U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C16H15N
Molecular Weight 221.297
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIZOCILPINE

SMILES

C[C@]12N[C@H](CC3=CC=CC=C13)C4=CC=CC=C24

InChI

InChIKey=LBOJYSIDWZQNJS-CVEARBPZSA-N
InChI=1S/C16H15N/c1-16-13-8-4-2-6-11(13)10-15(17-16)12-7-3-5-9-14(12)16/h2-9,15,17H,10H2,1H3/t15-,16+/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H15N
Molecular Weight 221.297
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:28:23 UTC 2023
Edited
by admin
on Fri Dec 15 15:28:23 UTC 2023
Record UNII
7PY8KH681I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIZOCILPINE
HSDB   INN   MI   WHO-DD  
INN  
Official Name English
Dizocilpine [WHO-DD]
Common Name English
DIZOCILPINE [MI]
Common Name English
MK-801
Code English
5H-DIBENZO(A,D)CYCLOHEPTEN-5,10-IMINE, 10,11-DIHYDRO-5-METHYL-, (+)-
Common Name English
(+)-10,11-DIHYDRO-5-METHYL-5H-DIBENZO(A,D)CYCLOHEPTEN-5,10-IMINE
Common Name English
DIZOCILPINE [HSDB]
Common Name English
dizocilpine [INN]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 605204
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
WIKIPEDIA Designer-drugs-Dizocilpine
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
WIKIPEDIA NMDA receptor antagonist
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
NCI_THESAURUS C264
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID3048447
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
EVMPD
SUB06341MIG
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
PUBCHEM
180081
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
HSDB
7641
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
FDA UNII
7PY8KH681I
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
NCI_THESAURUS
C65450
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
CHEBI
176788
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
CHEBI
34725
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
MERCK INDEX
m4700
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL284237
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
CAS
77086-21-6
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
SMS_ID
100000081843
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
INN
6320
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
WIKIPEDIA
DIZOCILPINE
Created by admin on Fri Dec 15 15:28:23 UTC 2023 , Edited by admin on Fri Dec 15 15:28:23 UTC 2023
PRIMARY
Related Record Type Details
TRANSPORTER -> INHIBITOR
TARGET -> INHIBITOR
TRANSPORTER -> INHIBITOR
TRANSPORTER -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY