KW-8232
目录号: PL10130 纯度: ≥98%
CAS No. :217813-15-5
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PL10130-5mg 5mg ¥8036.00 请登录
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中文名称
KW-8232
英文名称
KW-8232
英文别名
[4-[[2-[4-(2-chlorophenyl)piperazine-1-carbonyl]-1-[2-(dimethylamino)ethyl]indol-3-yl]-(4-hydroxyphenyl)methyl]phenyl] methanesulfonate;[3-[bis(4-hydroxyphenyl)methyl]-1-(2-dimethylaminoethyl)indol-2-yl]-[4-(2-chlorophenyl)piperazin-1-yl]methanone;methanesulfonate;KW-8232
Cas No.
217813-15-5
分子式
C36H37N4O3Cl.CH4O3S
分子量
705.26
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
KW-8232 是一种具有口服活性的抗骨质疏松剂,可以减少前列腺素 PGE2 的生物合成。
生物活性
KW-8232, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2.
性状
Solid
IC50 & Target[1][2]
Prostaglandin Receptor
体外研究(In Vitro)
KW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE2 in mouse osteoblastic cells.
KW-8232 possesses anti-viral activity against SARS-CoV-2 (EC50 ~1.2 μM ).
has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
KW-8232 (3, 10, 30 mg/kg, p.o.) potently increases the femoral bone mineral density (BMD) of immobilized legs of rats, and affects immobilization-induced abnormal bone turnovrer. KW-8232 markedly decreases urinary calcium excreation in the neurectomized rats only at 30 mg/kg, and highly reduces urinary pyridinoline and deoxypyridionline excretion which are markers of bone resorption in neurectomized rats. KW-8232 inhibits bone loss may be attributed to the lower prostaglandins (PGs)-stimulated bone resorption via regulation of PGE2 production. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Uchii M, et al. Effect of KW-8232, a novel anti-osteoporotic agent, on bone loss in sciatic neurectomized rats. Jpn J Pharmacol. 1998 Oct;78(2):241-3.
[2]. Shiwei Wang, et al. A Transferable Deep Learning Approach to Fast Screen Potent Antiviral Drugs against SARS-CoV-2. bioRxiv. 2020.
溶解度数据
In Vitro: DMSO : 125 mg/mL (177.24 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

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。

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