Chemical Structure : AN12855
货号: PC-36156Not For Human Use, Lab Use Only.
AN12855 (AN-12855) is potent, cofactor-independent M. tuberculosis InhA inhibitor, binds to and inhibits InhA with IC50 of 0.03 uM, shows potent activity against whole-cell M. tuberculosis H37Rv with IC90 of 0.09 uM.
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
AN12855 (AN-12855) is potent, cofactor-independent M. tuberculosis InhA inhibitor, binds to and inhibits InhA with IC50 of 0.03 uM, shows potent activity against whole-cell M. tuberculosis H37Rv with IC90 of 0.09 uM.
AN12855 demonstrates potent activity against drug-susceptible and drug-resistant strains of M. tuberculosis.
AN12855 exhibits comparable efficacy to the frontline antitubercular drug isoniazid (INH) in both acute and chronic models of TB infection with a lower potential for resistance development and shows in vitro activity against conventional KatG-mediated INH-resistant M. tuberculosis.
分子量 | 441.188 | |
分子式 | C17H15BF3N3O5S | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
1. Xia Y, et al. Life Sci Alliance. 2018 Jun 1;1(3):e201800025.
2. Robertson GT, et al. Antimicrob Agents Chemother. 2019 Mar 27;63(4). pii: e02071-18.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright