Chemical Structure : IHCH-3185
货号: PC-28312Not For Human Use, Lab Use Only.
IHCH-3185 is a potent, dual-targeting adenosine A2A receptor (A2AR) antagonist and HDAC inhibitor with Ki of 7.6 nM (A2AR) and IC50 of 102.9 nM (HDAC1) respectively.
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IHCH-3185 is a potent, dual-targeting adenosine A2A receptor (A2AR) antagonist and HDAC inhibitor with Ki of 7.6 nM (A2AR) and IC50 of 102.9 nM (HDAC1) respectively.
IHCH-3185 demonstrates broad-spectrum antiproliferative activity in vitro.
IHCH-3185 (20 mg/kg, oral) significantly inhibited CT26 and MC38 tumor growth in mice with tumor growth inhibition rates of 68.5% and 71.1%, respectively.
| 分子量 | 455.48 | |
| 分子式 | C24H21N7O3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Wenzhong Yan, et al. J Med Chem. 2026 Mar 12;69(5):6038-6062.
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