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Merck

79851

Sigma-Aldrich

Kaempferol-3-β-D-glucopyranosid

≥97.0% (HPLC)

Synonym(e):

3,4′,5,7-Tetrahydroxyflavon-3-glucosid, 3-(β-D-Glucopyranosyloxy)-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-on, 3-Glucosylkaempferol, Astragalin, Kaempferol-3-glucosid

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About This Item

Empirische Formel (Hill-System):
C21H20O11
CAS-Nummer:
Molekulargewicht:
448.38
MDL-Nummer:
UNSPSC-Code:
12352205
PubChem Substanz-ID:
NACRES:
NA.47

Assay

≥97.0% (HPLC)

Form

crystals

Lagertemp.

2-8°C

SMILES String

OC[C@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)cc4)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C21H20O11/c22-7-13-15(26)17(28)18(29)21(31-13)32-20-16(27)14-11(25)5-10(24)6-12(14)30-19(20)8-1-3-9(23)4-2-8/h1-6,13,15,17-18,21-26,28-29H,7H2/t13-,15-,17+,18-,21+/m1/s1

InChIKey

JPUKWEQWGBDDQB-QSOFNFLRSA-N

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Anwendung


  • Role in Ubiquinone Biosynthesis: The compound contributed to the biosynthesis of the benzenoid moiety of ubiquinone, a key component in plant biochemistry, highlighting its essential role in cellular energy production and plant health (Soubeyrand et al., 2018).

Biochem./physiol. Wirkung

Ähnliche Kaempferol-glucoside reduzieren die Nahrungsaufnahme und die entsprechenden Gewichtszunahme in Wistar Ratten.Das Glucosid wurde nicht geprüft.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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