General Information of Drug (ID: DMG5QJB)

Drug Name
(+)-MCPG Drug Info
Synonyms
(S)-Mcpg; (S)-MCPG; (+)-alpha-Methyl-4-carboxyphenylglycine; (S)-(ALPHA)-METHYL-4-CARBOXYPHENYLGLYCINE; 4-[(1S)-1-amino-1-carboxyethyl]benzoic acid; 4-(1-AMINO-1-CARBOXY-ETHYL)-BENZOIC ACID; UNII-61F6J48NHR; alpha-Mcpg; 61F6J48NHR; CHEMBL257626; CHEBI:43876; alpha-Methyl-cpgly; (S)-a-methyl-4-carboxyphenylglycine; (S)- -Methyl-4-carboxyphenylglycine; (S)-4-(1-amino-1-carboxyethyl)benzoic acid; (S)-(+)-alpha-methyl-4-carboxyphenylglycine; MCG; (S)-(+)-alpha-amino-4-carboxy-2-methylbenzeneacetic; alpha-Mcpg; alpha-methyl-4-carboxyphenylglycine; alpha-methyl-cpgly; 4-(1-Amino-1-Carboxy-Ethyl)-Benzoic Acid
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
446355
ChEBI ID
CHEBI:43876
CAS Number
CAS 150145-89-4
TTD Drug ID
DMG5QJB

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Patented Agent(s)
Discontinued Drug(s)
Preclinical Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
LY404039 DMWZIRJ Schizophrenia 6A20 Phase 3 [7]
RO-4995819 DMNTC7O Major depressive disorder 6A70.3 Phase 2 [8]
Oleoyl-estrone DM0RA8F Alzheimer disease 8A20 Phase 2 [9]
MP-101 DMYCITZ Alzheimer disease 8A20 Phase 2 [10]
BCI-838 DMRXDN3 Major depressive disorder 6A70.3 Phase 1 [11]
Pomaglumetad DMTOLI5 Schizophrenia 6A20 Phase 1 [12]
BCI-632 DMZYCWT Alzheimer disease 8A20 Phase 1 [13]
PMID25435285-Compound-16 DMKFX2G N. A. N. A. Patented [14]
PMID25435285-Compound-15 DMHBWNS N. A. N. A. Patented [14]
PMID25435285-Compound-20 DMG9FYH N. A. N. A. Patented [14]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
PF-1913539 DMXEU14 Alzheimer disease 8A20 Discontinued in Phase 3 [15]
AZD8529 DMEQ2N1 Schizophrenia 6A20 Discontinued in Phase 2 [16]
AZD-9272 DMYSBN3 Neuropathic pain 8E43.0 Discontinued in Phase 1 [17]
NPS-2390 DMMRY0Z Cerebrovascular ischaemia 8B1Z Preclinical [18]
A-841720 DMSO8IE Pain MG30-MG3Z Preclinical [19]
LY-367385 DM98POQ Neurological disorder 6B60 Terminated [20]
[3H]quisqualate DMDQBTX Discovery agent N.A. Investigative [21]
L-CCG-I DMPZ8XH Discovery agent N.A. Investigative [5]
(1S,3R)-ACPD DM5DOAF Discovery agent N.A. Investigative [5]
PHCCC DMNJY79 Discovery agent N.A. Investigative [22]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
L-serine-O-phosphate DMTJ1NH Discovery agent N.A. Investigative [6]
[3H]quisqualate DMDQBTX Discovery agent N.A. Investigative [23]
L-CCG-I DMPZ8XH Discovery agent N.A. Investigative [6]
(1S,3R)-ACPD DM5DOAF Discovery agent N.A. Investigative [6]
MAP4 DMUCE93 Discovery agent N.A. Investigative [6]
MPPG DMJHQ9T Discovery agent N.A. Investigative [6]
[3H]LY341495 DMGX0Y8 Discovery agent N.A. Investigative [6]
alpha-methylserine-O-phosphate DMCIH1X Discovery agent N.A. Investigative [6]
L-AP4 DMPJFGI Discovery agent N.A. Investigative [6]
LSP4-2022 DMBWHGP Discovery agent N.A. Investigative [24]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
RO-4995819 DMNTC7O Major depressive disorder 6A70.3 Phase 2 [8]
Oleoyl-estrone DM0RA8F Alzheimer disease 8A20 Phase 2 [9]
MP-101 DMYCITZ Alzheimer disease 8A20 Phase 2 [10]
JNJ-64281802 DMNMSVX Dengue 1D20-1D2Z Phase 2 [25]
BCI-838 DMRXDN3 Major depressive disorder 6A70.3 Phase 1 [11]
Pomaglumetad DMTOLI5 Schizophrenia 6A20 Phase 1 [12]
BCI-632 DMZYCWT Alzheimer disease 8A20 Phase 1 [13]
LY-2979165 DM16IX2 Bipolar disorder 6A60 Phase 1 [26]
JNJ-42491293 DMOL9JR Psychiatric disorder 6E8Z Phase 1 [27]
ADX71149 DMBUOX4 Epilepsy 8A60-8A68 Phase 1 [28]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
AFQ056 DMMHSLC Fragile X syndrome LD55 Phase 2/3 [29]
ADX-48621 DM6GTMD Parkinson disease 8A00.0 Phase 2/3 [30]
RG-7090 DMX8JYN Fragile X syndrome LD55 Phase 2 [31]
STX-107 DMLNKX7 Autism spectrum disorder 6A02 Phase 2 [32]
ADX10059 DMGVKHQ Anxiety disorder 6B00-6B0Z Phase 2 [33]
McN3377 DMTCADJ Fragile X syndrome LD55 Phase 1/2 [34]
MK-3328 DMW2O5D Alzheimer disease 8A20 Phase 1 [35]
[3H]fenobam DMBOXA1 Allodynia MB40.1 Phase 1 [36]
RG7342 DMIW5NG Schizophrenia 6A20 Phase 1 [37]
BMS-984923 DMFNDUL Alzheimer disease 8A20 Phase 1 [38]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Metabotropic glutamate receptor 1 (mGluR1) TTVBPDM GRM1_HUMAN Antagonist [2]
Metabotropic glutamate receptor 2 (mGluR2) TTXJ47W GRM2_HUMAN Antagonist [3]
Metabotropic glutamate receptor 3 (mGluR3) TT8A9EF GRM3_HUMAN Antagonist [4]
Metabotropic glutamate receptor 5 (mGluR5) TTHS256 GRM5_HUMAN Antagonist [5]
Metabotropic glutamate receptor 7 (mGluR7) TT0I76D GRM7_HUMAN Antagonist [6]

References

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4 [3H]-LY341495 as a novel antagonist radioligand for group II metabotropic glutamate (mGlu) receptors: characterization of binding to membranes of mGlu receptor subtype expressing cells. Neuropharmacology. 1999 Oct;38(10):1519-29.
5 Characterization of [(3)H]Quisqualate binding to recombinant rat metabotropic glutamate 1a and 5a receptors and to rat and human brain sections. J Neurochem. 2000 Dec;75(6):2590-601.
6 Binding of [3H](2S,1'S,2'S)-2-(9-xanthylmethyl)-2-(2'-carboxycyclopropyl) glycine ([3H]LY341495) to cell membranes expressing recombinant human group III metabotropic glutamate receptor subtypes. Naunyn Schmiedebergs Arch Pharmacol. 2000 Dec;362(6):546-54.
7 Positive allosteric modulators of the metabotropic glutamate receptor 2 for the treatment of schizophrenia. Expert Opin Ther Pat. 2009 Sep;19(9):1259-75.
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9 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
10 ClinicalTrials.gov (NCT03044249) A Study of MP-101 in Dementia-Related Psychosis and/or Agitation and Aggression. U.S. National Institutes of Health.
11 Metabotropic glutamate receptor subtype 2 (GRM2; MGLUR2); GRM3 (MGLUR3). SciBX 3(13); doi:10.1038/scibx.2010.413. April 1 2010
12 LY-2140023, a prodrug of the group II metabotropic glutamate receptor agonist LY-404039 for the potential treatment of schizophrenia. Curr Opin Investig Drugs. 2010 Jul;11(7):833-45.
13 Synthesis, in vitro pharmacology, structure-activity relationships, and pharmacokinetics of 3-alkoxy-2-amino-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid derivatives as potent and selective group II metabotropic glutamate receptor antagonists. J Med Chem. 2004 Aug 26;47(18):4570-87.
14 Novel metabotropic glutamate receptor 2/3 antagonists and their therapeutic applications: a patent review (2005 - present).Expert Opin Ther Pat. 2015 Jan;25(1):69-90.
15 Pfizer. Product Development Pipeline. March 31 2009.
16 Clinical pipeline report, company report or official report of AstraZeneca (2009).
17 Emerging drugs in neuropathic pain. Expert Opin Emerg Drugs. 2007 Mar;12(1):113-26.
18 Positive and negative modulation of group I metabotropic glutamate receptors. J Med Chem. 2008 Feb 14;51(3):634-47.
19 Comparison of the mGluR1 antagonist A-841720 in rat models of pain and cognition. Behav Pharmacol. 2007 Jul;18(4):273-81.
20 Anticonvulsant actions of LY 367385 ((+)-2-methyl-4-carboxyphenylglycine) and AIDA ((RS)-1-aminoindan-1,5-dicarboxylic acid). Eur J Pharmacol. 1999 Feb 26;368(1):17-24.
21 Mutational analysis and molecular modeling of the allosteric binding site of a novel, selective, noncompetitive antagonist of the metabotropic glut... J Biol Chem. 2003 Mar 7;278(10):8340-7.
22 URL: 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. (Target id: 289).
23 Excitatory amino acid receptor ligands: resolution, absolute stereochemistry, and enantiopharmacology of 2-amino-3-(4-butyl-3-hydroxyisoxazol-5-yl)... J Med Chem. 1998 Mar 12;41(6):930-9.
24 A novel selective metabotropic glutamate receptor 4 agonist reveals new possibilities for developing subtype selective ligands with therapeutic potential. FASEB J. 2012 Apr;26(4):1682-93.
25 Pharmacokinetic and pharmacodynamic characterisation of JNJ-40411813, a positive allosteric modulator of mGluR2, in two randomised, double-blind phase-I studies. J Psychopharmacol. 2015 Apr;29(4):414-25.
26 Annual Reports in Medicinal Chemistry. Volume 47, 2012, Page(78).
27 Opportunities and challenges in the discovery of allosteric modulators of GPCRs for treating CNS disorders. Nat Rev Drug Discov. 2014 Sep;13(9):692-708.
28 MGlu2 receptor-mediated modulation of conditioned avoidance behavior in rats. European journal of pharmacology. 01/2014; 727(1).
29 Metabolism and disposition of the metabotropic glutamate receptor 5 antagonist (mGluR5) mavoglurant (AFQ056) in healthy subjects. Drug Metab Dispos. 2013 Sep;41(9):1626-41.
30 Pipeline of Addex Pharma. Addex Pharma. 2009.
31 The challenges of clinical trials in fragile X syndrome. Psychopharmacology (Berl) 2014; 231(6): 1237-1250.
32 Social Communication is an Emerging Target for Pharmacotherapy in Autism Spectrum Disorder - A Review of the Literature on Potential Agents. J Can Acad Child Adolesc Psychiatry. 2014 February; 23(1):20-30.
33 A proof-of-concept study evaluating the effect of ADX10059, a metabotropic glutamate receptor-5 negative allosteric modulator, on acid exposure and... Gut. 2009 Sep;58(9):1192-9.
34 Glutamate- and GABA-based CNS therapeutics. Curr Opin Pharmacol. 2006 Feb;6(1):7-17.
35 URL: 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. (Target id: 293).
36 Fenobam: a clinically validated nonbenzodiazepine anxiolytic is a potent, selective, and noncompetitive mGlu5 receptor antagonist with inverse agon... J Pharmacol Exp Ther. 2005 Nov;315(2):711-21.
37 Clinical pipeline report, company report or official report of Roche.
38 Silent Allosteric Modulation of mGluR5 Maintains Glutamate Signaling while Rescuing Alzheimer's Mouse Phenotypes. Cell Rep. 2017 Jul 5;20(1):76-88.