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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8N2O
Molecular Weight 136.1512
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-Aminobenzamide

SMILES

NC(=O)C1=CC=C(N)C=C1

InChI

InChIKey=QIKYZXDTTPVVAC-UHFFFAOYSA-N
InChI=1S/C7H8N2O/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H2,9,10)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Capsaicin promotes a more aggressive gene expression phenotype and invasiveness in null-TRPV1 urothelial cancer cells.
2011-05
Bis(4-amino-benzoic acid-κN)dichloridozinc(II).
2010-11-24
A novel dietary supplement containing multiple phytochemicals and vitamins elevates hepatorenal and cardiac antioxidant enzymes in the absence of significant serum chemistry and genomic changes.
2010-08-19
Polyamide curvature and DNA sequence selective recognition: use of 4-aminobenzamide to adjust curvature.
2009-05
Bis(2,2'-bipyridine){ethyl 4'-[N-(4-carbamoylphen-yl)carbamo-yl]-2,2'-bi-pyridine-4-carboxyl-ate}ruthenium(II) bis-[hexa-fluorido-phosphate(V)].
2009-01-28
N-substituted 4-aminobenzamides (procainamide analogs): an assessment of multiple cellular effects concerning ion trapping.
2005-12
The effect of global compaction on the local secondary structure of folded dendrimers.
2003-11-26
Functional role for Tyr 31 in the catalytic cycle of chicken dihydrofolate reductase.
2003-05-01
Structures of Ser205 mutant plasmepsin II from Plasmodium falciparum at 1.8 A in complex with the inhibitors rs367 and rs370.
2002-12
Ca(2+)-calmodulin antagonist chlorpromazine and poly(ADP-ribose) polymerase modulators 4-aminobenzamide and nicotinamide influence hepatic expression of BCL-XL and P53 and protect against acetaminophen-induced programmed and unprogrammed cell death in mice.
2001-08-01
Differential effects of IH636 grape seed proanthocyanidin extract and a DNA repair modulator 4-aminobenzamide on liver microsomal cytochrome 4502E1-dependent aniline hydroxylation.
2001-02
[Preparation of novel magnetic dextran affinity adsorbents and their application to purify urokinase].
2001-01
Patents
Name Type Language
NSC-233920
Preferred Name English
4-Aminobenzamide
Systematic Name English
BENZAMIDE, 4-AMINO-
Systematic Name English
P-AMINOBENZAMIDE
Common Name English
4-CARBOXAMIDOANILINE
Common Name English
4-(AMINOCARBONYL)ANILINE
Systematic Name English
(4-(AMINOCARBONYL)PHENYL)AMINE
Systematic Name English
NSC-36963
Code English
4-CARBAMOYLANILINE
Systematic Name English
P-CARBAMOYLANILINE
Common Name English
4-AMINOBENZENECARBOXAMIDE
Systematic Name English
(4-AMINOPHENYL)CARBOXAMIDE
Common Name English
P-AMINOCARBONYLANILINE
Common Name English
BENZAMIDE, P-AMINO-
Systematic Name English
P-AMINOBENZENECARBOXAMIDE
Common Name English
Code System Code Type Description
PUBCHEM
76079
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
220-612-3
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY
NSC
233920
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY
FDA UNII
77722I6PAC
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID7038814
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY
CAS
2835-68-9
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY
NSC
36963
Created by admin on Mon Mar 31 21:09:21 GMT 2025 , Edited by admin on Mon Mar 31 21:09:21 GMT 2025
PRIMARY