, C1 to C4 alkyl, or C1 to C4 haloalkyl; R5 is hydrogen, C1 to C4 alkyl, or C1 to C4 haloalkyl; R6 is hydrogen, C1 to C4 alkyl, or C1 to C4 haloalkyl; and/or R7 is hydrogen, C1 to C4 alkyl, or C1 to C4 haloalkyl.
In certain compounds of formula (I), R1 is hydrogen, methyl, ethyl, propyl, halomethyl, haloethyl, or halopropyl; R4 is hydrogen, methyl, ethyl, propyl, halomethyl, haloethyl, or halopropyl; R5 is hydrogen, methyl, ethyl, propyl, halomethyl, haloethyl, or halopropyl; R6 is hydrogen, methyl, ethyl, propyl, halomethyl, haloethyl, or halopropyl; and/or R7 is hydrogen, methyl, ethyl, propyl, halomethyl, haloethyl, or halopropyl.
In some compounds of formula (I), at least one, at least two, at least three, at least four, or all of R1, R4, R5, R6, and R7 are each hydrogen. In certain compounds of formula (I), at least of one of R2, R4, R5, R6, and R7 is not hydrogen.
In various compounds of formula (I), R2 is C1 to C6 alkyl or C1 to C6 haloalkyl. In some compounds of formula (I), R2 is methyl, ethyl, propyl, halomethyl, haloethyl, or halopropyl. In certain compounds of formula (I), R2 is methyl.
In various compounds of formula (I), R3 is hydrogen, C1 to C6 alkyl, or C1 to C6 haloalkyl. In some compounds of formula (I), R3 is hydrogen, methyl, ethyl, or propyl. In certain compounds of formula (I), R3 is not hydrogen. In some compounds, R3 is not methyl.
In various compounds of formula (I), R3 is —CH2O(C═O)—RB and RB is C1 to C6 alkyl.
In various compounds of formula (I), X is OSO3H, OSO3−NH4+, SO3H, SO2H, COOH, NH(CH2)m—Y, H2PO4, HPO3R8, C(R9)2COOH, or C(R9)2—Y, and/or Y is OSO3H, OSO3−NH4+, SO3H, SO2H, COOH, H2PO4, or HPO3R8. In some compounds, X is OSO3H or COOH. In certain compounds of formula (I), X is OSO3H or salt thereof (e.g., OSO3−NH4+).
In various compounds of formula (I), m is an integer from 1 to 5, from 1 to 4, from 1 to 3, from 1 to 2, or is 1, 2, 3, 4, 5, or 6.
In various compounds of formula (I), n is an integer from 1 to 7, from 1 to 6, from 1 to 5, from 1 to 4, from 1 to 3, from 1 to 2, or is 1, 2, 3, 4, 5, 6, 7, or 8.
Some compounds of formula (I) have a structure of formula (II), or a pharmaceutically acceptable salt thereof:
where R1, R2, R3, R4, R5, R6, R7, and X are as defined above.
Some compounds of formula (I) have a structure of formula (III), or a pharmaceutically acceptable salt thereof:
where R1, R2, R3, R4, R5, R6, R7, and X are as defined above.
Certain compounds of formula (I) have a structure selected from the group consisting of:
and pharmaceutically acceptable salts thereof.
Various preferred compounds of formula (I) include those of the following structure:
and a pharmaceutically acceptable salts thereof. For example, one preferred salt has a structure of:
Various provisos may apply to the compounds of formulas (I)-(III) and pharmaceutically acceptable salts thereof. For example, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a single bond, R2 is methyl, R3 is hydrogen, X is COOH, and n is 1, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
Additionally or alternatively, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a single bond, R2 is methyl, R3 is methyl, X is COOH, and n is 1 or 2, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
Additionally or alternatively, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a double bond, R2 is methyl, R3 is methyl, X is COOH, and n is 1, 2 or 3, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
Additionally or alternatively, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a double bond, R2 is methyl, R3 is methyl, X is C(R9)2COOH, each R9 is halo, and n is 1, 2, or 3, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
Additionally or alternatively, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a double bond, R2 is methyl, R3 is methyl, X is C(R9)2COOH, each R9 is fluoro, and n is 1, 2, or 3, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
Additionally or alternatively, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a double bond, R2 is methyl, R3 is methyl, X is C(R9)2COOH, R9 is bromo, and n is 1, 2, or 3, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
These provisos may be applied in combination. For example, when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a single bond, R2 is methyl, R3 is hydrogen, X is COOH, and n is 1, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen;
when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a single bond, R2 is methyl, R3 is methyl, X is COOH, and n is 1 or 2, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen;
when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a double bond, R2 is methyl, R3 is methyl, X is COOH, and n is 1, 2 or 3, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen; and
when the bond at the 4,5 position is a single bond, the bond at the 5,6 position is a double bond, R2 is methyl, R3 is methyl, X is C(R9)2COOH, R9 is halo, and n is 1, 2, or 3, then at least of one of R1, R4, R5, R6, and R7 is not hydrogen.
In some embodiments, a NMDA receptor inhibiting/GABAA receptor potentiating agent can be, of the formula (IV):
or a pharmaceutically acceptable salt thereof, including all tautomers and stereoisomers, and optionally substituted analogues thereof.
In some embodiments, R1 is H or C1-4 alkyl; R2 is H or C1-4 alkyl; n=1-8; and X is OSO3H or COOH or other negatively charged group at physiological pH or salt thereof. In some embodiments, when the C5-C6 double bond is not present there is an α-H at position C5.
In various embodiments, the compound of formula (IV) is a compound of formula (V):
or a pharmaceutically acceptable salt thereof, wherein
R1 is H or C1-4 alkyl;
R2 is H or C1-4 alkyl;
n=1-8; and
X is OSO3H or COOH or other negatively charged group at physiological pH or salt thereof.
In some embodiments, the compound of formula (IV) can be
In some embodiments, the compounds of formulas (I)-(V) have NMDA receptor inhibitory activity and/or GABAA receptor potentiation activity.
Analogs of MQ-221 can include the addition or substitution with a variety of R groups which can be optionally substituted with one or more groups independently selected from the group consisting of hydroxyl; C1-10alkyl hydroxyl; amine; C1-10carboxylic acid; C1-10carboxyl; straight chain or branched C1-10alkyl, optionally containing unsaturation; a C2-10cycloalkyl optionally containing unsaturation or one oxygen or nitrogen atom; straight chain or branched C1-10alkyl amine; heterocyclyl; heterocyclic amine; and aryl comprising a phenyl; heteroaryl containing from 1 to 4 N, O, or S atoms; unsubstituted phenyl ring; substituted phenyl ring; unsubstituted heterocyclyl; and substituted heterocyclyl, wherein the unsubstituted phenyl ring or substituted phenyl ring can be optionally substituted with one or more groups independently selected from the group consisting of hydroxyl; C1-10alkyl hydroxyl; amine; C1-10carboxylic acid; C1-10carboxyl; straight chain or branched C1-10alkyl, optionally containing unsaturation; straight chain or branched C1-10alkyl amine, optionally containing unsaturation; a C2-10cycloalkyl optionally containing unsaturation or one oxygen or nitrogen atom; straight chain or branched C1-10alkyl amine; heterocyclyl; heterocyclic amine; aryl comprising a phenyl; and heteroaryl containing from 1 to 4 N, O, or S atoms; and the unsubstituted heterocyclyl or substituted heterocyclyl can be optionally substituted with one or more groups independently selected from the group consisting of hydroxyl; C1-10alkyl hydroxyl; amine; C1-10carboxylic acid; C1-10carboxyl; straight chain or branched C1-10alkyl, optionally containing unsaturation; straight chain or branched C1-10alkyl amine, optionally containing unsaturation; a C2-10cycloalkyl optionally containing unsaturation or one oxygen or nitrogen atom; heterocyclyl; straight chain or branched C1-10alkyl amine; heterocyclic amine; and aryl comprising a phenyl; and heteroaryl containing from 1 to 4 N, O, or S atoms. Any of the above can be further optionally functionalized or substituted with R groups.
The term “imine” or “imino”, as used herein, unless otherwise indicated, can include a functional group or chemical compound containing a carbon-nitrogen double bond. The expression “imino compound”, as used herein, unless otherwise indicated, refers to a compound that includes an “imine” or an “imino” group as defined herein. The “imine” or “imino” group can be optionally substituted.
The term “hydroxyl”, as used herein, unless otherwise indicated, can include —OH. The “hydroxyl” can be optionally substituted.
The terms “halogen” and “halo”, as used herein, unless otherwise indicated, include a chlorine, chloro, Cl; fluorine, fluoro, F; bromine, bromo, Br; or iodine, iodo, or I. Preferred “halo” groups include fluoro and bromo.
The term “haloalkyl” as used herein, unless otherwise indicated, includes chloroalkyl, fluoroalkyl, bromoalkyl, iodoalkyl groups and groups such as halomethyl, haloethyl, or halopropyl. The term “haloalkyl” also includes groups having multiple halo substituents, such as trifluoroalkyl (e.g., trifluoromethyl). Haloalkyls can be saturated, partially saturated, or unsaturated.
The term “acetamide”, as used herein, is an organic compound with the formula CH3CONH2. The “acetamide” can be optionally substituted.
The term “aryl”, as used herein, unless otherwise indicated, include a carbocyclic aromatic group. Examples of aryl groups include, but are not limited to, phenyl, benzyl, naphthyl, or anthracenyl. The “aryl” can be optionally substituted.
The terms “amine”, “aminyl”, and “amino”, as used herein, unless otherwise indicated, include a functional group that contains a nitrogen atom with a lone pair of electrons and wherein one or more hydrogen atoms have been replaced by a substituent such as, but not limited to, an alkyl group or an aryl group. The “amine” or “amino” group can be optionally substituted.
The term “alkyl”, as used herein, unless otherwise indicated, can include saturated monovalent hydrocarbon radicals having straight or branched moieties, such as but not limited to, methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl groups, etc. Representative straight-chain lower alkyl groups include, but are not limited to, -methyl, -ethyl, -n-propyl, -n-butyl, -n-pentyl, -n-hexyl, -n-heptyl and -n-octyl; while branched lower alkyl groups include, but are not limited to, -isopropyl, -sec-butyl, -isobutyl, -tert-butyl, -isopentyl, 2-methylbutyl, 2-methylpentyl, 3-methylpentyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 2,2-dimethylpentyl, 2,3-dimethylpentyl, 3,3-dimethylpentyl, 2,3,4-trimethylpentyl, 3-methylhexyl, 2,2-dimethylhexyl, 2,4-dimethylhexyl, 2,5-dimethylhexyl, 3,5-dimethylhexyl, 2,4-dimethylpentyl, 2-methylheptyl, 3-methylheptyl, unsaturated C1-10 alkyls include, but are not limited to, -vinyl, -allyl, -1-butenyl, -2-butenyl, -isobutylenyl, -1-pentenyl, -2-pentenyl, -3-methyl-1-butenyl, -2-methyl-2-butenyl, -2,3-dimethyl-2-butenyl, 1-hexyl, 2-hexyl, 3-hexyl, -acetylenyl, -propynyl, -1-butynyl, -2-butynyl, -1-pentynyl, -2-pentynyl, or -3-methyl-1 butynyl. An alkyl can be saturated, partially saturated, or unsaturated. The “alkyl” can be optionally substituted.
The term “carboxyl”, as used herein, unless otherwise indicated, can include a functional group consisting of a carbon atom double bonded to an oxygen atom and single bonded to a hydroxyl group (—COOH). The “carboxyl” can be optionally substituted.
The term “alkenyl”, as used herein, unless otherwise indicated, can include alkyl moieties having at least one carbon-carbon double bond wherein alkyl is as defined above and including E and Z isomers of said alkenyl moiety. An alkenyl can be partially saturated or unsaturated. The “alkenyl” can be optionally substituted.
The term “alkynyl”, as used herein, unless otherwise indicated, can include alkyl moieties having at least one carbon-carbon triple bond wherein alkyl is as defined above. An alkynyl can be partially saturated or unsaturated. The “alkynyl” can be optionally substituted.
The term “acyl”, as used herein, unless otherwise indicated, can include a functional group derived from an aliphatic carboxylic acid, by removal of the hydroxyl (—OH) group. The “acyl” can be optionally substituted.
The term “alkoxy” or “alkoxyl”, as used herein, unless otherwise indicated, can include O-alkyl groups wherein alkyl is as defined above and O represents oxygen. Representative alkoxyl groups include, but are not limited to, —O-methyl, —O-ethyl, —O-n-propyl, —O-n-butyl, —O-n-pentyl, —O-n-hexyl, —O-n-heptyl, —O-n-octyl, —O-isopropyl, —O-sec-butyl, —O-isobutyl, —O-tert-butyl, —O-isopentyl, —O-2-methylbutyl, —O-2-methylpentyl, —O-3-methylpentyl, —O-2,2-dimethylbutyl, —O-2,3-dimethylbutyl, —O-2,2-dimethylpentyl, —O-2,3-dimethylpentyl, —O-3,3-dimethylpentyl, —O-2,3,4-trimethylpentyl, —O-3-methylhexyl, —O-2,2-dimethylhexyl, —O-2,4-dimethylhexyl, —O-2,5-dimethylhexyl, —O-3,5-dimethylhexyl, —O-2,4dimethylpentyl, —O-2-methylheptyl, —O-3-methylheptyl, —O-vinyl, —O-allyl, —O-1-butenyl, —O-2-butenyl, —O-isobutylenyl, —O-1-pentenyl, —O-2-pentenyl, —O-3-methyl-1-butenyl, —O-2-methyl-2-butenyl, —O-2,3-dimethyl-2-butenyl, —O-1-hexyl, —O-2-hexyl, —O-3-hexyl, —O-acetylenyl, —O-propynyl, —O-1-butynyl, —O-2-butynyl, —O-1-pentynyl, —O-2-pentynyl and —O-3-methyl-1-butynyl, —O-cyclopropyl, —O-cyclobutyl, —O-cyclopentyl, —O-cyclohexyl, —O-cycloheptyl, —O-cyclooctyl, —O-cyclononyl and —O-cyclodecyl, —O—CH2-cyclopropyl, —O—CH2-cyclobutyl, —O—CH2-cyclopentyl, —O—CH2-cyclohexyl, —O—CH2-cycloheptyl, —O—CH2-cyclooctyl, —O—CH2-cyclononyl, —O—CH2-cyclodecyl, —O—(CH2)2-cyclopropyl, —O—(CH2)2-cyclobutyl, —O—(CH2)2-cyclopentyl, —O—(CH2)2-cyclohexyl, —O—(CH2)2-cycloheptyl, —O—(CH2)2-cyclooctyl, —O—(CH2)2-cyclononyl, or —O—(CH2)2-cyclodecyl. An alkoxy or alkoxyl can be saturated, partially saturated, or unsaturated. The “alkoxyl” can be optionally substituted.
The term “cycloalkyl”, as used herein, unless otherwise indicated, can include an aromatic, a non-aromatic, saturated, partially saturated, or unsaturated, monocyclic or fused, spiro or unfused bicyclic or tricyclic hydrocarbon referred to herein containing a total of from 1 to 10 carbon atoms (e.g., 1 or 2 carbon atoms if there are other heteroatoms in the ring), preferably 3 to 8 ring carbon atoms. Examples of cycloalkyls include, but are not limited to, C3-10 cycloalkyl groups include, but are not limited to, -cyclopropyl, -cyclobutyl, -cyclopentyl, -cyclopentadienyl, -cyclohexyl, -cyclohexenyl, -1,3-cyclohexadienyl, -1,4-cyclohexadienyl, -cycloheptyl, -1,3-cycloheptadienyl, -1,3,5-cycloheptatrienyl, -cyclooctyl, and -cyclooctadienyl. The term “cycloalkyl” also can include -lower alkyl-cycloalkyl, wherein lower alkyl and cycloalkyl are as defined herein. Examples of -lower alkyl-cycloalkyl groups include, but are not limited to, —CH2-cyclopropyl, —CH2-cyclobutyl, —CH2-cyclopentyl, —CH2-cyclopentadienyl, —CH2-cyclohexyl, —CH2-cycloheptyl, or —CH2-cyclooctyl. The “cycloalkyl” can be optionally substituted. A “cycloheteroalkyl”, as used herein, unless otherwise indicated, can include any of the above with a carbon substituted with a heteroatom (e.g., O, S, N).
The term “heterocyclic” or “heteroaryl”, as used herein, unless otherwise indicated, can include an aromatic or non-aromatic cycloalkyl in which one to four of the ring carbon atoms are independently replaced with a heteroatom from the group consisting of O, S and N. Representative examples of a heterocycle include, but are not limited to, benzofuranyl, benzothiophene, indolyl, benzopyrazolyl, coumarinyl, isoquinolinyl, pyrrolyl, pyrrolidinyl, thiophenyl, furanyl, thiazolyl, imidazolyl, pyrazolyl, triazolyl, quinolinyl, pyrimidinyl, pyridinyl, pyridonyl, pyrazinyl, pyridazinyl, isothiazolyl, isoxazolyl, (1,4)-dioxane, (1,3)-dioxolane, 4,5-dihydro-1H-imidazolyl, or tetrazolyl. Heterocycles can be substituted or unsubstituted. Heterocycles can also be bonded at any ring atom (i.e., at any carbon atom or heteroatom of the heterocyclic ring). A heterocyclic can be saturated, partially saturated, or unsaturated. The “heterocyclic” can be optionally substituted.
The term “indole”, as used herein, is an aromatic heterocyclic organic compound with formula C8H7N. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The “indole” can be optionally substituted.
The term “cyano”, as used herein, unless otherwise indicated, can include a —CN group. The “cyano” can be optionally substituted.
The term “alcohol”, as used herein, unless otherwise indicated, can include a compound in which the hydroxyl functional group (—OH) is bound to a carbon atom. In particular, this carbon center should be saturated, having single bonds to three other atoms. The “alcohol” can be optionally substituted.
The term “solvate” is intended to mean a solvate form of a specified compound that retains the effectiveness of such compound. Examples of solvates include compounds of the invention in combination with, for example: water, isopropanol, ethanol, methanol, dimethylsulfoxide (DMSO), ethyl acetate, acetic acid, or ethanolamine.
The term “mmol”, as used herein, is intended to mean millimole. The term “equiv”, as used herein, is intended to mean equivalent. The term “mL”, as used herein, is intended to mean milliliter. The term “g”, as used herein, is intended to mean gram. The term “kg”, as used herein, is intended to mean kilogram. The term “μg”, as used herein, is intended to mean micrograms. The term “h”, as used herein, is intended to mean hour. The term “min”, as used herein, is intended to mean minute. The term “M”, as used herein, is intended to mean molar. The term “L”, as used herein, is intended to mean microliter. The term “μM”, as used herein, is intended to mean micromolar. The term “nM”, as used herein, is intended to mean nanomolar. The term “N”, as used herein, is intended to mean normal. The term “amu”, as used herein, is intended to mean atomic mass unit. The term “° C.”, as used herein, is intended to mean degree Celsius. The term “wt/wt”, as used herein, is intended to mean weight/weight. The term “v/v”, as used herein, is intended to mean volume/volume. The term “MS”, as used herein, is intended to mean mass spectroscopy. The term “HPLC”, as used herein, is intended to mean high performance liquid chromatograph. The term “RT”, as used herein, is intended to mean room temperature. The term “e.g.”, as used herein, is intended to mean example. The term “N/A”, as used herein, is intended to mean not tested.
As used herein, the expression “pharmaceutically acceptable salt” refers to pharmaceutically acceptable organic or inorganic salts of a compound of the invention. One preferred salt includes the amine salt (NH4+). Other preferred salts include, but are not limited, various metal salts, such as alkali salts (e.g., lithium, sodium, and potassium salts). Preferred salts also include, but are not limited, to sulfate, citrate, acetate, oxalate, chloride, bromide, iodide, nitrate, bisulfate, phosphate, acid phosphate, isonicotinate, lactate, salicylate, acid citrate, tartrate, oleate, tannate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, or pamoate (i.e., 1,1′-methylene-bis-(2-hydroxy-3-naphthoate)) salts. A pharmaceutically acceptable salt may involve the inclusion of another molecule such as an acetate ion, a succinate ion or other counterion. The counterion may be any organic or inorganic moiety that stabilizes the charge on the parent compound. Furthermore, a pharmaceutically acceptable salt may have more than one charged atom in its structure. Instances where multiple charged atoms are part of the pharmaceutically acceptable salt can have multiple counterions. Hence, a pharmaceutically acceptable salt can have one or more charged atoms and/or one or more counterion. As used herein, the expression “pharmaceutically acceptable solvate” refers to an association of one or more solvent molecules and a compound of the invention. Examples of solvents that form pharmaceutically acceptable solvates include, but are not limited to, water, isopropanol, ethanol, methanol, DMSO, ethyl acetate, acetic acid, and ethanolamine. As used herein, the expression “pharmaceutically acceptable hydrate” refers to a compound of the invention, or a salt thereof, that further can include a stoichiometric or non-stoichiometric amount of water bound by non-covalent intermolecular forces.
Formulation
The agents and compositions described herein can be formulated by any conventional manner using one or more pharmaceutically acceptable carriers or excipients as described in, for example, Remington's Pharmaceutical Sciences (A. R. Gennaro, Ed.), 21st edition, ISBN: 0781746736 (2005), incorporated herein by reference in its entirety. Such formulations will contain a therapeutically effective amount of a biologically active agent described herein, which can be in purified form, together with a suitable amount of carrier so as to provide the form for proper administration to the subject.
The term “formulation” refers to preparing a drug in a form suitable for administration to a subject, such as a human. Thus, a “formulation” can include pharmaceutically acceptable excipients, including diluents or carriers.
The term “pharmaceutically acceptable” as used herein can describe substances or components that do not cause unacceptable losses of pharmacological activity or unacceptable adverse side effects. Examples of pharmaceutically acceptable ingredients can be those having monographs in United States Pharmacopeia (USP 29) and National Formulary (NF 24), United States Pharmacopeial Convention, Inc, Rockville, Md., 2005 (“USP/NF”), or a more recent edition, and the components listed in the continuously updated Inactive Ingredient Search online database of the FDA. Other useful components that are not described in the USP/NF, etc. may also be used.
The term “pharmaceutically acceptable excipient,” as used herein, can include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic, or absorption delaying agents. The use of such media and agents for pharmaceutical active substances is well known in the art (see generally Remington's Pharmaceutical Sciences (A. R. Gennaro, Ed.), 21st edition, ISBN: 0781746736 (2005)). One preferred excipient includes cyclodextrin.
Except insofar as any conventional media or agent is incompatible with an active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions.
A “stable” formulation or composition can refer to a composition having sufficient stability to allow storage at a convenient temperature, such as between about 0° C. and about 60° C., for a commercially reasonable period of time, such as at least about one day, at least about one week, at least about one month, at least about three months, at least about six months, at least about one year, or at least about two years.
The formulation should suit the mode of administration. The agents of use with the current disclosure can be formulated by known methods for administration to a subject using several routes which include, but are not limited to, parenteral, oral, topical, intradermal, intranasal, intramuscular, intraperitoneal, intravenous, subcutaneous, epidural, transdermal, buccal, and rectal. The individual agents may also be administered in combination with one or more additional agents or together with other biologically active or biologically inert agents. Such biologically active or inert agents may be in fluid or mechanical communication with the agent(s) or attached to the agent(s) by ionic, covalent, Van der Waals, hydrophobic, hydrophilic or other physical forces.
Controlled-release (or sustained-release) preparations may be formulated to extend the activity of the agent(s) and reduce dosage frequency. Controlled-release preparations can also be used to effect the time of onset of action or other characteristics, such as blood levels of the agent, and consequently affect the occurrence of side effects. Controlled-release preparations may be designed to initially release an amount of an agent(s) that produces the desired therapeutic effect, and gradually and continually release other amounts of the agent to maintain the level of therapeutic effect over an extended period of time. In order to maintain a near-constant level of an agent in the body, the agent can be released from the dosage form at a rate that will replace the amount of agent being metabolized or excreted from the body. The controlled-release of an agent may be stimulated by various inducers, e.g., change in pH, change in temperature, enzymes, water, or other physiological conditions or molecules.
Agents or compositions described herein can also be used in combination with other therapeutic modalities, as described further below. Thus, in addition to the therapies described herein, one may also provide to the subject other therapies known to be efficacious for treatment of the disease, disorder, or condition.
Therapeutic Methods
Also provided is a process of treating or preventing a psychiatric disease, disorder, or condition in a subject in need of administration of a therapeutically effective amount of an NMDA receptor inhibiting/GABAA receptor potentiating agent as described herein (e.g., one or more compounds of formulas (I)-(V)), so as to inhibit NMDAR and/or potentiate GABAAR.
Methods described herein are generally performed on a subject in need thereof. A subject in need of the therapeutic methods described herein can be a subject having, diagnosed with, suspected of having, or at risk for developing a psychiatric disease, disorder, or condition. A determination of the need for treatment will typically be assessed by a history, physical exam, or diagnostic tests consistent with the disease or condition at issue. Diagnosis of the various conditions treatable by the methods described herein is within the skill of the art. The subject can be an animal subject, including a mammal, such as horses, cows, dogs, cats, sheep, pigs, mice, rats, monkeys, hamsters, guinea pigs, and humans or chickens. For example, the subject can be a human subject.
Generally, a safe and effective amount of an NMDA receptor inhibiting/GABAA receptor potentiating agent is, for example, that amount that would cause the desired therapeutic effect in a subject while minimizing undesired side effects. In various embodiments, an effective amount of an NMDA receptor inhibiting/GABAA receptor potentiating agent described herein can substantially inhibit NMDAR, potentiate GABAAR, slow the progress of a psychiatric disease, disorder, or condition, or limit the development of a psychiatric disease, disorder, or condition.
According to the methods described herein, administration can be parenteral, pulmonary, oral, topical, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, ophthalmic, buccal, or rectal administration.
When used in the treatments described herein, a therapeutically effective amount of an NMDA receptor inhibiting/GABAA receptor potentiating agent can be employed in pure form or, where such forms exist, in pharmaceutically acceptable salt form and with or without a pharmaceutically acceptable excipient. For example, the compounds of the present disclosure can be administered, at a reasonable benefit/risk ratio applicable to any medical treatment, in a sufficient amount to potentiate GABAAR or inhibit NMDR.
The amount of a composition described herein that can be combined with a pharmaceutically acceptable carrier to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. It will be appreciated by those skilled in the art that the unit content of agent contained in an individual dose of each dosage form need not in itself constitute a therapeutically effective amount, as the necessary therapeutically effective amount could be reached by administration of a number of individual doses.
Toxicity and therapeutic efficacy of compositions described herein can be determined by standard pharmaceutical procedures in cell cultures or experimental animals for determining the LD50 (the dose lethal to 50% of the population) and the ED50, (the dose therapeutically effective in 50% of the population). The dose ratio between toxic and therapeutic effects is the therapeutic index that can be expressed as the ratio LD50/ED50, where larger therapeutic indices are generally understood in the art to be optimal.
The specific therapeutically effective dose level for any particular subject will depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the subject; the time of administration; the route of administration; the rate of excretion of the composition employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well known in the medical arts (see e.g., Koda-Kimble et al. (2004) Applied Therapeutics: The Clinical Use of Drugs, Lippincott Williams & Wilkins, ISBN 0781748453; Winter (2003) Basic Clinical Pharmacokinetics, 4th ed., Lippincott Williams & Wilkins, ISBN 0781741475; Sharqel (2004) Applied Biopharmaceutics & Pharmacokinetics, McGraw-Hill/Appleton & Lange, ISBN 0071375503). For example, it is well within the skill of the art to start doses of the composition at levels lower than those required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved. If desired, the effective daily dose may be divided into multiple doses for purposes of administration. Consequently, single dose compositions may contain such amounts or submultiples thereof to make up the daily dose. It will be understood, however, that the total daily usage of the compounds and compositions of the present disclosure will be decided by an attending physician within the scope of sound medical judgment. In some instances, the compound is administered in an amount of from about 0.1 mg to about 75 mg, from about 0.5 mg to about 50 mg, or from about 1 mg to about 25 mg per kg of bodyweight. Also, the composition can be administered once per day, twice per day, three times per day, or once every other day.
Again, each of the states, diseases, disorders, and conditions, described herein, as well as others, can benefit from compositions and methods described herein. Generally, treating a state, disease, disorder, or condition includes preventing or delaying the appearance of clinical symptoms in a mammal that may be afflicted with or predisposed to the state, disease, disorder, or condition but does not yet experience or display clinical or subclinical symptoms thereof. Treating can also include inhibiting the state, disease, disorder, or condition, e.g., arresting or reducing the development of the disease or at least one clinical or subclinical symptom thereof. Furthermore, treating can include relieving the disease, e.g., causing regression of the state, disease, disorder, or condition or at least one of its clinical or subclinical symptoms. A benefit to a subject to be treated can be either statistically significant or at least perceptible to the subject or to a physician.
Administration of an NMDA receptor inhibiting/GABAA receptor potentiating agent can occur as a single event or over a time course of treatment. For example, an NMDA receptor inhibiting/GABAA receptor potentiating agent can be administered daily, weekly, bi-weekly, or monthly. Treatment could extend from several weeks to several months or even a year or more.
Treatment in accord with the methods described herein can be performed prior to, concurrent with, or after conventional treatment modalities for a psychiatric disease, disorder, or condition.
An NMDA receptor inhibiting/GABAA receptor potentiating agent can be administered simultaneously or sequentially with another agent, such as an anti-psychotic, an anti-depressant, or anti-anxiety drug. For example, an NMDA receptor inhibiting/GABAA receptor potentiating agent can be administered simultaneously with another agent, such as an anti-psychotic, an anti-depressant, or anti-anxiety drug. Simultaneous administration can occur through administration of separate compositions, each containing one or more of an NMDA receptor inhibiting/GABAA receptor potentiating agent, an anti-psychotic, an anti-depressant, or anti-anxiety drug. Simultaneous administration can occur through administration of one composition containing two or more of an NMDA receptor inhibiting/GABAA receptor potentiating agent, an anti-psychotic, an anti-depressant, or anti-anxiety drug. An NMDA receptor inhibiting/GABAA receptor potentiating agent can be administered sequentially with an anti-psychotic, an anti-depressant, or anti-anxiety drug. For example, an NMDA receptor inhibiting/GABAA receptor potentiating agent can be administered before or after administration of an anti-psychotic, an anti-depressant, or anti-anxiety drug.
Administration
Agents and compositions described herein can be administered according to methods described herein in a variety of means known to the art. The agents and composition can be used therapeutically either as exogenous materials or as endogenous materials. Exogenous agents are those produced or manufactured outside of the body and administered to the body. Endogenous agents are those produced or manufactured inside the body by some type of device (biologic or other) for delivery within or to other organs in the body.
As discussed above, administration can be parenteral, pulmonary, oral, topical, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, ophthalmic, buccal, or rectal administration.
Agents and compositions described herein can be administered in a variety of methods well known in the arts. Administration can include, for example, methods involving oral ingestion, direct injection (e.g., systemic or stereotactic), implantation of cells engineered to secrete the factor of interest, drug-releasing biomaterials, polymer matrices, gels, permeable membranes, osmotic systems, multilayer coatings, microparticles, implantable matrix devices, mini-osmotic pumps, implantable pumps, injectable gels and hydrogels, liposomes, micelles (e.g., up to 30 μm), nanospheres (e.g., less than 1 μm), microspheres (e.g., 1-100 μm), reservoir devices, a combination of any of the above, or other suitable delivery vehicles to provide the desired release profile in varying proportions. Other methods of controlled-release delivery of agents or compositions will be known to the skilled artisan and are within the scope of the present disclosure.
Delivery systems may include, for example, an infusion pump which may be used to administer the agent or composition in a manner similar to that used for delivering insulin or chemotherapy to specific organs or tumors. Typically, using such a system, an agent or composition can be administered in combination with a biodegradable, biocompatible polymeric implant that releases the agent over a controlled period of time at a selected site. Examples of polymeric materials include polyanhydrides, polyorthoesters, polyglycolic acid, polylactic acid, polyethylene vinyl acetate, and copolymers and combinations thereof. In addition, a controlled release system can be placed in proximity of a therapeutic target, thus requiring only a fraction of a systemic dosage.
Agents can be encapsulated and administered in a variety of carrier delivery systems. Examples of carrier delivery systems include microspheres, hydrogels, polymeric implants, smart polymeric carriers, and liposomes (see generally, Uchegbu and Schatzlein, eds. (2006) Polymers in Drug Delivery, CRC, ISBN-10: 0849325331). Carrier-based systems for molecular or biomolecular agent delivery can: provide for intracellular delivery; tailor biomolecule/agent release rates; increase the proportion of biomolecule that reaches its site of action; improve the transport of the drug to its site of action; allow colocalized deposition with other agents or excipients; improve the stability of the agent in vivo; prolong the residence time of the agent at its site of action by reducing clearance; decrease the nonspecific delivery of the agent to nontarget tissues; decrease irritation caused by the agent; decrease toxicity due to high initial doses of the agent; alter the immunogenicity of the agent; decrease dosage frequency, improve taste of the product; or improve shelf life of the product.
Screening
Also provided are methods for screening for an NMDA receptor inhibiting/GABAA receptor potentiating agent.
The subject methods find use in the screening of a variety of different candidate molecules (e.g., potentially therapeutic candidate molecules). Candidate substances for screening according to the methods described herein include, but are not limited to, fractions of tissues or cells, nucleic acids, polypeptides, siRNAs, antisense molecules, aptamers, ribozymes, triple helix compounds, antibodies, and small (e.g., less than about 2000 mw, or less than about 1000 mw, or less than about 800 mw) organic molecules or inorganic molecules including but not limited to salts or metals.
Candidate molecules encompass numerous chemical classes, for example, organic molecules, such as small organic compounds having a molecular weight of more than 50 and less than about 2,500 Daltons. Candidate molecules can comprise functional groups necessary for structural interaction with proteins, particularly hydrogen bonding, and typically include at least an amine, carbonyl, hydroxyl or carboxyl group, and usually at least two of the functional chemical groups. The candidate molecules can comprise cyclical carbon or heterocyclic structures and/or aromatic or polyaromatic structures substituted with one or more of the above functional groups.
A candidate molecule can be a compound in a library database of compounds. One of skill in the art will be generally familiar with, for example, numerous databases for commercially available compounds for screening (see e.g., ZINC database, UCSF, with 2.7 million compounds over 12 distinct subsets of molecules; Irwin and Shoichet (2005) J Chem Inf Model 45, 177-182). One of skill in the art will also be familiar with a variety of search engines to identify commercial sources or desirable compounds and classes of compounds for further testing (see e.g., ZINC database; eMolecules.com; and electronic libraries of commercial compounds provided by vendors, for example: ChemBridge, Princeton BioMolecular, Ambinter SARL, Enamine, ASDI, Life Chemicals etc.).
Candidate molecules for screening according to the methods described herein include both lead-like compounds and drug-like compounds. A lead-like compound is generally understood to have a relatively smaller scaffold-like structure (e.g., molecular weight of about 150 to about 350 kD) with relatively fewer features (e.g., less than about 3 hydrogen donors and/or less than about 6 hydrogen acceptors; hydrophobicity character xlogP of about −2 to about 4) (see e.g., Angewante (1999) Chemie Int. ed. Engl. 24, 3943-3948). In contrast, a drug-like compound is generally understood to have a relatively larger scaffold (e.g., molecular weight of about 150 to about 500 kD) with relatively more numerous features (e.g., less than about 10 hydrogen acceptors and/or less than about 8 rotatable bonds; hydrophobicity character xlogP of less than about 5) (see e.g., Lipinski (2000) J. Pharm. Tox. Methods 44, 235-249). Initial screening can be performed with lead-like compounds.
When designing a lead from spatial orientation data, it can be useful to understand that certain molecular structures are characterized as being “drug-like”. Such characterization can be based on a set of empirically recognized qualities derived by comparing similarities across the breadth of known drugs within the pharmacopoeia. While it is not required for drugs to meet all, or even any, of these characterizations, it is far more likely for a drug candidate to meet with clinical successful if it is drug-like.
Several of these “drug-like” characteristics have been summarized into the four rules of Lipinski (generally known as the “rules of fives” because of the prevalence of the number 5 among them). While these rules generally relate to oral absorption and are used to predict bioavailability of compound during lead optimization, they can serve as effective guidelines for constructing a lead molecule during rational drug design efforts such as may be accomplished by using the methods of the present disclosure.
The four “rules of five” state that a candidate drug-like compound should have at least three of the following characteristics: (i) a weight less than 500 Daltons; (ii) a log of P less than 5; (iii) no more than 5 hydrogen bond donors (expressed as the sum of OH and NH groups); and (iv) no more than 10 hydrogen bond acceptors (the sum of N and O atoms). Also, drug-like molecules typically have a span (breadth) of between about 8 Å to about 15 Å.
A control sample or a reference sample as described herein can be a sample from a healthy subject. A reference value can be used in place of a control or reference sample, which was previously obtained from a healthy subject or a group of healthy subjects. A control sample or a reference sample can also be a sample with a known amount of a detectable compound or a spiked sample.
Definitions and methods described herein are provided to better define the present disclosure and to guide those of ordinary skill in the art in the practice of the present disclosure. Unless otherwise noted, terms are to be understood according to conventional usage by those of ordinary skill in the relevant art.
In some embodiments, numbers expressing quantities of ingredients, properties such as molecular weight, reaction conditions, and so forth, used to describe and claim certain embodiments of the present disclosure are to be understood as being modified in some instances by the term “about.” In some embodiments, the term “about” is used to indicate that a value includes the standard deviation of the mean for the device or method being employed to determine the value. In some embodiments, the numerical parameters set forth in the written description and attached claims are approximations that can vary depending upon the desired properties sought to be obtained by a particular embodiment. In some embodiments, the numerical parameters should be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of some embodiments of the present disclosure are approximations, the numerical values set forth in the specific examples are reported as precisely as practicable. The numerical values presented in some embodiments of the present disclosure may contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements. The recitation of ranges of values herein is merely intended to serve as a shorthand method of referring individually to each separate value falling within the range. Unless otherwise indicated herein, each individual value is incorporated into the specification as if it were individually recited herein. The recitation of discrete values is understood to include ranges between each value.
In some embodiments, the terms “a” and “an” and “the” and similar references used in the context of describing a particular embodiment (especially in the context of certain of the following claims) can be construed to cover both the singular and the plural, unless specifically noted otherwise. In some embodiments, the term “or” as used herein, including the claims, is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive.
The terms “comprise,” “have” and “include” are open-ended linking verbs. Any forms or tenses of one or more of these verbs, such as “comprises,” “comprising,” “has,” “having,” “includes” and “including,” are also open-ended. For example, any method that “comprises,” “has” or “includes” one or more steps is not limited to possessing only those one or more steps and can also cover other unlisted steps. Similarly, any composition or device that “comprises,” “has” or “includes” one or more features is not limited to possessing only those one or more features and can cover other unlisted features.
All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided with respect to certain embodiments herein is intended merely to better illuminate the present disclosure and does not pose a limitation on the scope of the present disclosure otherwise claimed. No language in the specification should be construed as indicating any non-claimed element essential to the practice of the present disclosure.
Groupings of alternative elements or embodiments of the present disclosure disclosed herein are not to be construed as limitations. Each group member can be referred to and claimed individually or in any combination with other members of the group or other elements found herein. One or more members of a group can be included in, or deleted from, a group for reasons of convenience or patentability. When any such inclusion or deletion occurs, the specification is herein deemed to contain the group as modified thus fulfilling the written description of all Markush groups used in the appended claims.
All publications, patents, patent applications, and other references cited in this application are incorporated herein by reference in their entirety for all purposes to the same extent as if each individual publication, patent, patent application or other reference was specifically and individually indicated to be incorporated by reference in its entirety for all purposes. Citation of a reference herein shall not be construed as an admission that such is prior art to the present disclosure.
Having described the present disclosure in detail, it will be apparent that modifications, variations, and equivalent embodiments are possible without departing the scope of the present disclosure defined in the appended claims. Furthermore, it should be appreciated that all examples in the present disclosure are provided as non-limiting examples.
The following non-limiting examples are provided to further illustrate the present disclosure. It should be appreciated by those of skill in the art that the techniques disclosed in the examples that follow represent approaches the inventors have found function well in the practice of the present disclosure, and thus can be considered to constitute examples of modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments that are disclosed and still obtain a like or similar result without departing from the spirit and scope of the present disclosure.
The synthesis of steroid MQ221 is described and shown in the scheme below.
Steroid 2
A solution of sodium ethoxide (26 mmol, formed in situ from 598 mg of sodium metal in 20 mL of ethanol) was added dropwise under N2 at 35-40° C. to stirred epiandrosterone (1, 1.8 g, 6.2 mmol) and triethyl phosphonoacetate (5.6 ml, 28 mmol) in anhydrous ethanol (50 mL). After addition, the reaction was refluxed for 16 h. Ethanol was removed under reduced pressure on a rotary evaporator and water was added. The product was extracted into dichloromethane (150 mL×2) and washed with brine (50 mL×2). The extract was dried over anhydrous Na2SO4, filtered and the solvents removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 2 (1.02 g, 46%) which had: 1H NMR (400 MHz, CDCl3) δ 5.48 (t, J=2.0 Hz, 1H), 4.12 (q, J=7.1 Hz, 2H), 3.57-3.49 (m, 1H), 2.79-2.75 (m, 2H), 2.18 (s, 1H), 1.79-0.60 (m, 23H), 0.78 (s, 3H), 0.77 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 176.4, 167.4, 108.3, 70.9, 59.4, 54.3, 53.4, 46.2, 44.7, 37.9, 36.9, 35.5, 35.2, 35.1, 31.8, 31.3, 30.3, 28.4, 24.2, 21.0, 18.4, 14.2, 12.2.
Steroid 3
5% Pd/C (400 mg) was added at room temperature to a flask containing steroid 2 (1.02 g, 2.83 mmol) dissolved in EtOAc (60 mL). The flask was evacuated and filled with H2 three times. The hydrogenation was carried out under 50 psi H2 pressure. After 3 h, the mixture was filtered through Celite and washed with EtOAc (200 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 3 (1.02 g, 100%) which had: 1H NMR (400 MHz, CDCl3) δ 4.15 (q, J=7.0 Hz, 2H), 3.66-3.56 (m, 1H), 2.38-0.63 (m, 29H), 0.81 (s, 3H), 0.59 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.0, 71.3, 60.1, 55.3, 54.5, 46.9, 44.9, 42.2, 38.2, 37.4, 37.0, 35.6, 35.5, 35.4, 32.1, 31.5, 28.7, 28.2, 24.5, 20.9, 14.2, 12.6, 12.3.
Steroid 4
Chloromethyl methyl ether (0.5 mL, 6.2 mmol) and i-Pr2NEt (2.0 mL, 14 mmol) were added at room temperature to a stirred solution of steroid 3 (1.02 g, 2.82 mmol) in dichloromethane. After 16 h, solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to give steroid 4 (1.05 g, 92%) which had: 1H NMR (400 MHz, CDCl3) δ 4.62 (s, 2H), 4.08 (q, J=7.1 Hz, 2H), 3.48-3.32 (m, 1H), 3.30 (s, 3H), 2.31-0.57 (m, 29H), 0.76 (s, 3H), 0.53 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 137.7, 94.4, 76.1, 59.9, 55.2, 54.9, 54.4, 46.8, 44.8, 42.0, 37.3, 36.9, 35.6, 35.4, 35.2, 35.1, 32.0, 28.6, 28.6, 28.0, 24.4, 20.8, 14.1, 12.5, 12.1.
Steroid 5
Lithium diisopropylamide (4 mL, 2.0 M in THF, 8.0 mmol) and hexamethylphosphoramide (10 mmol, 1.85 mL) were added at −78° C. to a stirred solution of steroid 4 (1.11 g, 2.72 mmol) in THF (50 mL). After 45 min, tert-butyl-(3-iodopropoxy)-dimethylsilane (3.0 g, 10 mmol) in THF (5 mL) was added and the reaction was allowed to warn to room temperature and stirred for 16 h. Water was added and the product was extracted into EtOAc (250 mL×2). The combined extracts were dried over anhydrous Na2SO4, filtered and the solvents removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to afford steroid 5 (1.21 g, 77%) which had: 1H NMR (400 MHz, CDCl3) δ 4.65 (s, 2H), 4.11-4.05 (m, 2H), 3.61-3.34 (m, 6H), 2.44-0.62 (m, 31H), 0.87 (s, 9H), 0.78 (s, 3H), 0.67 (s, 3H), 0.02 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 176.1, 94.4, 76.2, 62.7, 59.7, 55.7, 55.0, 54.3, 52.7, 47.1, 44.8, 42.1, 37.6, 36.9, 35.5, 35.4, 35.2, 32.0, 30.4, 28.7, 28.6, 28.2, 27.0, 25.9 (3×C), 23.7, 21.0, 18.2, 14.2, 12.2, 12.1, −5.4 (2×C).
Steroid 6
Lithium aluminum hydride (2.0 M in THF, 8 mL, 16 mmol) was added at room temperature to a stirred solution of the steroid 5 (1.1 g, 1.9 mmol) in diethyl ether (50 mL). After 2 h, water (0.64 mL), 10% aqueous NaOH (1.28 mL) and water (1.92 mL) were sequentially and slowly added. After stirring for 30 min, the mixture was filter through Celite and the Celite was washed with dichloromethane (200 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to afford steroid 6 (796 mg, 78%) which had: 1H NMR (400 MHz, CDCl3) δ 4.67 (s, 2H), 3.81-3.38 (m, 6H), 3.36 (s, 3H), 1.89-0.59 (m, 28H), 0.90 (s, 9H), 0.80 (s, 3H), 0.67 (s, 3H), 0.05 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.3, 63.6, 62.8, 56.3, 55.1, 54.3, 50.5, 44.8, 42.3, 42.1, 39.4, 37.0, 35.6, 35.4, 35.2, 32.0, 28.8, 28.7, 28.6, 27.6, 25.9 (3×C), 25.1, 24.0, 21.2, 18.3, 12.3, 12.2, −5.3, −5.3.
Steroid 7
Methanesulfonyl chloride (0.23 mL, 3 mmol) and Et3N (0.56 mL, 4 mmol) were added to a stirred solution of steroid 6 (796 mg, 1.49 mmol) in dichloromethane (30 mL) at 0° C. After 1 h, aqueous NaHCO3 (50 mL) was added and the product was extracted into dichloromethane (100 mL×2). The combined extracts were dried over anhydrous Na2SO4, filtered and the solvents removed on a rotary evaporator under reduced pressure. The residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 7 (775 mg, 95%) which had: 1H NMR (400 MHz, CDCl3) δ 4.75 (s, 2H), 4.38-4.35 (m, 1H), 4.29-4.09 (m, 2H), 3.63-3.38 (m, 3H), 3.36 (s, 3H), 2.99 (s, 3H), 1.83-0.59 (m, 27H), 0.89 (s, 9H), 0.80 (s, 3H), 0.68 (s, 3H), 0.04 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.2, 70.1, 63.2, 56.1, 55.1, 54.2, 50.1, 44.8, 42.3, 39.5, 39.3, 37.2, 36.9, 35.5, 35.4, 35.2, 31.9, 28.8, 28.7, 28.6, 27.4, 25.9 (3×C), 25.5, 23.9, 21.1, 18.3, 12.4, 12.2, −5.3 (2×C).
Steroid 8
Lithium aluminum hydride (2.0 M in THF, 4 mL, 8 mmol) was added to a stirred solution of steroid 7 (775 mg, 1.26 mmol) in diethyl ether (50 mL) at room temperature. After 2 h, water (0.64 mL), 10% aqueous NaOH (1.28 mL) and water (1.92 mL) were slowly added sequentially. After stirring for 30 min, the mixture was filter through Celite and the Celite was washed with dichloromethane (150 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to afford steroid 8 (532 mg, 81%) which had: 1H NMR (400 MHz, CDCl3) δ 4.67 (s, 2H), 3.58-3.46 (m, 3H), 3.36 (s, 3H), 1.97-0.59 (m, 31H), 0.89 (s, 9H), 0.80 (s, 3H), 0.64 (s, 3H), 0.04 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.3, 63.7, 56.4, 56.1, 55.0, 54.3, 44.8, 42.5, 40.0, 37.0, 35.6, 35.5, 35.4, 35.2, 32.0, 31.9, 29.4, 28.8, 28.7, 28.1, 25.9 (3×C), 24.2, 21.2, 18.6, 18.3, 12.2, 12.0, −5.28 (2×C).
Steroid 9
Tetra-n-butylammonium fluoride (3 mL, 1.0 M in THF, 3.0 mmol) was added to a stirred solution of steroid 8 (532 mg, 1.02 mmol) in THF (20 mL) at room temperature. After 4 h, the THF was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 25% EtOAc in hexanes) to give steroid 9 (336 mg, 81%) which had: 1H NMR (400 MHz, CDCl3) δ 4.64 (s, 2H), 3.57-3.35 (m, 3H), 3.33 (s 3H), 2.17-0.56 (m, 32H), 0.78 (s, 3H), 0.62 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 94.3, 76.2, 63.2, 56.3, 56.0, 55.0, 54.2, 44.7, 42.5, 39.9, 36.9, 35.5, 35.5, 35.3, 35.1, 31.9, 31.8, 29.3, 28.7, 28.5, 28.1, 24.1, 21.1, 18.5, 12.1, 12.0.
MQ-221
SO3-Et3N (209 mg, 1.5 mmol) was added to a stirred solution of steroid 9 (122 mg, 0.3 mmol) in pyridine (5 mL) at room temperature. The reaction was stirred for 16 h. Solvent was removed under reduced pressure on a rotary evaporator and the residue was redissolved in THF (5 mL) and acidified with aqueous 6 N HCl (5 mL). After 2 h, the product was extracted into dichloromethane (50 mL×2). Solvent was removed under reduced pressure on a rotary evaporator and the residue was added to 7 N ammonia in methanol (2 mL) and stirred at 23° C. for 1 h. After solvent removal under reduced pressure on a rotary evaporator, the residue was purified by flash chromatography (silica gel, eluted with 10% MeOH in dichloromethane) to give MQ-221 (75 mg, 54%) which had: mp 176-178° C.; [α]D20+16.7 (c=0.03, MeOH); 1H NMR (400 MHz, DMSO-d6) δ 3.74-3.69 (m, 2H), 3.37-3.30 (m, 1H), 1.89-0.51 (m, 36H), 0.71 (s, 3H), 0.58 (s, 3H); 13C NMR (100 MHz, DMSO-d6) δ9.4, 69.2, 66.1, 56.0, 55.8, 53.9, 44.4, 42.2, 39.6, 38.1, 36.7, 35.1, 35.1, 35.0, 31.8, 31.7, 28.5, 27.8, 25.8, 23.9, 20.9, 18.5, 12.1, 11.9.
An alternative synthesis for steroid MQ221 is described and shown in the scheme below.
Steroid 2
To a solution of 5-cholenic acid-3β-ol, methyl ester (1, 1.26 g, 3.25 mmol) in dichloromethane (30 mL) was added chloromethyl methyl ether (0.50 mL 6.5 mmol) and i-Pr2NEt (1.4 mL, 10 mmol) at 25° C. After 16 h, solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to give steroid 2 (1.19 g, 85%): 1H NMR (400 MHz, CDCl3) δ 5.30-5.28 (m, 1H), 4.63 (s, 2H), 3.61 (s, 3H), 3.40-3.32 (m, 1H), 3.31 (s, 3H), 2.34-0.84 (m, 28H), 0.96 (s, 3H), 0.63 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.4, 140.5, 121.5, 94.5, 76.7, 56.5, 55.6, 54.9, 51.3, 49.9, 42.2, 39.6, 39.4, 37.1, 36.5, 35.2, 31.7, 31.7, 30.8 (2×C), 28.7, 27.9, 24.1, 20.9, 19.2, 18.1, 11.7.
Steroid 4
To a solution of steroid 2 (1.19 g, 2.75 mmol) in EtOAc/MeOH (40 mL/10 mL) was added 10% Palladium on charcoal (200 mg) at 25° C. The hydrogenation flask was evacuated and refilled three times with H2. The hydrogenation was carried out under 55 psi for 6 h. the reaction mixture was filtered through Celite and washed with EtOAc (150 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to give steroid 4 (1.19 g, 100%): 1H NMR (400 MHz, CDCl3) δ 4.74 (s, 2H), 3.66 9s, 3H), 3.53-3.45 (m, 1H), 3.37 (s, 3H), 2.39-0.58 (m, 31H), 0.80 (s, 3H), 0.65 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.8, 94.5, 76.3, 56.4, 55.9, 55.1, 54.3, 51.5, 44.9, 42.6, 40.0, 37.0, 35.6, 35.5, 35.4, 35.2, 32.0, 31.0, 30.9, 28.8, 28.7, 28.1, 24.1, 21.2, 18.2, 12.2, 12.0.
Steroid 5
To a solution of steroid 4 (1.19 g, 2.74 mmol) in diethyl ether (60 mL) was added lithium aluminum hydride solution (2.0 M in THF, 5 mL, 10 mmol) at room temperature. After 2 h, 0.40 mL of water, 0.80 mL of 10% of NaOH, and 1.20 mL of water were slowly added. After stirring for 1 h, the mixture was filter through Celite and washed with dichloromethane (200 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 25% EtOAc in hexanes) to afford steroid 5 (1.11 g, 100%): 1H NMR (400 MHz, CDCl3) δ 5.35-5.33 (m, 1H), 4.68 (s, 2H), 3.60 (t, J=6.5 Hz, 2H), 3.58-3.80 (m, 1H), 3.36 (s, 3H), 2.33-0.87 (m, 29H), 1.00 (s, 3H), 0.68 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 140.7, 121.7, 94.6, 76.9, 63.6, 56.7, 56.0, 55.1, 50.1, 42.3, 39.7, 39.5, 37.2, 36.7, 35.6, 31.8 (2×C), 29.4, 28.9, 28.2, 24.2, 21.0, 19.3, 18.7, 11.8.
MQ221
To a solution of steroid 5 (768 mg, 1.89 mmol) in pyridine (25 mL) was added SO3-Me3N (1.39 g, 10 mmol) at room temperature. The mixture was stirred for 16 h. Solvent was removed under reduced pressure and the residue was redissolved in Methanol (10 mL) and then 6 N HCl (10 mL) was added. After 2 h, the product was extracted into dichloromethane (150 mL×4). Solvent was removed under reduced pressure, 7 N ammonia in methanol (6 mL) was added and the reaction was stirred at 23° C. for 1 h. After solvent removal under reduced pressure, the product was purified by flash chromatography (silica gel, eluted with 10%-25% MeOH in dichloromethane) to give MQ221 (710 mg, 82%): mp. 180-182° C.; [α]D20+18.0 (c=0.05, MeOH); 1H NMR (400 MHz, CD3OD) δ 3.99-3.96 (m, 2H), 3.58-3.44 (m, 1H), 2.13-0.82 (m, 36H), 0.84 (3H), 0.71 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 70.5, 68.3, 56.5, 56.2, 54.4, 44.8, 42.4, 40.0, 37.5, 36.8, 35.5, 35.4, 35.2, 31.9, 31.7, 30.7, 28.6, 27.8, 25.7, 23.8, 21.0, 17.7, 11.4, 11.1.
Synthesis for steroid MQ245 is described and shown in the scheme below.
Steroid 11
Acetyl chloride (5 mL) was added to a solution of lithocholic acid (10, 1.5 g, 4 mmol) in methanol (40 ml) at room temperature. After 2 h, water was added and the product was extracted into dichloromethane (150 mL×2). The organic layers were washed with aqueous NaHCO3. Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatograph (25% EtOAc in hexanes) to give lithocholic acid methy ester (11, 1.48 g, 95%): 1H NMR (CDCl3) 3.59 (s, 3H), 3.56-3.50 (m, 1H), 2.58 (s, 1H), 2.32-0.69 (m, 31H), 0.85 (s, 3H), 0.57 (s, 3H); 13C NMR (CDCl3) δ 174.6, 71.4, 56.3, 55.8, 51.3, 42.5, 41.9, 40.2, 40.0, 36.2, 35.6, 35.2, 35.1, 34.4, 30.8, 30.8, 30.2, 28.0, 27.0, 26.3, 24.0, 23.2, 20.6, 18.1, 11.8.
Steroid 12
Chloro(dimethyl)(2-methyl-2-propanyl)silane (450 mg, 3 mmol) and imidazole (6 mmol, 408 mg) were added to a stirred solution of steroid 11 (500 mg, 1.28 mmol) in dimethylforamide at room temperature. After 16 h, water was added and the product was extracted into EtOAc (150 mL×2). The organic layers were washed with brine (50 mL×2) dried over anhydrous Na2SO4, filtered and the solvent was removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatograph (10% EtOAc in hexanes) to give steroid 12 (646 mg, 100%): 1H NMR (400 MHz, CDCl3) 3.66 (d, J=1.1 Hz, 3H), 3.62-3.54 (m, 1H), 2.39-0.73 (m, 33H), 0.89 (m, 12H), 0.63 (s, 3H), 0.06 (s, 3H) 0.06 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.7, 72.8, 56.4, 55.9, 51.4, 42.7, 42.2, 40.2, 40.1, 36.9, 35.8, 35.5, 35.3, 34.5, 31.0, 31.0, 28.2, 27.3, 26.4, 25.9 (3×C), 25.7, 24.2, 23.4, 20.8, 18.3, 18.2, 12.0, −4.6 (2×C).
Steroid 13
Lithium aluminum hydride (1.0 M in THF, 6 mL, 6 mmol) was added to a solution of steroid 12 (646 mg, 1.28 mmol) in diethyl ether (40 mL) at room temperature. After 2 h, water (0.24 mL), 10% aqueous NaOH (0.48 mL) and water (0.72 ml) were slowly added dropwise in a sequential manner. The resultant mixture was stirred at room temperature for 45 min and then filtered through Celite. The Celite was washed with dichloromethane (200 mL). The solvents were removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (20% EtOAc in hexanes) to give steroid 13 (600 mg, 100%) which had: 1H NMR (400 MHz, CDCl3) 3.57-3.56 (m, 3H), 2.02-0.71 (m, 32H), 0.89 (s, 3H), 0.87 (s, 9H), 0.62 (s, 3H), 0.04 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 72.8, 63.3, 56.3, 56.1, 42.6, 42.2, 40.2, 40.1, 36.8, 35.8, 35.5, 35.5, 34.5, 31.8, 30.9, 29.3, 28.2, 27.2, 26.3, 25.9 (3×C), 24.1, 23.3, 20.7, 18.6, 18.2, 11.9, −4.69 (2×C).
MQ-245
SO3-Me3N (556 mg, 4 mmol) was added to a stirred solution of steroid 13 (300 mg, 0.637 mmol) in pyridine (15 mL) at room temperature. The reaction was stirred for 16 h. Solvent was removed under reduced pressure on a rotary evaporator and the residue was dissolved in methanol (4 mL) and then 6 N HCl (4 mL) was added. After 1 h, the product was extracted into dichloromethane (50 mL×4). Solvent was removed under reduced pressure on a rotary evaporator, 7 N ammonia in methanol (5 mL) was added and the reaction was stirred at 23° C. for 1 h. Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash chromatography (silica gel, eluted with 10%-25% MeOH in dichloromethane) to give MQ-245 (275 mg, 94%) which had: mp 195-197° C.; [α]D20+8.9 (c=0.09, MeOH); 1H NMR (400 MHz, CD3OD) δ 4.00 (t, J=6.3 Hz, 2H), 3.59-3.53 (m, 1H), 2.06-1.01 (m, 36H), 0.97 (s, 3H), 0.72 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 72.6, 69.8, 58.1, 57.7, 44.0, 43.7, 42.0, 41.7, 37.4, 37.3, 36.9, 36.6, 35.8, 33.2, 31.3, 29.4, 28.5, 27.8, 27.2, 25.4, 24.1, 22.1, 19.3, 12.7.
Synthesis for steroid MQ246 is described and shown in the scheme below.
Steroid 14
Dess-Martin periodinane (2.12 g, 5 mmol) was added to a stirred solution lithocholic acid methyl ester (11, 1.0 g, 2.56 mmol) at room temperature. After 2 h, water was added and the product was extracted into dichloromethane (150 mL×2). The combined extracts were dried over anhydrous Na2SO4, filtered and the solvent removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatograph (15% EtOAc in hexanes) to give steroid 14 (945 mg, 94%) which had: 1H NMR (400 MHz, CDCl3) δ 3.63 (s, 3H), 2.69-0.72 (m, 31H), 0.99 (s, 3H), 0.65 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 213.2, 174.6, 56.3, 55.8, 51.9, 44.2, 42.7, 42.4, 40.6, 39.9, 37.1, 36.9, 35.4, 35.2, 34.8, 30.9, 30.9, 28.0, 26.5, 25.7, 24.0, 22.5, 21.1, 18.2, 12.0.
Steroid 15
K-selectride (1.0 M in THF, 5 mL, 5 mmol) was added to a stirred solution of steroid 14 (945 mg, 2.44 mmol) in THF (930 mL) at −78° C. After 2 h, 3 N aqueous NaOH (10 mL) followed by H2O2 (3 mL) were added at −78° C. The reaction was then warmed to room temperature and stirring was continued for 45 min. The product was extracted into EtOAc (150 mL×2) and the combined organic layers were washed with brine (50 mL×2), dried over anhydrous Na2SO4 and filtered. Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (15% EtOAc in hexanes) to give steroid 15 (906 mg, 96%) which had: 1H NMR (400 MHz, CDCl3) δ 4.13-4.10 (m, 1H), 3.66 (s, 3H), 2.36-0.80 (m, 32H), 0.96 (s, 3H), 0.65 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.7, 67.1, 56.6, 56.0, 51.4, 42.7, 40.2, 39.7, 36.5, 35.6, 35.3, 35.1, 33.5, 31.0, 31.0, 29.9, 28.2, 27.8, 26.6, 26.2, 24.1, 23.9, 21.0, 18.2, 12.0.
Steroid 16
Chloro(dimethyl)(2-methyl-2-propanyl)silane (750 mg, 5 mmol) and imidazole (10 mmol, 680 mg) were added to a stirred solution of steroid 15 (906 mg, 2.32 mmol) in dimethylformide (20 mL) at room temperature. After 16 h, water was added and the product was extracted into EtOAc (150 mL×2). The combined organic layers were washed with brine (50 mL×2), dried over anhydrous Na2SO4, filtered and solvent was removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to give steroid 16 (1.09 g, 93%) which had: 1H NMR (400 MHz, CDCl3) δ 4.03-4.02 (m, 1H), 3.66 (s, 3H), 2.37-0.92 (m, 31H), 0.88 (s, 12H), 0.54 (s, 3H), 0.01 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 174.7, 67.4, 56.7, 56.0, 51.4, 42.8, 40.3, 39.9, 36.5, 35.7, 35.4, 35.0, 34.4, 31.0, 30.0, 28.6, 28.2, 26.9, 26.4, 25.8 (3×C), 25.7, 24.2, 24.0, 21.1, 18.3, 18.1, 12.0, −4.9 (2×C).
Steroid 17
Lithium aluminum hydride (1.0 M in THF, 6 mL, 6 mmol) was added to a stirred solution of steroid 16 (1.09 g, 2.16 mmol) in diethyl ether (60 mL) at room temperature. After 2 h, water (0.24 mL), 10% aqueous NaOH (0.48 mL) and water (0.72 ml) were slowly added dropwise in a sequential manner. The mixture was stirred at room temperature for 45 min then filtered through Celite. The Celite was washed with dichloromethane (200 mL) and the solvents were removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 17 (915 mg, 90%) which had: 1H NMR (400 MHz, CDCl3) 4.04-4.03 (m, 1H), 3.65-3.58 (m, 2H), 2.06-0.95 (m, 32H), 0.90 (s, 12H), 0.67 (s, 3H), 0.30 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 67.5, 63.6, 56.7, 56.2, 42.7, 40.3, 39.9, 36.5, 35.7, 35.6, 35.0, 34.4, 31.8, 30.0, 29.4, 28.6, 28.3, 26.9, 26.5, 25.8 (3×C), 24.2, 24.0, 21.1, 18.6, 18.1, 12.1, −4.8, −4.9.
MQ-246
SO3-Me3N (417 mg, 3 mmol) was added to a stirred solution of steroid 17 (213 mg, 0.53 mmol) in pyridine (10 mL) at room temperature. The reaction was stirred for 16 h and the solvent was removed under reduced pressure on a rotary evaporator. The residue was dissolved in methanol (3 mL) and aqueous 6 N HCl (3 mL) was added. After 1 h, the product was extracted into dichloromethane (50 mL×4). Solvent was removed under reduced pressure on a rotary evaporator, 7 N ammonia in methanol (7 mL) was added to the residue and the reaction was stirred at 23° C. for 1 h. After solvent removal under reduced pressure on a rotary evaporator, the residue was purified by flash column chromatography (silica gel eluted with 10%-25% MeOH in dichloromethane) to give MQ-246 (196 mg, 81%) which had: mp 191-193° C.; [α]D20+45.0 (c=0.06, MeOH); 1H NMR (400 MHz, CD3OD) δ 4.33-4.27 (m, 1H), 3.55-3.51 (m, 2H), 2.06-0.99 (m, 36H), 0.97 (s, 3H), 0.71 (s, 3H); 13C NMR (CD3OD) δ 80.5, 63.7, 58.0, 57.8, 44.0, 43.8, 42.0, 41.7, 37.4, 36.6, 35.7, 34.7, 33.3, 30.4, 29.5, 29.0, 28.4, 27.7, 25.4, 24.0, 23.9, 22.1, 19.4, 12.7.
Synthesis for steroid MQ254 is described and shown in the scheme below.
Steroid 18
Chloro(dimethyl)(2-methyl-2-propanyl)silane (0.5 mL, 6.2 mmol) and i-Pr2NEt (2.0 mL, 14 mmol) were added to a stirred solution of androsterone (800 mg, 2.76 mmol) in dichloromethane (50 mL) at room temperature. After 16 h, solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to give steroid 18 (875 mg, 95%) which had: 1H NMR (400 MHz, CDCl3) δ 4.62 (s, 2H), 3.79 (s, 1H), 3.31 (s, 3H), 2.41-2.34 (m, 1H), 2.06-0.93 (m, 21H), 0.81 (s, 3H), 0.77 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 221.1, 94.5, 71.4, 55.0, 54.3, 51.4, 47.7, 39.6, 35.9, 35.7, 34.9, 33.5, 32.7, 31.5, 30.7, 28.2, 26.2, 21.6, 19.9, 13.7, 11.3.
Steroid 19
Sodium ethoxide (generated in situ from 598 mg of sodium metal, 26 mmol, in 20 mL of ethanol) was added dropwise to a stirred solution of steroid 18 (875 mg, 2.62 mmol) and triethyl phosphonoacetate (5.6 ml, 28 mmol) in anhydrous ethanol (50 mL) under N2 at 35-40° C. After addition, the reaction was refluxed for 16 h. Ethanol was removed under reduced pressure on a rotary evaporator and water was added. The product was extracted into dichloromethane (150 mL×2) and washed with brine (50 mL×2). The extract was dried over anhydrous Na2SO4, filtered and the solvents removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 19 (805 mg, 76%) which had: 1H NMR (400 MHz, CDCl3) δ 5.44 (s, 1H), 4.59 (s, 2H), 4.08 (q, J=7.1 Hz, 2H), 3.75 (s, 1H), 3.28 (s, 3H), 2.76-2.74 (m, 2H), 1.76-0.74 (m, 23H), 0.74 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 176.3, 167.2, 108.2, 94.3, 71.3, 59.2, 54.9, 54.2, 53.5, 46.1, 39.5, 35.8, 35.2, 35.0, 33.4, 32.7, 31.6, 30.2, 28.3, 26.2, 24.1, 20.5, 18.3, 14.2, 11.2.
Steroid 20
5% Pd/C (500 mg) was added to a solution of steroid 19 (805 mg, 2 mmol) in EtOAc (60 mL) at room temperature. The flask was evacuated and charged with H2 three times. The hydrogenation was carried out under 50 psi H2. After 3 h, the reaction was filtered through Celite and the Celite was washed with EtOAc (200 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 20 (800 mg, 99%) which had: 1H NMR (400 MHz, CDCl3) δ 4.58 (s, 2H), 4.06-4.00 (m, 2H), 3.75 (s, 1H), 3.29 (s, 3H), 2.29-0.69 (m, 28H), 0.72 (s, 3H), 0.52 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 173.6, 94.3, 71.4, 59.8, 55.3, 54.9, 54.4, 46.7, 42.0, 39.6, 37.3, 35.8, 35.4, 35.2, 33.5, 32.7, 31.9, 28.4, 28.0, 26.2, 24.3, 20.3, 14.1, 12.4, 11.2.
Steroid 21
Lithium diisopropylamide (2 mL, 2.0 M in THF, 4.0 mmol) and hexamethylphoramide (6 mmol, 1.08 mL) was added to a stirred solution of steroid 20 (500 mg, 1.23 mmol) in THF (20 mL) at −78° C. After 45 min, tert-butyl-(3-iodopropoxy)-dimethylsilane (900 mg, 3 mmol) in THF (2 mL) was added and the reaction was allowed to warm to room temperature for 16 h. Water was added and the product was extracted into EtOAc (250 mL×2). The combined extracts were dried over anhydrous Na2SO4, filtered and the solvents removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to afford steroid 21 (635 mg, 89%) which had: 1H NMR (400 MHz, CDCl3) δ 4.66 (s, 2H), 4.11-4.06 (m, 2H), 3.80 (s, 1H), 3.60-3.56 (m, 2H), 3.35 (s, 3H), 2.27-0.69 (m, 31H), 0.87 (s, 9H), 0.76 (s, 3H), 0.67 (s, 3H), 0.02 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 176.1, 94.4, 71.6, 62.7, 59.7, 55.8, 55.1, 54.2, 52.7, 47.1, 42.2, 39.7, 37.7, 35.8, 35.4, 33.6, 32.8, 31.9, 30.4, 28.5, 28.3, 27.0, 26.3, 25.9 (3×C), 23.7, 20.6, 18.2, 14.2, 12.2, 11.3, −5.3 (2×C).
Steroid 22
Lithium aluminum hydride (2.0 M in THF, 6 mL, 12 mmol) was added to a stirred solution of steroid 21 (635 mg, 1.1 mmol) in diethyl ether (50 mL) at room temperature. After 2 h, water (0.48 mL), 10% aqueous NaOH (0.96 mL), and water (1.44 mL) of water were slowly added dropwise in sequential order. After stirring for 30 min, the mixture was filter through Celite and the Celite was washed with dichloromethane (200 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to afford steroid 22 (353 mg, 60%) which had: 1H NMR (400 MHz, CDCl3) δ 4.66 (s, 2H), 3.81-3.34 (m, 5H), 3.35 (s, 3H), 1.87-0.72 (m, 29H), 0.88 (s, 9H), 0.77 (s, 3H), 0.66 (s, 3H), 0.04 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.4, 71.6, 63.6, 62.8, 56.4, 55.1, 54.2, 50.5, 42.7, 42.1, 39.6, 39.5, 37.8, 35.4, 33.6, 32.8, 31.9, 28.8, 28.6, 27.6, 26.3, 25.9 (3×C), 25.2, 24.0, 20.7, 18.3, 12.3, 11.3, −5.4 (2×C).
Steroid 23
Methanesulfonyl chloride (0.16 mL, 2 mmol) and Et3N (0.42 mL, 3 mmol) were added to a stirred solution of the steroid 22 (353 mg, 0.66 mmol) in dichloromethane (20 mL) at 0° C. After 1 h, aqueous NaHCO3 (50 mL) was added and the product was extracted into dichloromethane (100 mL×2). The combined extracts were dried over anhydrous Na2SO4, filtered and the solvents removed under reduced pressure on a rotary evaporator. The residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give steroid 23 (323 mg, 80%) which had: 1H NMR (400 MHz, CDCl3) δ 4.64 (s, 2H), 4.38-4.35 (m, 1H), 4.15-4.12 (m, 1H), 3.81 (s, 1H), 3.62-3.57 (m, 2H), 3.36 (s, 3H), 2.98 (s, 3H), 1.83-0.72 (m, 28H), 0.88 (s, 9H), 0.77 (s, 3H), 0.67 (s, 3H), 0.03 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 71.6, 70.1, 63.2, 56.2, 55.1, 54.1, 50.1, 42.3, 39.6, 39.5, 39.3, 37.2, 35.8, 35.4, 33.6, 32.7, 31.8, 28.8, 28.5, 27.4, 26.2, 25.9 (3×), 25.5, 23.9, 20.7, 18.2, 12.4, 11.3, −5.4 (2×C).
Steroid 24
Lithium aluminum hydride (2.0 M in THF, 4 mL, 8 mmol) was added to a stirred solution of steroid 23 (323 mg, 0.526 mmol) in diethyl ether (40 mL) at room temperature. After 2 h, water (0.64 mL), 10% aqueous NaOH (1.28 mL), and water (1.92 mL) were slowly added dropwise in sequential order. After stirring for 30 min, the mixture was filter through Celite and the Celite was washed with dichloromethane (150 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to afford steroid 24 (207 mg, 76%) which had: 1H NMR (400 MHz, CDCl3) δ 4.66 (s, 2H), 3.82 (s. 1H), 3.58-3.55 (m, 2H), 3.37 (s, 3H), 1.97-0.73 (m, 31H), 0.90 (s, 9H), 0.78 (s, 3H), 0.65 (s, 3H), 0.05 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.3, 63.7, 56.4, 56.1, 55.0, 54.3, 44.8, 42.5, 40.0, 37.0, 35.6, 35.5, 35.4, 35.2, 32.0, 31.9, 29.4, 28.8, 28.7, 28.1, 25.9 (3×C), 24.2, 21.2, 18.6, 18.3, 12.2, 12.0, −5.28 (2×C).
Steroid 25
Tetra-n-butylammonium fluoride (1 mL, 1.0 M in THF, 1.0 mmol) was added to a stirred solution of steroid 24 (207 mg, 0.4 mmol) in THF (5 mL) at room temperature. After 16 h, the THF was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 25% EtOAc in hexanes) to give steroid 25 (139 mg, 86%); 1H NMR (400 MHz, CDCl3) δ 4.64 (s, 2H), 3.81 (s, 1H), 3.60-3.58 (m, 2H), 3.36 (s 3H), 1.96-0.71 (m, 32H), 0.77 (s, 3H), 0.64 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 94.4, 71.6, 63.4, 56.5, 56.0, 55.1, 54.2, 42.5, 39.9, 39.7, 35.8, 35.5, 35.4, 33.6, 32.8, 31.9, 31.8, 29.4, 28.6, 28.2, 26.3, 24.1, 20.7, 18.6, 12.0, 11.3.
MQ-254
SO3-Et3N (476 mg, 3.42 mmol) was added to a stirred solution of the steroid 25 (139 mg, 0.342 mmol) in pyridine (5 mL) at room temperature. The reaction was stirred for 16 h. Solvent was removed under reduced pressure on a rotary evaporator and the residue was dissolved in THF (5 mL) and acidified with aqueous 6 N HCl (5 mL). After 2 h, the product was extracted into dichloromethane (50 mL×2). Solvent was removed under reduced pressure on a rotary evaporator 7 N ammonia in methanol (3 mL) was added to the residue at 23° C. After stirring for 1 h, solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 10% MeOH in dichloromethane) to give MQ-254 (157 mg, 99%) which had: mp 179-181° C.; [α]D20+9.1 (c=0.11, MeOH); 1H NMR (400 MHz, CD3OD) δ 3.99 (s, 2H), 3.72 (s, 1H), 2.05-0.75 (m, 36H), 0.84 (s, 3H), 0.72 (s, 3H); 13C NMR (100 MHz, CD3OD) 69.8, 67.4, 58.1, 57.7, 56.0, 55.3, 43.9, 41.6, 40.4, 37.2, 37.0, 36.9, 36.8, 33.6, 33.5, 33.2, 29.9, 29.7, 27.3, 25.3, 22.0, 19.2, 12.7, 11.9.
Synthesis for steroid MQ260 is described and shown in the scheme below.
Steroid 2
To a solution of 5-cholenic acid-3β-ol, methyl ester (1, 1.26 g, 3.25 mmol) in dichloromethane (30 mL) was added chloromethyl methyl ether (0.50 mL 6.5 mmol) and i-Pr2NEt (1.4 mL, 10 mmol) at 25° C. After 16 h, solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to give steroid 2 (1.19 g, 85%): 1H NMR (400 MHz, CDCl3) δ 5.30-5.28 (m, 1H), 4.63 (s, 2H), 3.61 (s, 3H), 3.40-3.32 (m, 1H), 3.31 (s, 3H), 2.34-0.84 (m, 28H), 0.96 (s, 3H), 0.63 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.4, 140.5, 121.5, 94.5, 76.7, 56.5, 55.6, 54.9, 51.3, 49.9, 42.2, 39.6, 39.4, 37.1, 36.5, 35.2, 31.7, 31.7, 30.8 (2×C), 28.7, 27.9, 24.1, 20.9, 19.2, 18.1, 11.7.
Steroid 3
To a solution of steroid 2 (180 mg, 0.42 mmol) in diethyl ether (20 mL) was added lithium aluminum hydride solution (2.0 M in THF, 2 mL, 4 mmol) at room temperature. After 2 h, 0.16 mL of water, 0.32 mL of 10% aqueous NaOH, and 0.48 mL of water were added slowly. After stirring for 1 h, the mixture was filter through Celite and washed with dichloromethane (200 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 25% EtOAc in hexanes) to afford steroid 3 (170 mg, 100%): 1H NMR (400 MHz, CDCl3) δ 5.35-5.33 (m, 1H), 4.68 (s, 2H), 3.60 (t, J=6.5 Hz, 2H), 3.58-3.80 (m, 1H), 3.36 (s, 3H), 2.33-0.87 (m, 29H), 1.00 (s, 3H), 0.68 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 140.7, 121.7, 94.6, 76.9, 63.6, 56.7, 56.0, 55.1, 50.1, 42.3, 39.7, 39.5, 37.2, 36.7, 35.6, 31.8 (2×C), 29.4, 28.9, 28.2, 24.2, 21.0, 19.3, 18.7, 11.8.
MQ260
To a solution of steroid 3 (170 mg, 0.42 mmol) in pyridine (8 mL) was added SO3-Me3N (626 mg, 4.5 mmol) at room temperature. The mixture was stirred for 16 h. Solvent was removed under reduced pressure and the residue was redissolved in Methanol (5 mL) and then 6 N HCl (5 mL) was added. After 2 h, the product was extracted into dichloromethane (50 mL×4). Solvent was removed under reduced pressure, 7 N ammonia in methanol (4 mL) was added and the reaction was stirred at 23° C. for 1 h. After solvent removal under reduced pressure, the product was purified by flash chromatography (silica gel, eluted with 10%-25% MeOH in dichloromethane) to give MQ260 (185 mg, 96%): mp 164-166° C.; [α]D20-38.0 (c=0.05, MeOH); 1H NMR (400 MHz, CD3OD) δ 5.39-5.38 (m, 1H), 4.02 (t, J=6.5 Hz, 2H), 3.44-3.34 (m, 1H), 2.27-0.99 (m, 33H), 1.06 (s, 3H), 0.76 (s, 3H); 13C NMR (100 MHz, CD3OD) δ 143.2, 122.5, 72.5, 69.8, 58.3, 57.6, 51.8, 43.6, 43.1, 41.3, 38.7, 37.8, 36.9, 33.4, 33.2, 33.1, 32.4, 29.3, 27.2, 25.4, 22.3, 20.0, 19.3, 12.4.
Synthesis for a sulfonic acid analogue steroid is described below.
To a solution of olefin (400 mg, 1 mmol) in EtOAc (60 mL) was added 5% Pd/C (200 mg) at room temperature. The flask was evacuated and charged with H2 three time. The hydrogenation was carried out under 50 psi. After 3 h, the mixture was filtered through Celite and washed with EtOAc (200 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give product (400 mg, 100%): 1H NMR (CDCl3) δ 4.15 (q, J=7.0, 2H), 3.66-3.56 (m, 1H), 2.38-0.63 (m, 29H), 0.81 (s, 3H), 0.59 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 174.0, 71.3, 60.1, 55.3, 54.5, 46.9, 44.9, 42.2, 38.2, 37.4, 37.0, 35.6, 35.5, 35.4, 32.1, 31.5, 28.7, 28.2, 24.5, 20.9, 14.2, 12.6, 12.3.
To a solution of the ester (400 mg, 1 mmol) in THF (50 mL) was added LDA (1.25 mL, 2.0 M, 2.5 mmol) and HMPA (3 mmol, 0.54 mL) was added at −78° C. After 45 min, tert-butyl(3-iodopropoxy)dimethylsilane (900 mg, 3 mmol) in THF (5 mL) was added and the mixture was warmed up to room temperature for 16 h. Water was added and extracted with EtOAc (250 mL×2). The combined extracts were dried, filtered and the solvents removed. The residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to afford product (510 mg, 88%): 1H NMR (400 MHz, CDCl3) δ 4.65 (s, 2H), 4.11-4.05 (m, 2H), 3.61-3.34 (m, 6H), 2.44-0.62 (m, 31H), 0.87 (s, 9H), 0.78 (s, 3H), 0.67 (s, 3H), 0.02 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 176.1, 94.4, 76.2, 62.7, 59.7, 55.7, 55.0, 54.3, 52.7, 47.1, 44.8, 42.1, 37.6, 36.9, 35.5, 35.4, 35.2, 32.0, 30.4, 28.7, 28.6, 28.2, 27.0, 25.9 (3C), 23.7, 21.0, 18.2, 14.2, 12.2, 12.1, −5.4 (2C).
To a solution of the ester (510 mg, 0.88 mmol) in ether (40 mL) was added LAH (2.0 M in THF, 6 mL, 12 mmol) at room temperature. After 2 h, 0.48 mL of water, 0.96 mL of 10% of NaOH, and 1.44 mL of water were slowly added. After stirring for 30 min, the mixture was filter through Celite and washed with dichloromethane (200 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to afford product (216 mg, 46%): 1H NMR (400 MHz, CDCl3) δ 4.67 (s, 2H), 3.81-3.38 (m, 6H), 3.36 (s, 3H), 1.89-0.59 (m, 28H), 0.90 (s, 9H), 0.80 (s, 3H), 0.67 (s, 3H), 0.05 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.3, 63.6, 62.8, 56.3, 55.1, 54.3, 50.5, 44.8, 42.3, 42.1, 39.4, 37.0, 35.6, 35.4, 35.2, 32.0, 28.8, 28.7, 28.6, 27.6, 25.9 (3C), 25.1, 24.0, 21.2, 18.3, 12.3, 12.2, −5.3, −5.3.
To a solution of the alcohol (216 mg, 0.4 mmol) in dichloromethane (10 mL) was added MsCl (0.08 mL, 1 mmol) and Et3N (0.28 mL, 2 mmol) at 0° C. After 1 h, aqueous NaHCO3 (50 mL) was added and extracted with dichloromethane (100 mL×2). The combined extracts were dried, filtered and the solvents removed. The residue was purified by flash column chromatography (silica gel eluted with 20% EtOAc in hexanes) to give product (241 mg, 98%): 1H NMR (400 MHz, CDCl3) δ 4.75 (s, 2H), 4.38-4.35 (m, 1H), 4.29-4.09 (m, 2H), 3.63-3.38 (m, 3H), 3.36 (s, 3H), 2.99 (s, 3H), 1.83-0.59 (m, 27H), 0.89 (s, 9H), 0.80 (s, 3H), 0.68 (s, 3H), 0.04 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.2, 70.1, 63.2, 56.1, 55.1, 54.2, 50.1, 44.8, 42.3, 39.5, 39.3, 37.2, 36.9, 35.5, 35.4, 35.2, 31.9, 28.8, 28.7, 28.6, 27.4, 25.9 (3), 25.5, 23.9, 21.1, 18.3, 12.4, 12.2, −5.3 (2C).
To a solution of the mesylate (241 mg, 0.39 mmol) in ether (40 mL) was added LAH (2.0 M in THF, 4 mL, 8 mmol) at room temperature. After 2 h, 0.64 mL of water, 1.28 mL of 10% of NaOH, and 1.92 mL of water were slowly added. After stirring for 30 min, the mixture was filter through Celite and washed with dichloromethane (150 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 10% EtOAc in hexanes) to afford product (175 mg, 86%): 1H NMR (400 MHz, CDCl3) δ 4.67 (s, 2H), 3.58-3.46 (m, 3H), 3.36 (s, 3H), 1.97-0.59 (m, 31H), 0.89 (s, 9H), 0.80 (s, 3H), 0.64 (s, 3H), 0.04 (s, 6H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.3, 63.7, 56.4, 56.1, 55.0, 54.3, 44.8, 42.5, 40.0, 37.0, 35.6, 35.5, 35.4, 35.2, 32.0, 31.9, 29.4, 28.8, 28.7, 28.1, 25.9 (3C), 24.2, 21.2, 18.6, 18.3, 12.2, 12.0, −5.28 (2C).
To a solution of TBS ether (175 mg, 0.34 mmol) in THF (5 mL) was added TBAF (1 mL, 1.0 M in THF, 1.0 mmol) at room temperature. After 16 h, THF was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 25% EtOAc in hexanes) to give product (133 mg, 95%); 1H NMR (400 MHz, CDCl3) δ 1H NMR (400 MHz, CDCl3) δ 4.64 (s, 2H), 3.57-3.35 (m, 3H), 3.33 (s 3H), 2.17-0.56 (m, 32H), 0.78 (s, 3H), 0.62 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 94.3, 76.2, 63.2, 56.3, 56.0, 55.0, 54.2, 44.7, 42.5, 39.9, 36.9, 35.5, 35.5, 35.3, 35.1, 31.9, 31.8, 29.3, 28.7, 28.5, 28.1, 24.1, 21.1, 18.5, 12.1, 12.0.
To a solution of the alcohol (133 mg, 0.328 mmol) in benzene (8 mL) and dichloromethane (3 mL) was added PPh3 (524 mg, 2 mmol), imidazole (272 mg, 4 mmol), and I2 (508 mg, 2 mmol) at room temperature. After 3 h, aqueous NaHCO3 (20 mL) and aqueous Na2S2O3 (10 mL) were added and the product was extracted into diethyl ether (100 mL×2). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 4% EtOAc in hexanes) to give the iodo product (165 mg, 98%); 1H NMR (400 MHz, CDCl3) δ 4.62 (s, 2H), 3.46-3.40 (m, 1H), 3.30 (s, 3H), 3.13-3.05 (m, 2H), 1.89-0.52 (m, 31H), 0.74 (s, 3H), 0.58 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 94.5, 76.3, 56.4, 56.0, 55.1, 54.3, 44.9, 40.0, 37.0, 36.8, 35.5, 35.3, 35.1, 32.1, 30.3, 28.8, 28.7, 28.2, 24.2, 21.2, 18.7, 12.2, 12.1, 2.9.
To a solution of the iodo product (165 mg, 0.32 mmol) in methanol (8 mL) was added AcCl (2 mL) at room temperature. After 2 h, water (10 mL) was added and the product was extracted into dichloromethane (100 ml×3), the organic layers were washed with aqueous NaHCO3 (20 mL). Solvent was removed under reduced pressure on a rotary evaporator and the residue was purified by flash column chromatography (silica gel eluted with 25% EtOAc in hexanes) to give the iodo alcohol product (141 mg, 93%); 1H NMR (400 MHz, CDCl3) δ 3.60-3.54 (m, 1H), 3.21-3.08 (m, 2H), 1.96-0.58 (m, 32H), 0.79 (s, 3H), 0.64 (s, 3H).
To a solution of the iodo alcohol (141 mg, 0.3 mmol) in ethanol (25 mL) was added sodium sulfite (1.2 g, 9.44 mmol) at room temperature. The mixture was refluxed 48 h. Ethanol was removed and the aqueous layer was acidified with concentrated HCl to pH=1 and the product was extracted into EtOAc (150 mL×3). The organic layers were washed with water (50 mL). Solvent was removed under reduced pressure and the residue was purified by flash column chromatography (silica gel eluted with 10% MeOH in CH2Cl2) to give product (20 mg, 15%); 1H NMR (400 MHz, CD3OD) δ 3.72-3.66 (m, 1H), 2.83-2.80 (m, 2H), 1.91-0.70 (m, 33H), 1.02 (s, 3H), 0.87 (s, 3H).
Syntheses for various steroids are shown in the schemes below.
The pharmacological actions of MQ-221 at NMDA (negative allosteric modulator) and GABAA (positive allosteric modulator) receptors are shown in
Hippocampal Cultures.
Hippocampal cultures were maintained as described previously (Mennerick et al., 1995). Hippocampal tissue was harvested from postnatal 1-3 days old male and female Sprague-Dawley rats. A single-cell hippocampal suspension was plated on collagen-coated tissue culture plates and maintained in serum-containing medium on an astrocyte monolayer until use for recording. Recordings were performed 4-7 days after plating for exogenous agonist application and after 9 days for synaptic recordings in order to allow synaptic networks to mature.
N2a Cell Cultures and Transfection.
Murine neuro-2a (N2a; ATCC #CCL-131) cells were plated in Dulbecco's Modified Eagle's medium (DMEM) containing 10% fetal bovine serum, 2 mM glutamine, 100 U/ml penicillin, and 0.1 mg/ml streptomycin and maintained in a 5% CO2 humidified incubator. Cells were transfected with rat GluN1a and GluN2A or GluN2B subunit plasmids (pCDNA3), along with fluorescent protein plasmid to aid identification of transfected neurons, using Lipofectamine 2000 (ThermoFisher) as previously described (Warikoo et al., 2018).
Electrophysiology.
Hippocampal neurons were visualized with phase-contrast optics using an Eclipse TE2000-S inverted microscope. Voltage-clamp data were collected using a Multiclamp 700B amplifier, Digidata 1440 data acquisition board (Molecular Devices), and pClamp 10 software.
For study of exogenous agonist-induced currents, whole-cell pipette solution contained the following (in mM): 130 CsCl, 4 NaCl, 10 HEPES, 5 EGTA, and 0.5 CaCl2). The pH was adjusted to 7.25 with NaOH. Bath perfusion solution for study of NMDA current contained 138 mM NaCl, 4 mM KCl, 10 mM HEPES, 10 mM glucose, 0.2 mM CaCl2), 0 mM MgCl2, 1 μM NBQX, 10 μM glycine or 10 μM D-serine, and 10 μM gabazine. To isolate GABAAR currents and PSCs, 25 μM D-APV was used in place of 10 μM gabazine, and 1 mM MgCl2 was included in the bath. To isolate AMPAR PSCs, 25 μM D-APV was used instead of 1 μM NBQX. For synaptic studies, Ca2+ was increased to 2 mM. Whole-cell recording pipettes were pulled from borosilicate capillary glass (World Precision Instruments) and had final open-tip resistances of 3-6 MQ. Neuron membrane potential was clamped at −70 mV unless otherwise stated. Cells were constantly perfused with bath solution using a gravity-fed local perfusion stream, and drugs were applied by micromanifold with an exchange time of ˜100 ms. Transfected N2a cells expressing recombinant NMDAR subunits were recorded as with neurons, except receptor antagonists were omitted.
Data were analyzed using Clampfit 10 (MolecularDevices), processed in Excel spreadsheets (Microsoft), and plotted in Prism 8 (GraphPad). Concentration-response relationships were fit with inhibition or stimulation versions of the Hill equation using GraphPad Prism. Summary data in figures and text are given as mean±SEM. Statistical tests for comparison of means are described in the figure legends and were performed using Graphpad Prism. Comparisons were corrected where relevant for multiple comparisons as described in the legends. Statistical significance was defined as a corrected p-value<0.05. The reported n refers to the number of neurons recorded.
Compounds.
The synthesis of MQ-221, its stereoisomers MQ-245, MQ-246 and MQ-254, along with spectroscopic characterization data are reported above. The compounds were chromatographly pure as determined by thin layer chromatography on silica gel thin layer plates. KK-169 was synthesized as previously described (Chisari et al., 2019). 3α5βPS was obtained from Steraloids. Other salts and drugs were obtained from SigmaMillipore.
Results
Pharmacological Effects on NMDARs and GABAARs.
The same concentrations of MQ-221 also potentiated responses of neurons to 2 μM GABA (
To ascertain whether MQ-221 is likely to have other targets, we screened for interaction with a subset of other transmitter and hormone receptors present in the Psychoactive Drug Screening Program at the University of North Carolina. The screen, performed at 3 μM MQ-221, failed to clearly identify other targets of MQ-221 (see Table 1).
To gain a more detailed characterization of NMDAR inhibition and GABAAR potentiation, we examined the impact of systematically varied MQ-221 concentration on neuronal responses to 10 μM NMDA and 0.5 μM GABA (
Effects on Synaptic Function.
We addressed the impact of MQ-221 on physiological functioning by examining sEPSCs and sIPSCs in cultures of hippocampal neurons (
Comparison with Other Neuroactive Steroids.
The potentiation of GABAAR current by a sulfated steroid is the most surprising effect of MQ-221, because MQ-221 does not have structural attributes that characterize neurosteroid potentiation (Covey et al., 2001). To test whether MQ-221 shares a mechanism with conventional GABAAR-potentiating neurosteroids, we examined the effect of the al Q241L mutation, which eliminates potentiation by anesthetic neurosteroids (Hosie et al., 2006). Despite elimination of allopregnanolone (AlloP) potentiation of GABA current in N2a cells transfected with al (WT or Q241 mutant), β2, and γ2 subunits (
Characteristics of NMDAR Inhibition.
We next examined pharmacodynamic features of MQ-221 at NMDARs. Ketamine is an uncompetitive antagonist at NMDARs, requiring channel opening for entry and exit from the channel binding site (Johnson et al., 2014; MacDonald et al., 1987; Parsons et al., 1993). Although not likely a channel blocker, the sulfated neurosteroid pregnanolone sulfate, like ketamine, shows strong activation dependence (Petrovic et al., 2005). We queried the activation dependence of MQ-221 by comparing the impact of MQ-221 pre-application (in the absence of agonist), with the effect of MQ-221 co-applied during agonist presentation. Results demonstrated that MQ-221 interacted strongly with closed NMDAR channels (
The slight activation dependence of MQ-221 inhibition raises the possibility that MQ-221 could access a site in the NMDAR channel. If channel access is sufficiently deep, whereby the negative charge on MQ-221 experiences the voltage difference across the membrane, we would expect voltage dependence of MQ-221 inhibition. However, current voltage-response analysis of NMDA responses in the absence of extracellular Mg2+ showed no effect of MQ-221 inhibition on voltage between −110 mV and +70 mV (
Other activation dependent inhibitors, such as ketamine and memantine, exhibit faster onset and offset kinetics as channel open probability is manipulated with positive allosteric modulators or with increased NMDA concentration (Emnett et al., 2015). Consistent with the other evidence for some activation dependence in the mechanism of MQ-221 (
GluN2A versus GluN2B subtype-selective inhibitors of NMDARs are of interest for therapeutic purposes (Miller et al., 2014; Zanos and Gould, 2018). We tested subunit selectivity in native rat neuronal receptors by examining inhibition in the absence and presence of ifenprodil (10 μM), a selective inhibitor of NMDARs containing the GluN2B subunit. There appeared to be a modest reduction in MQ-221 sensitivity of cells challenged with MQ-221 in the presence of ifenprodil, suggesting that GluN2A-containing NMDARs may be less sensitive to MQ-221 (
Structure-Activity Characteristics
Given that MQ-221 seems unique in structure and in pharmacodynamics at GABAARs and NMDARs, we examined several stereoisomers of MQ-221. We focused on carbon 3 and carbon 5 stereoisomers because stereochemistry at these positions is important for NMDAR and GABAAR activity of other steroid analogues (Covey et al., 2001; Weaver et al., 2000). Examination of the effect of the four resulting stereoisomers on NMDAR currents in hippocampal neurons showed that the 30 hydroxylation appeared important for inhibition of NMDAR function, and both 3a stereoisomers exhibited NMDAR potentiation (
Neurosteroids and their analogues are emerging treatments for neuropsychiatric indications. The best understood targets of these compounds include GABAARs and NMDARs. Historically, neurosteroids that alter NMDAR function are sulfated and universally inhibit GABAAR function, potentially limiting usefulness. Here we describe a first-in-class compound, MQ-221, with a novel constellation of GABAAR PAM and NMDAR NAM activities. Two existing classes of compounds, represented by ketamine and brexanolone (allopregnanolone) have utility for treating depressive disorders. We propose that MQ-221, by possessing the major actions of both ketamine and brexanolone, may represent a clinically fortuitous compound.
In addition to ketamine and brexanolone, acamprosate is a clinically used drug with GABAARs and NMDARs as proposed targets. Acamprosate is FDA approved and modestly effective at treating alcohol use disorder (Kufahl et al., 2014). It may act at the same two receptor classes explored here and that are also responsible for acute actions of ethanol (GABAARs and NMDARs) (Abrahao et al., 2017). By mimicking ethanol, acamprosate may ease withdrawal symptoms. However, acamprosate suffers from low potency at its receptor targets (Kufahl et al., 2014). The enhanced potency of MQ-221 over acamprosate suggests that, as with depression, alcohol use disorder may be an indication worthy of exploration for MQ-221-like compounds.
MQ-221 possesses several interesting characteristics, including the concentration range over which it engages targets. GABAAR PAM neuroactive steroids (3β-hydroxy neurosteroids) typically are active in vitro in the high nanomolar to low micromolar range (Brown et al., 2002). Despite acting through a distinct mechanism from that of 3β-hydroxy neurosteroids, MQ-221 (a 3β-hydroxy neuroactive steroid) is an effective GABAAR PAM at similar concentrations. Higher MQ-221 concentrations promote GABAAR NAM effects in the late phase of prolonged GABA application (
Among pharmacodynamic effects on NMDARs is the weak use dependence of MQ-221 compared with pregnanolone sulfate (
Another pharmacodynamic effect of MQ-221 that may aid or may complicate clinical utility is the GABAAR NAM activity observed at high concentrations and with strong GABAAR activation. As noted above, this effect was not evident during spontaneous synaptic activity in cultures of hippocampal neurons. However, we cannot exclude the possibility that NAM effects might be relevant under certain physiological conditions in vivo. The NAM effect might self-limit GABAAR PAM actions and prevent sedation and other side effects of GABAAR PAMs at high concentrations. On the other hand, this feature may be a liability of MQ-221 by promoting convulsant activity observed with other GABAAR NAMs such as picrotoxin (Baker et al., 1965). The hope is that the concentration separation between PAM and NAM activity would limit negative consequences.
We found that MQ-221 preferred GluN2B-containing NMDARs. This effect was not as apparent in native rat hippocampal neurons as it was with recombinant rat NMDAR subunits transfected into N2a cells (
Finally, we considered structural features of MQ-221 that might account for the unusual dual GABAAR/NMDAR actions of the compound. MQ-221 might be considered a hybrid between neurosteroids and oxysterols. Oxysterols are direct oxidation products of cholesterol. Compounds in this class oxidized on the cholesterol side chain can have effects on NMDARs, including PAM or NAM activity (Hu et al., 2014; Linsenbardt et al., 2014; Paul et al., 2013). NMDAR NAM activity may derive from the oxysterol-like structure rather than a neurosteroid-like structure. To date, oxysterols are not known to have effects on GABAARs. Among possible additional structural manipulations of MQ-221, altering the side chain length is a straightforward change that could improve on the activity of MQ-221.
Bile acids are another class of cholesterol derivative with effects on GABAARs and NMDARs (Mennerick et al., 2001; Schubring et al., 2012). Bile acids, like MQ-221, have a negatively charged side chain. However, the major bile acids are 5β-reduced, while MQ-221 is 5α-reduced. Our structural modifications showed that conversion to the 5β stereoisomer of MQ-221 retained NMDAR effects but sacrificed GABAAR PAM activity in favor of NAM activity (
This invention was made with government support under MH110550 awarded by the National Institutes of Health. The government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2020/056171 | 10/16/2020 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63051713 | Jul 2020 | US | |
| 62926144 | Oct 2019 | US |
