Target Information
Target General Infomation | |||||
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Target ID |
T72458
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Former ID |
TTDC00072
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Target Name |
Melanocortin-4 receptor
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Gene Name |
MC4R
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Synonyms |
MC4-R; MC4R
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Target Type |
Clinical Trial
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Disease | Anorexia nervosa cachexia [ICD9: 307.1, 799.4; ICD10: F50.0-F50.1] | ||||
Cachexia [ICD9: 799.4; ICD10: R64] | |||||
Erectile dysfunction [ICD9: 302.72, 607.84; ICD10: F52.2, N48.4] | |||||
Female sexual dysfunction [ICD9: 302.7; ICD10: F52] | |||||
Metabolic disorders [ICD9: 270-279; ICD10: E70-E89] | |||||
Obesity [ICD9: 278; ICD10: E66] | |||||
Obesity; Sexual dysfunction [ICD9: 278, 302.7; ICD10: E66, F52] | |||||
Obesity; Diabetes [ICD9: 250, 278; ICD10: E08-E13, E66] | |||||
Sexual dysfunction; Obesity; Type 2 diabetes [ICD9: 250, 250.00, 250.02, 278, 302.7; ICD10: E08-E13, E11, E66, F52] | |||||
Sexual dysfunction; Obesity [ICD9: 278, 302.7; ICD10: E66, F52] | |||||
Sexual dysfunction [ICD9: 302.7; ICD10: F52] | |||||
Function |
Receptor specific to the heptapeptide core common to adrenocorticotropic hormone and alpha-, beta-, and gamma-MSH. Plays a central role in energy homeostasis and somatic growth. This receptor is mediated by G proteins that stimulate adenylate cyclase (cAMP).
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BioChemical Class |
GPCR rhodopsin
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Target Validation |
T72458
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UniProt ID | |||||
Sequence |
MVNSTHRGMHTSLHLWNRSSYRLHSNASESLGKGYSDGGCYEQLFVSPEVFVTLGVISLL
ENILVIVAIAKNKNLHSPMYFFICSLAVADMLVSVSNGSETIVITLLNSTDTDAQSFTVN IDNVIDSVICSSLLASICSLLSIAVDRYFTIFYALQYHNIMTVKRVGIIISCIWAACTVS GILFIIYSDSSAVIICLITMFFTMLALMASLYVHMFLMARLHIKRIAVLPGTGAIRQGAN MKGAITLTILIGVFVVCWAPFFLHLIFYISCPQNPYCVCFMSHFNLYLILIMCNSIIDPL IYALRSQELRKTFKEIICCYPLGGLCDLSSRY |
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Drugs and Mode of Action | |||||
Drug(s) | Amylin | Drug Info | Phase 4 | Discovery agent | [523879], [541936] |
Bremelanotide | Drug Info | Phase 3 | Erectile dysfunction | [536493] | |
Bremelanotide | Drug Info | Phase 2a | Sexual dysfunction | [536493] | |
PF-446687 | Drug Info | Phase 2 | Female sexual dysfunction | [522609] | |
AP-1030 | Drug Info | Phase 1/2 | Metabolic disorders | [522018], [538812] | |
CHIR-01020 | Drug Info | Preclinical | Obesity | [536122] | |
IDDBCP-150101 | Drug Info | Preclinical | Obesity; Sexual dysfunction | [536122] | |
MC-4 agonist | Drug Info | Preclinical | Obesity | [536122] | |
Melanotetan II | Drug Info | Preclinical | Sexual dysfunction; Obesity; Type 2 diabetes | [536122] | |
PT-15 | Drug Info | Preclinical | Sexual dysfunction; Obesity | [536122] | |
RM-493 | Drug Info | Preclinical | Obesity; Diabetes | [551045] | |
Ro-27-3225 | Drug Info | Preclinical | Obesity | [536122] | |
PT-14 | Drug Info | Discontinued in Phase 2 | Erectile dysfunction | [546757] | |
Inhibitor | 1-Benzyl-4-methyl-piperazine | Drug Info | [527746] | ||
1-Methyl-4-(1-phenyl-ethyl)-piperazine | Drug Info | [527746] | |||
4-(4-butylpiperidin-1-yl)-1-o-tolylbutan-1-one | Drug Info | [531079] | |||
Ac-dR[CEHdFRWC]-NH2 | Drug Info | [527529] | |||
Ac-His-D-Phe-Arg-2-Nal-NHCH3 | Drug Info | [528247] | |||
Ac-His-DPhe-Arg-Trp-NH2 | Drug Info | [534420] | |||
Ac-Nle-c[Asp-His-DNaI(2')-Pro-Trp-Lys]-NH2 | Drug Info | [530169] | |||
Ac-Nle-c[Asp-His-DNal(2')-Pro-Trp-Lys]-NH2 | Drug Info | [530169] | |||
Ac-Nle-c[Asp-His-DPhe-Arg-Trp-Lys]-NH2 | Drug Info | [530169] | |||
AC-Nle-c[Asp-His-DPhe-Pro-Trp-Lys]-NH2 | Drug Info | [530169] | |||
Ac-Phe-[Orn-Pro-cha-Trp-Arg] | Drug Info | [528343] | |||
Ac-R[CEHdFRWC]-NH2 | Drug Info | [527529] | |||
Ac-Tyr-D-Phe-Arg-2-Nal-NHCH3 | Drug Info | [528247] | |||
Ac-YCit[CEHdFRWC]-NH2 | Drug Info | [527529] | |||
Ac-YK[CEHdFRWC]-NH2 | Drug Info | [527529] | |||
Ac-YRC(Me)*EHdFRWC(Me)NH2 | Drug Info | [527529] | |||
Ac-YRMEHdFRWG-NH2 | Drug Info | [527529] | |||
Ac-YRMEHdFRWGSPPKD-NH2 | Drug Info | [527529] | |||
Ac-YR[CE(1-Me-H)dFRWC]-NH2 | Drug Info | [527529] | |||
Ac-YR[CEH(d-2alpha-Nal)RWC]-NH2 | Drug Info | [527529] | |||
Ac-YR[CEH(pCl-dF)RWC]-NH2 | Drug Info | [527529] | |||
Ac-YR[CEH(pF-dF)RWC]-NH2 | Drug Info | [527529] | |||
Ac-YR[CEHdFRWC]-NH2 | Drug Info | [527529] | |||
Ac-YR[CEHdFRWC]SPPKD-NH2 | Drug Info | [527529] | |||
Ac-YR[CEHFRWC]-NH2 | Drug Info | [527529] | |||
Ac-[CEHdFRWC]-NH2 | Drug Info | [527529] | |||
AEKKDEGPYRMEHFRWGSPPKD | Drug Info | [527529] | |||
C(his-D-phe-arg-trp-Abu) | Drug Info | [528187] | |||
C(his-D-phe-arg-trp-Ahp) | Drug Info | [528187] | |||
C(his-D-phe-arg-trp-Ahx) | Drug Info | [528187] | |||
C(his-D-phe-arg-trp-Aoc) | Drug Info | [528187] | |||
C(his-L-phe-arg-trp-Aoc) | Drug Info | [528187] | |||
C[CO-(CH2)2-CO-Nle-D-Nal(2)-Arg-Trp-Lys]-NH2 | Drug Info | [529226] | |||
C[CO-(CH2)2-CO-Nle-D-Phe-Arg-Trp-Lys]-NH2 | Drug Info | [529226] | |||
C[CO-(CH2)3-CO-Pro-D-Nal(2)-Arg-Trp-Lys]-NH2 | Drug Info | [529226] | |||
C[CO-o-C6H4-CO-Pro-D-Nal(2)-Arg-Trp-Lys]-NH2 | Drug Info | [529226] | |||
C[CO-o-C6H4-CO-Pro-D-Phe-Arg-Trp-Lys]-NH2 | Drug Info | [529226] | |||
C[Nle-Arg-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Arg-D-Phe-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Asp-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Asp-D-Phe-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Gln-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Glu-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-His-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-His-D-Phe-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Nle-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Nle-D-Phe-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Pro-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Pro-D-Phe-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Val-D-Nal(2')-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Nle-Val-D-Phe-Arg-Trp-Glu]-NH2 | Drug Info | [528082] | |||
C[Ser-Tyr-Thr-His-Dphe-Arg-Trp-Thr-Ile-Pro] | Drug Info | [527997] | |||
C[Thr-Tyr-Thr-His-DNaf-Arg-Trp-Thr-Ile-Pro] | Drug Info | [527997] | |||
D-Phe-Arg-2-Nal-NHCH3 | Drug Info | [528325] | |||
GPYRMEHFRWGSPPKD-NH2 | Drug Info | [527529] | |||
His-DPhe-Arg-Trp | Drug Info | [528799] | |||
Hoo-Phe-Orn-Pro-hle-Pff-Phe-NH2 | Drug Info | [528343] | |||
MCL-129 | Drug Info | [528626] | |||
MK-10 | Drug Info | [526348] | |||
MK-11 | Drug Info | [526348] | |||
ML-253764 | Drug Info | [527997] | |||
NDP-alpha-MSH | Drug Info | [529789] | |||
NDP-SYSMEHFRWGKPVG | Drug Info | [527529] | |||
Ser-Tyr-Ser-Nle-Glu-His-Dphe-Arg | Drug Info | [528799] | |||
Tic-D-Phe-Arg-2-Nal-NHCH3 | Drug Info | [527941] | |||
Agonist | AMSH | Drug Info | [536493] | ||
Amylin | Drug Info | [535068] | |||
Bremelanotide | Drug Info | [536747], [536858], [536984] | |||
CHIR-01020 | Drug Info | [536122] | |||
IDDBCP-150101 | Drug Info | [536122] | |||
MC-4 agonist | Drug Info | [536122] | |||
Melanotetan II | Drug Info | [536122] | |||
MT-II | Drug Info | [525923] | |||
MTII Melanotan-II | Drug Info | [536493] | |||
PT-14 | Drug Info | [532570] | |||
PT-15 | Drug Info | [536122] | |||
RM-493 | Drug Info | [551045] | |||
Ro-27-3225 | Drug Info | [536122] | |||
THIQ | Drug Info | [543735] | |||
Modulator | AP-1030 | Drug Info | [1572591] | ||
PF-446687 | Drug Info | [533131] | |||
Antagonist | BL-6020 | Drug Info | [543735] | ||
HS014 | Drug Info | [534856] | |||
MCL0129 | Drug Info | [543735] | |||
Melanocortin-4 Receptor antagonist | Drug Info | [536225] | |||
Target Expression Profile (TEP) and Drug Resistance Mutation (DRM) | |||||
TEP | EXP Info | ||||
Pathways | |||||
KEGG Pathway | Neuroactive ligand-receptor interaction | ||||
Pathway Interaction Database | Syndecan-3-mediated signaling events | ||||
Reactome | Peptide ligand-binding receptors | ||||
G alpha (s) signalling events | |||||
WikiPathways | GPCRs, Class A Rhodopsin-like | ||||
Peptide GPCRs | |||||
GPCR ligand binding | |||||
GPCR downstream signaling | |||||
References | |||||
Ref 522018 | ClinicalTrials.gov (NCT00464958) One Year Extension Study To Protocol C2/5/TZ:MS-05. U.S. National Institutes of Health. | ||||
Ref 522609 | ClinicalTrials.gov (NCT00862888) Study to Investigate Effect of a New Drug (PF-00446687) in Males Suffering From Erectile Dysfunction. U.S. National Institutes of Health. | ||||
Ref 523879 | ClinicalTrials.gov (NCT01580514) Myocardial Protection of Exenatide in AMI. U.S. National Institutes of Health. | ||||
Ref 536122 | Emerging drugs for obesity: linking novel biological mechanisms to pharmaceutical pipelines. Expert Opin Emerg Drugs. 2005 Aug;10(3):643-60. | ||||
Ref 536493 | Designing drugs for the treatment of female sexual dysfunction. Drug Discov Today. 2007 Sep;12(17-18):757-66. Epub 2007 Aug 27. | ||||
Ref 538812 | (http://www.guidetopharmacology.org/) Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 1322). | ||||
Ref 541936 | (http://www.guidetopharmacology.org/) Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 688). | ||||
Ref 525923 | Molecular determinants of ligand binding to the human melanocortin-4 receptor. Biochemistry. 2000 Dec 5;39(48):14900-11. | ||||
Ref 526348 | J Med Chem. 2002 Jun 6;45(12):2644-50.Novel cyclic templates of alpha-MSH give highly selective and potent antagonists/agonists for human melanocortin-3/4 receptors. | ||||
Ref 527529 | J Med Chem. 2005 May 5;48(9):3095-8.Discovery of a beta-MSH-derived MC-4R selective agonist. | ||||
Ref 527746 | Bioorg Med Chem Lett. 2005 Nov 15;15(22):4973-8.Privileged structure based ligands for melanocortin receptors--substituted benzylic piperazine derivatives. | ||||
Ref 527941 | Bioorg Med Chem Lett. 2006 Mar 15;16(6):1721-5. Epub 2005 Dec 20.Synthesis of Tic-D-Phe Psi[CH2-CH2] isostere and its use in the development of melanocortin receptor agonists. | ||||
Ref 527997 | J Med Chem. 2006 Feb 9;49(3):911-22.Mapping the binding site of melanocortin 4 receptor agonists: a hydrophobic pocket formed by I3.28(125), I3.32(129), and I7.42(291) is critical for receptor activation. | ||||
Ref 528082 | J Med Chem. 2006 Mar 23;49(6):1946-52.Development of cyclic gamma-MSH analogues with selective hMC3R agonist and hMC3R/hMC5R antagonist activities. | ||||
Ref 528187 | Bioorg Med Chem Lett. 2006 Jul 15;16(14):3723-6. Epub 2006 May 5.Design of cyclic peptides with agonist activity at melanocortin receptor-4. | ||||
Ref 528247 | Bioorg Med Chem Lett. 2006 Sep 1;16(17):4668-73.Design and synthesis of potent and selective 1,3,4-trisubstituted-2-oxopiperazine based melanocortin-4 receptor agonists. | ||||
Ref 528325 | J Med Chem. 2006 Jul 27;49(15):4745-61.Design, synthesis, and evaluation of proline and pyrrolidine based melanocortin receptor agonists. A conformationally restricted dipeptide mimic approach. | ||||
Ref 528343 | Bioorg Med Chem Lett. 2006 Oct 1;16(19):5088-92. Epub 2006 Jul 28.Peptidomimetic C5a receptor antagonists with hydrophobic substitutions at the C-terminus: increased receptor specificity and in vivoactivity. | ||||
Ref 528626 | Bioorg Med Chem. 2007 Mar 1;15(5):1989-2005. Epub 2006 Dec 30.Structure-activity relationships of novel piperazines as antagonists for the melanocortin-4 receptor. | ||||
Ref 528799 | Bioorg Med Chem Lett. 2007 Jun 15;17(12):3310-3. Epub 2007 Apr 6.Squalene-derived flexible linkers for bioactive peptides. | ||||
Ref 529226 | J Med Chem. 2008 Jan 24;51(2):187-95. Epub 2007 Dec 19.Structure-activity relationships of cyclic lactam analogues of alpha-melanocyte-stimulating hormone (alpha-MSH) targeting the human melanocortin-3 receptor. | ||||
Ref 529789 | J Med Chem. 2008 Nov 27;51(22):7094-8.cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11a-octahydrobenzofuro[2,3-h]quinazolin-2-amine (A-987306), a new histamine H4R antagonist that blocks pain responses against carrageenan-induced hyperalgesia. | ||||
Ref 530169 | J Med Chem. 2009 Jun 25;52(12):3627-35.Substitution of arginine with proline and proline derivatives in melanocyte-stimulating hormones leads to selectivity for human melanocortin 4 receptor. | ||||
Ref 531079 | J Med Chem. 2010 Sep 9;53(17):6386-97.Discovery of N-{1-[3-(3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-yl)propyl]piperidin-4-yl}-2-phenylacetamide (Lu AE51090): an allosteric muscarinic M1 receptor agonist with unprecedented selectivity and procognitive potential. | ||||
Ref 532570 | The protective effects of the melanocortin receptor (MCR) agonist, melanotan-II (MTII), against binge-like ethanol drinking are facilitated by deletion of the MC3 receptor in mice. Neuropeptides. 2014 Feb;48(1):47-51. | ||||
Ref 533131 | Melanocortin Receptor Agonists Facilitate Oxytocin-Dependent Partner Preference Formation in the Prairie Vole. Neuropsychopharmacology. 2015 Jul;40(8):1856-65. | ||||
Ref 534420 | J Med Chem. 1997 Jul 4;40(14):2133-9.Discovery of prototype peptidomimetic agonists at the human melanocortin receptors MC1R and MC4R. | ||||
Ref 534856 | Long-term administration of MC4 receptor antagonist HS014 causes hyperphagia and obesity in rats. Neuroreport. 1999 Mar 17;10(4):707-11. | ||||
Ref 536122 | Emerging drugs for obesity: linking novel biological mechanisms to pharmaceutical pipelines. Expert Opin Emerg Drugs. 2005 Aug;10(3):643-60. | ||||
Ref 536225 | Emerging drugs for eating disorder treatment. Expert Opin Emerg Drugs. 2006 May;11(2):315-36. | ||||
Ref 536493 | Designing drugs for the treatment of female sexual dysfunction. Drug Discov Today. 2007 Sep;12(17-18):757-66. Epub 2007 Aug 27. | ||||
Ref 536747 | Clinical applications of centrally acting agents in male sexual dysfunction. Int J Impot Res. 2008 Jul;20 Suppl 1:S17-23. |
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