Summary

IMPPAT Phytochemical identifier: IMPHY007498

Phytochemical name: [(1R,2S,19R,20R,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,

Synonymous chemical names:
laevigatin d

External chemical identifiers:
CID:16169195

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Chemical structure information

SMILES:
OC1O[C@@H]2COC(=O)c3cc(O)c(c(c3-c3c(C(=O)O[C@H]2[C@@H]([C@H]1OC(=O)c1cc(O)c(c(c1)Oc1c(cc(c(c1O)O)O)C(=O)O[C@H]1O[C@@H]2COC(=O)c4cc(O)c(c(c4-c4c(C(=O)O[C@H]2[C@H]2[C@H]1OC(=O)c1cc(O)c(c(c1-c1c(C(=O)O2)cc(c(c1O)O)O)O)O)cc(O)c(c4O)O)O)O)O)O)cc(O)c(c3O)O)O)O

InChI:
InChI=1S/C68H48O44/c69-20-1-12(59(93)109-56-52(92)54-29(105-67(56)101)10-102-60(94)13-3-21(70)38(78)45(85)31(13)33-15(62(96)107-54)5-23(72)40(80)47(33)87)2-28(37(20)77)104-53-19(9-27(76)44(84)51(53)91)66(100)112-68-58-57(110-64(98)17-7-25(74)42(82)49(89)35(17)36-18(65(99)111-58)8-26(75)43(83)50(36)90)55-30(106-68)11-103-61(95)14-4-22(71)39(79)46(86)32(14)34-16(63(97)108-55)6-24(73)41(81)48(34)88/h1-9,29-30,52,54-58,67-92,101H,10-11H2/t29-,30-,52+,54-,55-,56-,57+,58-,67?,68-/m1/s1

InChIKey:
BNKSPYAMWLMCHP-LWUVUOPPSA-N

DeepSMILES:
OCO[C@@H]COC=O)cccO)ccc6-ccC=O)O[C@H]%15[C@@H][C@H]%19OC=O)cccO)ccc6)Occcccc6O))O))O)))C=O)O[C@H]O[C@@H]COC=O)cccO)ccc6-ccC=O)O[C@H]%15[C@H][C@H]%19OC=O)cccO)ccc6-ccC=O)O%14))cccc6O))O))O))))))O))O))))))))))))ccO)cc6O))O)))))))O))O)))))))))))))))))O))))))))O)))))ccO)cc6O))O)))))))O))O

Functional groups:
CO, COC(C)O, cC(=O)OC, cC(=O)O[C@H](C)OC, cO, cOc

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C(OC1COC2COC(=O)c3ccccc3-c3ccccc3C(=O)OC2C1)c1cccc(Oc2ccccc2C(=O)OC2OC3COC(=O)c4ccccc4-c4ccccc4C(=O)OC3C3OC(=O)c4ccccc4-c4ccccc4C(=O)OC23)c1

Scaffold Graph/Node level:
OC(OC1COC2COC(O)C3CCCCC3C3CCCCC3C(O)OC2C1)C1CCCC(OC2CCCCC2C(O)OC2OC3COC(O)C4CCCCC4C4CCCCC4C(O)OC3C3OC(O)C4CCCCC4C4CCCCC4C(O)OC23)C1

Scaffold Graph level:
CC(CC1CCC2CCC(C)C3CCCCC3C3CCCCC3C(C)CC2C1)C1CCCC(CC2CCCCC2C(C)CC2CC3CCC(C)C4CCCCC4C4CCCCC4C(C)CC3C3CC(C)C4CCCCC4C4CCCCC4C(C)CC23)C1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Phenylpropanoids and polyketides

ClassyFire Class: Tannins

ClassyFire Subclass: Hydrolyzable tannins

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Phenolic acids (C6-C1)

NP Classifier Class: Gallotannins

NP-Likeness score: 0.864

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Chemical structure download