5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one (Q105257152)

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one

inferred from SMILES

1 reference

inferred from SMILES

mass

432.10564684 dalton

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

inferred from SMILES

stereoisomer of

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

2 references

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

1 reference

1 reference

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

1 reference

kaempferol-3-O-alpha-L-rhamnoside

1 reference

chemical formula

C₂₁H₂₀O₁₀

0 references

canonical SMILES

O=C1C(OC2OC(C)C(O)C(O)C2O)=C(OC=3C=C(O)C=C(O)C13)C=4C=CC(O)=CC4

0 references

isomeric SMILES

C[C@@H]1O[C@@H](Oc2c(-c3ccc(O)cc3)oc3cc(O)cc(O)c3c2=O)[C@@H](O)[C@H](O)[C@H]1O

0 references

found in taxon

Ajuga integrifolia

1 reference

Flavonol and iridoid glycosides of Ajuga remota aerial parts.

Alnus japonica

1 reference

New diarylheptanoids from Alnus japonica and their antioxidative activity.

Annona purpurea

1 reference

Antiplatelet aggregation constituents from Annona purpurea

Chamaecyparis formosensis

1 reference

Terpenes and lignans from leaves of Chamaecyparis formosensis

Chenopodium murale

1 reference

A flavonol triglycoside from Chenopodium murale

Cornus controversa

1 reference

Phenolic compounds from the leaves of Cornus controversa

Cornus kousa

1 reference

Lipid peroxidation, cyclooxygenase enzyme and tumor cell proliferation inhibitory compounds in Cornus kousa fruits

Davidsonia pruriens

1 reference

Flavonoids of Davidsonia pruriens

Dendrophthoe falcata

1 reference

Three new pentacyclic triterpenes and some flavonoids from the fruits of an Indian Ayurvedic plant Dendrophthoe falcata and their estrogen receptor binding activity.

Dryopteris crassirhizoma

1 reference

Two new triterpenes from the Rhizome of Dryopteris crassirhizoma, and inhibitory activities of its constituents on human immunodeficiency virus-1 protease

Epimedium sagittatum

1 reference

Prenylflavonol, acylated flavonol glycosides and related compounds from Epimedium sagittatum

Juglans mandshurica

1 reference

Inhibition of human immunodeficiency virus type 1 reverse transcriptase and ribonuclease H activities by constituents of Juglans mandshurica

Leptothyrsa sprucei

1 reference

Indolopyridoquinazoline alkaloid from Leptothyrsa sprucei

Mallotus metcalfianus

1 reference

Polyphenols isolated from antiradical extracts of Mallotus metcalfianus.

Nymphaea odorata

1 reference

Phenolic Compounds from Nymphaea odorata

Phellodendron amurense

1 reference

Constituents from the leaves of Phellodendron amurense and their antioxidant activity

Piper umbellatum

1 reference

Bioactive aristolactams from Piper umbellatum

Tetrapanax papyrifer

1 reference

Flavonoids and benzene derivatives from the flowers and fruit of Tetrapanax papyriferus.

Trachelospermum asiaticum

1 reference

Main phenolic compounds from the flower of Trachelospermum asiaticum var. intermedium (Apocynaceae).

Warburgia stuhlmannii

1 reference

Flavonol glycosides of Warburgia ugandensis leaves

Zanthoxylum culantrillo

1 reference

7,9′-Epoxylignan and other constituents of Zanthoxylum culantrillo

radish

1 reference

Deciphering the Nutraceutical Potential of -A Comprehensive Overview

Zingiber officinale

1 reference

Mechanism-based inhibition of CYP3A4 by constituents of Zingiber aromaticum

Phyllanthus emblica

1 reference

Two new acylated flavanone glycosides from the leaves and branches of Phyllanthus emblica

Foeniculum vulgare

1 reference

An Acylated Kaempferol Glycoside from Flowers of and

Rosa multiflora

1 reference

On the constituents of the fruits of Rosa multiflora Thunb. II. (author's transl)

Panax ginseng

1 reference

A novel acylated quercetin glycoside and compounds of inhibitory effects on α-glucosidase from Panax ginseng flower buds

Arabidopsis thaliana

1 reference

Expanded investigations of the aglycon promiscuity and catalysis characteristic of flavonol 3-O-rhamnosyltransferase AtUGT78D1 from Arabidopsis thaliana

broad bean

2 references

UHPLC-ESI-QTOF-MS-based metabolic profiling of Vicia faba L. (Fabaceae) seeds as a key strategy for characterization in foodomics

UHPLC/MS2-based approach for the comprehensive metabolite profiling of bean (Vicia faba L.) by-products: A promising source of bioactive constituents

Punica granatum

1 reference

Amelioration of diabetic nephropathy using pomegranate peel extract-stabilized gold nanoparticles: assessment of NF-κB and Nrf2 signaling system

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Ochna gamblei

1 reference

7-O-Methyltetrahydroochnaflavone, a new biflavanone from Ochna beddomei

Identifiers

InChI

InChI=1S/C21H20O10/c1-8-15(25)17(27)18(28)21(29-8)31-20-16(26)14-12(24)6-11(23)7-13(14)30-19(20)9-2-4-10(22)5-3-9/h2-8,15,17-18,21-25,27-28H,1H3/t8-,15-,17+,18-,21-/m0/s1

0 references

InChIKey

SOSLMHZOJATCCP-PADPQNGGSA-N

0 references

1 reference

17 September 2022