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Details

Stereochemistry ACHIRAL
Molecular Formula C16H22N4O
Molecular Weight 286.3721
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of A-620223

SMILES

CCCN1CCC(CC1)C2=NC3=C(N2)C(=CC=C3)C(N)=O

InChI

InChIKey=KXSIHXHEHABEJX-UHFFFAOYSA-N
InChI=1S/C16H22N4O/c1-2-8-20-9-6-11(7-10-20)16-18-13-5-3-4-12(15(17)21)14(13)19-16/h3-5,11H,2,6-10H2,1H3,(H2,17,21)(H,18,19)

HIDE SMILES / InChI

Molecular Formula C16H22N4O
Molecular Weight 286.3721
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
QSAR study of 2-(1-Propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide as PARP inhibitors for treatment of cancer.
2008-12
Discovery and SAR of 2-(1-propylpiperidin-4-yl)-1H-benzimidazole-4-carboxamide: A potent inhibitor of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer.
2008-07-15
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:00:06 GMT 2025
Edited
by admin
on Mon Mar 31 23:00:06 GMT 2025
Record UNII
01FPW436S6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
A-620223
Common Name English
1H-BENZIMIDAZOLE-4-CARBOXAMIDE, 2-(1-PROPYL-4-PIPERIDINYL)-
Preferred Name English
1H-BENZIMIDAZOLE-7-CARBOXAMIDE, 2-(1-PROPYL-4-PIPERIDINYL)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID40181726
Created by admin on Mon Mar 31 23:00:06 GMT 2025 , Edited by admin on Mon Mar 31 23:00:06 GMT 2025
PRIMARY
PUBCHEM
9925908
Created by admin on Mon Mar 31 23:00:06 GMT 2025 , Edited by admin on Mon Mar 31 23:00:06 GMT 2025
PRIMARY
DRUG BANK
DB07330
Created by admin on Mon Mar 31 23:00:06 GMT 2025 , Edited by admin on Mon Mar 31 23:00:06 GMT 2025
PRIMARY
CAS
272769-49-0
Created by admin on Mon Mar 31 23:00:06 GMT 2025 , Edited by admin on Mon Mar 31 23:00:06 GMT 2025
PRIMARY
FDA UNII
01FPW436S6
Created by admin on Mon Mar 31 23:00:06 GMT 2025 , Edited by admin on Mon Mar 31 23:00:06 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY