(Q909822)

(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22,23-octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.0^{4,9}.0^{10,15}]tricosa-4(9),5,7,10,12,14-hexaen-21-yl 3,4,5-trihydroxybenzoate

Corilagin (English)

5 October 2016

2 references

inferred from InChIKey

[(1R,19S,21S,22S,23S)-6,7,8,11,12,13,22,23-octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-21-yl] 3,4,5-trihydroxybenzoate

inferred from InChI

1 reference

[(1R,19S,21R,22R,23R)-6,7,8,11,12,13,22,23-octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-21-yl] 3,4,5-trihydroxybenzoate

inferred from InChI

1 reference

1 reference

[(1S,19R,21S,22R,23S)-6,7,8,11,12,13,22,23-octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-21-yl] 3,4,5-trihydroxybenzoate

1 reference

inferred from InChI

chemical formula

C₂₇H₂₂O₁₈

1 reference

Corilagin (English)

5 October 2016

C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O

1 reference

Corilagin (English)

5 October 2016

C1[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O

1 reference

Validated HPLC method for the standardization of Phyllanthus niruri (herb and commercial extracts) using corilagin as a phytochemical marker

Corilagin (English)

5 October 2016

4 references

Two new compounds from Phyllanthus niruri

Studies on aldose reductase inhibitors from natural products. II. Active components of a Paraguayan crude drug "Para-parai mí," Phyllanthus niruri

Niruriflavone, a New Antioxidant Flavone Sulfonic Acid from Phyllanthus niruri

Euphorbia hyssopifolia

1 reference

HIV-1 reverse transcriptase inhibitory principles from Chamaesyce hyssopifolia

Acalypha hispida

1 reference

Antimicrobial constituents of the leaves ofAcalypha wilkesiana and Acalypha hispida

Terminalia catappa

3 references

Antioxidant and hepatoprotective actions of medicinal herb, Terminalia catappa L. from Okinawa Island and its tannin corilagin

Terminalia chebula

2 references

Polyphenolic compounds in the fruits of Egyptian medicinal plants (Terminalia bellerica, Terminalia chebula and Terminalia horrida): characterization, quantitation and determination of antioxidant capacities

Cunonia macrophylla

1 reference

Bioactive ellagitannins from Cunonia macrophylla, an endemic Cunoniaceae from New Caledonia

Geranium thunbergii

5 references

Elaeocarpusin, a proto-type of geraniin from Geranium thunbergii.

Tannin production in hairy root culture of Geranium thunbergii

Inhibitory effect of tannins on reverse transcriptase from RNA tumor virus

Studies on the activities of tannins and related compounds from medicinal plants and drugs. IV. Effects of various extracts of Geranii herba and geraniin on liver injury and lipid metabolism in rats fed peroxidized oil

Constituents of Geranium thunbergii SIEB. et Zucc. XV. Modified Dehydroellagitannins, Geraniinic Acids B and C, and Phyllathusiin F.

Pelargonium reniforme

1 reference

Pelargoniins, new ellagitannins from Pelargonium reniforme

pomegranate

5 references

Two ellagitannins from Punica granatum heartwood

Polyphenols of the fruits of some varieties of pomegranate growing in Uzbekistan

Punicafolin, an ellagitannin from the leaves of Punica granatum

NMR spectral analysis of polyphenols from Punica granatum

Carbonic anhydrase inhibitors from the pericarps of Punica granatum L

Acalypha australis

1 reference

Phenolic compounds from Acalypha australis

Acalypha indica

2 references

Flavonoids from Acalypha indica

Phenolics fromAcalypha indica

1 reference

1 reference

Bischofianin, a dimeric dehydroellagitannin from Bischofia javanica

Carpinus laxiflora

1 reference

Two New Ellagitannin Metabolites, Carpinusin and Carpinusin from Carpinus laxiflora

Caryocar villosum

1 reference

Phenolic glycosides from the stem bark of Caryocar villosum and C. glabrum

Cercidiphyllum japonicum

1 reference

1 reference

2 references

Naturally occurring inhibitors of topoisomerase I mediated DNA relaxation

A strategy for identifying novel, mechanistically unique inhibitors of topoisomerase I

Euphorbia fischeriana

1 reference

Allose gallates from Euphorbia fischeriana

Euphorbia helioscopia

2 references

1 reference

2 references

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

1 reference

2 references

2 references

1 reference

Hydrolysable tannins from Euphorbia thymifolia

1 reference

1 reference

1 reference

Antihypertensive Activity of Corilagin and Chebulinic Acid, Tannins from Lumnitzera, racemosa

1 reference

1 reference

2 references

Bergenin derivatives from Mallotus japonicus

Mallotus philippinensis

1 reference

1 reference

2 references

Amariin, a di-dehydrohexahydroxydiphenoyl hydrolysable tannin from Phyllanthus amarus

Inhibition of wild-type human immunodeficiency virus and reverse transcriptase inhibitor-resistant variants by Phyllanthus amarus

Phyllanthus flexuosus

1 reference

Phyllanthus myrtifolius

1 reference

Antiviral tannins from two Phyllanthus species

Phyllanthus tenellus

1 reference

Two Tannins from Phyllanthus tenellus

Phyllanthus virgatus

1 reference

Tannins, flavonol sulfonates, and a norlignan from phyllanthus virgatus

Ricinus communis

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Falconeria insignis

1 reference

Diterpene esters and phenolic compounds from Sapium insigne (ROYLE) BENTH. ex HOOK. fil.

Terminalia citrina

2 references

Antimicrobial activity of tannins from Terminalia citrina

Tetradium glabrifolium

1 reference

Constituents of Leaves of Tetradium Glabrifolium

Excoecaria agallocha

1 reference

Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L.

Erodium cicutarium

1 reference

Tannins and Flavonoids from the Erodium cicutarium Herb

Geranium rectum

1 reference

Tanning substances ofGeranium rectum

Geranium sibiricum

1 reference

Antioxidant activities and xanthine oxidase inhibitory effects of extracts and main polyphenolic compounds obtained from Geranium sibiricum L.

Nephelium lappaceum

1 reference

Identification of major phenolic compounds from Nephelium lappaceum L. and their antioxidant activities.

Phyllanthus urinaria

2 references

Antiviral tannins from two Phyllanthus species

Evaluation of chemical constituents of Phyllanthus Niruri

Phyllanthus emblica

2 references

Novel norsesquiterpenoids from the roots of Phyllanthus emblica

Phyllanemblinins A-F, new ellagitannins from Phyllanthus emblica

Euphorbia maculata

2 references

Choerospondias axillaris

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Vernicia cordata

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Toxicodendron succedaneum

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Toxicodendron sylvestre

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Triadica sebifera

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Vernicia montana

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Identifiers

InChI

InChI=1S/C27H22O18/c28-9-1-6(2-10(29)16(9)32)24(39)45-27-22(38)23-19(35)13(43-27)5-42-25(40)7-3-11(30)17(33)20(36)14(7)15-8(26(41)44-23)4-12(31)18(34)21(15)37/h1-4,13,19,22-23,27-38H,5H2/t13-,19-,22-,23 ,27 /m1/s1

1 reference

Corilagin (English)

5 October 2016

2 references

Corilagin (English)

5 October 2016

ChEBI release 2020-09-01

1 reference

corilagin (English)

5 October 2016

1 reference

corilagin (English)

5 October 2016

2 references

English

title

Corilagin (English)

retrieved

5 October 2016

Reaxys registry number

76352

1 reference

corilagin (English)

5 October 2016

mapping relation type

2 references

English

title

corilagin (English)

retrieved

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C27H22O18/c28-9-1-6(2-10(29)16(9)32)24(39)45-27-22(38)23-19(35)13(43-27)5-42-25(40)7-3-11(30)17(33)20(36)14(7)15-8(26(41)44-23)4-12(31)18(34)21(15)37/h1-4,13,19,22-23,27-38H,5H2/t13-,19-,22-,23 ,27 /m1/s1

1 reference

CORILAGIN (English)

5 October 2016

2 references

inferred from InChIKey

1 reference

0 references

1 reference

DSSTOX compound identifier

DTXCID00813536

0 references

Human Metabolome Database ID

HMDB0031457

2 references

inferred from InChIKey

1 reference

corilagin (English)

5 October 2016

0 references

0 references

1 reference