Chemical Structure : ZK-316
Catalog No.: PC-24427Not For Human Use, Lab Use Only.
ZK-316 is a potent, HIV non-nucleoside reverse transcriptase inhibitor (NNRTI) with IC50 of 0.21 uM (WT HIV-1 RT), exhibits potent and broad-spectrum activity against wild-type and clinically observed mutant strains with EC50 of 0.99-75.1 nM.
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ZK-316 is a potent, HIV non-nucleoside reverse transcriptase inhibitor (NNRTI) with IC50 of 0.21 uM (WT HIV-1 RT), exhibits potent and broad-spectrum activity against wild-type and clinically observed mutant strains with EC50 of 0.99-75.1 nM.
ZK-316 exhibits the highest inhibitory activity against WT HIV-1 (EC50 = 0.99 nM) and selectivity index (SI > 227,273).
ZK-316 is exceptionally potent against single/double mutant strains with EC50 values of 2.61 nM (L100I), 1.13 nM (K103N), 5.86 nM (Y181C), 5.18 nM (Y188L), 7.75 nM (E138 K), 4.46 nM (F227L + V106A), and 75.1 nM (RES056) in MT-4 cells.
ZK-316 shows favorable pharmacokinetic profiles with a better oral bioavailability of 29%.
M.Wt | 554.72 | |
Formula | C27H22D6N6O3S2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Kun Zhang, et al. J Med Chem. 2025 Apr 5. doi: 10.1021/acs.jmedchem.5c00202.
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