Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C16H18O9 |
| Molecular Weight | 354.3087 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@@H]1C[C@@](O)(C[C@@H](O)[C@H]1OC(=O)\C=C/C2=CC=C(O)C(O)=C2)C(O)=O
InChI
InChIKey=GYFFKZTYYAFCTR-XYXZIBEBSA-N
InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(21)25-14-11(19)6-16(24,15(22)23)7-12(14)20/h1-5,11-12,14,17-20,24H,6-7H2,(H,22,23)/b4-2-/t11-,12-,14-,16+/m1/s1
Cryptochlorogenic acid is a structural isomer of chlorogenic acid; it is a cinnamate ester formed by the condensation of the carboxy group of trans-caffeic acid with the 4-hydroxy group of quinic acid. It can be isolated from several plant sources including apples, coffee, sunflowers, potatoes, and Hibiscus sabdariffa. Cryptochlorogenic acid mixed with related compounds has demonstrated potential anti-oxidant and anti-inflammatory properties and shown inhibitory activity against HBV DNA replication.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Identification, quantitative determination, and antioxidative activities of chlorogenic acid isomers in prune (Prunus domestica L. ). | 2000 Nov |
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| Quantitative comparison of caffeoylquinic acids and flavonoids in Chrysanthemum morifolium flowers and their sulfur-fumigated products by three-channel liquid chromatography with electrochemical detection. | 2015 |
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| [Degradation kinetics of chlorogenic acid, cryptochlorogenic acid, and neochlorogenic acid at neutral and alkaline pH values]. | 2016 Jan |
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| Hydroxycinnamic acids in cooked potato tubers from Solanum tuberosum group Phureja. | 2017 May |
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87099-76-1
Created by
admin on Sat Dec 16 05:01:08 GMT 2023 , Edited by admin on Sat Dec 16 05:01:08 GMT 2023
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765J6E4RXD
Created by
admin on Sat Dec 16 05:01:08 GMT 2023 , Edited by admin on Sat Dec 16 05:01:08 GMT 2023
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SUBSTANCE RECORD
