(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one CAS 115404-57-4

Introduction:Basic information about (23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one CAS 115404-57-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one Basic information

Product Name:(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one
Synonyms:(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one;Niloticin;Lanost-7-en-3-one,24,25-epoxy-23-hydroxy-, (13a,14b,17a,20S,23R,24S)-;Lanost-7-en-3-one, 24,25-epoxy-23-hydroxy-, (13α,14β,17α,20S,23R,24S)-
CAS:115404-57-4
MF:C30H48O3
MW:456.71
EINECS:
Product Categories:Triterpenoids
Mol File:115404-57-4.mol

(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one Chemical Properties

Melting point 149-151 °C
Boiling point 538.5±45.0 °C(Predicted)
density 1.07±0.1 g/cm3(Predicted)
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Cryst.
pka14.37±0.20(Predicted)
color White to off-white

Safety Information

(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one Usage And Synthesis

UsesNiloticin, tetracyclic triterpenoid compound, is a osteoclastogenesis inhibitor. Niloticin shows anti-viral, antioxidative, and mosquitocidal activities. Niloticin inhibits osteoclastogenesis by blocking RANKL-RANK interaction and suppressing the AKT, MAPK, and NF-κB signaling pathways[1].
References[1] Xu H, et al. Niloticin inhibits osteoclastogenesis by blocking RANKL-RANK interaction and suppressing the AKT, MAPK, and NF-κB signaling pathways. Biomed Pharmacother. 2022 May;149:112902. DOI:10.1016/j.biopha.2022.112902

(23R,24S)-24,25-Epoxy-23-hydroxy-5α-tirucall-7-en-3-one Preparation Products And Raw materials

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