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Merck
CN

85447

Sissotrin

~95% (TLC)

Synonym(s):

Biochanin A 7-O-β-D-glucopyranoside, Sissostrin

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About This Item

Empirical Formula (Hill Notation):
C22H22O10
CAS Number:
Molecular Weight:
446.40
UNSPSC Code:
51111800
NACRES:
NA.77
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1302648
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Product Name

Sissotrin, ~95% (TLC)

InChI

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

SMILES string

COc1ccc(cc1)C2=COc3cc(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)cc(O)c3C2=O

InChI key

LFEUICHQZGNOHD-RECXWPGBSA-N

assay

~95% (TLC)

form

powder

Biochem/physiol Actions

Sissotrin in the leaf exudate of chickpea inactivates nucleopolyhedroviruses (such as baculovirus) which can be used as biological pesticides..

General description

Flavonoid glycoside from Sophora japonica (Japanese pagoda tree), Cicer arietinum (chickpea), and other plant sources.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Max Norman Tandrup Lambert et al.
PloS one, 12(6), e0176590-e0176590 (2017-06-08)
Natural estrogen decline leads to vasomotor symptoms (VMS). Hormone therapy alleviates symptoms but increases cancer risk. Effective treatments against VMS with minimal cancer risks are needed. We investigate the effects of a highly bioavailable aglycone rich Red Clover isoflavone treatment

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