Patent Application
20220193068
The present invention relates to a GRK2 protein inhibitor compound. In particular, the invention relates to a GRK2 protein inhibitor compound of Formula I
wherein X is an atom selected from carbon and nitrogen, and
R1 is selected from methyl carboxylate and 1,3,4-oxadiazol-2-yl groups and wherein the compound is selected from methyl 4-(naphthalene-2-amide)benzoate and N[4-(1,3,4-oxadiazol-2-yl)phenyl]quinoline-3-carboxamide. In a preferred embodiment, the GRK2 protein inhibitor compound is methyl 4-(naphthalene-2-amido)benzoate.
The GRK2 protein is a key protein kinase in regulation of a large family of membrane receptors known as “G protein-coupled receptors” (GPCR). The main function described for GRK2 is physiological inhibition of the receptors, once they have been steadily stimulated. This phenomenon is known as “desensitization” and it allows cells to dynamically inactivate GPCR-dependent signaling pathways if necessary. The GRK2 protein is involved in the regulation of GPCRs related to cellular responses to adrenaline, histamine, serotonin, acetylcholine, and angiotensin, among others. Thus, excess GRK2 activity was associated with numerous pathologies, and obtaining GRK2 inhibitors is of interest for the pharmacological treatment of these pathologies. In particular, many efforts have been made in the search for GRK2 inhibitors for the treatment of cardiac diseases in which this kinase is known to be overactivated. However, the search for inhibitors has always been oriented to identifying compounds capable of blocking GRK2-mediated kinase or phosphorylation activity of receptors. Today, it is known that the GRK2 protein can not only phosphorylate receptors, but also inactivate them through its RGS domain by blocking the interaction between the receptor and the G-protein through which it signals or transfers the stimulus into the cell, to elicit a biological response. The present invention consists of the development of a new class of compounds capable of inhibiting the action of the RGS domain of GRK2 with high specificity and selectivity.
Although GRK2 protein kinase has been proposed as a target for the development of pharmacological inhibitors, to date only compounds that act by inhibiting the GRK2 kinase activity (of phosphorylation of other proteins) have been proposed. However, to date, no compounds that inhibit the RGS (or domain) activity of GRK2 (signaling regulator through G protein) have been proposed
The present invention relates to a GRK2 protein inhibitor compound. In particular, it relates to a GRK2 protein inhibitor compound that of Formula I
wherein X is an atom selected from carbon and nitrogen, and
R1 is selected from groups methyl carboxylate and 1,3,4-oxadiazol-2-yl and wherein the compound is selected from methyl 4-(naphthalene-2-amido)benzoate and N-[4-(1,3,4-oxadiazol-2-yl)phenyl]quinoline-3-carboxamide. In a preferred embodiment, the GRK2 protein inhibitor compound is methyl 4-(naphthalene-2-amido)benzoate.
Since GRK2 is a protein with great physiological relevance and which participates in the inactivation of numerous receptors, its deregulation is associated with the development of various pathologies such as hypertension, cardiac insufficiency, Alzheimer's disease, rheumatoid arthritis, cystic fibrosis and cancer, among others. In all cases, the signaling of a receptor (different for each pathology) is altered due to the over-activation of GRK2, therefore, inhibition of this protein would result in relief of the pathological case or reversal thereof. Thus, to date, there is a need to develop new GRK2 inhibitors that can be used in the treatment or control of the above-mentioned pathologies.
However, there are numerous suppliers who provide molecular tools to laboratories conducting research in the biomedical sciences and who may also be interested in marketing these molecules for in vitro, in vivo or ex vivo experimental testing where inhibiting the GRK2 RGS domain is useful.
Thus, the present invention refers to GRK2 protein inhibitor compounds. In particular, it refers to a GRK2 protein inhibitor compound of Formula I
wherein X is an atom selected from carbon and nitrogen, and R1 is selected from the methyl carboxylate and 1,3,4-oxadiazol-2-yl groups. In a particular manner, the compound of the invention is selected from methyl 4-(naphthalene-2-amido)benzoate and N-[4-(1,3,4-oxadiazol-2-yl)phenyl]quinoline-3-carboxamide. In a preferred embodiment, the GRK2 protein inhibitor compound is methyl 4-(naphthalene-2-amido)benzoate.
In a particular embodiment, the compound of the invention is of Formula II
In another particular embodiment, the compound of the invention is of Formula III
Another object of the invention is a pharmaceutical composition comprising at least a GRK2 protein inhibitor compound and pharmaceutically acceptable excipients. In a particular embodiment of the invention, the pharmaceutical composition comprises the methyl 4-(naphthalene-2-amido)benzoate compound and pharmaceutically acceptable excipients. In another particular embodiment of the invention, the pharmaceutical composition comprises the N-[4-(1,3,4-oxadiazol-2-yl)phenyl]quinoline-3-carboxamide compound. The expert in the art will be able to choose the most appropriate excipients for the composition of the invention, according to the chosen route of administration. Moreover, those pharmaceutical compositions comprising one or more of the compounds of the invention in combination with other therapeutically active substances are considered to be within the scope of the present invention.
Particularly, it is contemplated that the pharmaceutical composition of the invention may be administered by oral, parenteral or transdermal route. In particular, said composition may be in the form of a liquid, a suspension, a tablet, a capsule, a pill, a solution for injection or a transdermal patch. Also contemplated within the scope of the invention is formulating the composition of the invention so as to release in a controlled manner at least one of the compounds with inhibitory activity of a GRK2 cell protein that of formulas I, II and III. The expert in the art will be able to formulate the composition of the invention according to the chosen route of administration.
The present invention also encompasses the pharmaceutical compositions comprising, at least, a compound of Formula I, II or III in combination with other therapeutically active substances, which, along with the compounds of the invention, may provide a therapeutic addition or synergistic effect such as, for example, gemcitabine, capecitabine, decitabine, paclitaxel and docetaxel or other anti-tumor agents.
In another particular embodiment of the invention, the pharmaceutical composition comprises the therapeutically active substance(s) encapsulated in liposomes or microspheres. The expert in the art will be able to establish the necessary parameters and excipients, taking into account the available literature related to this type of encapsulation.
Moreover, another object of the invention is a method for the treatment of a condition, mediated by a GRK2 cell protein, comprising administering to a patient in need of said treatment a safe and effective amount of at least a compound of the invention.
In another embodiment of the invention, the described inhibitors may be used in basic research as pharmacological tools to promote the understanding of biological, physiological and pathological processes involving GRK2 through the RGS domain thereof, such as mechanisms of desensitization of various GPCRs. In this way, they will allow to identify and assign differential functions to the different GRK2 domains in in vitro, in vivo or ex vivo experimental assays.
The compounds of the invention may be of interest for the treatment or prevention of cardiac insufficiency (CI), heart hypertrophy and hypertension, as well as for cardiovascular complications in individuals with type 2 diabetes. CI is characterized by an elevated activity of the sympathetic nervous system. The resulting high levels of catecholamines have been associated with increased expression and activity of GRK2 in various tissues. In the heart, this overexpression leads to increased desensitization of GPCRs such as the β-adrenergic and angiotensin II receptors, which regulate contractility and blood flow to the body, respectively. Also, during myocardial ischemia, an increase in membrane GRK2 activity was observed, contributing to the inactivation of the β-adrenergic receptor. Cardiac performance has been shown to increase after inhibition of GRK2 activity. GRK2 has also been shown to play a central role in vasoconstrictor-mediated regulation of arterial tone. Increase in blood pressure induced by GRK2 increases is accompanied by vascular thickening and cardiac hypertrophy. In this sense, inhibition of GRK2 activity may reduce the alterations observed in the vasculature of hypertensive patients.
Moreover, the compounds of the invention could be used for the treatment of different types of cancer, in which an association between GRK2 and the development of cancer is determined. In this regard, the expression of a peptide inhibitor of GRK2, derived from its terminal carboxyl end (βARKct) showed a delay in the growth of prostate tumor cells in vitro and prevented the formation of prostate tumors in vivo in xenotransplant models.
Furthermore, GRK2 was found to be overexpressed in samples from patients with pancreatic ductal adenocarcinoma (PDAC). The study of GRK2 expression in various breast cancer-derived cell lines, in mammary glands from animal models and in patient samples, showed increased levels of said protein. In this context, xenotransplantation of breast tissue cancer cells that overexpress GRK2 generated larger and earlier tumors with respect to control, while inhibition of its expression prevented the formation of breast tumors in such models. As regards ovarian cancer, high expression of GRK2 was observed in the KGN cell line, derived from granulosa tumor cells, and also in primary and metastatic tumors of patients. This is consistent with the desensitizing function of GRK2 on the follicle-stimulating hormone receptor, responsible for modulating the proliferation and differentiation of granulosa cells and involved in the development of ovarian cancer, suggesting that exacerbated desensitization of this receptor may be part of the pathogenesis of ovarian cancer. In relation to acute myeloid leukemia, it has been demonstrated that the balance between production, degradation and exclusion of cAMP is essential for cell proliferation/differentiation. An increase in intracellular cAMP levels is desirable for differentiation therapy. Thus, histamine stimulation (acting through the H2/Gs receptor) in conjunction with GRK2 inhibitors would increase intracellular cAMP levels to induce the desired differentiation.
In addition, Alzheimer's disease (AD) is a neurodegenerative disorder in which altered expression of GRK2 is an early event in its pathogenesis and precedes the cognitive alterations that characterize the disease. The protein and mRNA levels of GRK2 have been increased in post-mortem hippocampuses and lymphocytes of patients with AD as well as in rat models with chronic cerebral hypoperfusion. Although the signaling pathways that would be altered have not yet been fully elucidated, GRK2 is known to participate in the desensitization of metabotropic glutamate receptors 1 and 5 and the M1 muscarinic receptor, which are involved in the development of AD. Thus, it is anticipated that the described GRK2 inhibitors may result in a therapeutic option.
Furthermore, the GRK2 protein constitutes an important regulator of the responses of the cells of the immune system to situations of inflammation, since it phosphorylates numerous receptors of chemokines and chemotactic responsible for the traffic of leukocytes towards the inflammatory focuses and the exit of T cells from the lymphoid organs. Although the pathogenesis of rheumatoid arthritis (RA), in its complexity, involves several cell types, synovial fibroblasts are responsible for the development of an invasive phenotype. They produce cytokines, which cause inflammation to persist, and proteases that destroy cartilage. It has been shown that during the development of the inflammatory process in rat models of CIA (collagen-induced arthritis), GRK2 levels in synovial fibroblasts increase as the condition progresses, and that GRK2 inhibitors are able to reverse this effect. Additionally, GRK2 inhibition with paroxetine has been shown to attenuate CIA symptoms by reducing T-cell infiltration into synovial tissue.
Results showing a decrease in GRK2 levels in mononuclear blood cells of rheumatoid arthritis have been published in specialized literature.
Moreover, cystic fibrosis (CF) is a disease caused by mutations in the gene that encodes CFTR protein (regulator of the transmembrane conductance of CF) and is characterized by abnormal, excessively thick and viscous secretions that mainly affect the lungs. The CFTR protein is found in the apical membrane of epithelial cells involved in exocrine secretion and acts as a channel for AMP-dependent Cl−. Thus, the composition of luminal secretion from the airways is regulated by the activity of the β2 adrenergic receptor (β2AR), which is coupled to the cAMP pathway. In airway samples from cystic fibrosis patients, a reduction in the density of this receptor has been observed, as well as an over-expression of GRK2. Accordingly, the culture of these epithelial cells showed a reduced secretion of Cl−in response to isoproterenol. Therefore, inhibition of GRK2 would be a potential target for increasing the activity of adenylate cyclase in response to activation of the β2 adrenergic receptor.
Additionally, sepsis is a complex clinical syndrome resulting from a host's harmful response to infection. Polymorphonuclear neutrophils (PMN) are the host's first line of defense against microorganisms, being recruited at the inflammatory sites by chemoattractants such as leukotriene B4 (LTB4) and chemokines. Once migrated, these leukocytes are capable of phagocyting and generating large quantities of reactive oxygen and nitrogen species, such as hydrogen peroxide and nitric oxide, which are crucial products for the microbicidal activity of these cells. Since neutrophils play a key role in the control of the infectious process, it can be hypothesized that poor neutrophil migration may aggravate infections. Data suggest that endogenous mediators produced during sepsis may continuously activate circulating neutrophils, leading to the activation of GRK2, which in turn may induce desensitization of neutrophils to chemoattractants. Inhibition of GRK2 may be beneficial by restoring the ability to migrate to neutrophils.
Finally, multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system. The infiltration of activated T-lymphocytes and macrophages into the brain and spinal cord is an important factor in the pathogenesis of this disease. In a mouse model of MS, a more benign course of the disease was demonstrated in GRK2+/− mice. It was also shown that GRK2 expression is reduced during the remission phase in MS patients, suggesting that the reduction of GRK2 activity during MS may be a new target for the therapy.
Thus, taking into account that the inhibition of GRK2 activity would be beneficial for controlling and/or treating the above mentioned disorders and diseases, the compounds of the invention could be used for controlling and/or treating such disorders and diseases. In particular, the compounds of the invention are useful in the treatment and/or control of heart disease, various types of cancer, inflammatory diseases, Alzheimer's disease (AD), rheumatoid arthritis, cystic fibrosis (CF), sepsis and multiple sclerosis (MS).
A particularly preferred object of the present invention is a pharmaceutical composition comprising a compound of Formula II or a compound of Formula III, one of their salts, one of their prodrugs or one of their pharmaceutically acceptable derivates. However, the invention also includes the pharmaceutical compositions comprising one or more of said compounds of the invention, in combination with one or more second therapeutically active substances.
According to the present invention, the term “administering” and variants thereof (for example, the “administration” of a compound) with reference to a compound of the invention, means to introduce a compound, a prodrug, a salt or a pharmaceutically acceptable derivative of the compound of the invention, into the system of the animal or human in need of said treatment. When a compound of the invention, a salt or a pharmaceutically acceptable derivative of the compound of the invention is provided in combination with one or more other active agents (for example, another therapeutically active substance that presents a complementary or synergistic therapeutic effect to that of the compound of the invention), “administration” and its variants must be, each one, understood as including the sequential and concurrent introduction of the compound, the salt, the derivative or the prodrug thereof and of the other agents.
The term “patient” for the purposes of the present invention includes humans. However, it should be understood that the compounds may also be administered to other animals, particularly mammals and other organisms. Thus, the methods are applicable both to human therapy and veterinary applications. Therefore, in some particular embodiments, the compounds are for administration to mammals, and in other applications they are for administration to humans.
According to the present invention, a “pharmaceutically acceptable salt or derivative” of a compound means a salt or derivative which is pharmaceutically acceptable, and which possesses the desired pharmacological activity of the starting compound. It should be understood that salts or pharmaceutically acceptable derivatives are not toxic. Additional information about suitable salts or pharmaceutically acceptable derivatives can be found in Remington the Science and Practice of Pharmacy 21st ed., Pharmaceutical Press, London, England, 2011, which is incorporated herein as reference. It should also be understood that the compounds of the invention may have one or more salts or one or more pharmaceutically acceptable derivates associated thereto.
By “prodrug” is meant compounds that are transformed (typically rapidly) in vivo, to obtain the starting compound of the above formula, for example, by hydrolysis in the blood. The expert in the art will know how to prepare prodrugs of the compounds of the invention in accordance with the appropriate practices to that purpose.
“Therapeutically effective amount of” or “safe and effective amount of” is an amount of a compound of the invention which, when administered to a patient, effectively treats a certain disease. The amount of a compound of the invention constituting a “therapeutically effective amount of” will vary depending upon a number of factors, including activity, metabolic stability, excretion rate and duration of compound action, age, weight, general health condition, sex, diet and species of the patient, route and time of administration of the compound, concurrent administration of adjuvants or additional therapies, and the severity of the disease for which the therapeutic effect is sought. The “therapeutically effective amount” or the “safe and effective amount” for a given circumstance can be determined without the need for extra experimentation. In preferred embodiments, the acceptable dose range is from 10 mg to 500 mg every 24 hours, via oral, intramuscular or intravenous route. As is known in the art, adjustments for systemic versus localized release, the age, weight, general health condition, sex, diet and species of the patient, and route and time of administration of the compound, concurrent administration of adjuvants or additional therapeutically active ingredients, and the severity of the disease for which the therapeutic effect is sought may be necessary, and will be ascertainable through routine experimentation. The effective amounts or doses of the compounds of the present invention may be determined by routine methods, such as modeling, dose escalation or clinical trials, taking into account routine factors. Actual dosage levels of active ingredients in pharmaceutical compositions may vary. In general, an adequate daily dosage of a compound and/or of the compositions and methods according to the present invention will be the amount of the compound that provides the lowest dose that is effective and produces the desired therapeutic effect.
The compounds of the invention can be administered to a patient by any acceptable route of administration. Acceptable routes of administration include, but are not limited to, oral, parenteral, transdermal, endocervical, endosinusal, enteral, intra-abdominal, intra-arterial, intrabronchial, intracerebral, intracoronary, intradermal, intraductal, intraduodenal, intradural, intraepidermal, intraesophageal, intragastric, intragingival, intraileal, intralymphatic, intrameninge, intramuscular, intraovarian, intraperitoneal, intraprostatic, intrapulmonary, intrasinal, intraspinal, intrasynovial, intratesticular, intrathecal, intratubular, intratumoral, intrauterine, intravascular, intravenous, nasal, nasogastric, buccal, percutaneous, peridural, rectal, respiratory (inhalation), subcutaneous, sublingual, submucosal, topical, transmucosal, transtracheal, ureteral, urethral and vaginal.
The compounds of the invention may be administered in any acceptable solid, semi-solid, liquid or gaseous dosage form. Acceptable dosage forms include, but are not limited to, tablets, capsules, solutions, sprays, creams, emulsions, gases, gels, grains, liniments, lotions, suppositories, ointments, pastes, powders, suspensions, syrups and tablets.
A dosage form of the invention may comprise only one compound of the invention, or the compound of the invention may be formulated together with conventional excipients, pharmaceutical carriers, adjuvants and/or other medicinal or pharmaceutical agents. Acceptable excipients include, but are not limited to, (a) anti-adherents, such as sodium croscarmellose, crospovidone, sodium glycolate starch, microcrystalline cellulose, starch and talc; (b) binders, such as cellulose, gelatin, hydroxypropyl cellulose, lactose, polyethylene glycol, polyvinylpyrrolidone, sorbitol, starch and xylitol (c) coatings, such as cellulose and shellac; (d) disintegrants, such as cellulose, polyvinylpyrrolidone, sodium carboxymethyl cellulose, methylcellulose, microcrystalline cellulose and sodium starch glycolate and starch; (e) fillers such as calcium carbonate, cellulose, dibasic calcium phosphate and mannitol; (f) flavoring agents/aromatizers; (g) coloring agents; (h) glidants such as calcium stearate and colloidal silicon dioxide; (i) lubricants, such as calcium stearate, magnesium stearate, polyethylene glycol, and talc; and (j) preservatives, such as citric acid, vitamin C and vitamin E. Pharmaceutical carriers include soluble polymers, microparticles made of polymers, natural or synthetic, insoluble or biodegradable, microcapsules, lipoproteins, liposomes, and micelles.
A pharmaceutical composition of the invention will include a therapeutically effective amount of a compound of the invention, a prodrug, a derivative or a pharmaceutically acceptable salt thereof, with the rest of the pharmaceutical composition being composed by one or more pharmaceutically acceptable excipients. Generally, a compound of the invention, a prodrug, a derivative or a pharmaceutically acceptable salt thereof, will be in a proportion from 1% to 99% by weight of the pharmaceutically acceptable composition, with the rest of the pharmaceutical composition being composed of one or more pharmaceutically acceptable excipients. Typically, a compound of the invention, an individual stereoisomer thereof or a mixture of stereoisomers thereof, a prodrug, a derivative or a pharmaceutically acceptable salt thereof, will be in a proportion from 5% to 75% by weight of the pharmaceutically acceptable composition, with the rest of the pharmaceutical composition being composed of one or more pharmaceutically acceptable excipients. Methods to prepare the dosage forms of the invention are known or will be apparent to those experts in the art; see, for example Remington the Science and Practice of Pharmacy 21st ed. (Pharmaceutical Press, London, England, 2011).
A therapeutically effective amount of a compound of the invention will vary depending on a series of factors, including activity, metabolic stability, excretion rate and duration of compound action, age, weight, general health condition, sex, diet and species of the patient, route and time of administration of the compound, presence of adjuvants, of additional therapeutically active ingredients in the composition, and the severity of the disease for which the therapeutic effect is sought.
The present invention also encompasses the procedures to be used for the obtention of the compounds of Formula I, II and III of the invention and intermediary compounds to be used in said procedure.
Step a: 4.0 g (29.2 mmol) of 4-aminobenzoic acid were dissolved in 40 mL of MeOH. This solution was cooled down to 0° C., 2.5 equivalents of SOCl2 were added dropwise and it was refluxed for 2.5 h, under vigorous stirring. Solvent was then evaporated, it was neutralized with NaHCO3 saturated solution (s.s.) and the mixture was extracted with EtOAc. The organic phase was washed with NaCl s.s., dried out over anhydrous Na2SO4 and the solvent was evaporated at reduced pressure. Purification of the raw residue by column chromatography (n-hexane/EtOAc) allowed to obtain methyl 4-aminobenzoate with a 70% yield (3.1 g). Step b: Afterwards, 500 mg (3.31 mmol) of the product of Step a were dissolved in CH2Cl2, triethylamine was added (3 equivalents) and 569 mg (3.31 mmol) of 2-naftoic acid were added to this solution. Then, SOCl2 was added dropwise at room temperature under vigorous stirring, until completing the reaction. Solvent was evaporated at reduced pressure, residue was dissolved in CH2Cl2 and washed with 1 N HCl, NaCl s.s., 1 N NaOH and finally with NaCl s.s., it was dried out over anhydrous Na2SO4 and the solvent was evaporated at reduced pressure. Purification of the raw residue by column chromatography (CH2Cl2) allowed to obtain methyl 4-(2-naphthamide)benzoate (L96B) with a 69% yield (700 mg).
M.p.: 142° C.
MS (ESI) m/z for M+H+:291.0890.
RMN-1H (500 MHz, CDCl3): 3·92 (CH3, 3H, s); 7.57-7.63 (2 H, m); 7.80 (2 H, d, J=8.7 Hz); 7.90-7.93 (2 H, m); 7.95 (2 H, t, J=8.2 Hz); 8.08 (2 H, d, J=8.7 Hz); 8.16 (NH, 1 H, s); 8.39 (1 H, s).
RMN-13C (125 MHz, CDCl3): 52.2 (CH3); 119.4; 123.5; 126.0; 127.3; 127.9; 128.0; 128.3; 129.1; 129.2; 131.1; 131.8; 132.7; 135.2; 142.3; 166.0 (CO amide); 166.7 (CO ester).
Methyl 4-(quinoline-3-carboxamide)benzoate (L94A) was obtained following a procedure similar to that described in Example 1, but using 3-quinolincarboxilic acid in Step b.
The compound obtained (200 g, 0.66 mmol) was dissolved in MeOH, 5 mL of hydrazine hydrate solution were added and left to stir at r.t. until the reaction was complete. The solvent was evaporated at reduced pressure. Purification of raw residue by CH2Cl2 crystallization allowed to obtain N-(4-(hydrazinecarbonyl)phenyl)quinoline-3-carboxamide with a 50% yield (100 mg). Finally, 25 mg (80 μmol) of the product obtained in the previous step were suspended in 3 mL of trimethyl orthoformate and it was heated to reflux under vigorous stirring until the reaction was complete. Solvent was evaporated at reduced pressure. Purification of raw residue by washing with ethyl ether and further recrystallization with CH2Cl2 allowed to obtain N-[4-(1,3,4-oxadiazol-2-yl)phenyl]quinoline-3-carboxamide (L94C) with a 15% total yield.
M.p.: 202° C.
MS (ESI) m/z for M+H+:317.10390.
RMN-1H (300 MHz, DMSO-d6): 7.65-7.82 (7H, m); 8.20 (1H, d, J=7.9 Hz); 8.37 (1H, d, J=7.9 Hz); 8.73 (1H, s); 9.25 (1H, s); 9.51 (NH, 1H, s).
RMN-13C (75 MHz, DMSO-d6): 123.3; 123.3; 123.6; 125.1; 126.1; 127.1; 127.1; 128.5; 128.7; 128.9; 131.6; 137.4; 143.0; 145.8; 149.9; 151.0; 162.2; 163.9.
Inhibiting activity of the compounds of the invention and of the following compounds from the Enamine library was studied:
In order to assess the effect of inhibitors of the RGS domain of GRK2, a cell model derived from HEK293 transfected cells was obtained. Such cells overexpress the histamine H2 receptor (rH2), a G-protein coupled receptor (GPCR) of the Gs type that, when activated, promotes cAMP synthesis and which is inactivated by regulatory domain-mediated desensitization of G-protein stimulation (RGS) of GRK2. The clone obtained not only overexpresses rH2 but also overexpresses a negative dominant mutant of GRK2, the GRK2-K220R variant, which cannot phosphorylate GPCRs but can inactivate them through its RGS domain. In this system, the desensitizing effect of the RGS domain of GRK2 on the cAMP response of rH2 is evident. When pre-treated with a compound, an enhancing effect of cAMP response to the agonist may be associated with an inhibition of RGS-domain mediated desensitization of GRK2.
Clones derived from HEK293 cells were obtained by stable and sequential transfection with pcDNA3.1Zeo(+)-HARH2 and pcDNA3-GRK2K22OR plasmids using K2 Transfection System (BIONTEX) reactive, following manufacturer's instructions and using, for a 35 mm diameter plate, a mixture A of 2.7 μg of total DNA and 150 μl of DMEM base and a mixture B of 6 μl of K2 transfection reactive and 150 μl of base DMEM. The following day, cells were plated in 96-well plates with 0.3 ml of complete DMEM per well. For clone selection, cells were incubated in selection agent-supplemented medium (50 μg/ml Zeocine or 1.2 mg/ml geneticin), following a limit dilution protocol. According to this protocol, cells were counted and plated performing serial dilutions, so as to obtain wells with con 1000, 100, 10 and 1 cell. The medium was renewed every other day by replacing 100 μl in each well with 100 μl of fresh medium of the same composition. After three weeks, several antibiotic-resistant clones were selected and afterwards plasmid expression was analyzed by Western blot.
Adhered clones were maintained in a humidified-atmosphere oven, with 5% CO2 at 37° C., in 10% FBS-supplemented DMEM medium, 50 μg/ml gentamicin, 0.8 mg/ml geneticin and 50 μg/ml zeocin. Cells were passed by adding 0.05% trypsin solution and 0.3 mM EDTA.
In order to assess the effect of GRK2 inhibitor compounds, clones were plated in 48-well plates at 50% confluence. After 24 h, cells were pretreated in minimum medium at 37° C. for 40 min with commercial compounds C2, C3, C4 and C5, at 10 μM or 100 μM concentrations or with compound L96B according to the invention at 100 nM or 1 μM concentrations. An equivalent amount of DMSO vehicle was used as negative control.
Next, cells were incubated for 3 min with 1 mM IBMX, a phosphodiesterase inhibitor that prevents degradation of the cAMP produced and afterwards the rH2-Gαs-adenylate-cyclase-cAMP signaling route was stimulated for 9 minutes with the rH2-specific agonist, amthamine, at a 10 μM concentration. Afterwards, cells were lysed and resuspended in absolute ethanol. This was evaporated and cAMP levels were determined.
cAMP in samples was quantified by adapting the linking protein-binding technique according to Davio et al, 1995.
In order to assess specificity of the effect of compounds over RGS domain of GRK2, assays were carried out in a second system that overexpresses rH2 and GRK2K220R/R106A, a GRK2 double mutant negative dominant construct that lacks both kinase activity and desensitization action through RGS domain. In this case, the overexpression of the inactive variant of GRK2 prevents regulation of the rH2response. The R106A mutation that inactivates the RGS domain is redundant to the effect of an inhibitory potential, thus constituting the selectivity control of the model and allowing to determine if the enhancement in the receiver response occurred as a result of an inhibition of the RGS domain, or if it was the result of a non-specific action of the compound on an unwanted target. Those compounds that also raise cAMP levels in this control system are considered to be of non-specific action.
The enhancing effect of compounds C2, C3, C4, C5 and L96B does not occur in clones derived from HEK293 cells which stably express rH2 and a double mutant GRK2 variant deficient in kinase activity and RGS activity. Since the latter mutation is redundant to the effect of a potential inhibitor of RGS domain of GRK2, this system allows us to discern whether the enhancement in the rH2 response occurred as a result of an RGS domain inhibition, or whether it resulted from a non-specific action of the compound on an unwanted target.
In order to assess the effect of GRK2-inhibitor compounds over cAMP response under more physiological conditions, cAMP response was determined in U937 cells that were not transfected as they endogenously express rH2.
400,000 cells were starved for two hours without fetal bovine serum, pretreated in minimum medium (RPMI), at 37° C. for 40 min, with compounds L96B and L94C of the invention, at 100 nM and 10 μM concentrations. An equivalent amount of vehicle, DMSO, was used as negative control.
Next, cells were incubated for 3 min with 1 mM IBMX, a phosphodiesterase inhibitor that prevents degradation of cAMP produced. Next, the rH2-Gαs-adenylate-cyclase-cAMP signaling route was stimulated for 9 minutes with the rH2-specific agonist, amthamine, at a 10 μM concentration. Afterwards, cells were lysed and resuspended in absolute ethanol. This was evaporated and cAMP levels were determined.
CAMP in samples was quantified by adapting the linking protein-binding technique according to Davio et al, 1995.
In order to assess the effect of the inhibitors of RGS domain of GRK2 on the response of GPCRs coupled to Gq-PLC-calcium intracellular signaling route, histamine H1 receptor was used as example, a Gq protein coupled receptor, which, upon activation, promotes calcium release from the endoplasmic reticulum into the cellular cytoplasm and is also inactivated by desensitization mediated by RGS domain of GRK2.
The system used for determining this biological activity consists of epithelial lung cell-line, A549, which endogenously express rH1 and GRK2. Calcium cytoplasmic levels were assessed using Fura2AM fluorescent probe, which is capable of binding to Ca2+ ion, whereby excitation wavelengths (2) are altered, varying from 380 nm (unbound) to 340 nm (bound). Accordingly, a calcium response by the receptor to stimuli is evidenced by an increase in fluorescence emitted by Fura2AM in its calcium-bound form and a decrease in signal emitted by its unbound form, giving an increase in fluorescence ratio F340/F380.
A549 cells were pleated at 40% confluence in 96-wells plates. The next day, the cells were incubated with FURA 2-AM 2 mM probe and 0.2% pluronic acid in buffer BSS (140 mM NaCl, 3.9 mM KCl, 0.7 mM KH2PO4, 0.5 mM Na2HPO4, Al2H2O, 1 mM CaCl2, 0.5 mM MgCl2, and 20 mM HEPES, 10 mM glucose and 0.1% BSA pH=7.5) for 90 min at 37° C. Then, the cells were washed with BSS twice. During the last 40 min of said incubation, the compound L96B according to the invention either was added at a 100 nM concentration or was not added at all. Intracellular calcium levels were recorded at 37° C. in real time, with a FlexStation 3 (MolDev) equipment alternating excitations at 340 nm and 380 nmen. Fluorescence emission was measured at 505 nm. Histamine ligand at a 100 μM concentration was pipetted in each well at 30 sec after initiating reading and without interrupting the same, and 0.1% Triton ×100 detergent was pipetted at 180 sec to estimate the amount of FURA2-AM incorporated by the cells.
In order to assess the response in desensitized cells, A549 cells were plated at 40% confluence in 96-well plates. The following day they were incubated with 2 mM FURA 2-AM and 0.2% pluronic acid, in BSS for 90 min at 37° C. During the last 10 min of said incubation, either histamine was added to the corresponding wells at a 33 μM concentration or only vehicle was added. Next, two BSS washes were performed, and procedure was followed as in response assays.
Induction of cell differentiation is a desirable event to achieve cell maturation and slow down leukemic cells proliferation. This process is closely related to the generation of the second cAMP messenger in response to different stimuli. The effect of the compounds on the differentiation of U937 leukemic cells was studied by measuring the expression of the terminal differentiation marker to CD88 monocytes after joint treatment with histamine (an agent that increases cAMP intracellular levels, but due to the fast desensitization of its receptor by GRK2, cAMP signal is insufficient to induce cell differentiation), the compounds C2 and C10 and compound L96B according to the invention.
Promonocytic leukemia U937 cells were cultivated in suspension in an oven with humidified atmosphere, with 5% CO2, at 37° C., in 10% FBS-supplemented RPMI 1640 medium and 50 μg/ml gentamicine, and maintained at a density of 4×105-1.6×106 cells/ml. U937 cells were treated for 48 h with a concentration of 100 μM of histamine and 1 μM of compounds C2 and C10 or with compound L96B of the invention.
Samples were lysed in Laemmli buffer (50 mM Tris-HCl pH 6.8; 2% SDS; 100 mM 2-mercaptoetanol; 10% glycerol and 0.05% bromophenol blue), sonicated and incubated in water bath for 5 minutes prior to seeding. Protein extracts were analyzed in polyacrylamide gel at 12%, under denaturalizing conditions (SDS-PAGE). The electrophoresis buffer used consisted in 25 mM Tris; 192 mM glycine; 0.1% SDS, pH 8.3. Electrophoresis was developed in minigels at a constant current of 30 mA (BioRad). After fractioning, the gel was balanced in transfer buffer (25 mM Tris HCl, pH 8.3, 150 mM glycine; 20% methanol) for 15 min and transferred to nitrocellulose membranes at 100 V, for 1 h at 4° C. The proteins transferred to the membranes were stained in a solution of 0.2% Ponceau; 0.5% acetic acid, to visualize the total proteins and to verify the transfer efficiency in all the lanes. Afterwards, the membranes were washed in PBS, until the staining disappeared. After treating the membranes with blocking solution (PBS-0.1% Tween20) for 1 h, they were incubated for 1 h with 1 μg/ml of goat anti-CD88 antibody or rabbit anti-beta-tubulin antibody. Detection was carried out by incubating with 0.2 μg/ml of secondary anti-goat or anti-rabbit antibody conjugated to peroxidase for 1 h, followed by exposure to a peroxidase substrate and chemiluminescence amplifier solution (Amersham Life Science). The result was displayed by autoradiography.
The intensity of the band corresponding to CD88 was quantified by optical densitometry using ImageJ software and expressed as relative to the value obtained for tubulin. Results were expressed considering the expression of CD88 in the cells treated with the DMSO vehicle as 100%. The data represent the mean±ESM of two independent experiments (n=2).
B-adrenergic receptors are responsible for controlling myocardial strength and contractility. The functioning of these receptors is regulated by GRK2 and their desensitization by GRK2 is exacerbated in patients with hypertension or cardiac insufficiency.
Cardiomyocytes were obtained from the ventricle of neonatal Sprague-Dawley rats by proteolytic digestion. Briefly, after decapitation, the ventricles were separated and transferred to iced PBS where they were cut with fine scissors into 1-3 mm3 portions. The tissue thus disintegrated was subjected to three rounds of enzymatic digestion in saline solution containing collagenase IV (1 mg/ml). The disintegrated cells were collected by centrifugation at 400 rpm for 5 minutes and kept in DEM-F12 medium containing 10% BFS, 10 μg/ml insulin, 10 μg/ml holo-transferrin, 100 μM bromodeoxyuridine (to avoid the proliferation of other cell types), 10,000 U/ml penicillin and 10 mg/ml streptomycin. The cells were plated in Petri dishes and kept for 1 h at 37° C. in atmosphere humidified with 5% CO2. The cells that did not adhere to the plate, corresponding to cardiomyocytes, were transferred at a density of 0.5×106 cells/well to 12-well multi-well plates. All of the experimentation with animals was carried out following the guidelines of the National Institute of Health Guide for the Care and Use of Laboratory Animals (2011) and were approved by the Institutional Committee for the Use and Care of Laboratory Animals of the School of Pharmacy and Biochemistry of the UBA (University of Buenos Aires) (Resolution (D) No. 19-16).
To perform the isoproterenol response tests, the cells were starved for 2h and pretreated for 40 min with compound L96B according to the invention at a 100 nM concentration or equivalent amounts of DMSO, in minimum medium, at 37° C. Then, cells were incubated for 3 min with 1 mM phosphodiesterase inhibitor, IBMX, and then stimulated for 9 min with 1 μM isoproterenol to activate the production of cAMP evoked by the (β-adrenergic receptors.
Afterwards, cells were lysed and resuspended in absolute ethanol. This was evaporated and cAMP levels were determined. cAMP in samples was quantified by adapting the linking protein-binding technique according to Davio et al, 1995.
Thirty percent of drug development processes are unsuccessful due to unexpected toxicity of a compound. Since hepatotoxicity is one of the main forms of toxicity in which drugs affect the body, the cytotoxicity of inhibitors was assessed using the human hepatocyte HEPG2 cell line.
Cells were plated in a 96-well plate at a 22,000 cell/well density and incubated for 48 hours with the compounds in a concentration range of between 0.33 μM and 200 μM. Afterwards, their viability was analyzed through trypan blue exclusion method and counted in Neubauer camera.
It can be observed in
The following examples disclose representative pharmaceutical compositions comprising one or more of the compounds according to the invention.
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| Number | Date | Country | Kind |
|---|---|---|---|
| P20190101103 | Apr 2019 | AR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2020/053874 | 4/23/2020 | WO | 00 |
