np-003686 (Q27102438)

beta-glucogallin-tetrakisgalloylglucose O-galloyltransferase activity

inferred from InChIKey

part of

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

mass

788.107223±0 dalton

1 reference

1,2,3,6-Tetragalloylglucose (English)

beta-D-Galactopyranose 1,2,3,6-tetrakis(3,4,5-trihydroxybenzoate)

5 October 2016

stereoisomer of

2 references

inferred from InChIKey

1-O,2-O,3-O,6-O-Tetragalloyl-beta-D-allopyranose

inferred from InChI

2 references

inferred from InChIKey

(2R,3S,4R,5S,6S)-5-hydroxy-3,4-bis(3,4,5-trihydroxybenzoyloxy)-6-[(3,4,5-trihydroxybenzoyloxy)methyl]oxan-2-yl 3,4,5-trihydroxybenzoate

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₃₄H₂₈O₂₂

1 reference

1,2,3,6-Tetragalloylglucose (English)

20 November 2016

canonical SMILES

C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O

1 reference

1,2,3,6-Tetragalloylglucose (English)

20 November 2016

isomeric SMILES

C1=C(C=C(C(=C1O)O)O)C(=O)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O

1 reference

Polyphenols from Cornulaca monacantha.

1,2,3,6-Tetragalloylglucose (English)

20 November 2016

2 references

Polyphenols from Cornulaca monacantha.

Juglans mandshurica

3 references

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

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

Anti-complement activity of constituents from the stem-bark of Juglans mandshurica

Chinese peony

2 references

Paeonianins A-E, new dimeric and monomeric ellagitannins from the fruits of Paeonia lactiflora

Rhodiola sachalinensis

3 references

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis

Acalypha indica

1 reference

Phenolics fromAcalypha indica

Agrobacterium rhizogenes

1 reference

A piperidone alkaloid from Hyoscyamus albus roots transformed with Agrobacterium rhizogenes

Rhizobium rhizogenes

1 reference

A piperidone alkaloid from Hyoscyamus albus roots transformed with Agrobacterium rhizogenes

Castanea crenata

1 reference

C-Glycosidic Ellagitannin Metabolites in the Heartwood of Japanese Chestnut Tree (Castanea crenata SIEB. et Zucc.).

Castanopsis fissa

1 reference

Triterpene hexahydroxydiphenoyl esters and a quinic acid purpurogallin carbonyl ester from the leaves of Castanopsis fissa

Cercidiphyllum japonicum

1 reference

Cornus officinalis

1 reference

Tannins of cornaceous plants. I. Cornusiins A, B and C, dimeric monomeric and trimeric hydrolyzable tannins from Cornus officinalis, and orientation of valoneoyl group in related tannins

Corylus heterophylla

1 reference

Heterophylliins A,B,C,D and E, ellagitannin monomers and dimers from Corylus heterophylla Fisch.

Cuphea hyssopifolia

1 reference

Macrocyclic ellagitannin dimers, cuphiins D1 and D2, and accompanying tannins from Cuphea hyssopifolia

Eucalyptus globulus

1 reference

Marker constituents of the natural antioxidant Eucalyptus leaf extract for the evaluation of food additives.

Eucalyptus viminalis

1 reference

Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis

Euphorbia helioscopia

1 reference

Euphorbia jolkinii

1 reference

Structure and biogenesis of jolkinin, a highly oxygenated ellagitannin from Euphorbia jolkinii

Fordia fruticosa

1 reference

Woodfordin C, a macro-ring hydrolyzable tannin dimer with antitumor activity, and accompanying dimers from Woodfordia fruticosa flowers

Geranium thunbergii

1 reference

Tannin production in hairy root culture of Geranium thunbergii

Haematoxylum campechianum

1 reference

Gallotannins and flavonoids from Haematoxylon campechianum.

Loropetalum chinense

1 reference

Hydrolysable tannins from Loropetalum chinense

Lotus corniculatus

1 reference

Gallic acid esters of bergenin and norbergenin from Mallotus japonicus

Mallotus japonicus

1 reference

Gallic acid esters of bergenin and norbergenin from Mallotus japonicus

Melaleuca leucadendra

1 reference

An hydrolysable tannin and accompanying polyphenols from Melaleuca leucadendron

Melaleuca squarrosa

1 reference

Flavonol glucuronides and C-glucosidic ellagitannins from Melaleuca squarrosa.

Phyllagathis rotundifolia

2 references

New cyanogenic and alkyl glycoside constituents from Phyllagathis rotundifolia

Characterisation of galloylated cyanogenic glucosides and hydrolysable tannins from leaves of Phyllagathis rotundifolia by LC-ESI-MS/MS.

Phyllanthus emblica

3 references

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

Phyllanemblinins A-F, new ellagitannins from Phyllanthus emblica

Novel norsesquiterpenoids from the roots of Phyllanthus emblica

1 reference

1 reference

1 reference

Taxifolin apioside and davuriciin M1, a hydrolysable tannin from Rosa davurica

Sanguisorba officinalis

1 reference

7-O-Galloyl-(+)-catechin and 3-O-galloylprocyanidin B-3 from Sanguisorba officinalis

1 reference

1 reference

Antiplasmodial activity of compounds from Sloanea rhodantha (Baker) Capuron var. rhodantha from the Madagascar rain forest.

1 reference

1 reference

Woodfordin C, a macro-ring hydrolyzable tannin dimer with antitumor activity, and accompanying dimers from Woodfordia fruticosa flowers

1 reference

1 reference

Benzophenone C-glucosides and gallotannins from mango tree stem bark with broad-spectrum anti-viral activity.

Ceratonia siliqua

1 reference

Extract from Ceratonia siliqua Exhibits Depigmentation Properties

Rhodiola rosea

2 references

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis

Eucalyptus consideniana

1 reference

Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis

Identifiers

InChI

InChI=1S/C34H28O22/c35-14-1-10(2-15(36)23(14)43)30(48)52-9-22-27(47)28(54-31(49)11-3-16(37)24(44)17(38)4-11)29(55-32(50)12-5-18(39)25(45)19(40)6-12)34(53-22)56-33(51)13-7-20(41)26(46)21(42)8-13/h1-8,22,27-29,34-47H,9H2/t22-,27-,28+,29-,34+/m1/s1

1 reference

1,2,3,6-Tetragalloylglucose (English)

20 November 2016

InChIKey

2 references

1,2,3,6-Tetragalloylglucose (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

79886-50-3

2 references

Global Substance Registration System

UNII

4648S0G699

np-003686 (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=79886-50-3

9 April 2021

1 reference

1,2,3,6-Tetrakis-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranose (English)

20 November 2016

2 references

1,2,3,6-Tetragalloylglucose (English)

matched by identifier from

20 November 2016

InChIKey

ChEBI ID

17527

mapping relation type

2 references

CHEMBL449947 (English)

matched by identifier from

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C34H28O22/c35-14-1-10(2-15(36)23(14)43)30(48)52-9-22-27(47)28(54-31(49)11-3-16(37)24(44)17(38)4-11)29(55-32(50)12-5-18(39)25(45)19(40)6-12)34(53-22)56-33(51)13-7-20(41)26(46)21(42)8-13/h1-8,22,27-29,34-47H,9H2/t22-,27-,28+,29-,34+/m1/s1

1 reference

splash10-014r-0920301200-06d646ba955cbc2f446f

CHEMBL449947 (English)

20 November 2016

1 reference

0 references

splash10-0udi-0910100000-8a07621bb9bff3cdb664

0 references

DSSTox substance ID

DTXSID80904234

0 references

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

4648S0G699

np-003686 (English)

matched by identifier from

20 November 2016

InChIKey