Taraxasterol - CAS 1059-14-9
Catalog number: 1059-14-9
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
C30H50O
Molecular Weight:
426.7
COA:
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Chemical Family:
Triterpenoids
Description:
Taraxasterol isolated from the herbs of Taraxacum officinale. It inhibits NO, PGE(2), TNF-α, IL-1β and IL-6 production in LPS-induced RAW 264.7 macrophages in a dose-dependent manner.
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Purity:
0.98
Appearance:
Powder
Synonyms:
(18α,19α)-5α-Urs-20(30)-en-3β-ol;Anthesterin;Taraxasta-20(30)-ene-3β-ol;
MSDS:
Inquire
Application:
anti-inflammatory activity
Quality Standard:
Enterprise Standard
Quantity:
Milligrams-Grams
1.Anti-carcinogenic activity of Taraxacum plant. II.
Takasaki M;Konoshima T;Tokuda H;Masuda K;Arai Y;Shiojima K;Ageta H Biol Pharm Bull. 1999 Jun;22(6):606-10.
Eleven triterpenoids (1-11) from the roots of Taraxacum japonicum (Compositae) were examined for their inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) induced by the tumor promoter, 12-O-tetrade-canoylphorbol-13-acetate (TPA), in Raji cells as a primary screening test for anti-tumor-promoters (cancer chemopreventive agents). Of these triterpenoids, taraxasterol (1) and taraxerol (7) exhibited significant inhibitory effects on EBV-EA induction, but the inhibitory effects of their acetates 2 and 8 were weaker than those of 1 and 7. Furthermore, 1 and 7 exhibited potent anti-tumor-promoting activity in the two-stage carcinogenesis tests of mouse skin using 7,12-dimethylbenz[a]anthracene (DMBA) as an initiator and TPA as a promoter, and 1 showed a remarkable inhibitory effect on mouse spontaneous mammary tumors using C3H/OuJ mouse. These results strongly suggested that taraxasterol (1) could be a valuable chemopreventive agent.
2.[Constituents of the leaves of Holodiscus discolor (Pursh) Maxim].
Haladová M;Eisenreichová E;Budĕsínský M;Ubik K;Grancai D Ceska Slov Farm. 2001 Nov;50(6):280-2.
The paper deals with the isolation of constituents from light petrol and methanol extracts of the leaves of Holodiscus discolor (PURSH) MAXIM., Rosaceae. beta-sitosterol and taraxasterol were isolated from the light petrol extract, luteolin-7-O-glucoside was isolated from the methanol extract. The isolated compounds were identified by spectroscopic means and by comparison with authentic samples.
3.Triterpene alcohol and fatty acid composition of shea nuts from seven African countries.
Akihisa T;Kojima N;Katoh N;Ichimura Y;Suzuki H;Fukatsu M;Maranz S;Masters ET J Oleo Sci. 2010;59(7):351-60.
The content and composition of triterpene alcohol fractions of the non-saponifiable lipids (NSL) along with the fatty acid composition of the kernel fats (n-hexane extracts) of the shea tree (Vitellaria paradoxa; Sapotaceae) were determined for 36 samples from seven sub-Saharan countries: Cote d' Ivoire, Ghana, Nigeria, Cameroun, Chad, Sudan, and Uganda. The fat content of the kernels, proportion of NSL in the fats, and triterpene alcohols in the NSL are in the range of 30-54, 2-12, and 22-72%, respectively. The triterpene alcohol fractions contained alpha-amyrin (1), beta-amyrin (2), lupeol (3), and butyrospermol (4) as the major constituents along with minor or trace amounts of psi-taraxasterol (5), taraxasterol (6), parkeol (7), 24-methylene-24-dihydroparkeol (8), 24-methylenecycloartanol (9), dammaradienol (10), and 24-methylenedammarenol (11). Fatty acid composition is dominated by stearic (28-56%) and oleic (34-61%) acids. Shea butters from West African provenances contained in general higher levels of triterpene alcohols and stearic acid than those from East African provenances. Both stearic acid and total triterpene alcohol contents were significantly correlated to the latitude and elevation of the source population, indicating that higher levels of these compounds are found at higher ambient temperatures.
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CAS 1059-14-9 Taraxasterol

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