| 中文名称 |
RP101988
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| 英文名称 |
RP101988
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| 包装储存 |
Powder -20°C 3 years;4°C 2 years
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| 详情描述 |
RP101442 是 Ozanimod 的主要的活性代谢物,是一种选择性强的 S1PR1 激动剂,对 S1PR1 和 S1P5R 的 EC50 分别为 0.19 nM 和 32.8 nM。
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| 产品详情 |
RP101442 是 Ozanimod 的主要的活性代谢物,是一种选择性强的 S1PR1 激动剂,对 S1PR1 和 S1P5R 的 EC50 分别为 0.19 nM 和 32.8 nM。
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| 生物活性 |
RP101988, the major active metabolite of Ozanimod, is a selective, potent S1PR1 (sphingosine-1-phosphate receptor 1) agonist, with EC 50 s of 0.19 nM and 32.8 nM for S1PR1 and S1PR5, respectivlely.
|
| 性状 |
Solid
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| IC50 & Target[1][2] |
S1PR1 0.19 nM (EC50) S1PR5 32.8 nM (EC
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| 体外研究(In Vitro) |
RP101988 is a substrate of P-gp and breast cancer resistance protein (BCRP) drug transporters. has not independently confirmed the accuracy of these methods. They are for reference only.
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| 运输条件 |
Room temperature in continental US; may vary elsewhere.
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| 储存方式 |
Powder -20°C 3 years;4°C 2 years
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| 参考文献 |
[1]. Tran JQ, et al. Cardiac Safety of Ozanimod, a Novel Sphingosine-1-Phosphate Receptor Modulator: Results of a Thorough QT/QTc Study. Clin Pharmacol Drug Dev. 2018;7(3):263-276.[2]. Gilardi D, et al. PK, PD, and interactions: the new scenario with JAK inhibitors and S1P receptor modulators, two classes of small molecule drugs, in IBD [published online ahead of print, 2020 Jul 1]. Expert Rev Gastroenterol Hepatol. 2020;1-10.
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| 溶解度数据 |
In Vitro: DMSO : 125 mg/mL (298.72 mM; Need ultrasonic)配制储备液
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[1]. Tran JQ, et al. Cardiac Safety of Ozanimod, a Novel Sphingosine-1-Phosphate Receptor Modulator: Results of a Thorough QT/QTc Study. Clin Pharmacol Drug Dev. 2018;7(3):263-276.[2]. Gilardi D, et al. PK, PD, and interactions: the new scenario with JAK inhibitors and S1P receptor modulators, two classes of small molecule drugs, in IBD [published online ahead of print, 2020 Jul 1]. Expert Rev Gastroenterol Hepatol. 2020;1-10.
1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。
2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。