(Q422305)

German Wikipedia

mass

320.053217344 dalton

1 reference

2 references

inferred from InChIKey

inferred from InChI

(2R,3S)-Dihydromyricetin

2 references

inferred from InChIKey

inferred from InChI

chemical formula

C₁₅H₁₂O₈

2 references

O=C1C=2C(O)=CC(O)=CC2OC(C3=CC(O)=C(O)C(O)=C3)C1O

0 references

isomeric SMILES

c1c(cc(c(c1O)O)O)[C@@H]2[C@H](C(=O)c3c(cc(cc3O2)O)O)O

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found in taxon

Pimenta dioica

1 reference

Phenolic glycosides from berries of Pimenta dioica

Berberis duclouxiana

1 reference

Constituents of Mahonia siamensis

Brassica carinata

1 reference

Pigmentation in the developing seed coat and seedling leaves of Brassica carinata is controlled at the dihydroflavonol reductase locus

Intsia bijuga

1 reference

Polyphenols of Intsia heartwoods

Manilkara zapota

3 references

Bioactive novel polyphenols from the fruit of Manilkara zapota (Sapodilla).

Bioactive novel polyphenols from the fruit of Manilkara zapota (Sapodilla).

Bioactive novel polyphenols from the fruit of Manilkara zapota (Sapodilla).

Rhododendron

1 reference

Leaf survey of flavonoids and simple phenols in the genus Rhododendron

Xanthoceras sorbifolia

2 references

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Burkea africana

1 reference

Oligomeric flavanoids. Part 2. The first profisetinidins with dihydroflavonol constituent units

Catharanthus roseus

1 reference

A flavonol O-methyltransferase from Catharanthus roseus performing two sequential methylations

Cyphostemma digitatum

1 reference

Flavonoids from Cissus digitata

Onobrychis cyri

1 reference

Biosynthesis of flavan-3-ols by leaf extracts of Onobrychis viciifolia

Onobrychis viciifolia

1 reference

Biosynthesis of flavan-3-ols by leaf extracts of Onobrychis viciifolia

Pinus contorta

1 reference

Isolation of dihydromyricetin and dihydroquercetin from bark of pinus contorta

Salix sachalinensis

1 reference

Ampelopsin, a Major Antifungal Constituent from Salix sachalinensis, and its Methyl Ethers.

Sedum reflexum

1 reference

Dihydroflavonols from Cedrus deodara

Sedum rupestre

1 reference

Dihydroflavonols from Cedrus deodara

Hovenia dulcis

2 references

Preparation, preliminary characterization and immunostimulatory activity of polysaccharide fractions from the peduncles of Hovenia dulcis

Hepatoprotective effect of Hovenia dulcis THUNB. on experimental liver injuries induced by carbon tetrachloride or D-galactosamine/lipopolysaccharide.

Catha edulis

2 references

Dihydromyricetin 3-O-rhamnoside from leaves of Catha edulis

Myricetin, Dihydromyricetin, and Quercetin Glycosides from Catha edulis

Cercidiphyllum japonicum

1 reference

Polyphenols from the heartwood of Cercidiphyllum japonicum and their effects on proliferation of mouse hair epithelial cells

Stachyurus himalaicus

1 reference

Flavonoids from leaves and twigs of Stachyurus himalaicus VAR. himalaicus

Glochidion zeylanicum

1 reference

New galloylated flavanonols from the Australian plant Glochidion sumatranum.

Shuteria vestita

2 references

Flavonoids from Erythrina schliebenii.

Phytochemical examination of the leaves of carica papaya L.

asparagus

1 reference

Transcriptome analysis of Asparagus officinalis reveals genes involved in the biosynthesis of rutin and protodioscin

Picea abies

1 reference

Ampelopsin 7-glucoside and other dihydroflavonol 7-glucosides from needles of Picea abies

Vitis rotundifolia

1 reference

Antibacterial Activities of Metabolites from (Muscadine) Roots against Fish Pathogenic Bacteria

Berberis napaulensis

1 reference

Constituents of Mahonia siamensis

Mahonia napaulensis

1 reference

Constituents of Mahonia siamensis

Great yellow gentian

1 reference

Differential accumulation of pelargonidin glycosides in petals at three different developmental stages of the orange-flowered gentian (Gentiana lutea L. var. aurantiaca)

Camellia sinensis

1 reference

Flavonoid biosynthesis in the tea plant Camellia sinensis: properties of enzymes of the prominent epicatechin and catechin pathways.

Xanthoceras sorbifolium

1 reference

Inhibitory effects on HIV-1 protease of constituents from the wood of Xanthoceras sorbifolia.

Nekemias grossedentata

1 reference

Chemical Constituents of Ampelopsis japonica

Melanthera prostrata

1 reference

Nuclear magnetic resonance studies of 5,7-dihydroxyflavonoids

Wollastonia dentata

1 reference

Nuclear magnetic resonance studies of 5,7-dihydroxyflavonoids

Sedum anglicum

1 reference

Dihydroflavonols from Cedrus deodara

Asteraceae

1 reference

Nuclear magnetic resonance studies of 5,7-dihydroxyflavonoids

Commons category

Ampelopsin

0 references

Identifiers

InChI

InChI=1S/C15H12O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,14-20,22H/t14-,15+/m0/s1

1 reference

PubChem

2 references

PubChem

ChEBI release 2020-09-01

CAS Registry Number

27200-12-0

2 references

German Wikipedia

https://commonchemistry.cas.org/detail?cas_rn=27200-12-0

9 April 2021

ChemSpider ID

16735660

1 reference

English Wikipedia

PubChem CID

161557

2 references

German Wikipedia

PubChem Substance ID (SID)

5833

0 references

Reaxys registry number

4269977

0 references

ChEBI ID

28429

mapping relation type

exact match

2 references

English Wikipedia

International Chemical Identifier

InChI

InChI=1S/C15H12O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,14-20,22H/t14-,15+/m0/s1

SureChEMBL ID

SCHEMBL723736

2 references

inferred from InChIKey

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

1 reference

2 references

DSSTOX compound identifier

DTXCID90104167

0 references

DrugBank ID

DB15645

1 reference

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

0 references

0 references

1 reference

retrieved

15 January 2022