Blumenol C glucoside - CAS 135820-80-3
Catalog number: B0005-164891
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Molecular Formula:
C19H32O7
Molecular Weight:
372.5
COA:
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Chemical Family:
Sesquiterpenoids
Description:
Blumenol C glucoside isolated from the barks of Pseudolarix amabilis.
Ordering Information
Catalog Number Size Price Stock Quantity
B0005-164891 1 mg $399 In stock
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Purity:
0.93
Appearance:
Oil
Synonyms:
(2S)-4-[(1R)-2,6,6-Trimethyl-4-oxo-2-cyclohexen-1-yl]-2-butanyl β -D-glucopyranoside
MSDS:
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Quality Standard:
Enterprise Standard
Quantity:
Milligrams-Grams
1.Norsesquiterpenoids and triterpenoids from strawberry cv. Falandi.
Yang D1, Liang J2, Xie H3, Wei X4. Food Chem. 2016 Jul 15;203:67-72. doi: 10.1016/j.foodchem.2016.02.036. Epub 2016 Feb 4.
Falandi is a common strawberry (Fragaria × ananassa Duch.) cultivar in southern China. Further study of the chemical constituents in Falandi fruit led to the isolation of nine norsesquiterpenoids and three triterpenoids. Falandioside D (1) and falandins A (2) and B (3) were new norsesquiterpenoids, and the others excluding tormentic acid (11) were found in strawberry for the first time. Compounds 1 and 11 exhibited potent α-glucosidase inhibitory activity with the half maximal inhibitory concentration (IC50) values of 565.0 and 27.4μM in comparison to acarbose (619.9μM). Compounds 3, 7 (blumenol C glucoside), and 11 showed cytotoxicity against human nasopharyngeal carcinoma cell line CNE1 with the IC50 values of 57.6, 56.4, and 36.0μM, respectively. Among new compounds, 1 showed 2,2'-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical cation scavenging capacity (IC50=36.2μM). These results suggested that non-phenolic constituents were also involved in the antidiabetic, antitumour, and antioxidant effects of strawberry fruit.
2.[Chemical constituents from the seed coat of Juglans regia].
Liu C1, Tai Z, Feng S, Fang Y, Cai L, Ding Z. Zhongguo Zhong Yao Za Zhi. 2012 May;37(10):1417-21.
Fifteen compounds were isolated from the seed coat of Juglans regia by silica gel, MCI gel and Sephadex LH-20 gel column chromatography, as well as high preparative performance liquid chromatography. Their structures were identified as salidroside (1), (6S, 9S)-roseoside (2), (6S, 9R)-roseoside (3), blumenol C glucoside (4), byzantionoside B (5), 5-hydroxy-2-methoxy-1, 4-naphthoquinone (6), gallic acid (7), glycerol 1-(9Z-octadecenoate)-2-(9Z, 12Z-octadecadienoate)-3-(9Z, 12Z, 15Z-octadecatrienoate) (8), glycerol 1, 2, 3-tri-(9Z, 12Z-octadecadienoate) (9), glycerol 1, 2, 3-tri-(9Z, 12Z, 15Z-octadecatrienoate) (10), glycerol 1-hexadecanoate-2, 3-di-(9Z, 12Z-octadecadienoate) (11) on the basis of EI-MS, FAB-MS and NMR spectra. Moreover, 35 volatile compounds were identified by GC-MS.
3.Structural revisions of blumenol C glucoside and byzantionoside B.
Matsunami K1, Otsuka H, Takeda Y. Chem Pharm Bull (Tokyo). 2010 Mar;58(3):438-41.
The absolute stereochemistry of blumenol C glucoside and byzantionoside B was revised here as (6R,9S)- and (6R,9R)-9-hydroxymegastigman-4-en-3-one 9-O-beta-D-glucopyranosides, respectively, by modified Mosher's method. The empirical rules of (13)C-NMR chemical shift to determine the absolute stereochemistry of C-9 of 9-hydroxymegastigmane 9-O-beta-D-glucopyranoside were also discussed.
4.[Chemical constituents from Faeces bombycis].
Cui XQ1, Li XC, Wang L, Chen RY. Zhongguo Zhong Yao Za Zhi. 2008 Nov;33(21):2493-6.
OBJECTIVE: To study the chemical constituents from Faeces bombycis.
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CAS 135820-80-3 Blumenol C glucoside

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