(Q105149869)

English

Phyllanthusiin C

group of stereoisomers with the chemical formula C₄₀H₃₀O₂₆

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Statements

group of stereoisomers

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1 reference

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926.1025310800003 dalton

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based on heuristic

inferred from isomeric SMILES

chemical formula

C₄₀H₃₀O₂₆

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canonical SMILES

O=C1OCC2OC(OC(=O)C3=CC(O)=C(O)C(O)=C3)C4OC(=O)C5=CC(O)=C(O)C=6OC7(O)C(O)CC(O)(C(=O)OC2C4OC(=O)C8=CC(O)=C(O)C(O)=C8C=9C(O)=C(O)C(O)=CC19)C7C65

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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]3[C@H]1OC(=O)c1cc(O)c(O)c4c1C1C(O)(CC(O)C1(O)O4)C(=O)O[C@@H]32)c1cc(O)c(O)c(O)c1

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Acalypha hispida

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Acalyphidins M1, M2 and D1, ellagitannins from Acalypha hispida1Part 16 in the series of Tannins and Related Polyphenols of Euphorbiaceous Plants. For Part 15, see Amakura, Kawada, Hatano, Agata, Sugaya et al., 1997.1

Geranium thunbergii

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

Phyllanthus flexuosus

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Tannins and Related Polyphenols of Euphorbiaceous Plants. IX. Hydrolyzable Tannins with 1C4 Glucose Core from Phyllanthus flexuosus MUELL. ARG.

Phyllanthus myrtifolius

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Antiviral tannins from two Phyllanthus species

Identifiers

InChI=1S/C40H30O26/c41-12-1-8(2-13(42)22(12)47)33(53)65-37-31-30-28(64-38(57)39(58)6-18(46)40(59)32(39)21-11(36(56)63-31)5-16(45)25(50)29(21)66-40)17(61-37)7-60-34(54)9-3-14(43)23(48)26(51)19(9)20-10(35(55)62-30)4-15(44)24(49)27(20)52/h1-5,17-18,28,30-32,37,41-52,58-59H,6-7H2/t17-,18?,28-,30+,31-,32?,37+,39?,40?/m1/s1

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LCJOXNIMFDLZJH-KCRIIDRDSA-N

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1 reference

17 September 2022

based on heuristic

inferred from InChIKey

UniChem compound ID

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