(Q104200389)

English

5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate

group of stereoisomers with the chemical formula C₂₂H₁₈O₁₁

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Statements

instance of

group of stereoisomers

0 references

1 reference

458.084911396 dalton

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based on heuristic

inferred from SMILES

chemical formula

C₂₂H₁₈O₁₁

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canonical SMILES

O=C(OC1CC=2C(O)=CC(O)=CC2OC1C3=CC(O)=C(O)C(O)=C3)C4=CC(O)=C(O)C(O)=C4

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found in taxon

Diospyros kaki

1 reference

stated in

Inhibitory effects of persimmon (Diospyros kaki) extract and related polyphenol compounds on growth of human lymphoid leukemia cells

Distylium racemosum

1 reference

stated in

Compounds with tyrosinase inhibition, elastase inhibition and DPPH radical scavenging activities from the branches of Distylium racemosum Sieb. et Zucc

Phyllanthus

1 reference

stated in

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

Cistus salviifolius

1 reference

stated in

Flavan-3-ols and proanthocyanidins from Cistus incanus

Averrhoa

1 reference

stated in

Analysis of CYP3A inhibitory components of star fruit (Averrhoa carambola L.) using liquid chromatography-mass spectrometry

Myrica rubra

2 references

stated in

Antitumor principle constituents of Myrica rubra Var. acuminata

stated in

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

Acacia pycnantha

1 reference

stated in

Determination of the predominant catechins in Acacia catechu by liquid chromatography/electrospray ionization-mass spectrometry

Camellia sinensis

8 references

stated in

Tea catechins and flavonoids from the leaves of Camellia sinensis inhibit yeast alcohol dehydrogenase

stated in

Bioactive saponins and glycosides. XXVIII. New triterpene saponins, foliatheasaponins I, II, III, IV, and V, from Tencha (the leaves of Camellia sinensis).

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Medicinal flowers. XIV. New acylated oleanane-type triterpene oligoglycosides with antiallergic activity from flower buds of chinese tea plant (Camellia sinensis).

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Floratheasaponins A-C, acylated oleanane-type triterpene oligoglycosides with anti-hyperlipidemic activities from flowers of the tea plant (Camellia sinensis).

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New Flavonol Triglycosides from Tea (Camellia sinensis)

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The use of green tea (Camellia sinensis) leaf flavan-3-ol composition in predicting plain black tea quality potential

stated in

Acylated oleanane-type triterpene saponins with acceleration of gastrointestinal transit and inhibitory effect on pancreatic lipase from flower buds of chinese tea plant (Camellia sinensis).

Morella rubra

2 references

stated in

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

stated in

Antitumor principle constituents of Myrica rubra Var. acuminata

Identifiers

InChI

InChI=1S/C22H18O11/c23-10-5-12(24)11-7-18(33-22(31)9-3-15(27)20(30)16(28)4-9)21(32-17(11)6-10)8-1-13(25)19(29)14(26)2-8/h1-6,18,21,23-30H,7H2

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InChIKey

WMBWREPUVVBILR-UHFFFAOYSA-N

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2 references

26 December 2021

matched by identifier from

InChIKey

WMBWREPUVVBILR-UHFFFAOYSA-N

ChEBI ID

182308

mapping relation type

exact match

2 references

stated in

ChEBI release 2022-06-13

matched by identifier from

International Chemical Identifier

InChI

InChI=1S/C22H18O11/c23-10-5-12(24)11-7-18(33-22(31)9-3-15(27)20(30)16(28)4-9)21(32-17(11)6-10)8-1-13(25)19(29)14(26)2-8/h1-6,18,21,23-30H,7H2

SureChEMBL ID

SCHEMBL161547

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

WMBWREPUVVBILR-UHFFFAOYSA-N

1 reference

1 reference

matched by identifier from

InChIKey

WMBWREPUVVBILR-UHFFFAOYSA-N

Human Metabolome Database ID

HMDB0243513

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

InChIKey

WMBWREPUVVBILR-UHFFFAOYSA-N

Probes And Drugs ID

PD056514

0 references

(Q104200389)

5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate

Statements

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