- Hepatoprotective constituents from the roots and stems of erycibe hainanesis
-
Eleven new diglycosides, erycibosides A-K (1-11), four new chlorogenic acid derivatives (14-17), and a new biscoumarin (18), together with 21 known compounds, have been isolated from an EtOH extract of the roots and stems of Erycibe hainanesis. Their structures were elucidated by means of spectroscopic methods and chemical evidence. Inhibitory activities of some of the compounds on D-galactosamine-induced cytotoxicity in WB-F344 rat hepatic epithelial stemlike cells were screened, and compounds 2, 6, 10, 18, and 32 showed potent hepatoprotective activities at concentrations of 1 × 10-5 to 1 × 10-4 M.
- Song, Shuang,Li, Yixiu,Feng, Ziming,Jiang, Jianshuang,Zhang, Peicheng
-
-
Read Online
- Efficient and versatile synthesis of 5-O-acylquinic acids with a direct esterification using a p-methoxybenzyl quinate as a key intermediate
-
An efficient and versatile synthesis of 5-O-acylquinic acids from commercially available (-)-quinic acid was accomplished. We designed p-methoxybenzyl quinate as a key intermediate, and two problems, the esterification of the sterically hindered 5-OH group for the concise divergent synthesis and the low yield of the final deprotection step, were solved. For the first problem, we improved Tanabe's method, TsCl/NMI-mediated esterification using free carboxylic acids, by the addition of i-Pr2NEt. For the second problem, we established a TFA- or BCl3/C6HMe5-catalyzed deprotection reaction for the final deprotection step. 5-O-Acylquinic acids were synthesized in seven steps with 45-60% overall yield.
- Oyama, Kin-Ichi,Watanabe, Noriyuki,Yamada, Tomomi,Suzuki, Masako,Sekiguchi, Yukiko,Kondo, Tadao,Yoshida, Kumi
-
p. 3120 - 3130
(2015/05/04)
-
- Identification and quantification of phenolic compounds from the forage legume sainfoin (Onobrychis viciifolia)
-
Phenolic compounds of sainfoin (Onobrychis viciifolia) variety Cotswold Common are assumed to contribute to its nutritive value and bioactive properties. A purified acetone/water extract was separated by Sephadex LH-20 gel chromatography. Sixty-three phen
- Regos, Ionela,Urbanella, Andrea,Treutter, Dieter
-
body text
p. 5843 - 5852
(2010/06/17)
-
- Polyphenols are intensively metabolized in the human gastrointestinal tract after apple juice consumption
-
Polyphenols are secondary plant compounds showing anticarcinogenic effects both in vitro and in animal experiments and may thus reduce the risk of colorectal cancer in man. The identification of polyphenol metabolites formed via their passage through the small intestine of healthy ileostomy subjects after apple juice consumption is presented. Identification and quantification of polyphenols and their metabolites were performed using HPLC-DAD as well as HPLC-ESI-MS/MS. Total procyanidin content (TPA) was measured, and additionally the mean degree of polymerization (DPm) of the procyanidins was determined in the apple juice and ileostomy effluents. As products of polyphenol metabolism, D-(-)-quinic acid and methyl esters of caffeic acid and p-coumaric acid are liberated from the corresponding hydroxycinnamic acid esters. 1-Caffeoylquinic acid and 3-caffeoylquinic acid were determined as products of isomerization. Phloretin 2′-O-glucoside (phloridzin) and phloretin 2′-O-xyloglucoside were metabolized into the corresponding aglycons phloretin and phloretin 2′-Oglucuronide and all were found in the ileostomy effluent. Ninety percent of the consumed procyanidins were recovered in the ileostomy effluent and therefore would reach the colon under physiologic circumstances. The DPm was reduced (DPm of apple juice = 5.7) and varied depending on the time point of excretion. The gastrointestinal passage seems to play an important role in the colonic availability of apple polyphenols.
- Kahle, Kathrin,Huemmer, Wolfgang,Kempf, Michael,Scheppach, Wolfgang,Erk, Thomas,Richling, Elke
-
experimental part
p. 10605 - 10614
(2009/10/02)
-
- Synthesis of designed acylquinic acid derivatives involved in blue color development of hydrangea and their co-pigmentation effect
-
The blue sepal color of hydrangea may be developed by an unstable stipramolecular metal-complex pigment composed of delphinidin 3-glucoside (1), 5-O-caffeoylquinic acid (2) and 5-O-p-coumaroylquinic acid (3) as co-pigments and Al3+ in aqueous s
- Toyama-Kato, Yuki,Kondo, Tadao,Yoshida, Kumi
-
p. 239 - 254
(2008/03/12)
-
- Essential structure of co-pigment for blue sepal-color development of hydrangea
-
Blue sepal-color of Hydrangea macrophylla might be due to a supramolecular metal-complex pigment consisting of delphinidin 3-glucoside (1), co-pigments (5-O-caffeoylquinic acid (2), and/or 5-O-p-coumaroylquinic acid (3)) and Al 3+ in an aqueous
- Kondo, Tadao,Toyama-Kato, Yuki,Yoshida, Kumi
-
p. 6645 - 6649
(2007/10/03)
-
- Antioxidant constituents of almond [Prunus dulcis (Mill.) D.A. Webb] hulls
-
Almond hulls (Nonpareil variety) were extracted with methanol and analyzed by reversed phase HPLC with diode array detection. The extract contained 5-O-caffeoylquinic acid (chlorogenic acid), 4-O-caffeoylquinic acid (cryptochlorogenic acid), and 3-O-caffe
- Takeoka, Gary R.,Dao, Lan T.
-
p. 496 - 501
(2007/10/03)
-
- First efficient syntheses of 1-, 4-, and 5-caffeoylquinic acid
-
Efficient synthesis of 1-, 4-, and 5-caffeoylquinic acid was achieved in three or four steps with suitably protected quinic acid precursors, in overall yields of 41%, 36%, and 60% [from quinic acid (1)]. 1-Caffeoylquinic acid was prepared by esterificatio
- Sefkow, Michael,Kelling, Alexandra,Schilde, Uwe
-
p. 2735 - 2742
(2007/10/03)
-
- Rapid and easy identification of isomers of coumaroyl- and caffeoyl-D-quinic acid by gas chromatography/mass spectrometry
-
The 3-O-, 4-O- and 5-O-isomers of caffeoyl-D-quinic acid and the corresponding ethyl esters were separated by high-performance liquid chromatography and the structures were verified by NMR spectrometry. Trimethylsilylation of the compounds allowed a rapid
- Fuchs, Claus,Spiteller, Gerhard
-
p. 602 - 608
(2007/10/03)
-
