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CAS No. : 2088453-21-6
MCE 国际站:OATD-01
产品活性:OATD-01 是一种高效、口服活性、 first-in-class、选择性几丁质酶 (chitinase) 抑制剂,对 CHIT1 具有低纳摩尔活性 (hCHIT1, IC50=23 nM)。OATD-01 在多个物种中显示出良好的药代动力学特征。OATD-01 在体内具有显著的抗纤维化活性,用于肺纤维化 (IPF) 研究。
研究领域:Others
作用靶点:Others
In Vitro: OATD-01 exhibits high affinity toward h/mCHIT1 and h/mAMCase, and the inhibitory constants (Ki) for all four enzymes are 17.3 nM, 26.05 nM, 4.8 nM and 5.7 nM, respectively. These Ki values reveals good correlation with earlier established IC50 data, the IC50 values are 23 nM, 28 nM, 9 nM and 7.8 nM for hCHIT1,mCHIT1, hAMCase and mAMCase, respectively..Off-target in vitro effects of compound OATD-01 have been evaluated at 10 μM in the Eurofins Panlabs panel of 98 in vitro binding and enzymatic assays, involving diverse molecular classes of proteins.
In Vivo: OATD-01 (oral gavage; 30 mg/kg, 100 mg/kg; once daily; 21 days) shows significant antifibrotic efficacy in an animal model of bleomycin-induced pulmonary fibrosis. It reduces the degree of lung fibrosis in a dose-dependent manner, ultimately achieving comparable therapeutic efficacy to reference treatment with Nintedanib in this animal model.
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