Name | 1-Caffeoylquinic acid |
Synonyms | 1-Caffeoylquinicaci 1-Kaffeylchinasaeure 1-Caffeoylquinic acid 1-O-caffeoylquinic acid 3,4-Dihydroxycinnamic acid (-)-1-carboxy-3,4,5-trihydroxycyclohexyl ester Cinnamic acid, 3,4-dihydroxy-, (-)-1-carboxy-3,4,5-trihydroxycyclohexyl ester 1-[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-3,4,5-trihydroxy-,(1a,3R,4a,5R) 1-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3,4,5-trihydroxycyclohexanecarboxylic acid Cyclohexanecarboxylic acid, 1-[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-3,4,5-trihydroxy-, (1α,3R,4α,5R)- |
CAS | 1241-87-8 |
InChI | InChI=1/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(21)25-16(15(23)24)6-11(19)14(22)12(20)7-16/h1-5,11-12,14,17-20,22H,6-7H2,(H,23,24)/b4-2+ |
Molecular Formula | C16H18O9 |
Molar Mass | 354.31 |
Density | 1.65 |
Boling Point | 636.2±55.0 °C(Predicted) |
Flash Point | 234.5°C |
Vapor Presure | 4.66E-17mmHg at 25°C |
Appearance | White powder |
pKa | 2.94±0.50(Predicted) |
Storage Condition | 2-8℃ |
Refractive Index | 1.69 |
Physical and Chemical Properties | Yellow crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from honeysuckle. |
Reference Show more | 1. Cai, Z, Liao, H, Wang, C, et al. A comprehensive study of the aerial parts of Lonicera japonica Thunb. based on metabolite profiling coupled with PLS-DA. Phytochemical Analysis. 2020; 31: 786– 800. https://doi.org/10.1002/pca.2943 2. [IF=3.373] Zhichen Cai et al."A comprehensive study of the aerial parts of Lonicera japonica Thunb. based on metabolite profiling coupled with PLS-DA."Phytochem Analysis. 2020 Nov;31(6):786-800 3. [IF=6.475] Guoping Lai et al."Free, soluble conjugated and insoluble bonded phenolic acids in Keemun black tea: From UPLC-QQQ-MS/MS method development to chemical shifts monitoring during processing."Food Res Int. 2022 May;155:111041 4. [IF=3.645] Lewen Xiong et al."Study on phenolic acids of Lonicerae japonicae Flos based on ultrahigh performance liquid chromatography-tandem mass spectrometry combined with multivariate statistical analysis."JOURNAL OF SEPARATION SCIENCE |
uses | 1-caffeoylquinic acid is used as a standard reference substance in biochemical research for content determination/identification/pharmacological experiments, etc. |
biological activity | 1-Caffeoylquinic acid 1-caffeoylquinic acid is an effective NF-κB inhibitor, showing high binding affinity for RH domain of p105, Ki value is 0.002 μM, and binding energy is 1.50 Kcal/mol. 1-Caffeoylquinic acid has anti-oxidative stress ability. 1-Caffeoylquinic acid inhibits PD-1/PD-L1 interactions. |
target | Ki: 0.002 μM (1-Cateoylquinic acid) |