Chemical Structure : BVL3572S
Catalog No.: PC-27995Not For Human Use, Lab Use Only.
BVL3572S is a potent bactericidal compound potently inhibits Mtb growth (MIC90=1.7 uM, Mtb H37Rv) and is bactericidal, inhibits two essential pyridoxal phosphate (PLP)-dependent aminotransferases HisC and AlaA, disrupting L-His and L-Ala biosynthesis.
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BVL3572S is a potent bactericidal compound potently inhibits Mtb growth (MIC90=1.7 uM, Mtb H37Rv) and is bactericidal, inhibits two essential pyridoxal phosphate (PLP)-dependent aminotransferases HisC and AlaA, disrupting L-His and L-Ala biosynthesis.
BVL3572S shows broad-spectrum activity against Gram-positive and Gram-negative bacteria.
BVL3572S inhibits Mtb growth by targeting histidine and alanine biosynthesis, has a broad impact on intrabacterial amino acid levels.
BVL3572S synergizes with the second-line antibiotic D-cycloserine.
| M.Wt | 257.09 | |
| Formula | C9H9BrN2O2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Zainab Edoo, et al. Cell Chem Biol. 2026 Aug 11:S2451-9456(26)00281-3.

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