目錄:MedChemExpress LLC>>生化試劑>> BAY-1316957 | MCE
參考價(jià) | ¥ 1500 |
參考價(jià) | ¥ 1500 |
更新時(shí)間:2023-07-05 09:20:19瀏覽次數(shù):106評(píng)價(jià)
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CAS | 1613264-40-6 | 純度 | 98.94% |
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分子量 | 441.52 | 分子式 | C??H??N?O? |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 5 mg |
貨號(hào) | HY-111539 | 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. : 1613264-40-6
產(chǎn)品活性:BAY-1316957 is a potent, selective and orally active prostaglandin E2 receptor subtype 4 (EP4-R) antagonist with an IC50 of 15.3 nM for human EP4-R. BAY-1316957 has excellent agent metabolism and pharmacokinetics properties, and can be used for endometriosis research.
研究領(lǐng)域:GPCR/G Protein
作用靶點(diǎn):Prostaglandin Receptor
In Vitro: BAY-1316957 (Compound 32) shows high solubility and permeability using the Caco-2 cellular assay.
In Vivo: BAY-1316957 (Compound 32; 0.2-5 mg/kg; oral administration; once) treatment significantly reduces mechanical allodynia in dmPGE2 pain model.
The pharmacokinetic parameters of BAY-1316957 (Compound 32) shows a low clearance, long half-life, and high bioavailability (F%=90%) in Wistar rats. Investigation of the metabolic pathways of BAY-1316957 (Compound 32) in human, rat, mouse, dog, and monkey hepatocytes revealed that the formation of the acyl glucuronide was also the common and predominant route of biotransformation, mainly catalyzed by UGT1A1 and to a lesser extent by UGT1A3.
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