Preliminary communicationSynthesis and biological evaluation of indazole derivatives
-
Add time:08/30/2019 Source:sciencedirect.com
The inhibition of neuronal and inducible nitric oxide synthases (nNOS and iNOS) by a series of 36 indazoles has been evaluated, showing that most of the assayed derivatives are better iNOS than nNOS inhibitors. A parabolic model relating the iNOS inhibition percentage with the difference, Erel, between stacking and apical interaction energies of indazoles with the active site of the NOS enzyme has been established.
► synthetic indazoles are good inhibitors of NOS isoforms. ► fluorine atoms in the molecule increase the inhibitory potency against NOS. ► 4,5,6,7-tetrafluoroindazole is a potent and selective iNOS inhibitor. ► a parabolic model relates the interaction between inhibitory indazoles and iNOS.
We also recommend Trading Suppliers and Manufacturers of 3-BROMO (1H) INDAZOLE CARBOXYLIC ACID (cas 114086-30-5). Pls Click Website Link as below: cas 114086-30-5 suppliers
Prev:ReviewFluorine-containing indazoles: Synthesis and biological activity
Next:Research paperDiscovery and optimization of a series of 3-substituted indazole derivatives as multi-target kinase inhibitors for the treatment of lung squamous cell carcinoma) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Research paperDiscovery and optimization of a series of 3-substituted indazole derivatives as multi-target kinase inhibitors for the treatment of lung squamous cell carcinoma08/31/2019
- ReviewFluorine-containing indazoles: Synthesis and biological activity08/29/2019
- Research paperCarboxamides vs. methanimines: Crystal structures, binding interactions, photophysical studies, and biological evaluation of (indazole-5-yl)methanimines as monoamine oxidase B and acetylcholinesterase inhibitors08/28/2019
- Mini-reviewSynthesis of indazole motifs and their medicinal importance: An overview08/27/2019
- Chapter Three - Indazoles: Synthesis and Bond-Forming Heterocyclization08/26/2019


