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(E)- 1- (4- tert- butylbenzyl)- N'- (1- (5- chloro- 2- hydroxyphenyl) ethylidene)- 3- (4- chlorophenyl)- 1H- pyrazole- 5- carbohydrazide
structure in first source
Also Known As:
4-TCH-CP-CH cpd
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Bio-Agent Context: Research Results
Organic Chemicals: 133
Hydrazines: 379
(E)-1-(4-tert-butylbenzyl)-N'-(1-(5-chloro-2-hydroxyphenyl) ethylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide: 1
Heterocyclic Compounds: 198
1-Ring Heterocyclic Compounds
Azoles: 2138
Pyrroles: 369
(E)-1-(4-tert-butylbenzyl)-N'-(1-(5-chloro-2-hydroxyphenyl) ethylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide: 1
Experts
1.
Dong, Wen-Liang
: 1 article (03/2009)
2.
Miao, Jun-Ying
: 1 article (03/2009)
3.
Wu, Ling-Ling
: 1 article (03/2009)
4.
Zhao, Bao-Xiang
: 1 article (03/2009)
5.
Zheng, Liang-Wen
: 1 article (03/2009)
Related Diseases
1.
Lung Neoplasms (Lung Cancer)
03/01/2009 - "
The results showed that all compounds had inhibitory effects on the growth of A549 lung cancer cells and compound (E)-1-(4-tert-butylbenzyl)-N'-(1-(5-chloro-2-hydroxyphenyl) ethylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide (3e) possessed the highest growth inhibitory effect and induced apoptosis of A549 lung cancer cells.
"