نتایج جستجو برای: glucosidase inhibitors

تعداد نتایج: 194978  

2015
Senhua Chen Zhaoming Liu Yayue Liu Yongjun Lu Lei He Zhigang She

Three new depsidones, botryorhodines E-G (1-3), and two new isoindolinones, meyeroguillines A and B (7 and 9), along with five known compounds were isolated from an endophytic fungus Meyerozyma guilliermondii, derived from the mangrove plant Kandelia obovata. Their structures were elucidated by 1D and 2D NMR spectroscopy and high resolution mass spectrometry (HREIMS). Compounds 1-6 exhibited st...

2016
Lovemore Nkhata Malunga Peter Eck Trust Beta

The effect of feruloylated arabinoxylan mono- and oligosaccharides (FAXmo) on mammalian α-glucosidase and glucose transporters was investigated using human Caco-2 cells, rat intestinal acetone powder, and Xenopus laevis oocytes. The isolated FAXmo from wheat aleurone and corn bran were identified to have degree of polymerization (DP) of 4 and 1, respectively, by HPLC-MS. Both FAXmo extracts wer...

2018
Diganta Kalita David G Holm Daniel V LaBarbera J Mark Petrash Sastry S Jayanty

Diabetes mellitus is a chronic disease that is becoming a serious global health problem. Diabetes has been considered to be one of the major risks of cataract and retinopathy. Synthetic and natural product inhibitors of carbohydrate degrading enzymes are able to reduce type 2 diabetes and its complications. For a long time, potatoes have been portrayed as unhealthy for diabetic patients by some...

Journal: :The Journal of antibiotics 2002
Hung-Bae Chang Sun-Ho Kim Young-In Kwon Dong-Ho Choung Won-Kyu Choi Tae Won Kang Sungsook Lee Jong-Gwan Kim Hyoung-Sik Chun Soon Kil Ahn Chung Il Hong Kyou-Hoon Han

We have isolated two novel a-glucosidase inhibitors, O-[4-deoxy-4-(2,3-epoxy-3-hydroxymethyl-4,5,6-trihydroxycyclohexane-1-yl-amino)-alpha-D-glucopyranosyl]-(1-->4)-O-alpha-D-glucopyranosyl-(1-->4)-alpha-D-glucopyranose (named CKD-711) and its hexameric analog CKD-711a, from the fermentation broth of Streptomyces sp. CK-4416. HRFAB-MS and NMR analyses reveal that molecular formulae of CKD-711 a...

Journal: :Archives of internal medicine 2001
V S Catalan J A Couture J LeLorier

BACKGROUND A carbose is the first of a new class of antidiabetic agents, the alpha-glucosidase inhibitors. This study characterizes and identifies predictors of persistence of use of acarbose. METHODS Medical, pharmaceutical, and demographic records were extracted for 2 cohorts of patients (social assistance recipients and seniors) from the databases of Quebec's provincial health plan. Patien...

 Hyperglycemia and hyperlipidemia have been symptoms of many serious diseases such as diabetes and atherosclerosis overall the world. Thus, drug researchers have focused on new, natural and healthy drug alternatives. Marine macroalgae is a great source of hypoglycemic, hypolipidemic or hypocholesterolemic agents. In this study, we investigated that hypoglycemic, hypolipidemic a...

Journal: :Indian Journal of Endocrinology and Metabolism 2014

Journal: :نامه انجمن حشره شناسی ایران 0
میسره شابراری گروه گیاه پزشکی، دانشکده ی و منابع طبیعی، دانشگاه محقق اردبیلی، اردبیل، ایران. بهرام ناصری گروه گیاه پزشکی، دانشکده ی و منابع طبیعی، دانشگاه محقق اردبیلی، اردبیل، ایران.

the imported willow leaf beetle, plagiodera versicolora is one of the main pests of forest trees worldwide including iran. activities of α- and β-glucosidases in the midgut of p. versicolora adults were studied in this research. the results showed a higher α- glucosidase activity of adultsthan β-glucosidase. the optimal phs for α- and β-glucosidases activities were found to be 6 and 9, respecti...

Journal: :Journal of the American Chemical Society 2017
Saeideh Shamsi Kazem Abadi Michael Tran Anuj K Yadav Pal John Pal Adabala Saswati Chakladar Andrew J Bennet

The design of covalent inhibitors in glycoscience research is important for the development of chemical biology probes. Here we report the synthesis of a new carbocyclic mechanism-based covalent inhibitor of an α-glucosidase. The enzyme efficiently catalyzes its alkylation via either an allylic cation or a cationic transition state. We show this allylic covalent inhibitor has different catalyti...

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