casuarictin (Q5050928)

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chemical compound

Language	Label	Description	Also known as
English	casuarictin	chemical compound

Statements

type of chemical entity

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1(beta)-O-Galloylpedunculagin

1 reference

based on heuristic

inferred from SMILES

chemical structure

Casuarictin.svg
1,035 × 885; 46 KB

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936.086881016 dalton

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based on heuristic

inferred from SMILES

stereoisomer of

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based on heuristic

inferred from InChI

chemical formula

C₄₁H₂₈O₂₆

2 references

imported from Wikimedia project

English Wikipedia

canonical SMILES

C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O

2 references

imported from Wikimedia project

English Wikipedia

isomeric SMILES

O=C(O[C@@H]1O[C@@H]2COC(=O)c3cc(O)c(O)c(O)c3-c3c(cc(O)c(O)c3O)C(=O)O[C@H]2[C@@H]2OC(=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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Agrimonia pilosa

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Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Camellia oleifera

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A dimeric hydrolysable tannin from Camellia oleifera

Castanopsis cuspidata

1 reference

Tannins and related compounds. LXXVI. Isolation and characterization of cercidinins A and B and cuspinin, unusual 2,3-(R)-hexahydroxydiphenoyl glucoses from Cercidiphyllum japonicum and Castanopsis cuspidata var. sieboldii.

Corylus heterophylla

1 reference

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

Eucalyptus nitens

1 reference

Identification of hydrolysable tannins in the reaction zone of Eucalyptus nitens wood by high performance liquid chromatography--electrospray ionisation mass spectrometry

Fragaria iinumae

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Fragaria nipponica

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

1 reference

Gemins D, E and F, ellagitannins from Geum japonicum

Heterocentron subtriplinervium

2 references

Ellagitannin formation in callus cultures of Heterocentron roseum

Tannins and Related Polyphenols of Melastomataceous Plants. III. Nobotanins G, H and I, Dimeric Hydrolyzable Tannins from Heterocentron roseum.

Hippophae rhamnoides

1 reference

Tannins from Hippophae rhamnoides

1 reference

Antioxidative polyphenols from walnuts (Juglans regia L.).

Liquidambar formosana

1 reference

Seasonal changes in the tannins of Liquidambar formosana reflecting their biogenesis

Melastoma dodecandrum

1 reference

Inhibitory effects of hydrolyzable tannins from Melastoma dodecandrum Lour. on nitric oxide production by a murine macrophage-like cell line, RAW264.7, activated with lipopolysaccharide and interferon-gamma

Potentilla centigrana

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Quercus coccifera

1 reference

Dimeric and trimeric hydrolyzable tannins from Quercus coccifera and Quercus suber

1 reference

Polyphenols and chemical defence of the leaves of Quercus robur

2 references

Hydrolysable tannin oligomers from Rosa davurica

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

Rosa multiflora

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Rosa roxburghii

1 reference

Tannins and related polyphenols of rosaceous medicinal plants. IV. Roxbins A and B from Rosa roxburghii fruits

2 references

Tannins of rosaceous plants. VIII. Hydrolyzable tannin monomers having a valoneoyl group from flower petals of Rosa rugosa Thunb.

Tellimagrandin I, HCV invasion inhibitor from Rosae Rugosae Flos

Rubus pseudochingii

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Rubus toyorensis

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Sieversia pentapetala

1 reference

Hydrolysable tannins as chemotaxonomic markers in the rosaceae

Stachyurus praecox

3 references

Tannins of Stachyurus Species. II. Praecoxins A, B, C and D, Four New Hydrolyzable Tannins from Stachyurus praecox Leaves.

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

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

3 references

Alpha-glucosidase inhibitors from clove (Syzgium aromaticum).

Isolation of virus-cell fusion inhibitory components from Eugenia caryophyllata

Tannins and Related Compounds. CXXIII. Chromone, Acetophenone and Phenylpropanoid Glycosides and Their Galloyl and /or Hexahydroxydiphenoyl Esters from the Leaves of Syzygium aromaticum MERR. et PERRY.

Tibouchina semidecandra

1 reference

Tannins and Related Polyphenols of Melastomataceous Plants. I. Hydrolyzable Tannins from Tibouchina semidecandra COGN.

Alnus sieboldiana

1 reference

Alnusnins A and B from the leaves of Alnus sieboldiana

Castanopsis fissa

1 reference

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

Casuarina stricta

2 references

Ellagitannins of the casuarinaceae, stachyuraceae and myrtaceae

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

Euscaphis japonica

1 reference

Euscaphinin, a new ellagitannin dimer from Euscaphis japonica (THUNB.) KANITZ

Staphylea japonica

1 reference

Euscaphinin, a new ellagitannin dimer from Euscaphis japonica (THUNB.) KANITZ

Lotus corniculatus

1 reference

Tannins and related compounds. LXXXIV. Isolation and characterization of five new hydrolyzable tannins from the bark of Mallotus japonicus

Mallotus japonicus

1 reference

Tannins and related compounds. LXXXIV. Isolation and characterization of five new hydrolyzable tannins from the bark of Mallotus japonicus

Melaleuca squarrosa

1 reference

Flavonol glucuronides and C-glucosidic ellagitannins from Melaleuca squarrosa.

Monochaetum multiflorum

1 reference

Oligomeric hydrolyzable tannins from Monochaetum multiflorum

1 reference

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

Platycarya strobilacea

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ent-Eudesmane sesquiterpenoids, galloyl esters of the oak lactone precursor, and a 3-O-methylellagic acid glycoside from the wood of Platycarya strobilacea

Psidium guajava

1 reference

Phenolic compounds from the leaves of Psidium guajava. I. Hydrolysable tannins and benzophenone glycosides

1 reference

Tannins and related compounds. CIX. Isolation of alienanins A and B, novel C,C-linked ellagitannin dimers from Quercus aliena Blume.

Quercus phillyraeoides

1 reference

Tannins and related compounds. LXXXIII. Isolation and structures of hydrolyzable tannins, phillyraeoidins A-E from Quercus phillyraeoides.

Rhoiptelea chiliantha

2 references

Three novel C-glycosidic ellagitannins, rhoipteleanins H, I, and J, from rhoiptelea chiliantha

Structures and Biogenesis of Rhoipteleanins, Ellagitannins Formed by Stereospecific Intermolecular C-C Oxidative Coupling, Isolated from Rhoiptelea chiliantha

1 reference

Inhibitory effects of Rosa gallica on the digestive enzymes

1 reference

Tannis of rosaceous medicinal plants. V. Hydrolyzable tannis with dehydrodigalloyl group from Rosa laevigata MICHX.

Rubus lambertianus

1 reference

Tannins and related compounds. CXXII. New dimeric, trimeric and tetrameric ellagitannins, lambertianins A-D, from Rubus lambertianus Seringe

Rubus chingii var. suavissimus

1 reference

Rubusuaviins A-F, monomeric and oligomeric ellagitannins from Chinese sweet tea and their alpha-amylase inhibitory activity

Allocasuarina distyla

2 references

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

Ellagitannins of the casuarinaceae, stachyuraceae and myrtaceae

Melastoma malabathricum

1 reference

Dimeric hydrolysable tannins from melastoma Malabathricum

Geum macrophyllum

1 reference

Gemins D, E and F, ellagitannins from Geum japonicum

Allocasuarina verticillata

2 references

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

Ellagitannins of the casuarinaceae, stachyuraceae and myrtaceae

Pleroma heteromallum

1 reference

Oligomeric hydrolysable tannins from Tibouchina multiflora

Syzygium aqueum

1 reference

Tannins and Related Compounds. CXIX. Samarangenins A and B, Novel Proanthocyanidins with Doubly Bonded Structures, from Syzygium samarangens and S. aqueum.

Identifiers

InChI=1S/C41H28O26/c42-13-1-8(2-14(43)24(13)48)36(57)67-41-35-34(65-39(60)11-5-17(46)27(51)31(55)22(11)23-12(40(61)66-35)6-18(47)28(52)32(23)56)33-19(63-41)7-62-37(58)9-3-15(44)25(49)29(53)20(9)21-10(38(59)64-33)4-16(45)26(50)30(21)54/h1-6,19,33-35,41-56H,7H2/t19-,33-,34+,35-,41+/m1/s1

1 reference

SWRFKGRMQVLMKA-JIZJWZDPSA-N

2 references

ChEBI release 2020-09-01

CAS Registry Number

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imported from Wikimedia project

English Wikipedia

1 reference

imported from Wikimedia project

English Wikipedia

mapping relation type

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ChEBI release 2019-10-02

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imported from Wikimedia project

English Wikipedia

UniChem compound ID

1 reference

DSSTox substance ID

DTXSID401000730

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DSSTOX compound identifier

DTXCID701427690

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Microsoft Academic ID

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Sitelinks

Wikipedia(7 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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