目錄:MedChemExpress LLC>>生化試劑>> BI 1015550 | MCE
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更新時(shí)間:2023-07-05 09:20:19瀏覽次數(shù):140評(píng)價(jià)
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CAS | 1423719-30-5 | 分子量 | 448.97 |
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分子式 | C??H??ClN?O?S | 供貨周期 | 現(xiàn)貨 |
貨號(hào) | HY-153192 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 1423719-30-5
產(chǎn)品活性:BI 1015550 is an orally active inhibitor of PDE4B with an IC50 value of 7.2 nM. BI 1015550 has good safety and potential applications in inflammation, allergic diseases, pulmonary fibrosis, and chronic obstructive pulmonary disease (COPD).
研究領(lǐng)域:Metabolic Enzyme/Protease
作用靶點(diǎn):Phosphodiesterase (PDE)
In Vitro: BI 1015550 inhibits Lipopolysaccharides (HY-D1056) induced TNF-α release and Phytohemagglutinin P (HY-N7038A) induced IL-2 release in human PBMCs with IC50 values of 35 nM and 9 nM, respectively.
BI 1015550 inhibits TNF-α release in rat whole blood with an IC50 value of 91 nM.
In Vivo: BI 1015550 (Example 2) (0, 0.3, 1.0 and 3.0 mg/kg; p.o.; single dose) weakens intestinal transport in rats at 1.0 mg/kg without significantly affecting body weight.
BI 1015550 prevents inflammation in rat lung tissue with an ED50 value of 0.1 mg/kg.
BI 1015550 (0.01, 0.1 and 1.0 mg/kg; p.o.; single dose) reduces the Lipopolysaccharides (HY-D1056) induced TNF-α release with dose-dependent manner in mice plasma.
BI 1015550 (0.1, 0.3 and 1.0 mg/kg; p.o.; single dose) inhibits lipopolysaccharides induced neutrophil entry into bronchoalveolar lavage fluid of male Suncus Murinus and Wistar rats.
BI 1015550 (2.5 mg/kg and 12.5 mg/kg; p.o.; twice daily for 6 days) effectively improves the damage of Bleomycin (HY-108345) to mice.
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