(Q105349619)

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1-Desgalloyleugeniin

chemical compound

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instance of

type of chemical entity

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subclass of

[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate

1 reference

based on heuristic

inferred from SMILES

[(10R,12S,13R)-3,4,5,13,21,22,23-heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate

1 reference

based on heuristic

inferred from SMILES

mass

786.091572472 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

[(10R,11S,12R,13S,15R)-3,4,5,13,21,22,23-heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate

1 reference

based on heuristic

inferred from InChI

chemical formula

C₃₄H₂₆O₂₂

0 references

canonical SMILES

O=C(OC1C(O)OC2COC(=O)C=3C=C(O)C(O)=C(O)C3C4=C(O)C(O)=C(O)C=C4C(=O)OC2C1OC(=O)C5=CC(O)=C(O)C(O)=C5)C6=CC(O)=C(O)C(O)=C6

0 references

isomeric SMILES

O=C(O[C@@H]1[C@@H](OC(=O)c2cc(O)c(O)c(O)c2)[C@H](O)O[C@@H]2COC(=O)c3cc(O)c(O)c(O)c3-c3c(cc(O)c(O)c3O)C(=O)O[C@@H]12)c1cc(O)c(O)c(O)c1

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found in taxon

Chinese peony

2 references

stated in

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

stated in

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

Alnus hirsuta

1 reference

stated in

Hirsunin, an ellagitannin with a diarylheptanoid moiety, from Alnus hirsuta var. Microphylla

Alnus sieboldiana

1 reference

stated in

Alnusnins A and B from the leaves of Alnus sieboldiana

Micromeles japonica

1 reference

stated in

Tannins of Coriaria japonica A. Gray. I Coriariins A and B, new dimeric and monomeric hydrolyzable tannins.

Allocasuarina verticillata

1 reference

stated in

Tannis of Casuarina and Stachyurus species. Part 1. Structures of pendunculagin, casuarictin, strictinin, casuarinin, casuariin, and stachyurin

Casuarina stricta

1 reference

stated in

Tannis of Casuarina and Stachyurus species. Part 1. Structures of pendunculagin, casuarictin, strictinin, casuarinin, casuariin, and stachyurin

Coriaria japonica

1 reference

stated in

Tannins of Coriaria japonica A. Gray. I Coriariins A and B, new dimeric and monomeric hydrolyzable tannins.

Cornus officinalis

4 references

stated in

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

stated in

Cornusiin A, a dimeric ellagitannin forming four tautomers, and accompanying new tannins in Cornus officinalis.

stated in

Revised Structure of Isoterchebin, Isolated from Cornus officinalis

stated in

Tannins of cornaceous plants. II. Cornusiins D, E and F, new dimeric and trimeric hydrolyzable tannins from Cornus officinalis.

Eucalyptus alba

1 reference

stated in

Eucalbanins A,B and C, Monomeric and Dimeric Hydrolyzable Tannins from Eucalyptus alba REINW.

Eucalyptus consideniana

1 reference

stated in

Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis

Eucalyptus globulus

1 reference

stated in

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

Eucalyptus camaldulensis

1 reference

stated in

Antioxidant activity of tannins and flavonoids in Eucalyptus rostrata

Eucalyptus viminalis

1 reference

stated in

Polyphenols from Eucalyptus consideniana and Eucalyptus viminalis

1 reference

1 reference

1 reference

Hydrolysable tannins from Euphorbia thymifolia

Fordia fruticosa

1 reference

stated in

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

Geranium collinum

1 reference

stated in

Polyphenolic compounds ofGeranium collinum. IV

Hippophae rhamnoides

1 reference

stated in

Tannins from Hippophae rhamnoides

Juglans regia

1 reference

stated in

Antioxidative polyphenols from walnuts (Juglans regia L.).

Liquidambar formosana

1 reference

stated in

Seasonal changes in the tannins of Liquidambar formosana reflecting their biogenesis

Loropetalum chinense

1 reference

stated in

Hydrolysable tannins from Loropetalum chinense

Oenothera laciniata

2 references

stated in

Oenotheins D, F and G, hydrolysable tannin dimers from Oenothera laciniata

stated in

Production of macrocyclic ellagitannin oligomers by Oenothera laciniata callus cultures

Quercus suber

2 references

stated in

Antioxidant and biological properties of bioactive phenolic compounds from Quercus suber L.

stated in

Dimeric and trimeric hydrolyzable tannins from Quercus coccifera and Quercus suber

Reaumuria hirtella

1 reference

stated in

Tannins of Tamaricaceous Plants. II. New Monomeric and Dimeric Hydrolyzable Tannins from Reaumuria hirtella and Tamarix pakistanica.

Rosa gallica

1 reference

stated in

Inhibitory effects of Rosa gallica on the digestive enzymes

Rosa rugosa

1 reference

stated in

Tellimagrandin I, HCV invasion inhibitor from Rosae Rugosae Flos

1 reference

2 references

Casuariin, stachyurin and strictinin, new ellagitannins from Casuarina stricta and Stachyurus praecox.

stated in

Tannis of Casuarina and Stachyurus species. Part 1. Structures of pendunculagin, casuarictin, strictinin, casuarinin, casuariin, and stachyurin

1 reference

1 reference

Hydrolyzable tannins of tamaricaceous plants. III. Hellinoyl- and macrocyclic-type ellagitannins from Tamarix nilotica

Tamarix parviflora

1 reference

stated in

Hydrolyzable tannins of tamaricaceous plants. IV: Micropropagation and ellagitannin production in shoot cultures of Tamarix tetrandra

Tamarix tetrandra

1 reference

stated in

Hydrolyzable tannins of tamaricaceous plants. IV: Micropropagation and ellagitannin production in shoot cultures of Tamarix tetrandra

Tellima grandiflora

1 reference

stated in

Ellagitannins from Tellima grandiflora

1 reference

1 reference

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

Alniaria japonica

1 reference

stated in

Tannins of Coriaria japonica A. Gray. I Coriariins A and B, new dimeric and monomeric hydrolyzable tannins.

Punica granatum

1 reference

stated in

Diverse Phytochemicals and Bioactivities in the Ancient Fruit and Modern Functional Food Pomegranate (Punica granatum).

Allocasuarina distyla

1 reference

stated in

Tannis of Casuarina and Stachyurus species. Part 1. Structures of pendunculagin, casuarictin, strictinin, casuarinin, casuariin, and stachyurin

Tamarix senegalensis

1 reference

stated in

Hydrolyzable tannins of tamaricaceous plants. III. Hellinoyl- and macrocyclic-type ellagitannins from Tamarix nilotica

Castanea sativa

1 reference

stated in

Chestnut (Castanea sativa Miller.) Burs Extracts and Functional Compounds: UHPLC-UV-HRMS Profiling, Antioxidant Activity, and Inhibitory Effects on Phytopathogenic Fungi

Identifiers

InChI

InChI=1S/C34H26O22/c35-12-1-8(2-13(36)21(12)41)30(47)55-28-27-18(53-34(51)29(28)56-31(48)9-3-14(37)22(42)15(38)4-9)7-52-32(49)10-5-16(39)23(43)25(45)19(10)20-11(33(50)54-27)6-17(40)24(44)26(20)46/h1-6,18,27-29,34-46,51H,7H2/t18-,27-,28+,29-,34-/m1/s1

0 references

InChIKey

YKDNTEQLKGYZHT-JSAIFSMWSA-N

0 references

1 reference

26 December 2021

1 reference

(Q105349619)

1-Desgalloyleugeniin

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Identifiers

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