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KW-8232 free base
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
KW-8232 free base图片
CAS NO:170365-25-0
包装与价格:
包装价格(元)
1mg电议
5mg电议
10mg电议

产品介绍
KW-8232 free base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 free base, an orally active anti-osteoporotic agent, and can reduces the biosynthesis ofPGE2[1].

IC50& Target

Prostaglandin Receptor[1]

体外研究
(In Vitro)

KW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE2in mouse osteoblastic cells[1].
KW-8232 possesses anti-viral activity against SARS-CoV-2 (EC50~1.2 μM )[2].

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[1].

Animal Model:male Sprague-Dawley rats (5-week-old)[1].
Dosage:1, 3, 10, and 30 mg/kg.
Administration:Orally once daily beginning 1 day prior to neurectomy for 28 days.
Result:Decreased urinary calcium excreation in the neurectomized rats only at 30 mg/kg.
分子量

609.16

性状

Solid

Formula

C36H37ClN4O3

CAS 号

170365-25-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month