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SMB00195

Sigma-Aldrich

Maesopsin

≥90% (LC/MS-ELSD)

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About This Item

Empirical Formula (Hill Notation):
C15H12O6
CAS Number:
5989-16-2
Molecular Weight:
288.25
MDL number:
MFCD24849354
UNSPSC Code:
12352205
PubChem Substance ID:
329824858
NACRES:
NA.25

assay

≥90% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

Oc1ccc(CC2(O)Oc3cc(O)cc(O)c3C2=O)cc1

InChI

1S/C15H12O6/c16-9-3-1-8(2-4-9)7-15(20)14(19)13-11(18)5-10(17)6-12(13)21-15/h1-6,16-18,20H,7H2

InChI key

LOFYFDPXORJJEE-UHFFFAOYSA-N

General description

Natural product derived from plant source.

pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

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Liselotte Krenn et al.
Journal of natural products, 66(8), 1107-1109 (2003-08-23)
A sulfated emodin glucoside, emodin 8-O-beta-D-glucopyranosyl-6-O-sulfate (1), was isolated from the roots of Rheum emodi in an investigation of the active constituents of this Nepalese medicinal plant, and its structure was determined by spectroscopic and chemical methods. Additionally, two rare
R Chao et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 22(4), 233-234 (1997-04-01)
A reversed-phase HPLC method was developed for the determination of maesopsin, a fliavonoid, in the xylem parts of the traditional Tibetan medicinal herb Shengdeng (Rhamnella gilgitica). An ODS column was used and the mobile phase was methanol-water (28:27) with 0.05
X C Li et al.
Phytochemistry, 46(1), 97-102 (1997-09-01)
During the search for antimicrobial compounds from higher plant sources, a methanol extract of Ceanothus americanus demonstrated antimicrobial activity against selected oral pathogens. Through further bioassay-guided fractionation and purification, three triterpenes (ceanothic acid, 27-hydroxy ceanothic acid and ceanothetric acid) and
R Bekker et al.
Journal of natural products, 64(3), 345-347 (2001-03-30)
Resolution of racemic 2-benzyl-2-hydroxy-1-benzofuran-3(2H)-ones (auronols) and CD data of the ensuing enantiomers permit assessment of the absolute configuration at the single stereocenter.

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