Summary

IMPPAT Phytochemical identifier: IMPHY011961

Phytochemical name: Cyclohexanecarboxylic acid, 3-[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1,4,5-trihydroxy-, (1S,3R,4S,5R)-

Synonymous chemical names:
iso-chlorogenic acid, isochlorogenic acid, isochlorogenic-acid

External chemical identifiers:
CID:73081

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Chemical structure information

SMILES:
O=C(O[C@@H]1C[C@@](O)(C[C@H]([C@@H]1O)O)C(=O)O)C=Cc1ccc(c(c1)O)O

InChI:
InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(20)25-12-7-16(24,15(22)23)6-11(19)14(12)21/h1-5,11-12,14,17-19,21,24H,6-7H2,(H,22,23)/t11-,12-,14+,16+/m1/s1

InChIKey:
CWVRJTMFETXNAD-HLSYRSCKSA-N

DeepSMILES:
O=CO[C@@H]C[C@@]O)C[C@H][C@@H]6O))O)))C=O)O))))))C=Ccccccc6)O))O

Functional groups:
CC(=O)O, CO, cC=CC(=O)OC, cO

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C(C=Cc1ccccc1)OC1CCCCC1

Scaffold Graph/Node level:
OC(CCC1CCCCC1)OC1CCCCC1

Scaffold Graph level:
CC(CCC1CCCCC1)CC1CCCCC1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Organic oxygen compounds

ClassyFire Class: Organooxygen compounds

ClassyFire Subclass: Alcohols and polyols

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Phenylpropanoids (C6-C3)

NP Classifier Class: Cinnamic acids and derivatives

NP-Likeness score: 2.246

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Chemical structure download