Synthesis, characterization, and biological evaluation of benzimidazole derivatives as potential anxiolytics.

about

Synthesis and evaluation of antimicrobial, antitubercular and anticancer activities of 2-(1-benzoyl-1H-benzo[d]imidazol-2-ylthio)-N-substituted acetamides.

P2860

Q55346818-DE685B33-1809-43F5-B0F1-6FE46984BC1C

P2860

Synthesis, characterization, and biological evaluation of benzimidazole derivatives as potential anxiolytics.

Item

http://www.wikidata.org/entity/Q42396778

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

Synthesis, characterization, a ...... ives as potential anxiolytics.

@en

Synthesis, characterization, a ...... ives as potential anxiolytics.

@nl

type

Item

label

Synthesis, characterization, a ...... ives as potential anxiolytics.

@en

Synthesis, characterization, a ...... ives as potential anxiolytics.

@nl

prefLabel

Synthesis, characterization, a ...... ives as potential anxiolytics.

@en

Synthesis, characterization, a ...... ives as potential anxiolytics.

@nl

P1476

Synthesis, characterization, a ...... ives as potential anxiolytics.

@en

P2093

Atyam Vsss Gupta

http://www.w3.org/2001/XMLSchema#string

Dt Nannapaneni

http://www.w3.org/2001/XMLSchema#string

Mi Reddy

http://www.w3.org/2001/XMLSchema#string

Raidu Ch Sarva

http://www.w3.org/2001/XMLSchema#string

P2860

Discovery of novel benzimidazoles as potent inhibitors of TIE-2 and VEGFR-2 tyrosine kinase receptors

Diarylamidine derivatives with one or both of the aryl moieties consisting of an indole or indole-like ring. Inhibitors of arginine-specific esteroproteases

Synthesis, pharmacology and molecular modeling of N-substituted 2-phenyl-indoles and benzimidazoles as potent GABA(A) agonists.

Synthesis and evaluation of a series of novel 2-[(4-chlorophenoxy)methyl]benzimidazoles as selective neuropeptide Y Y1 receptor antagonists.

A review of the validity and variability of the elevated plus-maze as an animal model of anxiety.

Structure-activity relationships of benzimidazoles and related heterocycles as topoisomerase I poisons.

Novel cyano- and amidino-substituted derivatives of styryl-2-benzimidazoles and benzimidazo[1,2-a]quinolines. Synthesis, photochemical synthesis, DNA binding, and antitumor evaluation, part 3.

P304

273-279

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.4103/0975-1483.66809

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2010-07-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

47645721

http://www.w3.org/2001/XMLSchema#string

P698

21042485

http://www.w3.org/2001/XMLSchema#string

P932

2964780

http://www.w3.org/2001/XMLSchema#string

Synthesis, characterization, and biological evaluation of benzimidazole derivatives as potential anxiolytics.

about

P2860

P2860

Synthesis, characterization, and biological evaluation of benzimidazole derivatives as potential anxiolytics.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932