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Details

Stereochemistry ACHIRAL
Molecular Formula C21H23N5O2
Molecular Weight 377.4396
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BMS-433771

SMILES

OCCCCN1C(CN2C(=O)N(C3CC3)C4=C2C=NC=C4)=NC5=CC=CC=C15

InChI

InChIKey=KSHJXDWYTZJUEI-UHFFFAOYSA-N
InChI=1S/C21H23N5O2/c27-12-4-3-11-24-17-6-2-1-5-16(17)23-20(24)14-25-19-13-22-10-9-18(19)26(21(25)28)15-7-8-15/h1-2,5-6,9-10,13,15,27H,3-4,7-8,11-12,14H2

HIDE SMILES / InChI

Molecular Formula C21H23N5O2
Molecular Weight 377.4396
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Orally active fusion inhibitor of respiratory syncytial virus.
2004 Feb
Antiviral activity and molecular mechanism of an orally active respiratory syncytial virus fusion inhibitor.
2005 Mar
Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.
2007 Feb 15
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:40:59 GMT 2023
Edited
by admin
on Sat Dec 16 04:40:59 GMT 2023
Record UNII
G2427554NW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BMS-433771
Common Name English
1-CYCLOPROPYL-3-((1-(4-HYDROXYBUTYL)-1H-BENZIMIDAZOL-2-YL)METHYL)-1,3-DIHYDROIMIDAZO(4,5-C)PYRIDIN-2-ONE
Systematic Name English
2H-IMIDAZO(4,5-C)PYRIDIN-2-ONE, 1-CYCLOPROPYL-1,3-DIHYDRO-3-((1-(4-HYDROXYBUTYL)-1H-BENZIMIDAZOL-2-YL)METHYL)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID20202746
Created by admin on Sat Dec 16 04:40:59 GMT 2023 , Edited by admin on Sat Dec 16 04:40:59 GMT 2023
PRIMARY
FDA UNII
G2427554NW
Created by admin on Sat Dec 16 04:40:59 GMT 2023 , Edited by admin on Sat Dec 16 04:40:59 GMT 2023
PRIMARY
PUBCHEM
6478034
Created by admin on Sat Dec 16 04:40:59 GMT 2023 , Edited by admin on Sat Dec 16 04:40:59 GMT 2023
PRIMARY
CAS
543700-68-1
Created by admin on Sat Dec 16 04:40:59 GMT 2023 , Edited by admin on Sat Dec 16 04:40:59 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY