Design, Synthesis, X-ray Crystallographic Analysis, and Biological Evaluation of Thiazole Derivatives as Potent and Selective Inhibitors of Human Dihydroorotate Dehydrogenase

2015 ◽  
Vol 58 (3) ◽  
pp. 1123-1139 ◽  
Author(s):  
Junsheng Zhu ◽  
Le Han ◽  
Yanyan Diao ◽  
Xiaoli Ren ◽  
Minghao Xu ◽  
...  
Keyword(s):  
Biological Evaluation ◽  
Crystallographic Analysis ◽  
Dihydroorotate Dehydrogenase ◽  
Selective Inhibitors ◽  
Thiazole Derivatives ◽  
Design Synthesis ◽  
X Ray

Anilinopyrazole as Selective CDK2 Inhibitors: Design, Synthesis, Biological Evaluation, and X-Ray Crystallographic Analysis.

ChemInform ◽  
2003 ◽  
Vol 34 (50) ◽  
Author(s):  
Jun Tang ◽  
Lisa M. Shewchuk ◽  
Hideyuki Sato ◽  
Masaichi Hasegawa ◽  
Yoshiaki Washio ◽  
...  
Keyword(s):  
Biological Evaluation ◽  
Crystallographic Analysis ◽  
Design Synthesis ◽  
X Ray

Isolation and structure of combretastatin

1982 ◽  
Vol 60 (11) ◽  
pp. 1374-1376 ◽  
Author(s):  
George R. Pettit ◽  
Gordon M. Cragg ◽  
Delbert L. Herald ◽  
Jean M. Schmidt ◽  
Prasert Lohavanijaya
Keyword(s):  
Total Synthesis ◽  
South African ◽  
Spectral Methods ◽  
Biological Evaluation ◽  
Crystallographic Analysis ◽  
Structural Elucidation ◽  
The South ◽  
X Ray

The South African tree Combretumcaffrum has been shown to contain a constituent capable of significantly reversing astrocyte formation employing the National Cancer Institute's 9ASK system. The constituent responsible for astrocyte reversal was isolated and designated combretastatin (1). Structural elucidation was initiated employing spectral methods and completed by X-ray crystallographic analysis. By this means combretastatin was assigned structure 1. Further biological evaluation and a total synthesis are now in progress.

scholarly journals Design, synthesis, X-ray studies, and biological evaluation of novel macrocyclic HIV-1 protease inhibitors involving the P1′-P2′ ligands

2017 ◽  
Vol 27 (21) ◽  
pp. 4925-4931 ◽  
Author(s):  
Arun K. Ghosh ◽  
W. Sean Fyvie ◽  
Margherita Brindisi ◽  
Melinda Steffey ◽  
Johnson Agniswamy ◽  
...  
Keyword(s):  
Protease Inhibitors ◽  
Biological Evaluation ◽  
Design Synthesis ◽  
X Ray ◽  
Hiv 1

scholarly journals Probing Lipophilic Adamantyl Group as the P1-Ligand for HIV-1 Protease Inhibitors: Design, Synthesis, Protein X-ray Structural Studies, and Biological Evaluation

2016 ◽  
Vol 59 (14) ◽  
pp. 6826-6837 ◽  
Author(s):  
Arun K. Ghosh ◽  
Heather L. Osswald ◽  
Kristof Glauninger ◽  
Johnson Agniswamy ◽  
Yuan-Fang Wang ◽  
...  
Keyword(s):  
Protease Inhibitors ◽  
Biological Evaluation ◽  
Structural Studies ◽  
Design Synthesis ◽  
X Ray ◽  
Protein X ◽  
Hiv 1

scholarly journals Structure-based design, synthesis, X-ray studies, and biological evaluation of novel HIV-1 protease inhibitors containing isophthalamide-derived P2-ligands

2015 ◽  
Vol 25 (21) ◽  
pp. 4903-4909 ◽  
Author(s):  
Arun K. Ghosh ◽  
Jun Takayama ◽  
Luke A. Kassekert ◽  
Jean-Rene Ella-Menye ◽  
Sofiya Yashchuk ◽  
...  
Keyword(s):  
Protease Inhibitors ◽  
Biological Evaluation ◽  
Design Synthesis ◽  
X Ray ◽  
Hiv 1
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