Chemical Structure : ACT-1016-0707
货号: PC-21751Not For Human Use, Lab Use Only.
ACT-1016-0707 is a potent, selective, and orally active lysophosphatidic acid receptor subtype 1 receptor (LPA1 receptor, LPAR1) antagonist with IC50 of 3.1 nM, highly selective over LPAR2 or LPAR3.
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ACT-1016-0707 is a potent, selective, and orally active lysophosphatidic acid receptor subtype 1 receptor (LPA1 receptor, LPAR1) antagonist with IC50 of 3.1 nM, highly selective over LPAR2 or LPAR3.
ACT-1016-0707 suppressed the LPA-induced vascular leakage at a p.o. dose of 30 mg/kg.
分子量 | 438.93 | |
分子式 | C19H23ClN4O4S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Lescop C, et al. J Med Chem. 2024 Feb 13. doi: 10.1021/acs.jmedchem.3c01827.
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