Chemical Structure : TST1N-224
货号: PC-22813Not For Human Use, Lab Use Only.
TST1N-224 is a potent inhibitor targeting the response regulator VraRC of S. aureus, inhibits the formation of the VraRC-DNA complex with IC50 of 60.2 uM, shows strong binding to VraRC (KD=23.4 uM), enhances the susceptibility of vancomycin-intermediate S. aureus (VISA) to both vancomycin and methicillin.
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TST1N-224 is a potent inhibitor targeting the response regulator VraRC of S. aureus, inhibits the formation of the VraRC-DNA complex with IC50 of 60.2 uM, shows strong binding to VraRC (KD=23.4 uM), enhances the susceptibility of vancomycin-intermediate S. aureus (VISA) to both vancomycin and methicillin.
分子量 | 460.62 | |
分子式 | C10H20O8S6 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Ying-Chu Hsu, et al. J Chem Inf Model. 2024 Jul 30. doi: 10.1021/acs.jcim.4c01046.
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