𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: 4,5-Diaryl-3-aminopyrazole Derivatives as Analogues of Combretastatin A-4: Synthesis and Biological Evaluation.

✍ Scribed by Tao Liu; Rong Cui; Jing Chen; Jun Zhang; Qiaojun He; Bo Yang; Yongzhou Hu

Publisher
John Wiley and Sons
Year
2011
Weight
26 KB
Volume
42
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Synthesis and Biolo
ChemInform Abstract: Synthesis and Biological Evaluation of 4-Chloro-3,5-dinitrobenzotrifluoride Analogues as Antileishmanial Agents.
✍ Kevin K. Pitzer; Karl A. Werbovetz; James J. Brendle; John P. Scovill πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 28 KB πŸ‘ 1 views

## Synthesis and Biological Evaluation of 4-Chloro-3,5dinitrobenzotrifluoride Analogues as Antileishmanial Agents. -Investigation of 17 desnitro analogues of title compound chloralin in vitro against amastigote-like Leishmania donovani parasites shows that compound (If) possesses excellent in vit

ChemInform Abstract: Synthesis and Antic
ChemInform Abstract: Synthesis and Anticonvulsant Activity of New 4-Aminopyrazoles and 5-Aminopyrazol-3-ones.
✍ H.-J. Lankau; M. Menzer; A. Rostock; Th. Arnold; Ch. Rundfeldt; K. Unverferth πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: Design, Synthesis,
ChemInform Abstract: Design, Synthesis, and Biological Evaluation of 1,5-Diaryl-1,2,4-triazole Derivatives as Selective Cyclooxygenase-2 Inhibitors.
✍ Bo Jiang; Yi Zeng; Meng-Jie Li; Jin-Yi Xu; Yong-Na Zhang; Qiu-Juan Wang; Ni-Yue πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 24 KB πŸ‘ 1 views

## Abstract The results of biological tests show that compound (I) is a potent and selective inhibitor of COX‐2 (IC~50~ = 0.37 ΞΌM) being equipotent to celecoxib.