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SMB00190

Sigma-Aldrich

Aloenin

≥95% (LC/MS-ELSD)

Synonym(s):

6-[2-(β-D-Glucopyranosyloxy)-4-hydroxy-6-methylphenyl]-4-methoxy-2H-pyran-2-one, Aloearbonaside

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About This Item

Empirical Formula (Hill Notation):
C19H22O10
CAS Number:
38412-46-3
Molecular Weight:
410.37
MDL number:
MFCD08275450
UNSPSC Code:
12352200
PubChem Substance ID:
329824855
NACRES:
NA.25

assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

COC1=CC(=O)OC(=C1)c2c(C)cc(O)cc2O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O

InChI

1S/C19H22O10/c1-8-3-9(21)4-11(15(8)12-5-10(26-2)6-14(22)27-12)28-19-18(25)17(24)16(23)13(7-20)29-19/h3-6,13,16-21,23-25H,7H2,1-2H3/t13-,16-,17+,18-,19-/m1/s1

InChI key

KFJNVVJUICKJEQ-LQDZTQBFSA-N

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General description

Natural product derived from plant source.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
12222852V
122228-52V

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Guang-Zhu Jin et al.
Cancer letters, 218(1), 15-20 (2005-01-11)
The cytotoxic effects on HCT 116, Hep G2 and HCT 116/VCR 100-1-1 cell lines of synthetic 4'-O-alkylaloenins (2-17), 4'-O-benzylaloenin (18) and 4'-O-allylaloenin (19) were examined by MTT assay, and compared with that of aloenin (1) isolated from Aloe arborescens Mill.
M Yokohira et al.
Journal of food science, 74(2), T24-T30 (2009-03-28)
A 2-y carcinogenicity study of Aloe, Aloe arborescens Miller var. natalensis Berger, a food additive, was conducted for assessment of toxicity and carcinogenic potential in the diet at doses of 4% or 0.8% in groups of male and female Wistar
Gas chromatographic and mass spectral determination of aloenin in skin-care cosmetics.
H Nakamura et al.
Journal of chromatography, 509(2), 377-382 (1990-06-22)
Zonggen Shen et al.
Ying yong sheng tai xue bao = The journal of applied ecology, 13(11), 1381-1384 (2003-03-11)
Aloe plants are the succulents mainly distributed in arid or semi-arid desert in South Africa. TLC analysis indicated that Aole arborescens and Aloe hereroensis contained the high concentration of phenolic derivative metabolites, anthraquinones such as barbaloin, homonataloin, aloeresin and aloenin.
Hidehiko Beppu et al.
Journal of ethnopharmacology, 103(3), 468-477 (2006-01-13)
We carried out three experimental trials to determine antidiabetic effects of Aloe arborescens Miller components. Firstly, ICR mice which received frequent injections of streptozotocin (Sz) in small doses (low-dose Sz-induced diabetes mice) were fed ad libitum with basal diets supplemented
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