Chemical Structure : MK-7762
Catalog No.: PC-25987Not For Human Use, Lab Use Only.
MK-7762 (TBD09) is a new broadly active oxazolidinone Mycobacterium tuberculosis (Mtb) inhibitor with MIC95 of 0.93 uM, inhibits the mycobacterial ribosome.
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MK-7762 (TBD09) is a new broadly active oxazolidinone Mycobacterium tuberculosis (Mtb) inhibitor with MIC95 of 0.93 uM, inhibits the mycobacterial ribosome.
MK-7762 shows no inhibition in a panel of 106 off-targets except for monoamine oxidase-B (IC50=6.9 uM).
MK-7762 showsminimal inhibition of MPS (half-maximal effective concentration (EC50) of 98 µM) compared to linezolid (EC50 of 16 µM), suggesting a low risk for mitochondrial toxicity in humans compared to linezolid.
MK-7762 has a more potent minimum bactericidal concentration (MBC) than that of linezolid with an observed MBC99 of 18.1 µM compared to 52.7 µM.
MK-7762 is active against a wide range of diverse drug-sensitive and drug-resistant clinical isolates and showed similar bactericidal activity as linezolid.
| M.Wt | 419.40 | |
| Formula | C16H19F2N3O6S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Crowley BM, et al. Nat Med. 2026 Jan 13. doi: 10.1038/s41591-025-04164-x.

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