General Information of Drug (ID: DMMGYXR)

Drug Name
Dizocilpine Drug Info
Synonyms
DIZOCILPINE; 77086-21-6; MK-801 (Dizocilpine); UNII-7PY8KH681I; MK-801; Lopac-M-108; Lopac-M-107; MK 801; Prestwick0_000109; (5S,10R)-5-methyl-10,11-dihydro-5H-5,10-epiminodibenzo[a,d][7]annulene; 7PY8KH681I; CHEMBL284237; CHEBI:34725; Dizocilpine [INN]; Dizocilpinum [INN-Latin]; Dizocilpina [INN-Spanish]; Dizocilpinum; Dizocilpina; MK801; MK-801(Dizocilpine); HSDB 7641; (+)MK-801; (+)-MK-801; (+/-)-MK801; Prestwick2_000109; Prestwick3_000109; Prestwick1_000109; Biomol-NT_000210; SCHEMBL34528; Lopac0_000872; BSPBio_000098; SPBio_002037
Indication
Disease Entry ICD 11 Status REF
Cerebrovascular ischaemia 8B1Z Terminated [1] , [2]
Cross-matching ID
PubChem CID
180081
ChEBI ID
CHEBI:34725
CAS Number
CAS 77086-21-6
TTD Drug ID
DMMGYXR
VARIDT Drug ID
DR00506

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Discontinued Drug(s)
Preclinical Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Glycine DMIOZ29 Malnutrition 5B50-5B71 Approved [5]
NBQX DMPHZI5 Neurological disorder 6B60 Phase 1 [6]
YM-90K DMWRT4L Convulsion 8A68.Z Discontinued in Phase 2 [7]
Spermine DMD4BFY N. A. N. A. Terminated [8]
L-689560 DMCVY4U Neurodegenerative disorder 8A20-8A23 Terminated [9]
L-698544 DMLRBN1 Alzheimer disease 8A20 Terminated [10]
RPR-104632 DM9L50N N. A. N. A. Terminated [11]
L-698532 DMO9HM7 Neurological disorder 6B60 Terminated [12]
L-695902 DMT1DNS N. A. N. A. Terminated [10]
L-701324 DMAIJSX Cerebrovascular ischaemia 8B1Z Terminated [12]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
IB-MECA DM9G5XD Psoriasis vulgaris EA90 Phase 3 [13]
Tonapofylline DMBH316 Acute and chronic heart failure BD1Z Phase 2 [14]
NITD609 DMQHBSX Malaria 1F40-1F45 Phase 2 [15]
CF102 DMP56WJ Hepatocellular carcinoma 2C12.02 Phase 2 [16]
SCH-442416 DMQ2K1V N. A. N. A. Phase 1 [17]
BEMESETRON DMSPJX9 N. A. N. A. Discontinued in Phase 3 [3]
BAY 60-6583 DMTEJV1 Myocardial ischemia BA6Z Preclinical [18]
CF602 DM0ULO2 Inflammation 1A00-CA43.1 Preclinical [16]
CF502 DMQSJ20 Inflammation 1A00-CA43.1 Preclinical [16]
Methylthioadenosine DMC8J6F Multiple sclerosis 8A40 Terminated [19]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Cycloserine DMT1I52 Bacterial infection 1A00-1C4Z Approved [20]
D-Serine DM3YH4I N. A. N. A. Phase 4 [21]
ELIPRODIL DMIOGZM Multiple sclerosis 8A40 Phase 2 [22]
NBQX DMPHZI5 Neurological disorder 6B60 Phase 1 [6]
YM-90K DMWRT4L Convulsion 8A68.Z Discontinued in Phase 2 [7]
Spermine DMD4BFY N. A. N. A. Terminated [8]
L-689560 DMCVY4U Neurodegenerative disorder 8A20-8A23 Terminated [23]
L-698544 DMLRBN1 Alzheimer disease 8A20 Terminated [10]
RPR-104632 DM9L50N N. A. N. A. Terminated [11]
L-698532 DMO9HM7 Neurological disorder 6B60 Terminated [12]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Alpha 1-PI DMXC1K9 Alpha-1 antitrypsin deficiency 5C5A Approved [24]
ELIPRODIL DMIOGZM Multiple sclerosis 8A40 Phase 2 [22]
CP-101,606 DMIU19E Parkinson disease 8A00.0 Phase 2 [25]
CERC-301 DMSABRI Major depressive disorder 6A70.3 Phase 2 [26]
RGH-896 DMCHZAN Peripheral neuropathy 8C0Z Phase 2 [27]
MIJ821 DMN45RI Major depressive disorder 6A70.3 Phase 2 [28]
NBQX DMPHZI5 Neurological disorder 6B60 Phase 1 [6]
Neu-2000 DMNJTLC Cardiac arrest MC82 Phase 1 [29]
EVT100 DMAKWQD Major depressive disorder 6A70.3 Phase 1 [30]
YM-90K DMWRT4L Convulsion 8A68.Z Discontinued in Phase 2 [7]
⏷ 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
Adenosine A3 receptor (ADORA3) TTJFY5U AA3R_HUMAN Inhibitor [3]
Glutamate receptor ionotropic NMDA 1 (NMDAR1) TTLD29N NMDZ1_HUMAN Inhibitor [4]
Glutamate receptor ionotropic NMDA 2A (NMDAR2A) TTKJEMQ NMDE1_HUMAN Inhibitor [4]
Glutamate receptor ionotropic NMDA 2B (NMDAR2B) TTN9D8E NMDE2_HUMAN Inhibitor [4]

References

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2 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800000713)
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5 Glycine transport inhibitors for the treatment of schizophrenia: Symptom and disease modification. Curr Opin Drug Discov Devel. 2009 Jul;12(4):468-78.
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8 Bivalent beta-carbolines as potential multitarget anti-Alzheimer agents. J Med Chem. 2010 May 13;53(9):3611-7.
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11 Indeno[1,2-b]pyrazin-2,3-diones: a new class of antagonists at the glycine site of the NMDA receptor with potent in vivo activity. J Med Chem. 2000 Jun 15;43(12):2371-81.
12 Synthesis of thieno[2,3-b]pyridinones acting as cytoprotectants and as inhibitors of [3H]glycine binding to the N-methyl-D-aspartate (NMDA) receptor. J Med Chem. 2006 Feb 9;49(3):864-71.
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15 Spiroindolones, a potent compound class for the treatment of malaria. Science. 2010 Sep 3;329(5996):1175-80.
16 2011 Pipeline of Can-Fite BioPharm.
17 Synthesis and evaluation of 1,2,4-triazolo[1,5-c]pyrimidine derivatives as A2A receptor-selective antagonists. Bioorg Med Chem Lett. 2010 Oct 1;20(19):5690-4.
18 Protein kinase C protects preconditioned rabbit hearts by increasing sensitivity of adenosine A2b-dependent signaling during early reperfusion. J Mol Cell Cardiol. 2007 Sep;43(3):262-71.
19 Novel amino acid derived natural products from the ascidian Atriolum robustum: identification and pharmacological characterization of a unique aden... J Med Chem. 2004 Apr 22;47(9):2243-55.
20 How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
21 Therapeutic Target Database. Nucleic Acids Res. 2002 Jan 1;30(1):412-5.
22 4-Hydroxy-1-[2-(4-hydroxyphenoxy)ethyl]-4-(4-methylbenzyl)piperidine: a novel, potent, and selective NR1/2B NMDA receptor antagonist. J Med Chem. 1999 Jul 29;42(15):2993-3000.
23 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: 455).
24 NMDA receptor stimulation induces reversible fission of the neuronal endoplasmic reticulum. PLoS One. 2009;4(4):e5250.
25 NMDA receptors as targets for drug action in neuropathic pain. Eur J Pharmacol. 2001 Oct 19;429(1-3):71-8.
26 Inhibition of in vivo [(3)H]MK-801 binding by NMDA receptor open channel blockers and GluN2B antagonists in rats and mice. Eur J Pharmacol. 2015 Nov 5;766:1-8.
27 Emerging drugs in neuropathic pain. Expert Opin Emerg Drugs. 2007 Mar;12(1):113-26.
28 Clinical pipeline report, company report or official report of Cadent Therapeutics.
29 Neu2000, an NR2B-selective, moderate NMDA receptor antagonist and potent spin trapping molecule for stroke. Drug News Perspect. 2010 Nov;23(9):549-56.
30 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)