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Details

Stereochemistry ACHIRAL
Molecular Formula C13H11NO
Molecular Weight 197.2325
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZANILIDE

SMILES

O=C(NC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=ZVSKZLHKADLHSD-UHFFFAOYSA-N
InChI=1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)

HIDE SMILES / InChI

Molecular Formula C13H11NO
Molecular Weight 197.2325
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Joint QSAR analysis using the Free-Wilson approach and quantum chemical parameters.
2001
Activation of the aryl hydrocarbon receptor by methyl yellow and related congeners: structure-activity relationships in halogenated derivatives.
2002 Apr
N-Methylbenzanilide derivatives as a novel class of selective V(1A) receptor antagonists.
2002 Jan 21
On the relationship between the substitution pattern of thiobenzanilides and their antimycobacterial activity.
2002 Sep
Lipophilicity parameter from high-performance liquid chromatography on an immobilized artificial membrane column and its relationships to bioactivity of the group of 2,4-dihydroxythiobenzanilides.
2002 Sep-Oct
A triclinic polymorph of benzanilide: disordered molecules form hydrogen-bonded chains.
2003 Jan
Preparation of non-peptide, highly potent and selective antagonists of arginine vasopressin V1A receptor by introduction of alkoxy groups.
2003 Sep
CG base pair recognition by substituted phenylimidazole nucleosides.
2004 Apr 21
Synthesis and biological activity of novel substituted benzanilides as potassium channel activators. V.
2004 Jun
Biological activity of 2-hydroxythiobenzanilides and related compounds.
2004 Mar
Dual fluorescence of diphenyl carbazide and benzanilide: effect of solvents and pH on electronic spectra.
2005 Dec
Unprecedented control over polymerization of n-hexyl isocyanate using an anionic initiator having synchronized function of chain-end protection.
2005 Mar 30
Neutron vibrational spectroscopy gives new insights into the structure of poly(p-phenylene terephthalamide).
2005 May 11
Structural modifications of benzanilide derivatives, effective potassium channel openers. X.
2006 Dec
Heterocyclic analogs of benzanilide derivatives as potassium channel activators. IX.
2006 Jun
Inhibitors of type III secretion in Yersinia: design, synthesis and multivariate QSAR of 2-arylsulfonylamino-benzanilides.
2007 Nov 15
Synthesis of 2-arylbenzoxazoles by copper-catalyzed intramolecular oxidative C-O coupling of benzanilides.
2008
New amido derivatives as potential BKCa potassium channel activators. XI.
2008 Apr
2,4-Dichloro-N-cyclo-hexyl-benzamide.
2008 Apr 2
N-(2-Methoxy-phen-yl)-2-nitro-benzamide.
2008 Feb 20
N-(4-Chloro-phen-yl)-3,4,5-trimethoxy-benzamide.
2008 Jul 31
Benzanilides with spasmolytic activity: chemistry, pharmacology, and SAR.
2008 Jun 1
4-Chloro-N-(2,6-dimethyl-phen-yl)benzamide.
2008 Jun 28
N-(2-Chloro-4-nitro-phen-yl)-2-nitro-benzamide.
2008 Mar 12
N-(4-Chloro-phen-yl)benzamide.
2008 Mar 29
Synthesis and biological evaluation of thiobenzanilides as anticancer agents.
2008 May 1
N-(2,4-Dichloro-phen-yl)benzamide.
2008 May 3
N-Butyl-4-chloro-benzamide.
2008 Nov 13
Mechanism based QSAR studies of N-phenylbenzamides as antimicrobial agents.
2008 Sep
N-(4-Nitro-phen-yl)cinnamamide.
2009 Aug 8
N-(4-Methoxy-phen-yl)pivalamide.
2009 Aug 8
[External stimulus-responsive conformational alterations of aromatic amides].
2009 Dec
Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA.
2009 Dec 15
Determination of a benzamide histone deacetylase inhibitor, MS-275, in human plasma by liquid chromatography with mass-spectrometric detection.
2009 Jan 15
N-Benzoyl-N'-(2-chloro-3-pyrid-yl)thio-urea.
2009 Jul 18
4-Chloro-N-cyclo-hexyl-benzamide.
2009 Jun 10
4-Chloro-N-(2,6-dichloro-phen-yl)benzamide.
2009 Jun 20
2-Fluoro-N-(4-methoxy-phen-yl)benzamide.
2009 Mar 19
4-Chloro-N-m-tolyl-benzamide.
2009 May 20
N-(3,4-Diethoxy-phen-yl)acetamide.
2009 May 20
Pharmacokinetics and tissue distribution of dodeca-2E,4E,8E,10E/Z-tetraenoic acid isobutylamides after oral administration in rats.
2009 Oct
Unusual spectral shifts on fast violet-B and benzanilide: Effect of solvents, pH and beta-cyclodextin.
2009 Oct 1
4-Chloro-N-(3-chloro-phen-yl)benzamide.
2009 Sep 12
4-Chloro-N-(3,4-dimethyl-phen-yl)benzamide.
2010 Apr 28
N-(4-Ferrocenylphenyl)benzamide.
2010 Jun 23
N-(2-Chloro-phen-yl)-3-methyl-benzamide.
2010 Mar 20
2-Methyl-N-p-tolyl-benzamide: a second monoclinic polymorph.
2010 Mar 24
N-(3-Chloro-phen-yl)-3-methyl-benzamide hemihydrate.
2010 Mar 31
N-(2,6-Dimethyl-phen-yl)-3-methyl-benzamide.
2010 Mar 31
Enantioseparation of benzazoles and benzanilides on polysaccharide-based chiral columns.
2010 May 5
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:14:46 GMT 2023
Edited
by admin
on Sat Dec 16 04:14:46 GMT 2023
Record UNII
AK1B12366O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZANILIDE
MI  
Systematic Name English
N-BENZOYLANILINE
Systematic Name English
BENZANILIDE [MI]
Common Name English
N-PHENYLBENZENECARBOXAMIDE
Systematic Name English
N-PHENYLBENZAMIDE
Systematic Name English
NSC-3131
Code English
Code System Code Type Description
ECHA (EC/EINECS)
202-292-7
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
CAS
93-98-1
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
EPA CompTox
DTXSID9059096
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
PUBCHEM
7168
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
MESH
C034595
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
WIKIPEDIA
BENZANILIDE
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
MERCK INDEX
m2333
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY Merck Index
FDA UNII
AK1B12366O
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY
NSC
3131
Created by admin on Sat Dec 16 04:14:46 GMT 2023 , Edited by admin on Sat Dec 16 04:14:46 GMT 2023
PRIMARY