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170365-25-0

170365-25-0 Structure

170365-25-0 Structure
IdentificationBack Directory
[Name]

KW-8232 free base
[CAS]

170365-25-0
[Synonyms]

KW-8232 free base
Methanone, [3-[bis(4-hydroxyphenyl)methyl]-1-[2-(dimethylamino)ethyl]-1H-indol-2-yl][4-(2-chlorophenyl)-1-piperazinyl]-
[Molecular Formula]

C36H37ClN4O3
[MDL Number]

MFCD30533346
[MOL File]

170365-25-0.mol
[Molecular Weight]

609.16
Chemical PropertiesBack Directory
[Boiling point ]

805.5±65.0 °C(Predicted)
[density ]

1.26±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

9.95±0.10(Predicted)
[color ]

Off-white to pink
Hazard InformationBack Directory
[Uses]

KW-8232 free base, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2[1].
[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.
[IC 50]

EP
[storage]

Store at -20°C
[References]

[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. DOI:10.1254/jjp.78.241
[2] Shiwei Wang, et al. A Transferable Deep Learning Approach to Fast Screen Potent Antiviral Drugs against SARS-CoV-2. bioRxiv. 2020.
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