Summary

IMPPAT Phytochemical identifier: IMPHY014851

Phytochemical name: Camellin

Synonymous chemical names:
camellin

External chemical identifiers:
CID:73989750

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Chemical structure information

SMILES:
OCC1OC(Oc2cc(O)cc3c2c(=O)cc(o3)c2ccc(cc2)O)C(C(C1OC1OC(C)C(C(C1O)O)O)O)O

InChI:
InChI=1S/C27H30O14/c1-10-20(32)21(33)23(35)26(37-10)41-25-18(9-28)40-27(24(36)22(25)34)39-17-7-13(30)6-16-19(17)14(31)8-15(38-16)11-2-4-12(29)5-3-11/h2-8,10,18,20-30,32-36H,9H2,1H3

InChIKey:
LRFDUPNLCDXZOE-UHFFFAOYSA-N

DeepSMILES:
OCCOCOcccO)ccc6c=O)cco6)cccccc6))O)))))))))))))))CCC6OCOCC)CCC6O))O))O)))))))O))O

Functional groups:
CO, COC(C)OC, c=O, cO, cOC(C)OC, coc

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=c1cc(-c2ccccc2)oc2cccc(OC3CCC(OC4CCCCO4)CO3)c12

Scaffold Graph/Node level:
OC1CC(C2CCCCC2)OC2CCCC(OC3CCC(OC4CCCCO4)CO3)C12

Scaffold Graph level:
CC1CC(C2CCCCC2)CC2CCCC(CC3CCC(CC4CCCCC4)CC3)C12

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Phenylpropanoids and polyketides

ClassyFire Class: Flavonoids

ClassyFire Subclass: Flavonoid glycosides

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Flavonoids

NP Classifier Class: Flavones

NP-Likeness score: 2.081

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Chemical structure download