Name | [4-[[2-[4-(2-chlorophenyl)piperazine-1-carbonyl]-1-[2-(dimethylamino)ethyl]indol-3-yl]-(4-hydroxyphenyl)methyl]phenyl] methanesulfonate |
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Synonyms | kw8232 |
Description | KW-8232, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2[1]. |
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Related Catalog | |
Target |
Prostaglandin Receptor[1] |
In Vitro | KW-8232 is an anti-osteoporotic agent. KW-8232 reduces the biosynthesis of PGE2 in mouse osteoblastic cells[1]. KW-8232 possesses anti-viral activity against SARS-CoV-2 (EC50 ~1.2 μM )[2]. |
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. |
References |
Boiling Point | 805.5ºC at 760 mmHg |
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Molecular Formula | C37H39ClN4O5S |
Molecular Weight | 687.24700 |
Flash Point | 440.9ºC |
Exact Mass | 686.23300 |
PSA | 103.70000 |
LogP | 7.12660 |
Vapour Pressure | 5.44E-27mmHg at 25°C |