scholarly journals Anti-nociceptive and Anti-inflammatory Properties of Ilex latifolia and its Active Component, 3,5-Di-caffeoyl Quinic Acid Methyl Ester

2018 ◽  
Vol 25 (1) ◽  
pp. 64
Author(s):  
Joo Youn Kim ◽  
Hong Kyu Lee ◽  
Yeon Hee Seong
1984 ◽  
Vol 39 (1-2) ◽  
pp. 167-170 ◽  
Author(s):  
Denis Barron ◽  
Mourad Kaouadji ◽  
Anne-Marie Mariotte

Abstract Two new cinnamoyl quinic acid esters were isolated from the methanolic extract of Meumathamanticum rhizome. They were identified as l-trans-O-caffeoyl quinic acid methyl ester and l-trans-O-feruloyl quinic acid methyl ester by the spectral data of the natural products and those of the acetylated derivatives.


2010 ◽  
Vol 5 (5) ◽  
pp. 1934578X1000500 ◽  
Author(s):  
Manuela Jehle ◽  
Johanna Bano ◽  
Ernst P. Ellmerer ◽  
Christian Zidorn

The aerial parts of Scorzonera aristata Ramond ex DC., collected in the South Tyrolean Dolomites, yielded the flavonoids quercetin 3- O-glucoside, rutin, and isoorientin, and the caffeic acid derivatives chlorogenic acid, 4,5-dicaffeoyl quinic acid, and 3,5-dicaffeoyl quinic acid. Sub-aerial parts contained caffeic acid methyl ester, 3,5-dicaffeoyl quinic acid, and the triterpenes 3α-hydroxyolean-5-ene, lupeol, and magnificol. Chemosystematic implications of the isolated compounds are discussed briefly.


2018 ◽  
Vol 9 (12) ◽  
pp. 6155-6164 ◽  
Author(s):  
Lang Zhang ◽  
Ya Fan ◽  
Hanwen Su ◽  
Li Wu ◽  
Yuying Huang ◽  
...  

In vivoandin vitrostudies show that chlorogenic acid methyl ester (CME) has been proven to be a potential nutraceutical for preventing inflammation.


Author(s):  
Alain S. Leutou ◽  
Jennifer R. McCall ◽  
Robert York ◽  
Rajeshwar R. Govindapur ◽  
Andrea J. Bourdelais

A New monogalactosyldiacylglycerol (MGDG), a known monogalactosylmonoacylglycerol (MGMG) and a known polyunsaturated fatty acid methyl ester (PUFAME) were isolated from the marine dinoflagellate Karenia mikimotoi. The planar structure of the glycolipids was elucidated using MS and NMR spectroscopic analyses and comparisons to the known glycolipid to confirm its structure. The isolation of PUFAME strongly supports the polyunsaturated fatty acid fragment of these glycolipids. The relative configuration of the sugar was deduced by comparisons of 3JHH values and proton chemical shifts with those of known glycolipids. All isolated compounds MGDG, MGMG and PUFAME (1-3) were evaluated for their antimicrobial and anti-inflammatory activity. All compounds modulated macrophage responses, with compound 3 exhibiting the greatest anti-inflammatory activity.


RSC Advances ◽  
2015 ◽  
Vol 5 (23) ◽  
pp. 17786-17796 ◽  
Author(s):  
Young-Yeon Choo ◽  
Suhyun Lee ◽  
Phi-Hung Nguyen ◽  
Wanju Lee ◽  
Mi-Hee Woo ◽  
...  

Caffeoylglycolic acid methyl ester, a major constituent of sorghum, exhibits anti-inflammatory activityviaactivating the Nrf2/HO-1 pathway.


2016 ◽  
Vol 18 (10) ◽  
pp. 945-951 ◽  
Author(s):  
Yong-Fen Yang ◽  
Hong-Mei Ma ◽  
Gang Chen ◽  
Hai-Feng Wang ◽  
Zheng Xiang ◽  
...  

Author(s):  
M. Amin Mir ◽  
Waqar Ashraf Muhammad ◽  
Priya Singh

The anti-inflammatory activity and the phytochemical analysis of Lilium polyphyllum showed that the plant does possess a large of phytochemicals which can be used solely or in combination to over the problem of inflammation. The analysis was carried out by using three solvent systems, in which it had been found that water extract possess more anti inflammation property followed by ethanol and less activity were found associated with DCM extract. The HPLC, GC-MS, 1HNMR and 13CNMR analysis showed the presence of various important phytochemicals viz, Methyl 2-furoate, 5-hydroxymethyl furfural, Methyl piperate, Piperine, 7, 10-Hexadecadienoic acid methyl ester, Palmitic acid, Methyl palmitate, which are responsible wither individually or in combination for the property in reference.


Marine Drugs ◽  
2020 ◽  
Vol 18 (3) ◽  
pp. 138 ◽  
Author(s):  
Alain S. Leutou ◽  
Jennifer R. McCall ◽  
Robert York ◽  
Rajeshwar R. Govindapur ◽  
Andrea J. Bourdelais

A new monogalactosyldiacylglycerol (MGDG), a known monogalactosylmonoacylglycerol (MGMG) and a known polyunsaturated fatty acid methyl ester (PUFAME) were isolated from the marine dinoflagellate Karenia mikimotoi. The planar structure of the glycolipids was elucidated using mass spectroscopy (MS) and nuclear magnetic resonance (NMR) analyses and comparisons to the known glycolipid to confirm its structure. The MGDG was characterized as 3-O-β-D-galactopyranosyl-1-O-3,6,9,12,15-octadecapentaenoyl-2-O-tetradecanoylglycerol 1. The MGMG and PUFAME were characterized as (2S)-3-O-β-D-galactopyranosyl-1-O-3,6,9,12,15-octadecapentaenoylglycerol 2 and Methyl (3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoate 3, respectively. The isolation of the PUFAME strongly supports the polyunsaturated fatty acid (PUFA) fragment of these glycolipids. The relative configuration of the sugar was deduced by comparisons of 3JHH values and proton chemical shifts with those of known glycolipids. All isolated compounds MGDG, MGMG and PUFAME 1-3 were evaluated for their antimicrobial and anti-inflammatory activity. All compounds modulated macrophage responses, with compound 3 exhibiting the greatest anti-inflammatory activity.


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