نتایج جستجو برای: flavonol aglycon

تعداد نتایج: 1629  

B Nickavar G Amin N Mehregan

From the aerial parts of Tanacetum balsamita L. (Compositae) a flavonol aglycon was iso­lated using chromatographic techniques. The structure of this compound was determined using spectroscopic methods (UV, H-NMR and MS) as 3',4',5,7-Tetrahydroxy flavonol (Quercetin).

B Nickavar G Amin N Mehregan

From the aerial parts of Tanacetum balsamita L. (Compositae) a flavonol aglycon was iso­lated using chromatographic techniques. The structure of this compound was determined using spectroscopic methods (UV, H-NMR and MS) as 3',4',5,7-Tetrahydroxy flavonol (Quercetin).

Journal: :iranian journal of pharmaceutical research 0
g amin n mehregan

from the aerial parts of tanacetum balsamita l. (compositae) a flavonol aglycon was iso­lated using chromatographic techniques. the structure of this compound was determined using spectroscopic methods (uv, h-nmr and ms) as 3',4',5,7-tetrahydroxy flavonol (quercetin).

2003
Ö. Tokuşoğlu M. K. Ünal Z. Yıldırım Celal Bayar

The amounts of three flavonoids, quercetin, kaempferol, and myricetin, in tomatoes (Solanum lycopersicum L.) and tomato-based products produced in Turkey has been determined by reversed phase high-performance liquid chromatography (RPHPLC) with UV detection. The HPLC profiles of five types of tomato, one commercial composite tomato juice, and three types of tomato paste, were obtained after aci...

2003
ALBERT N. BOOTH FRANCIS T. JONES

Three metabolites appearing in the urine of animals after the ingestion of the flavonol quercetin (1, 2) having been identified, our interests were next centered on similar studies of several citrus flavonoids. Here again our primary concern was to find evidence, if any, that these compounds are absorbed from the gastrointestinal tract after oral ingestion and, secondly, if absorption does take...

Journal: :The Journal of biological chemistry 1958
A N BOOTH F T JONES F DeEDS

Three metabolites appearing in the urine of animals after the ingestion of the flavonol quercetin (1, 2) having been identified, our interests were next centered on similar studies of several citrus flavonoids. Here again our primary concern was to find evidence, if any, that these compounds are absorbed from the gastrointestinal tract after oral ingestion and, secondly, if absorption does take...

2015
Yuta Morishita Emi Saito Eri Takemura Ryoma Fujikawa Ryohei Yamamoto Masanori Kuroyanagi Osamu Shirota

We isolated three active constituents from an aqueous extract of spinach leaves by evaluating the inhibitory activity of IgE-mediated degranulation in rat basophilic leukemia RBL-2H3 cells, and determined their chemical structures. These compounds, referred to as SO-1, SO-2 and SO-3, were assessed to be flavonol glucuronides with the same fundamental structure. Among them, SO-1 exhibited the mo...

Journal: :F1000Research 2022

Hyperoside, also known as quercetin-3-O-?-D-galactopyranoside, belongs to the class of flavonol glycosides. Its aglycon is quercetin, and sugar base galactopyranoside. It made quercetin. The O atom at 3rd position element connected group by a ?-glycosidic bond. Hyperoside, which widely present in planted objects, such fruits whole plants Hypericaceae, Rosac...

Journal: :The Journal of antibiotics 1998
H Hori Y Igarashi T Kajiura T Furumai K Higashi T Ishiyama M Uramota Y Uehara T Oki

The structure of hibarimicins A, B, C, D and G which are inhibitors for tyrosine specific protein kinase are determined using spectroscopic techniques. Hibarimicins described in this report consist of a common aglycon and six deoxyhexoses. The aglycon contains a highly oxidized naphtylnaphthoquinone as a chromophore. Among them, hibarimicin B was identical with angelmicin B.

2016
Amandine Kolleth Julian Gebauer Abdelatif ElMarrouni Raphael Lebeuf Céline Prévost Eric Brohan Stellios Arseniyadis Janine Cossy

We report here the total synthesis of 11-epi-lyngbouilloside aglycon. Our strategy features a Boeckman-type esterification followed by a RCM to form the 14-membered ring macrolactone and a late-stage side chain introduction via a Wittig olefination. Overall, the final product was obtained in 20 steps and 2% overall yield starting from commercially available 3-methyl-but-3-enol. Most importantly...

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