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Details

Stereochemistry RACEMIC
Molecular Formula C24H19ClN4O4
Molecular Weight 462.885
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BMS-908662

SMILES

COC(=O)NC1=NC2=CC(=CC=C2N1)C3(O)N(C(=O)C4=C3C=CC=C4)C5=C(C)C=CC(Cl)=C5

InChI

InChIKey=MMNNTJYFHUDSKL-UHFFFAOYSA-N
InChI=1S/C24H19ClN4O4/c1-13-7-9-15(25)12-20(13)29-21(30)16-5-3-4-6-17(16)24(29,32)14-8-10-18-19(11-14)27-22(26-18)28-23(31)33-2/h3-12,32H,1-2H3,(H2,26,27,28,31)

HIDE SMILES / InChI

Molecular Formula C24H19ClN4O4
Molecular Weight 462.885
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:32 UTC 2023
Edited
by admin
on Fri Dec 15 16:04:32 UTC 2023
Record UNII
DW2NWI3TFN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BMS-908662
Common Name English
CARBAMIC ACID, N-(6-(2-(5-CHLORO-2-METHYLPHENYL)-2,3-DIHYDRO-1-HYDROXY-3-OXO-1H-ISOINDOL-1-YL)-1H-BENZIMIDAZOL-2-YL)-, METHYL ESTER
Common Name English
METHYL (5-(2-(5-CHLORO-2-METHYLPHENYL)-1-HYDROXY-3-OXO-2,3-DIHYDRO-1H-ISOINDOL-1-YL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
Systematic Name English
CARBAMIC ACID, (5-(2-(5-CHLORO-2-METHYLPHENYL)-2,3-DIHYDRO-1-HYDRO
Common Name English
(±)-METHYL (5-(2-(5-CHLORO-2-METHYLPHENYL)-1-HYDROXY-3-OXO-2,3-DIHYDRO-1H-ISOINDOL-1-YL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE
Systematic Name English
METHYL (5-(2-(5-CHLORO-2-METHYLPHENYL)-1-HYDROXY-3-OXO-2,3-DIHYDRO-1H-ISOINDOL-1-YL)-1H-BENZIMIDAZOL-2-YL)CARBAMATE, (±)-
Systematic Name English
BMS-908662 FREE BASE
Common Name English
XL 281 [WHO-DD]
Common Name English
Code System Code Type Description
SMS_ID
100000174997
Created by admin on Fri Dec 15 16:04:32 UTC 2023 , Edited by admin on Fri Dec 15 16:04:32 UTC 2023
PRIMARY
FDA UNII
DW2NWI3TFN
Created by admin on Fri Dec 15 16:04:32 UTC 2023 , Edited by admin on Fri Dec 15 16:04:32 UTC 2023
PRIMARY
DRUG BANK
DB12854
Created by admin on Fri Dec 15 16:04:32 UTC 2023 , Edited by admin on Fri Dec 15 16:04:32 UTC 2023
PRIMARY
CAS
870603-16-0
Created by admin on Fri Dec 15 16:04:32 UTC 2023 , Edited by admin on Fri Dec 15 16:04:32 UTC 2023
PRIMARY
ChEMBL
CHEMBL3545027
Created by admin on Fri Dec 15 16:04:32 UTC 2023 , Edited by admin on Fri Dec 15 16:04:32 UTC 2023
PRIMARY
PUBCHEM
56931136
Created by admin on Fri Dec 15 16:04:32 UTC 2023 , Edited by admin on Fri Dec 15 16:04:32 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY