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106518-63-2

106518-63-2 structure
106518-63-2 structure
  • Name: Ganodermanontriol
  • Chemical Name: (5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R,5S)-5,6,7-trihydroxy-6-methylheptan-2-yl]-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one
  • CAS Number: 106518-63-2
  • Molecular Formula: C30H48O4
  • Molecular Weight: 472.700
  • Catalog: Natural product Moss
  • Create Date: 2018-05-10 08:00:00
  • Modify Date: 2025-08-25 17:52:07
  • Ganodermanontriol, a sterol isolated from Ganoderma lucidum, induces anti-inflammatory activity in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells through the expression of HO-1. Ganodermanontriol exhibits hepatoprotective activity[1][2].

Name (5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R,5S)-5,6,7-trihydroxy-6-methylheptan-2-yl]-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one
Synonyms Ganodermanontriol
Lanosta-7,9(11)-dien-3-one, 24,25,26-trihydroxy-, (24S,25R)-
(24S,25R)-24,25,26-Trihydroxylanosta-7,9(11)-dien-3-one
Description Ganodermanontriol, a sterol isolated from Ganoderma lucidum, induces anti-inflammatory activity in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells through the expression of HO-1. Ganodermanontriol exhibits hepatoprotective activity[1][2].
Related Catalog
In Vitro Ganodermanontriol inhibits breast cancer cell lines MCF-7 and MDA-MB-231with IC50 values of 5.8 and 9.7 μM, respectively[2].
References

[1]. Ha do T, et al. In vitro and in vivo hepatoprotective effect of ganodermanontriol against t-BHP-induced oxidative stress. Ethnopharmacol. 2013 Dec 12;150(3):875-85.

[2]. Kennedy EM, et al. Semisynthesis and biological evaluation of ganodermanontriol and its stereoisomeric triols. J Nat Prod. 2011 Nov 28;74(11):2332-7.

Density 1.1±0.1 g/cm3
Boiling Point 623.2±55.0 °C at 760 mmHg
Molecular Formula C30H48O4
Molecular Weight 472.700
Flash Point 344.7±28.0 °C
Exact Mass 472.355255
PSA 77.76000
LogP 5.66
Vapour Pressure 0.0±4.1 mmHg at 25°C
Index of Refraction 1.559
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