Chemical Structure : ZG-2492
货号: PC-24993Not For Human Use, Lab Use Only.
ZG-2492 is a potent, orally bioavailable inhibitor of lactate dehydrogenase A (LDHA) with IC50 of 156 nM.
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ZG-2492 is a potent, orally bioavailable inhibitor of lactate dehydrogenase A (LDHA) with IC50 of 156 nM.
ZG-2492 exhibits cytotoxicity activity against pancreatic Mia PaCa-2 cells with IC50 of 2.4 uM, shows no toxicity to normal HUVEC cells (IC50>40 uM).
ZG-2492 inhibits lactate production in pancreatic Mia PaCa-2 cells with IC50 of 3.6 uM.
ZG-2492 binds LDHA with a dissociation constant (Kd) of 3.99 μM in SPR assays.
ZG-2492 (1-10 uM) induces apoptosis in Mia PaCa-2 cells.
ZG-2492 (100 mg/kg, oral) exhibited antitumor effects in Mia PaCa-2 xenograft nude mouse model.
分子量 | 448.92 | |
分子式 | C20H21ClN4O4S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Qijie Gong, et al. J Med Chem. 2025 Jul 11. doi: 10.1021/acs.jmedchem.5c00359.
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