(Q105359928)

English

Oenothein B

group of stereoisomers with the chemical formula C₆₈H₄₈O₄₄

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Statements

group of stereoisomers

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chemical compound

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1,568.151844816 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₆₈H₄₈O₄₄

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canonical SMILES

O=C1OCC2OC(O)C3OC(=O)C4=CC(O)=C(O)C(O)=C4OC=5C=C6C(=O)OCC7OC(O)C(OC(=O)C8=CC(O)=C(O)C(O)=C8OC=9C=C(C(=O)OC2C3OC(=O)C%10=CC(O)=C(O)C(O)=C%10)C(=C(O)C9O)C%11=C(O)C(O)=C(O)C=C1%11)C(OC(=O)C%12=CC(O)=C(O)C(O)=C%12)C7OC(=O)C%13=CC(O)=C(O)C(O)=C%13C6=C(O)C5O

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Eucalyptus alba

1 reference

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

Melaleuca leucadendra

1 reference

An hydrolysable tannin and accompanying polyphenols from Melaleuca leucadendron

Oenothera tetraptera

1 reference

A macrocyclic ellagitannin trimer, oenotherin T(1), from Oenothera species

Epilobium capense

1 reference

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Epilobium roseum

1 reference

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Epilobium montanum

1 reference

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Epilobium hirsutum

1 reference

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Epilobium parviflorum

2 references

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Determination of oenothein B as the active 5-alpha-reductase-inhibiting principle of the folk medicine Epilobium parviflorum

Epilobium salignum

1 reference

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Epilobium stereophyllum

1 reference

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Oenothera laciniata

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Production of macrocyclic ellagitannin oligomers by Oenothera laciniata callus cultures

Cuphea hyssopifolia

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Antitumor activity of four macrocyclic ellagitannins from Cuphea hyssopifolia

Eugenia uniflora

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EBV DNA polymerase inhibition of tannins from Eugenia uniflora

Oenothera glazioviana

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Oenothein B, a dimeric hydrolyzable tannin of cyclic structure.

Chamaenerion dodonaei

2 references

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Induction of neutral endopeptidase activity in PC-3 cells by an aqueous extract of Epilobium angustifolium L. and oenothein B.

Epilobium dodonaei

2 references

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Induction of neutral endopeptidase activity in PC-3 cells by an aqueous extract of Epilobium angustifolium L. and oenothein B.

Epilobium prantlii

2 references

Inhibition of 5 alpha-reductase and aromatase by the ellagitannins oenothein A and oenothein B from Epilobium species

Induction of neutral endopeptidase activity in PC-3 cells by an aqueous extract of Epilobium angustifolium L. and oenothein B.

Oenothera erythrosepala

2 references

Oenothein B, a dimeric, hydrolysable tannin with macrocyclic structure, and accompanying tannins from Oenothera erythrosepala

Oenothein B, a dimeric hydrolyzable tannin of cyclic structure.

Identifiers

InChI=1S/C68H48O44/c69-21-1-13(2-22(70)37(21)77)59(91)109-55-53-32-12-102-62(94)17-9-29(43(83)47(87)35(17)34-16(63(95)107-53)6-26(74)40(80)46(34)86)103-51-19(7-27(75)41(81)49(51)89)65(97)112-58-56(110-60(92)14-3-23(71)38(78)24(72)4-14)54-31(105-68(58)100)11-101-61(93)15-5-25(73)39(79)45(85)33(15)36-18(64(96)108-54)10-30(44(84)48(36)88)104-52-20(8-28(76)42(82)50(52)90)66(98)111-57(55)67(99)106-32/h1-10,31-32,53-58,67-90,99-100H,11-12H2

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YSLFLCIPPPJEHH-UHFFFAOYSA-N

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2 references

15 September 2022

matched by identifier from

YSLFLCIPPPJEHH-UHFFFAOYSA-N

UniChem compound ID

1 reference

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