Patent Application
20230212222
The present invention relates to a novel compound and a composition for an anti-diabetes and anti-obesity comprising the same as an active ingredient.
About 880 G protein-coupled receptors (GPCRs), which are the most abundant membrane proteins in all mammals, are currently known. Of these, about 60% are related to the senses of sight, smell, taste, and the like, and about 400 GPCRs, including the remaining orphan GPCRs, are regulated by various ligands (e.g., proteins, peptide hormones, amino acids, amines and lipids) in vivo and are involved in various life phenomena. In particular, GPCRs are associated with diseases such as metabolic diseases, cardiovascular diseases, degenerative diseases and carcinogenesis. Therefore, it is an important drug target for new drug development, and more than 50% of the drugs developed to date are directly or indirectly related to the activity of GPCR.
On the other hand, GPR39 (G protein-coupled receptor 39) is one of the orphan GPCRs, and an intrinsic ligand has not been discovered to date. GPR39 belongs to the Ghrelin receptor (GHSR, growth hormone secretagogue receptor) family, and is known to be distributed in the stomach, intestine, pancreas, liver, kidney, reproductive and adipose tissue (Cellular and Molecular Life Sciences, January 2011, Volume 68, Issue 1, pp 85-95). GPR39 was found to be associated with body weight gain and body fat accumulation through in vitro GPR39 silencing and metabolic function studies through high-fat or low-fat diet control in GPR39 knockout (KO) mice (Gastroenterology 2006, 131:1131-1141). In addition, through the study of GPR39 KO mice, it was confirmed that the blood glucose level of GPR39 KO mice was increased in high-fat diet control, whereas insulin secretion was impaired and glucose-dependent insulin secretion (glucose stimulated insulin secretion) was decreased (Endocrinology 2009, 150:2577-2585).
The above results suggest that GPR39 plays an important role in the physiological function of the body, and a modulator for GPR39 is expected to be a new drug candidate for the treatment of metabolic diseases such as diabetes mellitus and obesity.
The present inventors have completed the present invention by confirming that a peptide consisting of a specific amino acid sequence or a variant thereof effectively regulates the activity of GPR39 to exhibit anti-diabetic and anti-obesity effects.
Therefore, an object of the present invention is to provide a compound represented by Formula 1 below or a pharmaceutically acceptable salt thereof.
In order to achieve the above object, in one aspect of the present invention, there is provided a compound represented by Formula 1 below or a pharmaceutically acceptable salt thereof:
in Formula 1
A is —C(—R0)—, —N═ or —N(—R1)—,
Cy is C6-14 aryl or 5 to 6-membered heteroaryl,
R1 and R3 are each independently hydrogen, Ra, an amine protecting group, C1-6 alkyl substituted with 1 to 3 Ra, C3-10 cycloalkyl, or 5 to 6-membered heterocyclyl, wherein said heterocyclyl has or does not have 1 to 3 substituents selected from phenylethyl and cyclohexylethyl,
R2 is hydrogen, Ra, or 5 to 6-membered heterocyclyl,
R0 is hydrogen, or R0 and R2 are linked to each other to form a benzene ring together with the two carbon atoms to which they are attached,
Ra is each independently C3-10 cycloalkyl or C6-14 aryl, wherein said aryl has or does not have one or more substituents selected from the group consisting of halogen, —OH, C6-14 aryl substituted with 5 to 6-membered heteroaryl, C1-6 alkyl and C1-6 alkoxy,
n is 1 to 10,
R4 is hydrogen, C1-10 alkyl or C1-C20 alkylcarbonyl,
R5 is hydrogen, halogen, CF3 or C1-6 alkyl,
R6 is hydrogen, C1-10 alkyl or —S(═O)2OH,
R7 and R8 are each independently hydrogen, halogen, nitro, amine or C1-6 alkyl,
R9 is —OH or —NH2, and
R10 is hydrogen, an amine protecting group or biotin, wherein said heterocyclyl and heteroaryl each independently contain at least one heteroatom selected from the group consisting of N, S and O.
In another aspect of the present invention, there is provided a pharmaceutical composition for preventing or treating diabetes mellitus, comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient.
In another aspect of the present invention, there is provided a method for preventing or treating diabetes mellitus, comprising administering the compound or pharmaceutically acceptable salt thereof to a mammal.
In another aspect of the present invention, there is provided the use of the compound or pharmaceutically acceptable salt thereof, for the manufacture of a medicament for preventing or treating diabetes mellitus.
In another aspect of the present invention, there is provided a health functional food composition for preventing or improving diabetes mellitus, comprising the compound or nutritionally acceptable salt thereof as an active ingredient.
In another aspect of the present invention, there is provided a pharmaceutical composition for preventing or treating obesity, comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient.
In another aspect of the present invention, there is provided a method for preventing or treating obesity, comprising administering the compound or pharmaceutically acceptable salt thereof to a mammal.
In another aspect of the present invention, there is provided the use of the compound or pharmaceutically acceptable salt thereof, for the manufacture of a medicament for preventing or treating obesity.
In another aspect of the present invention, there is provided a health functional food composition for preventing or improving obesity, comprising the compound or nutritionally acceptable salt thereof as an active ingredient.
In another aspect of the present invention, there is provided a cosmetic composition for preventing or improving obesity, comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient.
The compound or pharmaceutically acceptable salt thereof according to the present invention selectively and specifically acts as an agonist of GPR39, activates the mechanism of glucose-dependent insulin secretion in pancreatic beta cells, and significantly increases glucose tolerance and an anti-diabetic effect, and therefore can be utilized as a composition for improving, preventing, or treating diabetes mellitus. In addition, the compound or pharmaceutically acceptable salt thereof according to the present invention acts on GPR39 so as to have lipolytic ability in adipocytes and adipose tissue, and therefore can be utilized as a composition for improving, preventing, or treating obesity.
Hereinafter, the present invention will be described in more detail.
In one aspect of the present invention, there is provided a compound represented by Formula 1 below or a pharmaceutically acceptable salt thereof.
in Formula 1
A is —C(—R0)—, —N═ or —N(—R1)—,
Cy is C6-14 aryl or 5 to 6-membered heteroaryl,
R1 and R3 are each independently hydrogen, Ra, an amine protecting group, C1-6 alkyl substituted with 1 to 3 Ra, C3-10 cycloalkyl, or 5 to 6-membered heterocyclyl, wherein said heterocyclyl has or does not have 1 to 3 substituents selected from phenylethyl and cyclohexylethyl,
R2 is hydrogen, Ra, or 5 to 6-membered heterocyclyl, and
R0 is hydrogen, or R0 and R2 are linked to each other to form a benzene ring together with the two carbon atoms to which they are attached,
Ra is each independently C3-10 cycloalkyl or C6-14 aryl, wherein said aryl has or does not have one or more substituents selected from the group consisting of halogen, —OH, C6-14 aryl substituted with 5 to 6-membered heteroaryl, C1-6 alkyl and C1-6 alkoxy,
n is 1 to 10,
R4 is hydrogen, C1-10 alkyl or C1-C20 alkylcarbonyl,
R5 is hydrogen, halogen, CF3 or C1-6 alkyl,
R6 is hydrogen, C1-10 alkyl or —S(═O)2OH,
R7 and R8 are each independently hydrogen, halogen, nitro, amine or C1-6 alkyl,
R9 is —OH or —NH2, and
R10 is hydrogen, an amine protecting group or biotin,
wherein said heterocyclyl and heteroaryl each independently contain at least one heteroatom selected from the group consisting of N, S and O.
In one embodiment of the present invention, the compound may be a peptide, and the peptide may be a derivative of a peptide having a four amino acid sequence, and the four amino acid sequence may be His-Lys-Phe-Tyr (SEQ ID NO: 1).
In accordance with convention used in the art, in the Formula herein, is used to denote a bond that is the point of attachment of a moiety or substituent to a nucleus or framework structure.
As used herein, the term “alkyl” is a hydrocarbon having normal (primary), secondary, tertiary or cyclic carbon atoms. For example, an alkyl group may have 1 to 20 carbon atoms (i.e., C1-C20 alkyl), 1 to 10 carbon atoms (i.e., C1-C10 alkyl), or 1 to 6 carbon atoms (i.e., C1-C6 alkyl). Examples of suitable alkyl groups include methyl (Me, —CH3), ethyl (Et, —CH2CH3), 1-propyl (n-Pr, n-propyl, —CH2CH2CH3), 2-propyl (i-Pr, i-propyl, —CH(CH3)2), 1-butyl (n-Bu, n-butyl, —CH2CH2CH2CH3), 2-methyl-1-propyl (i-Bu, i-butyl, —CH2CH(CH3)2), 2-butyl (s-Bu, s-butyl, —CH(CH3)CH2CH3), 2-methyl-2-propyl (t-Bu, t-butyl, —C(CH3)3), 1-pentyl (n-pentyl, —CH2CH2CH2CH2CH3), 2-pentyl (—CH(CH3)CH2CH2CH3), 3-pentyl (—CH(CH2CH3)2), 2-methyl-2-butyl (—C(CH3)2CH2CH3), 3-methyl-2-butyl (—CH(CH3)CH(CH3)2), 3-methyl-1-butyl (—CH2CH2CH(CH3)2), 2-methyl-1-butyl (—CH2CH(CH3)CH2CH3), 1-hexyl (—CH2CH2CH2CH2CH2CH3), 2-hexyl (—CH(CH3)CH2CH2CH2CH3), 3-hexyl (—CH(CH2CH3)(CH2CH2CH3)), 2-methyl-2-pentyl (—C(CH3)2CH2CH2CH3), 3-methyl-2-pentyl (—CH(CH3)CH(CH3)CH2CH3), 4-methyl-2-pentyl (—CH(CH3)CH2CH(CH3)2), 3-methyl-3-pentyl (—C(CH3)(CH2CH3)2), 2-methyl-3-pentyl (—CH(CH2CH3)CH(CH3)2), 2,3-dimethyl-2-butyl (—C(CH3)2CH(CH3)2), 3,3-dimethyl-2-butyl (—CH(CH3)C(CH3)3, and octyl (—(CH2)7CH3), but are not limited thereto.
As used herein, the term “cycloalkyl” refers to a saturated monocycle or poly-cycle containing only carbon atoms in the ring. A cycloalkyl may have 3 to 7 carbon atoms as a monocycle, 7 to 12 carbon atoms as a bicyclic cycloalkyl, and up to about 20 carbon atoms as a poly-cycle. A monocyclic cycloalkyl has 3 to 6 ring atoms, and more typically 5 or 6 ring atoms. A bicyclic cycloalkyl has 7 to 12 ring atoms arranged in a bicyclo [4,5], [5,5], [5,6] or [6,6] system, or 9 to 10 ring atoms arranged in a bicyclo [5,6] or [6,6] system or a spiro-fused ring. Non-limiting examples of monocyclic cycloalkyls may include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl (each of which may be substituted or unsubstituted).
As used herein, the term “heterocyclyl” includes the radicals of heterocycles described in the literature [Paquette, Leo A.; Principles of Modern Heterocyclic Chemistry (W. A. Benjamin, New York, 1968), specifically Chapters 1, 3, 4, 6, 7 and 9; The Chemistry of Heterocyclic Compounds, A Series of Monographs” (John Wiley & Sons, New York, from 1950 to present), specifically Volumes 13, 14, 16, 19 and 28; and J. Am. Chem. Soc. (1960) 82:5566], but is not limited thereto. The term “heterocyclyl” refers to an aromatic or non-aromatic ring radical that is formed as saturated or unsaturated single or multiple rings and has one or more heteroatoms. For example, “5 to 6-membered heterocyclyl” may refer to a heterocyclyl having a total of 5 to 6 heteroatoms and/or carbon atoms. As used herein, when “heterocyclyl” is described as a substituent, it can be used as a term encompassing “heterocycloalkyl” and “heteroaryl.” Herein, “heterocycloalkyl” refers to a saturated ring radical that is formed as single or multiple rings and has one or more heteroatoms, and “heteroaryl” refers to an aromatic ring radical that is formed as single or multiple rings and has one or more heteroatoms, and “heteroatom” may be selected from N, O and S. Non-limiting examples of heteroaryl rings include all those listed in the definition of “heterocyclyl,” including pyridinyl, pyrrolyl, oxazolyl, indolyl, isoindolyl, purinyl, furanyl, thienyl, benzofuranyl, benzothiophenyl, carbazolyl, imidazolyl, thiazolyl, isoxazolyl, pyrazolyl, isothiazolyl, quinolyl, isoquinolyl, pyridazyl, pyrimidyl, pyrazyl (which may be substituted or unsubstituted), and the like.
As used herein, the term “heteroaryl” refers to an aromatic heterocyclyl having one or more heteroatoms in the ring. Non-limiting examples of suitable heteroatoms that may be included in the aromatic ring include oxygen, sulfur and nitrogen. Non-limiting examples of heteroaryl rings include all those listed in the definition of “heterocyclyl,” including pyridinyl, pyrrolyl, oxazolyl, indolyl, isoindolyl, purinyl, furanyl, thienyl, benzofuranyl, benzothiophenyl, carbazolyl, imidazolyl, thiazolyl, isoxazolyl, pyrazolyl, isothiazolyl, quinolyl, isoquinolyl, pyridazyl, pyrimidyl, pyrazyl (which may be substituted or unsubstituted), and the like.
As used herein, the term “alkoxy” refers to a group having the Formula —O-alkyl, in which an alkyl group as defined above is attached to a parent compound through an oxygen atom. The alkyl portion of the alkoxy group may have 1 to 20 carbon atoms (i.e., C1-C20 alkoxy), 1 to 12 carbon atoms (i.e., C1-C12 alkoxy), or 1 to 6 carbon atoms (i.e., C1-C6 alkoxy). Examples of suitable alkoxy groups include methoxy (—O—CH3 or -OMe), ethoxy (—OCH2CH3 or -OEt), t-butoxy (—O—C(CH3)3 or —O-tBu), and the like, but are not limited thereto.
As used herein, the term “alkylcarbonyl” refers to a group having the Formula —C(═O)-alkyl, in which an alkyl group as defined above is attached to a parent compound through a carbon atom. The alkyl portion of the alkylcarbonyl group may have 1 to 20 carbon atoms (i.e., C1-C20 alkylcarbonyl) or 5 to 17 carbon atoms (i.e., C5-C17 alkylcarbonyl). Examples of suitable alkylcarbonyl groups include caprylic (—C(═O)(CH2)6CH3), capric (—C(═O)(CH2)8CH3), lauric (—C(═O)(CH2)10CH3), myristic (—C(═O)(CH2)12CH3), palmitic (—C(═O)(CH2)14CH3), and the like, but are not limited thereto.
The term “substituted” with respect to alkyl, aryl, heteroaryl, heterocyclyl, carbocyclyl (for example, cycloalkyl), and the like, for example, “substituted alkyl”, “substituted aryl”, “substituted heteroaryl”, “substituted heterocyclyl” and “substituted carbocyclyl (for example, substituted cycloalkyl)” refer to alkyl, aryl, heteroaryl, heterocyclyl, carbocyclyl (for example, cycloalkyl) in which one or more hydrogen atoms are each independently substituted with a non-hydrogen substituent. Typical substituents include —X, —R, —O—, ═O, —OR, —SR, —S—, —NR2, —N+R3, =NR, —C(X)3, —CN, —OCN, —SCN, —N═C═O, —NCS, —NO, —NO2, ═N—OH, =N2, —N3, —NHC(═O)R, —C(═O)R, —C(═O)NRR—S(═O)2O—, —S(═O)2OH, —S(═O)2R, —OS(═O)2OR, —S(═O)2NR, —S(═O)R, —OP (=O)(OR)2, —C(═O)R, alkylene-C(═O)R, —C(S)R, —C(═O)OR, alkylene-C(═O)OR, —C(═O)O—, alkylene-C(═O)O—, —C(═S)OR, —C(═O)SR, —C(═S)SR, —C(═O)NRR, alkylene-C(═O)NRR, —C(═S)NRR, —C(—NR)NRR (wherein, each X is independently halogen: F, Cl, Br, or I, and R is independently H, alkyl, aryl, arylalkyl or heterocycle), but are not limited thereto. Alkylene, alkenylene, and alkynylene groups may also be similarly substituted.
In addition, the present invention includes pharmaceutically acceptable salts and addition salts of the compounds of the present invention, such as hydrochloride, hydrobromide or trifluoroacetate addition salts and sodium, potassium and magnesium salts, but is not limited thereto.
It will be appreciated by one of ordinary skill in the art that when a moiety such as “alkyl”, “aryl”, “heterocyclyl” is substituted by one or more substituents, it may optionally be referred to as a moiety such as “alkylene”, “arylene”, “heterocyclylene” (i.e., meaning that one or more hydrogen atoms of the parent “alkyl”, “aryl”, “heterocyclyl” moiety are substituted with the substituents as stated above). When a moiety such as “alkyl”, “aryl”, “heterocyclyl,” etc. is referred to herein as “substituted” or shown as substituted in the drawings (or optionally substituted, for example, when the number of substituents is from 0 to a positive number), the terms “alkyl”, “aryl”, “heterocyclyl” and the like should be understood as interchangeable with “alkylene”, “arylene”, “heterocyclylene” and the like.
It will be appreciated by one of ordinary skill in the art that the substituents and other moieties of the compound of Formula 1 should be selected to provide a compound that is sufficiently stable to provide a pharmaceutically useful compound that can be formulated into an acceptable stable pharmaceutical composition. The compound of Formula 1 having such stability is considered to be included in the scope of the present invention.
As used herein, the term “optionally substituted” refers to a particular moiety of a compound of Formula 1 having one, two, or more substituents.
In the present invention, the compound represented by Formula 1 may be an optical isomer of an L-form or a D-form.
In the present invention, in the compound represented by Formula 1, A may be —C(—R0)— or —N(—R1)—, and R1 may be hydrogen,
but is not limited thereto. In addition, R0 may be hydrogen, and R2 may be hydrogen,
or, or R0 and R2 may be linked to each other to form a benzene ring together with the two carbon atoms to which they are attached, but is not limited thereto. In addition, R3 may be one selected from the group consisting of
and
preferably, it may be
but is not limited thereto.
In addition, n may be 3 or 4, R4 may be heptylcarbonyl, R5 may be methyl or CF3, R6 may be hydrogen or S(═O)2OH, and R7 and R8 may be each independently hydrogen or amine. In addition, R7 and R8 may be each independently hydrogen, R9 may be —OH, and R10 may be hydrogen, p-toluenesulfonyl (p-Ts), t-butoxycarbonyl (t-Boc) or biotin, but is not limited thereto. In addition, R5, R7 and R8 are not particularly limited at positions to be substituted on the benzene ring. For example, R5 may be substituted at an ortho (o-), meta (m-) or para (p-) position.
It may be any one selected from the group consisting of:
In the present invention, the compound may be (X1)—(X2)-[His(trt)-Lys(caprylic)-Phe-Tyr], wherein X1 and X2 may be each independently any one amino acid selected from 20 amino acids or derivatives thereof, and specifically, it may be 37) Gly-Ser-His(trt)-Lys(caprylic)-Phe-Tyr (SEQ ID NO: 2).
In the present invention, in the compound represented by Formula 1, 1 to 10 amino acids or derivatives thereof may be further bound to the C-terminus of the compound. Specifically, the compound may be [His(trt)-Lys(caprylic)-Phe-Tyr]-(X3)a—(X4)b—(X5)c—(X)a—(X7)e—(X8)f—(X9)g, wherein X3 to X9 may be each independently any one amino acid selected from 20 amino acids or derivatives thereof, and a to g may be 0 or 1, and at least one of them may be 1. More specifically, the compound may be any one selected from the group consisting of 38) His(trt)-Lys(caprylic)-Phe-Tyr-Ser-Asp-Gln-Gln-Ala-Arg-Phe (SEQ ID NO: 3), 39) His(trt)-Lys(caprylic)-Phe-Tyr-Ser-Gln-Asn-Gly-Ala-Arg-Phe (SEQ ID NO: 4), 40) His(trt)-Lys(caprylic)-Phe-Tyr-Ser-His-Gln-Gln-Ala-Arg-Phe (SEQ ID NO: 5), 41) His(trt)-Lys(caprylic)-Phe-Tyr-Gln-Asn-Gly-Ala-Arg-Phe (SEQ ID NO: 6), 42) His(trt)-Lys(caprylic)-Phe-Tyr-His-Gln-Gln-Ala-Arg-Phe (SEQ ID NO: 7), 43) His(trt)-Lys(caprylic)-Phe-Tyr-Gln-Asn-Gln-Ala-Arg-Phe (SEQ ID NO: 8), and 44) His(trt)-Lys(caprylic)-Phe-Tyr-Trp (SEQ ID NO: 9).
In another aspect of the present invention, there is provided a compound or a pharmaceutically acceptable salt thereof, wherein the compound consists of [His(trt)-Lys(caprylic)]-(X10)h-(X11)i, wherein X10 to X11 may be each independently any one amino acid selected from 20 amino acids or derivatives thereof, and h and i may be 0 or 1, and at least one of them may be 1. Specifically, the compound may be any one selected from the group consisting of 45) Biotin-His(trt)-Lys(caprylic)-Ala(biphenyl)-Tyr (SEQ ID NO: 10), 46) His(trt)-Lys(caprylic)-Phe-Trp (SEQ ID NO: 11), 47) His(trt)-Lys(caprylic)-Tyr-Phe (SEQ ID NO: 12), 48) His(trt)-Lys(caprylic)-Tyr-Tyr (SEQ ID NO: 13), 49) His(trt)-Lys(caprylic)-Phe, 50) His(trt)-Lys(caprylic)-Phe-Ser (SEQ ID NO: 14), and 51) His(trt)-Lys(caprylic)-Leu-Tyr (SEQ ID NO: 15).
In another aspect of the present invention, there is provided any one selected from the group consisting of 52) His(trt)-Phe-Tyr-Asp-Gln-Gln-Ala-Arg-Phe (SEQ ID NO: 16), 53) His(trt)-Gly-Ser-Lys(caprylic)-Phe-Tyr (SEQ ID NO: 17), 54) Lys(caprylic)-Phe-Tyr, 55) Lys(caprylic)-His(trt)-Phe-Tyr (SEQ ID NO: 18), 56) His(trt)-Lys(caproic)-Phe-Tyr-Asp-Gln-Gln-Ala-Arg-Phe (SEQ ID NO: 19) and 79) His(benzhydryl)Lys(caprylic).
In the present invention, the compound may be present in a mixture of L-form and D-form amino acids (for example, which may be any one amino acid selected from the group consisting of His, Lys, Phe, Tyr, Ser, Asp, Gln, Ala, Arg and Asn, but is not limited thereto), where “d” means a D-form amino acid.
In the present invention, “trt” is triphenylmethyl, “Boc” is t-butyloxycarbonyl, “tBu” is t-butyl, “Fmoc” is 9-fluorenylmethoxyoxycarbonyl, “dde” is 1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl, and “Bip” is biphenylalanine.
In the present invention, the “biotin” is a kind of vitamin B complex required for the growth of animals and plants. The natural one is a D-form isomer, in which the bond of the two pentagonal rings is in the cis configuration. The other seven isomers, such as L-biotin in cis form or allobiotin in trans form, do not exhibit coenzyme activity.
In the present invention, the “amine protecting group” may be a protecting group selected from the group consisting of t-butyloxycarbonyl (Boc), p-toluenesulfonyl (Ts), fluorenylmethyloxycarbonyl, benzyl, triphenylmethyl and carboxybenzyl, and it may be preferably p-toluenesulfonyl or t-butyloxycarbonyl.
In the present invention, when R10 in the compound represented by Formula 1 is biotin, the biotin may be a compound represented by Formula 2 below.
In Formula 2, n may be 1 to 10, and it may be preferably 4, but is not limited thereto.
In addition, in the present invention, the compound represented by Formula 1 may be represented by Formula 3 below, when A is —N═, R2 is hydrogen, R3 is
n is 4, R4 is heptylcarbonyl, Cy is phenyl, R5 is methyl, R6 is S(═O)2OH, R7, R8 and R10 are each independently hydrogen, and R9 is —OH, and the amino acid of SEQ ID NO: 1 may be a substituted form, such as His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr. The IUPAC name of the compound represented by Formula 3 below is ((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octanamidoh exanamido)-3-(p-tolyl)propanoyl)-L-tyrosine, and in one embodiment of the present invention, it was named HKFY-34.
In one embodiment of the present invention, it was confirmed that the peptide derivative, which is a compound having the structure of Formula 1 according to the present invention, selectively and specifically binds to GPR39 (G protein-coupled receptor 39), one of the orphan G protein-coupled receptor (orphan GPCR), which is a membrane protein (Tables 3 to 5 and
In addition, in one embodiment of the present invention, when rat insulinoma cells or rat islet cells were treated with the peptide derivative according to the present invention, glucose-dependent insulin secretion ability was enhanced through the GPR39 receptor (
Therefore, in another aspect of the present invention, there is provided a pharmaceutical composition for preventing or treating diabetes mellitus, comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient.
As used herein, the term “diabetes mellitus” is a type of metabolic diseases such as insufficient insulin secretion or failure to function normally. Diabetes mellitus is characterized by high blood glucose in which the concentration of glucose in the blood is elevated, and high blood glucose causes various symptoms and signs and causes the excretion of glucose in the urine. Diabetes mellitus is divided into type 1 and type 2. Type 1 diabetes mellitus, previously called ‘juvenile diabetes mellitus’, is a disease caused by the inability to produce insulin at all. Type 2 diabetes mellitus, which is relatively deficient in insulin, is characterized by insulin resistance. Type 2 diabetes mellitus seems to be largely caused by environmental factors such as high calorie, high fat, high protein diet due to westernization of diet, lack of exercise, and stress, but in addition to the above, diabetes mellitus can be caused by a defect in a specific gene, and can also be caused by pancreatic surgery, infection, or drugs. In the present invention, the “diabetes mellitus” may include type 1 or type 2, and may refer to a chronic disease caused by a lack of insulin causing glucose tolerance.
In addition, the present invention provides a method for preventing or treating diabetes mellitus, comprising administering the compound or pharmaceutically acceptable salt thereof to a mammal.
In addition, the present invention provides the use of the compound or pharmaceutically acceptable salt thereof, for the manufacture of a medicament for preventing or treating diabetes mellitus.
The “pharmaceutical composition” may be administered orally, intramuscularly or subcutaneously. Formulations for oral administration may take various forms such as syrups, tablets, capsules, creams and lozenges. Syrup formulations generally comprise a suspension or solution of the compound or a salt thereof in a liquid carrier such as ethanol, peanut oil, olive oil, glycerin or water, and optionally comprise a sweetening agent or a coloring agent. When the composition is in the form of a tablet, any pharmaceutical carrier generally used for the preparation of solid formulations may be used. Examples of such carriers include magnesium stearate, white clay, talc, gelatin, acacia, stearic acid, starch, lactose and sucrose. When the composition is in the form of a capsule, any conventional encapsulation process may be used, for example, the carrier may be included in a hard gelatin capsule shell. When the composition is formulated in the form of a soft gelatin capsule shell, any pharmaceutical carrier generally used for the preparation of dispersions or suspensions may be used, and such carriers are aqueous gum, cellulose, silicate or oil. Formulations for intramuscular or subcutaneous administration may be prepared in a liquid form, such as solutions, suspensions and emulsions including aqueous solvents such as water, physiological saline and Ringer's solution; or lipophilic solvents such as fatty oil, sesame oil, corn oil and synthetic fatty acid esters.
The composition is preferably formulated in a dosage form specific to a particular patient.
For each unit dose for oral administration, it is preferable to contain the compound of Formula 1 or a pharmaceutically acceptable salt thereof in an amount of 0.1 mg/kg to 500 mg/kg, 1 mg/kg to 100 mg/kg, or 10 mg/kg to 50 mg/kg.
A daily administration dose suitable for oral administration is about 0.01 to 40 mg/kg of the compound of Formula 1 or a pharmaceutically acceptable salt thereof, and may be administered 1 to 6 times a day depending on the condition of the patient.
In another aspect of the present invention, there is provided a health functional food composition for preventing or improving diabetes mellitus, comprising the compound or nutritionally acceptable salt thereof as an active ingredient.
The health functional food according to the present invention may be in the form of powder, granule, tablet, capsule or beverage, and may be candy, chocolate, gum, tea, vitamin complex, health supplement food, and the like.
In this case, the content of the compound or pharmaceutically acceptable salt thereof according to the present invention included in the health functional food may be typically 0.01 to 50% by weight, or 0.1 to 20% by weight of the total food weight. In addition, in the case of the health beverage composition, it may be included in an amount of 0.02 to 10 g, or 0.3 to 1 g, based on 100 mL of the health beverage composition.
The food may further include a nutritionally acceptable food supplementary additive together with the compound or pharmaceutically acceptable salt thereof of the present invention.
In one embodiment of the present invention, it was confirmed that the lipolytic ability was excellent when 3T3-L1 cells and WAT cells were treated with the peptide derivative according to the present invention (
Therefore, in another aspect of the present invention, there is provided a pharmaceutical composition for preventing or treating obesity, comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient.
As used herein, the term “obesity” refers to a state in which adipose tissue is excessive in the body, and when an excessive amount of nutrients is consumed compared to energy consumption over a long period of time, obesity is induced by energy imbalance. There are cases where it is caused by a problem with the function of the appestat due to genetic mutations in specific genes, or it is caused by endocrine diseases such as Cushing's syndrome and various drugs that increase appetite, but in general, it occurs because energy intake is greater than energy consumption. In general, obesity is caused by a combination of genetic and environmental influences. In particular, the modem living environment, which is rich in high-calorie foods and does not cause inconvenience even with less physical activity, is causing an explosive increase in obesity.
In addition, the present invention provides a method for preventing or treating obesity, comprising administering the compound or pharmaceutically acceptable salt thereof to a mammal.
In addition, the present invention provides the use of the compound or pharmaceutically acceptable salt thereof, for the manufacture of a medicament for preventing or treating obesity.
In another aspect of the present invention, there is provided a health functional food composition for preventing or improving obesity, comprising the compound or nutritionally acceptable salt thereof as an active ingredient.
In another aspect of the present invention, there is provided a cosmetic composition for preventing or improving obesity, comprising the compound or pharmaceutically acceptable salt thereof as an active ingredient.
Hereinafter, the present invention will be described in detail by way of Examples. However, the following examples are only for illustrating the present invention, and the present invention is not limited to the following examples.
In order to prepare His(trt)-Lys(caprylic)-Phe-Tyr (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine, HKFY-1), Fmoc-Tyr(tBu) and DMF (dimethylformamide) were loaded onto the trityl resin to prepare Fmoc-Tyr(tBu)-trityl resin. DMF containing 20% piperidine and Fmoc-Phe-OH and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Tyr(tBu)-trityl resin to prepare Fmoc-Phe-Tyr(tBu)-trityl resin.
DMF containing 2% NH2NH2·H2O was added to Fmoc-Lys(dde)-OH, and dde was removed to prepare Fmoc-Lys-OH. DMF containing caprylic acid and HOBt and DIC was added to the Fmoc-Lys-OH to prepare Fmoc-Lys(caprylic acid)-OH.
DMF containing 20% piperidine was added to the Fmoc-Phe-Tyr(tBu)-trityl resin, and HOBt (hydroxyl-benzo triazole) was added to the Fmoc-Lys(caprylic acid)-OH to prepare Fmoc-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin.
DMF containing 20% piperidine was added to the Fmoc-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin, and Boc-His(trt)-OH and HOBt (hydroxyl-benzo triazole) were added to prepare Boc-His(trt)-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin.
The protecting group was cleaved from the Boc-His(trt)-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin and then purified to prepare His(trt)-Lys(caprylic acid)-Phe-Tyr.
The purity, molecular weight and 1H NMR of the HKFY-1 are shown in
In order to prepare biotin ((S)-3-([1,1′-biphenyl]-4-yl)-2-((S)-6-octanamido-2-((S)-2-(5-((3aS,4S,6aR)-2-oxohexahydro -1H-thieno[3,4-d]imidazol-4-yl)pentanamido)-3-(1-trityl-1H-imidazol-4-yl)propanamido)hex anamido)propanoyl)-L-tyrosine, DMF containing 20% piperidine was added to the Fmoc-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin obtained from Example 1.1, and Fmoc-His(trt)-OH was added to prepare Fmoc-His(trt)-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin. D-biotin was added to the resin in the same manner to prepare D-biotin-His(trt)-Lys(caprylic acid)-Phe-Tyr(tBu)-trityl resin.
The protecting group of the resin was cleaved and then purified to prepare biotin-His(trt)-Lys(caprylic acid)-Phe-Tyr (N6-octanoyl-N2—(Na-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pent anoyl)-Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine).
The purity, molecular weight and 1H NMR of the HKFY-2 are shown in
His(benzyl)-Lys(caprylic)-Phe-Tyr (N2-(Nt-benzyl-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(benzyl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-3 are shown in
d-His(trt)-Lys(caprylic)-Phe-Tyr (N6-octanoyl-N2-(Nt-trityl-D-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-d-His(trt) was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-4 are shown in
His(4-methyltrityl)-Lys(caprylic)-Phe-Tyr (N2-(Nt-(diphenyl (p-tolyl)methyl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(4-methyltrityl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-5 are shown in
His(DAMP-3)-Lys(caprylic)-Phe-Tyr (N2-((S)-2-amino-3-(1,3-diphenethyl-2,3-dihydro-1H-imidazol-4-yl)propanoyl)-N6-octanoyl -L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(DAMP-3)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-6 are shown in
His(DAMP-5)-Lys(caprylic)-Phe-Tyr (N2-((S)-2-amino-3-(3-(2-cyclohexvlethyl)-2,3-dihydro-1H-imidazol-4-yl)propanoyl)-N6-oct anoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(DAMP-5)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-7 are shown in
His(DAMP-2)-Lys(caprylic)-Phe-Tyr (N2-((S)-2-amino-3-(1,3-bis(2-cyclohexylethyl)-2,3-dihydro-1H-imidazol-4-yl)propanoyl)-N 6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(DAMP-2)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-8 are shown in
His(DAMP-2)-Lys(caprylic)-Phe-Tyr (N6-octanoyl-N2-(Nt-phenethyl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(2-phenylethyl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-9 are shown in
His(2-naphthalen-1-methyl)-Lys(caprylic)-Phe-Tyr (N2-(Nt-(naphthalen-1-ylmethyl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(2-naphthalen-1-methyl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-10 are shown in
His(2-cyclohexylethyl)-Lys(caprylic acid)-Phe-Tyr (N2-(Nt-(2-cyclohexylethyl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(2-cyclohexylethyl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-11 are shown in
In order to prepare His(trt)-Lys(caprylic)-d-Phe-Tyr (N6-decanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-D-phenylalanyl-L-tyrosine, HKFY-12), Fmoc-Tyr(tBu) and DMF (dimethylformamide) were loaded onto the trityl resin to prepare Fmoc-Tyr(tBu)-trityl resin. DMF containing 20% piperidine and Fmoc-d-Phe-OH of Formula 8 and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Tyr(tBu)-trityl resin to prepare Fmoc-d-Phe-Tyr(tBu)-trityl resin.
Fmoc-Lys(caprylic acid)-OH and HOBt (hydroxyl-benzo triazole) were added to the Fmoc-d-Phe-Tyr(tBu)-trityl resin to prepare Fmoc-Lys(caprylic acid)-d-Phe-Tyr(tBu)-trityl resin. DMF containing 20% piperidine was added to Fmoc-Lys(caprylic acid)-d-Phe-Tyr(tBu)-trityl resin, and Boc-His(trt)-OH and HOBt (hydroxyl-benzo triazole) were added to prepare Boc-His(trt)-Lys(caprylic acid)-d-Phe-Tyr(tBu)-trityl resin.
The protecting group was cleaved from the Boc-His(trt)-Lys(caprylic acid)-d-Phe-Tyr(tBu)-trityl resin and then purified to prepare His(trt)-Lys(caprylic)-d-Phe-Tyr.
The purity and molecular weight of the HKFY-12 are shown in
His(trt)-Lys(caprylic)-d-Phe(4-Cl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-(non-1-en-2-ylami no)hexanamido)-3-(4-chlorophenyl)propanoyl)-L-tyrosine, HKFY-13) was prepared in the same manner except that Fmoc-d-Phe(4-Cl)—OH was used instead of Fmoc-d-Phe-OH obtained during the preparation process of Example 1.6.
The purity and molecular weight of the HKFY-13 are shown in
Fmoc-d-Tyr(tBu)-trityl resin was prepared in the same manner except that Fmoc-d-Tyr(tBu)-OH was used instead of Fmoc-Tyr(tBu)-OH obtained during the preparation process of Example 1.13. During the subsequent process, Boc-His(trt)-OH was changed to Boc-d-His(trt)-OH to prepare d-His(trt)-Lys(caprylic)-d-Phe(4-Cl)-d-Tyr (((R)-2-((S)-2-((R)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(4-chlorophenyl)propanoyl)-D-tyrosine).
The purity and molecular weight of the HKFY-14 are shown in
His(trt)-Lys(caprylic)-d-Phe(4-Cl)-d-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(4-chlorophenyl)propanoyl)-D-tyrosine) was prepared in the same manner except that Boc-His(trt)-OH was used instead of Boc-d-His(trt)-OH obtained during the preparation process of Example 1.14.
The purity and molecular weight of the HKFY-15 are shown in
His(trt)-d-Lys(caprylic)-d-Phe(4-Cl)-Tyr (((R)-2-((R)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(4-chlorophenyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Fmoc-d-Lys(caprylic)-OH was used by replacing Fmoc-Lys(dde)-OH with Fmoc-d-Lys(dde)-OH in the preparation process using Fmoc-Lys(caprylic)-OH instead of Fmoc-Lys(dde)-OH obtained during the preparation process of Example 1.13.
The purity and molecular weight of the HKFY-16 are shown in
His(3,3-diphenylethyl)-Lys(caprylic acid)-Phe-Tyr (N2-(Nt-(2,2-diphenylethyl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(3,3-diphenylethyl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-17 are shown in
His(Fm)-Lys(caprylic acid)-Phe-Tyr (N2-(Nt-(9H-fluoren-9-yl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(Fm)—OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-18 are shown in
His(phenylethyl)-Lys(caprylic acid)-Phe-Tyr (N6-octanoyl-N2-(Nt-phenethyl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(phenylethyl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-19 are shown in
His(methoxylbenzhydryl)-Lys(caprylic acid)-Phe-Tyr (N2-(Nt-((4-methoxyphenyl)(phenyl)methyl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalany 1-L-tyrosine) was prepared in the same manner except that Boc-His(methoxylbenzhydryl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-20 are shown in
His(4-chlorobenzhydryl)-Lys(caprylic acid)-Phe-Tyr (N2-(Nt-((R)-(4-chlorophenyl)(phenyl)methyl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylala nyl-L-tyrosine) was prepared in the same manner except that Boc-His(4-chlorobenzhydryl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-21 are shown in
His(methylbenzhydryl)-Lys(caprylic acid)-Phe-Tyr (N6-octanoyl-N2-(Nt-((R)-phenyl (p-tolyl)methyl)-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(methylbenzhydryl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-22 are shown in
His(adamantan-1-yl)-Lys(caprylic acid)-Phe-Tyr (N2-(Nt-(adamantan-1-yl)-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(adamantan-1-yl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-23 are shown in
His(trt)-Lys(capric)-Phe-Tyr (N6-decanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine, HKFY-24) was prepared in the same manner except that capric acid instead of caprylic acid was added to Fmoc-Lys-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-24 are shown in
His(trt)-Lys(lauric)-Phe-Tyr (N6-dodecanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine, HKFY-25) was prepared in the same manner except that lauric acid instead of caprylic acid was added to Fmoc-Lys-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-25 are shown in
His(trt)-Lys(myristic)-Phe-Tyr (N6-tetradecanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine, HKFY-26) was prepared in the same manner except that myristic acid instead of caprylic acid was added to Fmoc-Lys-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-26 are shown in
His(trt)-Lys(palmitic)-Phe-Tyr (N6-palmitoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosine, HKFY-27) was prepared in the same manner except that palmitic acid instead of caprylic acid was added to Fmoc-Lys-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-27 are shown in
His(trt)-Lys(caprylic)-d-Phe(4-F)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(4-fluorophenyl)propanoyl)-L-tyrosine, HKFY-28) was prepared in the same manner except that Fmoc-d-Phe(4-F)—OH was used instead of Fmoc-d-Phe-OH obtained during the preparation process of Example 1.6.
The purity and molecular weight of the HKFY-28 are shown in
His(trt)-Lys(caprylic)-d-Phe(4-Br)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(4-bromophenyl)propanoyl)-L-tyrosine, HKFY-29) was prepared in the same manner except that Fmoc-d-Phe(4-Br)—OH was used instead of Fmoc-d-Phe-OH obtained during the preparation process of Example 1.6.
The purity and molecular weight of the HKFY-29 are shown in
His(trt)-Lys(caprylic)-d-Phe(4-methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(p-tolyl)propanoyl)-L-tyrosine, HKFY-30) was prepared in the same manner except that Fmoc-d-Phe(4-methyl)-OH was used instead of Fmoc-d-Phe-OH obtained during the preparation process of Example 1.6.
The purity and molecular weight of the HKFY-30 are shown in
d-His(trt)-Lys(caprylic)-d-Phe(4-methyl)-Tyr ((R)-2-((S)-2-((R)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-d-His(trt)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.30.
The purity and molecular weight of the HKFY-31 are shown in
His(1,3-difluorobenzhydryl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((2R)-2-((2S)-2-((2S)-2-amino-3-(1-((2,4-difluorophenyl)(phenyl)methyl)-1H-imidazol-4-yl)propanamido)-6-octanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(1,3-difluorobenzhydryl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34. below.
The purity and molecular weight of the HKFY-32 are shown in
His(benzhydryl)-Lys(caprylic)-Phe-Tyr (N2-(Nt-benzhydryl-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine) was prepared in the same manner except that Boc-His(benzhydryl)-OH was used instead of Boc-His(trt)-OH obtained during the preparation process of Example 1.1.
The purity and molecular weight of the HKFY-33 are shown in
In order to prepare His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octanamidoh exanamido)-3-(p-tolyl)propanoyl)-L-tyrosine, HKFY-34), Fmoc-Tyr(tBu) and DMF (dimethylformamide) were loaded onto the trityl resin to prepare Fmoc-Tyr(tBu)-trityl resin. DMF containing 20% piperidine and Fmoc-d-Phe(4-methyl)-OH and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Tyr(tBu)-trityl resin to prepare Fmoc-d-Phe(4-methyl)-Tyr(tBu)-trityl resin.
DMF containing 2% NH2NH2H2O was added to Fmoc-Lys(dde)-OH, and dde was removed to prepare Fmoc-Lys-OH. DMF containing caprylic acid, HOBt and DIC was added to the Fmoc-Lys-OH to prepare Fmoc-Lys(caprylic acid)-OH, and Boc-His(trt)-OH was used to prepare Boc-His(benzhydryl)-OH.
DMF containing 20% piperidine was added to the Fmoc-d-Phe(4-methyl)-Tyr(tBu)-trityl resin, and HOBt (hydroxyl-benzo triazole) was added to the Fmoc-Lys(caprylic acid)-OH to prepare Fmoc-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr(tBu)-trityl resin. DMF containing 20% piperidine was added to Fmoc-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr(tBu)-trityl resin, and Boc-His(benzhydryl)-OH and HOBt (hydroxyl-benzo triazole) were added to prepare a peptide of Boc-His(benzhydryl)-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr(tBu)-trityl resin.
The protecting group was cleaved from the Boc-His(benzhydryl)-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr(tBu)-trityl resin and then purified to prepare His(benzhydryl)-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr-OH.
The purity, molecular weight and 1H NMR of the HKFY-34 are shown in
His(benzhydryl)-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr ((SO3H)—OH (S)-2-((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanamido)-3-(4-(sulfooxy)phenyl)propanoic acid) was prepared in the same manner except that Fmoc-Tyr(SO3H)—OH was used instead of Fmoc-Tyr(tBu)-OH obtained during the preparation process of Example 1.34.
The purity and molecular weight of the HKFY-35 are shown in
His(benzhydryl)-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr ((2.6-di-methyl)-OH (S)-2-((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanamido)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid) was prepared in the same manner except that Fmoc-Tyr(2.6-di-methyl)-OH was used instead of Fmoc-Tyr(tBu)-OH obtained during the preparation process of Example 1.34.
The purity and molecular weight of the HKFY-36 are shown in
DMF containing 20% piperidine was added to Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr-OH-trityl resin obtained during the preparation process of Example 1.1., and HOBt (hydroxyl-benzo triazole) was added to Fmoc-Ser(tBu)-OH to prepare Fmoc-Ser(tBu)-His(trt)-Lys(caprylic)-Phe-Tyr-OH-trityl resin. DMF containing 20% piperidine was added to the resin, and HOBt (hydroxyl-benzo triazole) was added to Fmoc-Gly-OH to prepare Fmoc-Gly-Ser(tBu)-His(trt)-Lys(caprylic)-Phe-Tyr-OH-trityl resin.
The protecting group was cleaved from the Fmoc-Gly-Ser(tBu)-His(trt)-Lys(caprylic)-Phe-Tyr-OH-trityl resin and then purified to prepare Gly-Ser-His(trt)-Lys(caprylic acid)-Phe-Tyr (N2-(Na-glycyl-L-seryl-Nt-trityl-L-histidyl)-N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine).
The purity and molecular weight of the HKFY-37 are shown in
In order to prepare HKFY-38 ((3S,6S,9S,12S,15S)-15-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-12-benzyl-3-(((6S,9S,12S,15S)-1,18-diamino-6-(((S)-1-amino-1-oxo-3-phenylpropan-2-yl)carbamoyl)-1 2-(3-amino-3-oxopropyl)-1-imino-9-methyl-8,11,14,18-tetraoxo-2,7,10,13-tetraazaoctadecan-15-yl)carbamoyl)-9-(4-hydroxybenzyl)-6-(hydroxymethyl)-5,8,11,14,21-pentaoxo-4,7,10,13, 20-pentaazaoctacosanoic acid), Fmoc-Phe-OH and DMF (dimethylformamide) were loaded onto the trityl resin to prepare Fmoc-Phe-trityl resin. DMF containing 20% piperidine and Fmoc-Arg(pbf)-OH and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Phe-trityl resin to prepare Fmoc-Arg(pbf)-Phe-trityl resin. DMF containing 20% piperidine and Fmoc-Ala-OH and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Arg(pbf)-Phe-trityl resin to prepare Fmoc-Ala-Arg(pbf)-Phe-trityl resin. Fmoc-Gln(trt)-OH, Fmoc-Gln(trt)-OH, Fmoc-Asp(tBu)-OH, Fmoc-Ser(tBu)-OH, Fmoc-Tyr(tbu)-OH, Fmoc-Phe-OH were sequentially added in the same manner as above to prepare Fmoc-Phe-Tyr(tBu)-Ser(tBu)-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin.
DMF containing 20% piperidine and Fmoc-Lys(caprylic)-OH obtained from Example 1.1. and HOBt (hydroxyl-benzo triazole) were added to the resin to prepare Fmoc-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trit yl resin.
DMF containing 20% piperidine and Fmoc-His(trt)-OH obtained from Example 1.1. and HOBt (hydroxyl-benzo triazole) were added to the resin to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin.
The protecting group was cleaved from the Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin and then purified to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Ser-Asp-Gln-Gln-Ala-Arg-Phe.
The purity and molecular weight of the HKFY-38 are shown in
In order to prepare HKFY-39 ((3S,6S,9S,12S,15S,18S)-3-((2-(((S)-1-(((S)-1-(((S)-1-amino-1-oxo-3-phenylpropan-2-yl)ami no)-5-guanidino-1-oxopentan-2-yl)amino)-1-oxopropan-2-yl)amino)-2-oxoethyl)carbamoyl)-18-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-(3-amino-3-oxopropyl)-15-be nzyl-12-(4-hydroxybenzyl)-9-(hydroxymethyl)-5,8,11,14,17,24-hexaoxo-4,7,10,13,16,23-hex aazahentriacontanoic acid), DMF containing 20% piperidine and Fmoc-Gly-OH and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Ala-Arg(pbf)-Phe-trityl resin obtained from Example 1.38. to prepare Fmoc-Gly-Ala-Arg(pbf)-Phe-trityl resin. DMF containing 20% piperidine and Fmoc-Asn(trt)-OH and HOBt (hydroxyl-benzo triazole) were added to Fmoc-Gly-Ala-Arg(pbf)-Phe-trityl resin to prepare Fmoc-Asn(trt)-Gly-Ala-Arg(pbf)-Phe-trityl resin. Fmoc-Gln(trt)-OH, Fmoc-Ser(tBu)-OH, Fmoc-Tyr(tbu)-OH, Fmoc-Phe-OH were sequentially added in the same manner as above to prepare Fmoc-Phe-Tyr(tBu)-Ser(tBu)-Gln(trt)-Asn(trt)-Gly-Ala-Arg(pbf)-Phe-trityl resin. Fmoc-Lys(caprylic)-OH obtained from Example 1.1. and HOBt (hydroxyl-benzo triazole) were added to the resin to prepare Fmoc-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-Gln(trt)-Asn(trt)-Gly-Ala-Arg(pbf)-Phe-trityl resin.
DMF containing 20% piperidine and Fmoc-His(trt)-OH obtained from Example 1.1. and HOBt (hydroxyl-benzo triazole) were added to the resin to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-Gln(trt)-Asn(trt)-Gly-Ala-Arg(pbf)-Phe-t rityl resin.
The protecting group was cleaved from the Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-Gln(trt)-Asn(trt)-Gly-Ala-Arg(pbf)-Phe-t rityl resin and then purified to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Ser-Gln-Asn-Gly-Ala-Arg-Phe.
The purity and molecular weight of the HKFY-39 are shown in
DMF containing 20% piperidine and Fmoc-Gln(trt)-OH and HOBt (hydroxyl-benzo triazole) were added to the Fmoc-Ala-Arg(pbf)-Phe-trityl resin obtained from Example 1.39. to prepare Fmoc-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin.
Fmoc-Gln(trt)-OH, Fmoc-His(trt)-OH, Fmoc-Ser(tBu)-OH, Fmoc-Tyr(tBu)-OH, Fmoc-Phe( )-OH were sequentially added in the same manner to prepare Fmoc-Phe-Tyr(tBu)-Ser(tBu)-His(trt)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin.
Fmoc-Lys(caprylic)-OH obtained from Example 1.1. and Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-His(trt)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-P he-trityl resin.
The protecting group was cleaved from the Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Ser(tBu)-His(trt)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-P he-trityl resin and then purified to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Ser-His-Gln-Gln-Ala-Arg-Phe ((S)-2-((2S,5S,8S,11S,14S)-2-((1H-imidazol-4-yl)methyl)-14-((S)-2-amino-3-(1-trityl-1H-im idazol-4-yl)propanamido)-11-benzyl-8-(4-hydroxybenzyl)-5-(hydroxymethyl)-4,7,10,13,20-pentaoxo-3,6,9,12,19-pentaazaheptacosanamido)-N1-((S)-5-amino-1-(((S)-1-(((S)-1-(((S)-1-a mino-1-oxo-3-phenylpropan-2-yl)amino)-5-guanidino-1-oxopentan-2-yl)amino)-1-oxopropan -2-yl)amino)-1,5-dioxopentan-2-yl)pentanediamide).
The purity and molecular weight of the HKFY-40 are shown in
DMF containing 20% piperidine and Fmoc-Gly-OH and HOBt (hydroxyl-benzo triazole) were added to the Fmoc-Ala-Arg(pbf)-Phe-trityl resin obtained from Example 1.39. to prepare Fmoc-Gly-Ala-Arg(pbf)-Phe-trityl resin. Fmoc-Asn(trt)-OH, Fmoc-Gln(trt)-OH, Fmoc-Tyr(tBu)-OH, Fmoc-Phe-OH, Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Gln(trt)-Asn(trt)-Gly-Ala-Arg(pbf)-Phe-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Gln-Asn-Gly-Ala-Arg-Phe ((3S,6S,9S,12S,15S,18S)-3-((2-(((S)-1-(((5)-1-(((5)-1-amino-1-oxo-3-phenylpropan-2-yl)ami no)-5-guanidino-1-oxopentan-2-yl)amino)-1-oxopropan-2-yl)amino)-2-oxoethyl)carbamoyl)-18-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-(3-amino-3-oxopropyl)-15-be nzyl-12-(4-hydroxybenzyl)-9-(hydroxymethyl)-5,8,11,14,17,24-hexaoxo-4,7,10,13,16,23-hex aazahentriacontanoic acid).
The purity and molecular weight of the HKFY-41 are shown in
DMF containing 20% piperidine and Fmoc-Gln(trt) and HOBt (hydroxyl-benzo triazole) were added to the Fmoc-Ala-Arg(pbf)-Phe-trityl resin obtained from Example 1.39. to prepare Fmoc-Gly-Ala-Arg(pbf)-Phe-trityl resin. Fmoc-Gln(trt)-OH, Fmoc-His(trt)-OH, Fmoc-Tyr(tBu)-OH, Fmoc-Phe-OH, Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-His(trt)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe-Tyr-His-Gln-Gln-Ala-Arg-Phe ((S)-2-((2S,5S,8S,11S)-2-((1H-imidazol-4-yl)methyl)-11-((S)-2-amino-3-(1-trityl-1H-imidaz ol-4-yl)propanamido)-8-benzyl-5-(4-hydroxybenzyl)-4,7,10,17-tetraoxo-3,6,9,16-tetraazatetr acosanamido)-N1-((S)-5-amino-1-(((S)-1-(((S)-1-(((S)-1-amino-1-oxo-3-phenylpropan-2-yl)a mino)-5-guanidino-1-oxopentan-2-yl)amino)-1-oxopropan-2-yl)amino)-1,5-dioxopentan-2-yl)pentanediamide).
The purity and molecular weight of the HKFY-42 are shown in
Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Gln(trt)-Asn(trt)-Gln(trt)-Ala-Arg(pbf)-P he-trityl resin was prepared in the same manner except that Fmoc-Gln(trt)-OH was used instead of Fmoc-Gly-OH among the constituent amino acids of Example 1.41. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Gln-Asn-Gln-Ala-Arg-Phe ((S)-N1-((S)-1-(((S)-1-(((S)-1-amino-1-oxo-3-phenylpropan-2-yl)amino)-5-guanidino-1-oxop entan-2-yl)amino)-1-oxopropan-2-yl)-2-((2S,5S,8S,11S,14S)-2-(2-amino-2-oxoethyl)-14-((S) -2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-5-(3-amino-3-oxopropyl)-11-benzyl-8-(4-hydroxybenzyl)-4,7,10,13,20-pentaoxo-3,6,9,12,19-pentaazaheptacosanamido)pentanediam ie).
The purity and molecular weight of the HKFY-43 are shown in
In order to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Trp, Fmoc-Trp(Boc)-OH and DMF were loaded onto the trityl resin to prepare Fmoc-Trp(Boc)-trityl resin. DMF containing 20% piperidine and Fmoc-Tyr(tBu)-OH and HOBt (hydroxyl-benzo triazole) were added to the Fmoc-Trp(Boc)-trityl resin to prepare Fmoc-Tyr(tBu)-Trp(Boc)-trityl resin.
Fmoc-Phe-OH, Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Tyr(tBu)-Trp(Boc)-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe-Tyr-Trp (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-tyrosvl-L-tryptophan).
The purity and molecular weight of the HKFY-44 are shown in
D-biotin-His(trt)-K(caprylic)-Ala(biphenyl)-Tyr(Boc)-trityl resin was prepared in the same manner except that Fmoc-Ala(biphenyl)-OH was used instead of Fmoc-Phe-OH during the preparation process of Example 1.2. The protecting group of the resin was cleaved to prepare biotin-His(trt)-K(caprylic)-Ala(biphenyl)-Tyr (((S)-3-(1,1′-biphenyl-4-yl)-2-((S)-6-octanamido-2-((S)-2-(5-((3aS,4S,6aR)-2-oxohexahydr o-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)-3-(1-trityl-1H-imidazol-4-yl)propanamido)he xanamido)propanoyl)-L-tyrosine).
The purity and molecular weight of the HKFY-45 are shown in
Fmoc-Phe-OH and DMF were loaded onto the Fmoc-Trp(Boc)-trityl resin obtained from Example 1.44. to prepare Fmoc-Trp(Boc)-trityl resin. Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Trp(Boc)-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe-Trp(N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl -L-tryptophan).
The purity and molecular weight of the HKFY-46 are shown in
In order to prepare N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-tyrosyl-L-phenylalanine, Fmoc-Phe-OH and DMF were loaded onto the trityl resin to prepare Fmoc-Phe-trityl resin. Fmoc-Tyr(Boc)-OH, Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Tyr(Boc)-Phe-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Tyr-Phe (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-tyrosyl-L-phenylalanine).
The purity and molecular weight of the HKFY-47 are shown in
In order to prepare HKFY-48 (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-tyrosyl-L-tyrosine), Fmoc-Tyr(Boc)-OH and DMF were loaded onto the trityl resin to prepare Fmoc-Tyr(Boc)-trityl resin. Fmoc-Tyr(Boc)-OH, Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Tyr(Boc)-Tyr(Boc)-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Tyr-Tyr(N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-tyrosyl-L-tyr osine).
The purity and molecular weight of the HKFY-48 are shown in
In order to prepare HKFY-49 (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanine), Fmoc-Lys(caprylic)-OH obtained from Example 1.1., and Fmoc-His(trt)-OH were sequentially added to the Fmoc-Phe-trityl resin obtained from Example 1.47. in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe.
The purity and molecular weight of the HKFY-49 are shown in
In order to prepare HKFY-50 (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-phenylalanyl-L-serine), Fmoc-Ser(tBu)-OH and DMF were loaded onto the trityl resin to prepare Fmoc-Ser(tBu)-trityl resin. Fmoc-Phe-OH, Fmoc-Lys(caprylic)-OH obtained from Example 1.1., and Fmoc-His(trt)-OH were sequentially added to the resin in the same manner to prepare Fmoc-His(trt)-Lys(caprylic)-Phe-Ser-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caprylic)-Phe-Ser.
The purity and molecular weight of the HKFY-50 are shown in
His(trt)-Lys(caprylic)-Leu-Tyr (N6-octanoyl-N2-(Nt-trityl-L-histidyl)-L-lysyl-L-leucyl-L-tyrosine) was prepared in the same manner except that Fmoc-Leu-OH was used instead of Fmoc-Tyr(Boc)-OH among the constituent amino acids of Example 1.48.
The purity and molecular weight of the HKFY-51 are shown in
Fmoc-Asp(tBu)-OH, Fmoc-Tyr(Boc)-OH, Fmoc-Phe-OH, and Fmoc-His(trt)-OH were sequentially added to the Fmoc-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin obtained from Example 1.38. in the same manner to prepare Fmoc-His(trt)-Phe-Tyr(Boc)-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Phe-Tyr-Asp-Gln-Gln-Ala-Arg-Phe ((6S,9S,12S,15S,18S)-1-amino-6-(((S)-1-amino-1-oxo-3-phenylpropan-2-yl)carbamoyl)-18-((S)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-3-phenylpropanamido) -3-(4-hydroxyphenyl)propanamido)-12,15-bis(3-amino-3-oxopropyl)-1-imino-9-methyl-8,11, 14,17-tetraoxo-2,7,10,13,16-pentaazaicosan-20-oic acid).
The purity and molecular weight of the HKFY-52 are shown in
Fmoc-Lys(caprylic)-OH obtained from Example 1.1., Fmoc-Ser(tBu)-OH, Fmoc-Gly-OH, and Fmoc-His(trt)-OH were sequentially added to the Fmoc-Phe-Tyr(Boc)-trityl resin obtained from Example 1.47. in the same manner to prepare Fmoc-His(trt)-Gly-Ser(tBu)-Lys(caprylic)-Phe-Tyr(Boc)-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Gly-Ser-Lys(caprylic)-Phe-Tyr (N6-octanoyl-N2-(Nt-trityl-L-histidylglycyl-L-seryl)-L-lysyl-L-phenylalanyl-L-tyrosine).
The purity and molecular weight of the HKFY-53 are shown in
Fmoc-Lys(caprylic)-OH obtained from Example 1.1. and DMF and HOBt were added to the Fmoc-Phe-Tyr(Boc)-trityl resin obtained from Example 1.47. to prepare Fmoc-Lys(caprylic)-Phe-Tyr(Boc)-trityl resin. The protecting group of the resin was cleaved to prepare Lys(caprylic)-Phe-Tyr (N6-octanoyl-L-lysyl-L-phenylalanyl-L-tyrosine).
The purity and molecular weight of the HKFY-54 are shown in
Fmoc-His(trt)-OH, and Fmoc-Lys(caprylic)-OH obtained from Example 1.1. were sequentially added to the Fmoc-Phe-Tyr(Boc)-trityl resin obtained from Example 1.47. in the same manner to prepare Fmoc-Lys(caprylic)-His(trt)-Phe-Tyr(Boc)-trityl resin. The protecting group of the resin was cleaved to prepare Lys(caprylic)-His(trt)-Phe-Tyr (Na—(N6-octanoyl-L-lysyl)-Nt-trityl-L-histidyl-L-phenylalanyl-L-tyrosine).
The purity and molecular weight of the HKFY-55 are shown in
Fmoc-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin was prepared in the same manner except that Fmoc-Asp(tBu)-OH was used instead of Fmoc-Ser(tBu)-OH during the preparation process of Example 1.38. DMF containing 2% NH2NH2H2O was added to Fmoc-Lys(dde)-OH, and dde was removed to prepare Fmoc-Lys-OH. DMF containing caproic acid and HOBt and DIC was added to the Fmoc-Lys-OH to prepare Fmoc-Lys(caproic acid)-OH.
Fmoc-Lys(caproic)-OH and Fmoc-His(trt)-OH were sequentially added in the same manner to prepare Fmoc-His(trt)-Lys(caproic)-Phe-Tyr(Boc)-Asp(tBu)-Gln(trt)-Gln(trt)-Ala-Arg(pbf)-Phe-trityl resin. The protecting group of the resin was cleaved to prepare His(trt)-Lys(caproic)-Phe-Tyr-Asp-Gln-Gln-Ala-Arg-Phe ((6S,9S,12S,15S,18S)-1-amino-6-(((S)-1-amino-1-oxo-3-phenylpropan-2-yl)carbamoyl)-18-((S)-2-((S)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-(non-1-en-2-y lamino)hexanamido)-3-phenylpropanamido)-3-(4-hydroxyphenyl)propanamido)-12,15-bis(3-amino-3-oxopropyl)-1-imino-9-methyl-8,11,14,17-tetraoxo-2,7,10,13,16-pentaazaicosan-20-oic acid).
The purity and molecular weight of the HKFY-56 are shown in
His(2-phenyl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(2-phenyl-1H-imidazol-4-yl)propanamido)-6-octanamidohexa namido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(2-phenyl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-57 are shown in
His(1-phenyl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-phenyl-1H-imidazol-4-yl)propanamido)-6-octanamidohexa namido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(1-phenyl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-58 are shown in
His(1,2-diphenyl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1,2-diphenyl-1H-imidazol-4-yl)propanamido)-6-octanamidoh exanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(1,2-diphenyl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-59 are shown in
His(2-(4-tert-butyl)phenyl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(2-(4-(tert-butyl)phenyl)-1H-imidazol-4-yl)propanamido)-6-oc tanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(2-(4-tert-butyl)phenyl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-60 are shown in
His(1-(4-tert-butyl)phenyl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-(4-(tert-butyl)phenyl)-1H-imidazol-4-yl)propanamido)-6-octanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(1-(4-tert-butyl)phenyl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-61 are shown in
d-His(benzhydryl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((R)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octanamido hexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-d-His(benzhydryl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-62 are shown in
His(thiophene)-Lys(caprylic)-d-Phe(methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(2-(thiophen-2-yl)-1H-imidazol-4-yl)propanamido)-6-octanam idohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(thiophene)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-63 are shown in
His(4-methoxybenzhydryl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((2R)-2-((2S)-2-((2S)-2-amino-3-(1-((4-methoxyphenyl)(phenyl)methyl)-1H-imidazol-4-yl) propanamido)-6-octanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(4-methoxybenzhydryl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-64 are shown in
His(4-hydroxybenzhydryl)-Lys(caprylic)-d-Phe(methyl)-Tyr (((2R)-2-((2S)-2-((2S)-2-amino-3-(1-((4-hydroxyphenyl)(phenyl)methyl)-1H-imidazol-4-yl)p ropanamido)-6-octanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(4-hydroxybenzhydryl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-65 are shown in
His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr-NH2, (N—((S)-5-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-(((R)-1-(((S)-1-a mino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)amino)-1-oxo-3-(p-tolyl)propan-2-yl)amino)-6-oxohexyl)octanamide) was prepared in the same manner except that Fmoc-Tyr-wang resin was used instead of the trityl resin among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-66 are shown in
His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr(3-chloro) ((S)-2-((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanamido)-3-(3-chloro-4-hydroxyphenyl)propanoic acid) was prepared in the same manner except that Fmoc-Tyr(3-chloro) was used instead of Fmoc-Tyr(tBu) among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-67 are shown in
His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr(3-nitro) ((S)-2-((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanamido)-3-(4-hydroxy-3-nitrophenyl)propanoic acid) was prepared in the same manner except that Fmoc-Tyr(3-nitro) was used instead of Fmoc-Tyr(tBu) among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-68 are shown in
His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr(3,5-nitro) ((S)-2-((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanamido)-3-(4-hydroxy-3,5-dinitrophenyl)propanoic acid) was prepared in the same manner except that Fmoc-Tyr(3,5-nitro) was used instead of Fmoc-Tyr(tBu) among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-69 are shown in
His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr(3-amino) ((S)-2-((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanamido)-3-(3-amino-4-hydroxyphenyl)propanoic acid) was prepared in the same manner except that Fmoc-Tyr(3-amino) was used instead of Fmoc-Tyr(tBu) among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-70 are shown in
His(benzhydryl)-Orn(caprylic)-d-Phe(4-methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-benzhydryl-1H-imidazol-4-yl)propanamido)-5-octanamidop entanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Fmoc-Orn(dde) was used instead of Fmoc-Lys(dde) among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-71 are shown in
Biotin-His(benzhydryl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr (((S)-2-((S)-2-((S)-3-(1-benzhydryl-1H-imidazol-4-yl)-2-(5-((3aS,4S,6aR)-2-oxohexahydro-1 H-thieno[3,4-d]imidazol-4-yl)pentanamido)propanamido)-6-octanamidohexanamido)-3-(p-to lyl)propanoyl)-L-tyrosine) was prepared in the same manner as in the synthesis process of D-biotin of Example 1.2. using His(benzhydryl)-Lys(caprylic acid)-d-Phe(4-methyl)-Tyr-OH of Example 1.34.
The purity and molecular weight of the HKFY-72 are shown in
H(trt)Lys(caprylic)-d-3Pal-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(pyridin-3-yl)propanoyl)-L-tyrosine) was prepared in the same manner except that Fmoc-d-3Pal was used instead of Fmoc-d-Phe-OH among the constituent amino acids of Example 1.12.
The purity and molecular weight of the HKFY-73 are shown in
H(trt)Lys(caprylic)-d-2Nal-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(naphthalen-2-yl)propanoyl)-L-tyrosine) was prepared in the same manner except that Fmoc-d-2Nal was used instead of Fmoc-d-3Pal among the constituent amino acids of Example 1.73.
The purity and molecular weight of the HKFY-74 are shown in
His(tosyl)-Lys(caprylic)-d-Phe(4-methyl)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-tosyl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(tosyl)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-75 are shown in
His(trityl)-Lys(caprylic)-d-Phe(4-CF3)-Tyr (((R)-2-((S)-2-((S)-2-amino-3-(1-trityl-1H-imidazol-4-yl)propanamido)-6-octanamidohexana mido)-3-(4-(trifluoromethyl)phenyl)propanovl)-L-tyrosine) was prepared in the same manner except that Fmoc-d-Phe(4-CF3) was used instead of Fmoc-d-3Pal among the constituent amino acids of Example 1.73.
The purity and molecular weight of the HKFY-76 are shown in
His(tbm)-Lys(caprylic)-d-Phe(4-CF3)-Tyr (((R)-2-((S)-2-((S)-3-(1-((2′-(1H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-1H-imidazol-4-yl)-2-aminopropanamido)-6-octanamidohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-His(tbm)-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-77 are shown in
Boc-Trp-Lys(caprylic)-d-Phe(4-methyl)-Tyr (((R)-2-((S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-(1H-indol-3-yl)propanamido)-6-octana midohexanamido)-3-(p-tolyl)propanoyl)-L-tyrosine) was prepared in the same manner except that Boc-Trp-OH was used instead of Boc-His(benzhydryl)-OH among the constituent amino acids of Example 1.34.
The purity and molecular weight of the HKFY-78 are shown in
Fmoc-Lys(dde) and DMF (dimethylformamide) were loaded onto the trityl resin to prepare Fmoc-Lys(dde)-trityl resin. Fmoc-Lys(caprylic acid)-trityl resin was prepared in the same manner as in the synthesis process of Example 1.1. Thereafter, Boc-His(benzhdyryl)-OH was used to prepare His(benzhydryl)-Lys(caprylic) (N2-(Nt-benzhydryl-L-histidyl)-N6-octanoyl-L-lysine).
The HKFY peptide derivatives prepared by the above preparation method are shown in Table 1 below.
The HKFY derivatives prepared in Examples 1.1 to 1.79 were analyzed for purity and molecular weight using HPLC and Ion-Mass. The results are shown in Table 2 below, and the HPLC analysis results of the HKFY derivatives are shown in
In order to investigate the binding capacity of the HKFY derivatives prepared in Examples 1.1. to 1.79 above to GPR39, a luciferase assay system was used. The luciferase assay system is a method for confirming the degree of activity of a receptor in a cell through the binding of a ligand to a receptor in a cell.
Specifically, the fibroblast cell line CV-1 (1×105 cells/ml, Korea Cell Line Bank) was cultured in a 96 well cell culture plate for 24 hours, and then treated with GPR39 inserted into adenovirus and SRE (serum response element) luciferase at 50 MOI (multiplicity of infection) and 25 MOI virus for 3 hours, respectively, and then cultured for 24 hours. In order to give a fasting process, after 24 hours, the medium was replaced with a serum-free medium and cultured for 16 hours, and then treated with each HJKFY and HJKFY derivative for 6 hours and cultured, and then the expression level of luciferase, a reporter gene, by activated GPR39 was quantified using a luminometer (Table 3).
16 ± 1.7
16 ± 2.2
22 ± 2.2
18 ± 1.7
16 ± 1.7
13 ± 1.7
16 ± 1.5
As a result, referring to Table 3, it was confirmed that all HJKFY derivatives had high activity at nM to μM level for GPR39. In addition, among the analogs in which various fatty acids were conjugated to Lys, the analog conjugated to caprylic acid showed the most excellent activity. Derivatives exhibiting nM level of activity are considered to have highly selective and specific activity for GPR39.
On the other hand, HJKFY-30, HKFY-34, HJKFY-63, HJKFY-64, and HJKFY-65 derivatives exhibited a higher activity level than other HJKFY derivatives. In particular, HIKFY-30 and HIKFY-34 composed of d-Phe(methyl) exhibited the most excellent activity and high ECmax value.
In order to confirm the selectivity and specificity of the HJKFY derivatives for GPR39, the degree of activity was confirmed by a luciferase assay system and a calcium influx assay system (
Specifically, the luciferase assay system analyzed the degree of activity using HKFY-34 among the HKFY derivatives in Experimental Example 2 above (top in
In the calcium influx assay system, the fibroblast cell line CV-1 (1×105 cells/ml) was transfected with a mixture of human GPR39 (pCDNA3.1_hGPR39, American Type Culture Collection), Gαq (pCDNA3.1_Gaq, American Type Culture Collection), Aequrin (pCDNA3.1_aequrin, American Type Culture Collection) and lipofectamine (American Type Culture Collection), and then the medium was replaced with a serum-free medium, and after 16 hours of fasting, treated with HKFY-34 for 6 hours and cultured, and then the degree of binding of calcium activated by activated GPR39 to aequrin was quantified using a luminometer (bottom in
As a result, referring to
In addition, through the activity test of the HKFY derivatives for similar receptors to GPR39, ghrelin receptor family (ghrelin receptor (GHSR), motilin receptor (MTLR), neurotensin receptor (NTSR1 & NTSR2), neuromedin U receptor (NMU1 & NMU2), TRH (thyrotropin releasing hormone) receptor (TRHR)), the selectivity and specificity for the GPR39 receptor were confirmed.
Specifically, the degree of activity between the intrinsic ligand and HKFY-34 for each receptor was analyzed using a luciferase assay system (
As a result, referring to
These results suggest that the HKFY derivative can be used as an agonist that selectively and specifically binds to the GPR39 receptor.
The GPR39 receptor is widely distributed in the pancreas, and it is known that glucose-dependent insulin secretion ability is impaired in GPR39 KO mice (Endocrinology 2009, 150:2577-2585).
In this regard, in order to confirm the effect of the HKFY derivative, a candidate GPR39 agonist, on insulin secretion ability, a glucose-dependent insulin secretion ability test was performed in INS-1 (Korea Cell Line Bank), a rat insulinoma cell (
Specifically, when INS-1 cells were treated with 1 or 10 μM of HKFY-34 in 2.8 mM glucose similar to a physiological blood glucose level or 11.1 mM glucose, a high blood glucose level, the insulin secretion ability was confirmed using a rat insulin ELISA.
As a result, referring to
In addition, through GPR39 knock-down experiment using GPR39 siRNA, it was confirmed that HKFY-34 enhances insulin secretion through the GPR39 receptor. In particular, the fact that the insulin secretion ability was not increased in cells treated with GPR39 siRNA compared to scrambled siRNA in 11.1 mM glucose suggests that HKFY-34 enhances the glucose-dependent insulin secretion ability through the GPR39 receptor.
In addition, the glucose-dependent insulin secretion ability of the HKFY derivative for rat islet was confirmed (
Specifically, the pancreas was extracted from a 8-week-old SD rat (Damul Science), and islets were isolated. The isolated islets were treated with HKFY-34 at different concentrations (1 nM, 10 nM, 100 nM, 1 μM, 10 μM and 100 μM) in 2.8 mM or 28 mM glucose, and then the amount of the secreted insulin was measured using a rat insulin ELISA.
As a result, referring to
The mRNA expression levels of Irs2 and Ins2, which are important factors for proliferation and differentiation of pancreatic beta cells, were analyzed through RT-PCR (
As a result, referring to
Lipolysis is regulated by β-adrenergic receptors, which are mainly distributed in adipocytes, and obesity due to hyper-proliferation of adipocytes can be regulated through normal lipolysis.
In a study through the control of a high-fat or low-fat diet for GPR39 KO, it was confirmed that the increase in body weight and the accumulation of body fat were enhanced in GPR39 KO mice (Gastroenterology 2006, 131:1131-1141).
Accordingly, the expression level of the GPR39 receptor in adipocytes and adipose tissue was analyzed using western blot (
In addition, the mRNA expression levels of HSL (hormone-sensitive lipase), ATGL (adipose triglyceride lipase) and Perilipin A, which are important factors for lipolysis signaling according to HKFY-34 treatment, were analyzed through RT-PCR (
In addition, lipolytic ability according to the HKFY-34 treatment by concentration (100 nM, 500 nM, 1 confirmed (
As a result, referring to
In order to analyze the mechanism of lipolytic ability according to the HKFY derivative treatment in 3T3-L1 cells and WAT cells, the expression levels of pERK and pPKA were analyzed (
Specifically, protein was purified from 3T3L-1 cells (Korea Cell Line Bank) and WAT (tissue culture using mice purchased from Central Lab. Animal Inc.) treated with the HKFY derivatives, and then each antibody for pERK, ERK, pPKA, and PKA expressed in mice was used, and the expression level of each protein due to the derivatives was measured through western blot.
As a result, referring to
Experimental Example 7. Glucose Tolerance Test According to HKFY Derivative Treatment
The glucose tolerance level in a mouse model of diabetes mellitus disease according to the HKFY derivative treatment was analyzed (
Specifically, male db/db mice (5 to 7-week-old, Central Lab. Animal Inc.), which is a mouse model of diabetes mellitus disease, were fasted for 16 hours, and then HKFY-34 was administered subcutaneously at a concentration of 0.5, 1, 5 and 10 mg/kg, respectively. After 30 minutes, glucose (1.5 g/kg) was intraperitoneally administered. After 0, 15, 30, 45, 60, 90, 120 and 180 minutes, blood was collected from the tail of the mice, and the blood glucose was measured with a blood glucose meter (acc-check, Roche, Germany) to analyze the glucose tolerance.
As a result, referring to
In addition, the blood insulin level was analyzed simultaneously with the glucose tolerance test for the mouse model of diabetes mellitus disease (
Specifically, after 0, 15, 30, 60, 90, 120 and 180 minutes, blood was collected from the orbital veins of mice, and the insulin level in plasma was analyzed using mouse ELISA.
As a result, referring to
In addition, the glucose tolerance level and insulin level according to HKFY-34 treatment in a mouse model of obesity disease were analyzed (
Specifically, in the glucose tolerance level and insulin level analysis experiment, the experiment was performed by changing the mouse model of diabetes mellitus disease into a mouse model of obesity disease (DIO), in which obesity was induced by providing male C57BL6/J mice (6 to 7-week-old, Central Lab. Animal Inc.) with a high-fat feed (60% fat chow) for 5-6 weeks.
As a result, referring to
In addition, the glucose tolerance level in the GPR39 KO mouse model induced by a high-fat diet according to the HKFY derivative treatment was analyzed (
Specifically, obesity was induced by providing male GPR39 KO mice (6 to 7-week-old, Central Lab. Animal Inc.) with a high-fat feed (60% fat chow) for 5-6 weeks. HKFY-34 was administered subcutaneously at a concentration of 0.5, 1, 5 and 10 mg/kg, respectively, to the 16, 17 or 18-week-old GPR39 KO mice, in which obesity was induced. After 30 minutes, glucose (1.5 g/kg) was intraperitoneally administered. After 0, 15, 30, 45, 60, 90, 120 and 180 minutes, blood was collected from the tail of the mice, and the blood glucose was measured with a blood glucose meter (acc-check, Roche, Germany) to analyze the glucose tolerance.
As a result, referring to
Experimental Example 8. Confirmation of Anti-Diabetic Effect According to HKFY Derivative Treatment
The drop in blood glucose level in a mouse model of diabetes mellitus disease according to the HKFY derivative treatment was analyzed (
Specifically, HKFY-34 was subcutaneously administered at a concentration of 0.5, 1, 5 and 10 mg/kg, respectively, to male db/db mice (5 to 7-week-old), which is a mouse model of diabetes mellitus disease. After 0, 1, 2, 4, 6, 8, 12, 18 and 24 hours, blood was collected from the tail of the mice, and the blood glucose was measured with a blood glucose meter (acc-check, Roche, Germany) to confirm the anti-diabetic effect.
As a result, referring to
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2020-0030303 | Mar 2020 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2021/003045 | 3/11/2021 | WO |
