3-METHOXYBENZAMIDE

COC1=CC(=CC=C1)C(N)=O

InChIKey=VKPLPDIMEREJJF-UHFFFAOYSA-N

InChI=1S/C8H9NO2/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5H,1H3,(H2,9,10)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Characterization of ftsZ mutations that render Bacillus subtilis resistant to MinC.	2010-08-11	20711458
Creating an antibacterial with in vivo efficacy: synthesis and characterization of potent inhibitors of the bacterial cell division protein FtsZ with improved pharmaceutical properties.	2010-05-27	20426423
Deciphering the stem cell machinery as a basis for understanding the molecular mechanism underlying reprogramming.	2009-11	19662495
Antibacterial alkoxybenzamide inhibitors of the essential bacterial cell division protein FtsZ.	2009-01-15	19064318
In silico characterization of the family of PARP-like poly(ADP-ribosyl)transferases (pARTs).	2005-10-04	16202152
Recoupled long-range C-H dipolar dephasing in solid-state NMR, and its use for spectral selection of fused aromatic rings.	2003-05	12762998
1,5-isoquinolinediol increases the frequency of gene targeting by homologous recombination in mouse fibroblasts.	2003-02	12683632

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:36:46 GMT 2025` Edited by `admin` on `Mon Mar 31 21:36:46 GMT 2025`
Record UNII	M8502TLK98
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

3-METHOXYBENZAMIDE

Systematic Name

English

NSC-209527

Preferred Name

English

3MBA

Common Name

English

NSC-28589

Code

English

M-METHOXYBENZAMIDE

Systematic Name

English

BENZAMIDE, 3-METHOXY-

Systematic Name

English

M-ANISAMIDE

Systematic Name

English

Code System Code Type Description

NSC

209527