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SMB00126

Sigma-Aldrich

Isoprunetin 7-O-glucoside

≥90% (LC/MS-ELSD)

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About This Item

Empirical Formula (Hill Notation):
C22H22O10
CAS Number:
128856-77-9
Molecular Weight:
446.40
MDL number:
MFCD24849317
UNSPSC Code:
12352205
PubChem Substance ID:
329824804
NACRES:
NA.25

assay

≥90% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

COc1cc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc3OC=C(C(=O)c13)c4ccc(O)cc4

InChI

1S/C22H22O10/c1-29-14-6-12(31-22-21(28)20(27)19(26)16(8-23)32-22)7-15-17(14)18(25)13(9-30-15)10-2-4-11(24)5-3-10/h2-7,9,16,19-24,26-28H,8H2,1H3/t16-,19-,20+,21-,22-/m1/s1

InChI key

KSVVGBSBNPMXJF-RECXWPGBSA-N

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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D J De Rodriguez et al.
Planta medica, 56(1), 59-62 (1990-02-01)
Extracts from Ulex europaeus L. (Fabaceae) were tested for antiviral activity against HSV-1 and poliovirus. It was found that the n-butanolic extract significantly inhibited the replication of these viruses, as shown by inhibition of cytophathic effects and reduction of plaques;

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