(Q105300454)

English

WASNQMYMYFXZHF-UHFFFAOYSA-N

group of stereoisomers with the chemical formula C₇₅H₅₂O₄₈

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Statements

group of stereoisomers

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chemical compound

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1,721.1895 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₇₅H₅₂O₄₈

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canonical SMILES

O=CC1OC(=O)C2=CC(O)=C(O)C(O)=C2OC=3C=C4C(=O)OC5C(OC(OC(=O)C6=CC(O)=C(O)C(O)=C6OC=7C=C8C(=O)OCC(O)C(OC(=O)C9=CC(O)=C(O)C(O)=C9C8=C(O)C7O)C1OC(=O)C%10=CC(O)=C(O)C(O)=C%10)C(OC(=O)C%11=CC(O)=C(O)C(O)=C%11)C5OC(=O)C%12=CC(O)=C(O)C(O)=C%12)COC(=O)C%13=CC(O)=C(O)C(O)=C%13C4=C(O)C3O

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Camellia sasanqua

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Tannins of theaceous plants. II. Camelliins A and B, two new dimeric hydrolyzable tannins from flower buds of Camellia japonica L. and Camellia sasanqua Thunb.

Polyspora axillaris

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Camelliin B induced apoptosis in HeLa cell line

Loropetalum chinense

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Hydrolysable tannins from Loropetalum chinense

Camellia japonica

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Tannins of theaceous plants. II. Camelliins A and B, two new dimeric hydrolyzable tannins from flower buds of Camellia japonica L. and Camellia sasanqua Thunb.

Camellia oleifera

2 references

Tannins of theaceous plants. II. Camelliins A and B, two new dimeric hydrolyzable tannins from flower buds of Camellia japonica L. and Camellia sasanqua Thunb.

A dimeric hydrolysable tannin from Camellia oleifera

Identifiers

InChI=1S/C75H52O48/c76-13-38-62(119-66(103)16-1-25(77)44(88)26(78)2-16)61-35(87)14-112-70(107)21-11-36(51(95)55(99)42(21)41-20(71(108)118-61)8-32(84)48(92)54(41)98)114-60-24(10-34(86)50(94)58(60)102)74(111)123-75-65(122-68(105)18-5-29(81)46(90)30(82)6-18)64(121-67(104)17-3-27(79)45(89)28(80)4-17)63-39(117-75)15-113-69(106)19-7-31(83)47(91)53(97)40(19)43-22(72(109)120-63)12-37(52(96)56(43)100)115-59-23(73(110)116-38)9-33(85)49(93)57(59)101/h1-13,35,38-39,61-65,75,77-102H,14-15H2

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WASNQMYMYFXZHF-UHFFFAOYSA-N

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CAS Registry Number

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CAS (formerly Chemical Abstracts Service)

25 January 2022

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15 September 2022

matched by identifier from

WASNQMYMYFXZHF-UHFFFAOYSA-N

UniChem compound ID

1 reference

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