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Merck
CN

SML2429

3,3′,4-Tri-O-methylellagic acid

≥95% (HPLC)

Synonym(s):

3,3’,4-Tri-O-methylellagic acid, 2,3,8-Tri-O-methylellagic acid, 3-hydroxy-2,7,8-trimethoxy- [1]Benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione, Nasutin B

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About This Item

Empirical Formula (Hill Notation):
C17H12O8
CAS Number:
5145-53-9
Molecular Weight:
344.27
UNSPSC Code:
12352106
NACRES:
NA.77
MDL number:
MFCD20260578

Key Documents

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Product Name

3,3′,4-Tri-O-methylellagic acid, ≥95% (HPLC)

SMILES string

[o]1c2c3c4c([o][c](c3cc(c2OC)OC)=O)c(c(cc4[c]1=O)O)OC

InChI

1S/C17H12O8/c1-21-9-5-7-11-10-6(16(19)25-15(11)13(9)23-3)4-8(18)12(22-2)14(10)24-17(7)20/h4-5,18H,1-3H3

InChI key

LXEQIOGTMDLLEC-UHFFFAOYSA-N

assay

≥95% (HPLC)

form

solid

storage temp.

−20°C

Related Categories

General description

3,3′,4-Tri-O-methylellagic acid is the methylated analogue of Ellagic acid. 3,3′,4-Tri-O-methylellagic acid was initially isolated from the rhizomes of Euphorbia acaulis.
3,3′,4-Tri-O-methylellagic acid was found to have anti-diabetic properties in mice models treated with Alloxan. Furthermore, 3,3′,4-Tri-O-methylellagic acid was reported to possess anti-bacterial activity against several bacterial strains including, Klebsiella pneumoniae, Enterobacter aerogenes and Staphylococcus aureus.

Other Notes

Solubility: 5mg/ml in DMSO (requires heat), in case of precipitation reheat solution.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
019M4128V
32181005
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Igor K Voukeng et al.
BMC complementary and alternative medicine, 17(1), 28-28 (2017-01-08)
Elaeophorbia drupifera (Thonn.) Stapf. (Euphorbiaceae) is used in Cameroonian folk medicine to treat several ailments including bacterial-related diseases such as skin infections. In this study, the methanol extract from the leaves (EDL), fractions (EDLa-d), sub-fractions EDLc1-7 and EDLc31-35 as well
Philip F Uzor et al.
EXCLI journal, 15, 290-296 (2016-06-15)
The root of Combretum dolichopetalum (Combreatacea) is used in ethnomedicine for the management of diabetes mellitus. Though some compounds have been isolated from it, the antidiabetic principles have not been identified. The present study was designed to evaluate the chemical

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