Compound

kaempferol 3-O-beta-D-glucoside

CHEBI:169942ChEBI

Structure

2D depiction · 3D model shown

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A generated conformer of kaempferol 3-O-beta-D-glucoside — one low-energy arrangement PubChem computed, not a measured structure. Hydrogens are not drawn; the formula counts them.

Class: Organic compound, anion
Formula: C21H19O11
Mass: 447.372 g/mol
Charge: -1
InChIKey: JPUKWEQWGBDDQB-QSOFNFLRSA-M
SMILES: O=c1c(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c(-c2ccc(O)cc2)oc2cc([O-])cc(O)c12
Look it up: ChEBI PubChem By InChIKey

Identity from ChEBI, geometry from PubChem. Not evidence.

What it touches on the way

Mechanistic reach

1 entity

1 entities reached.

0 reported hops1 assembled from the scaffold

LCTProteinUNIPROT:P09848substrate ofInferred only8 paths8 endpoints

What the reference databases state

Statements

1 statement

1 statement · 1 reference database · Subject: kaempferol 3-O-beta-D-glucoside · Sources: Rhea

Order

kaempferol 3-O-beta-D-glucoside is a substrate of LCTProteinRhea RHEA:69659Inferred only

Reactions

2 reactions

kaempferol 3-O-beta-D-glucoside+malonyl-CoACHEBI:169943+coenzyme A(4-)
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:67336CC BY 4.0Reference data
kaempferol 3-O-beta-D-glucoside+waterkaempferol+beta-D-glucose
Catalysed by LCT
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:69659CC BY 4.0Reference data