نتایج جستجو برای: glucosidase inhibitors

تعداد نتایج: 194978  

2015
Yingbo Yang Lihua Gu Ying Xiao Qing Liu Haijun Hu Zhengtao Wang Kaixian Chen

Alpha-glucosidase inhibitors currently form an important basis for developing novel drugs for diabetes treatment. In our preliminary tests, the ethyl acetate fraction of Phlomis tuberosa extracts showed significant α-glucosidase inhibitory activity (IC₅₀ = 100 μg/mL). In the present study, a combined method using Sepbox chromatography and thin-layer chromatography (TLC) bioautography was develo...

Journal: :علوم و فنون زنبور عسل 0

abstract bee venom is a complex mixture of proteins, peptides and low molecular components: proteins (enzymes) :( phospholipase, a2phospholipase b, hyaluronidase α – glucosidase) - , peptides (melittin, apamine mcd peptide,adolapine ,procamine a and b, protease inhibitors)- low molecular components: biogenic amines:( histamine, dopamine and noradrenalin) - pheromones: complex ethers- sugars :( ...

Journal: :Diabetic medicine : a journal of the British Diabetic Association 2011
O J Phung N A Sood B E Sill C I Coleman

AIM To determine the comparative efficacy of oral anti-diabetic drugs in preventing the development of Type 2 diabetes. METHODS A systematic literature search of MEDLINE, EMBASE and Cochrane CENTRAL was conducted for randomized controlled trials evaluating oral anti-diabetic drugs in patients at high risk for developing Type 2 diabetes. Mixed-treatment comparison meta-analysis methods were us...

Journal: :Glycobiology 1996
S Muniruzzaman Y T Pan Y Zeng B Atkins K Izumori A D Elbein

A number of unusual and rare carbohydrates were tested as potential inhibitors of various glycosidases, as well as inhibitors of N-linked oligosaccharide processing. The best inhibitors of several arylglycosidases and of glucosidase I were L-xylulose and L-fructose. Both of these sugars showed some inhibitory activity towards yeast alpha-glucosidase but were inactive against beta-glucosidase an...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
N Zitzmann A S Mehta S Carrouée T D Butters F M Platt J McCauley B S Blumberg R A Dwek T M Block

One function of N-linked glycans is to assist in the folding of glycoproteins by mediating interactions of the lectin-like chaperone proteins calnexin and calreticulin with nascent glycoproteins. These interactions can be prevented by inhibitors of the alpha-glucosidases, such as N-butyl-deoxynojirimycin (NB-DNJ) and N-nonyl-DNJ (NN-DNJ), and this causes some proteins to be misfolded and retain...

Journal: :Medicinal Chemistry Research 2022

High postprandial hyperglycaemia is an important determinant of the development and progression type 2 diabetes. Thus, inhibition key digestive enzymes such as α-amylase α-glucosidase considered efficient approach to control glycaemic levels in diabetics. In search inhibitors, root bark Paeonia suffruticosa was screened for resulting isolation eleven phenolic compounds (1–11). Their inhibitory ...

Journal: :Archives of Biochemistry and Biophysics 1975

Journal: :Internal medicine 2015
Amihai Rottenstreich Yahel Agmon Ram Elazary

Alpha glucosidase inhibitors have been shown to be associated with pneumatosis intestinalis (PI) in recent reports. We herein report the case of a 73-year old man who received treatment with an alpha glucosidase inhibitor (acarbose) and presented with acute abdomen. A computed tomography scan demonstrated PI in addition to intrahepatic portal air and pneumoperitoneum. During exploratory laparot...

Journal: :European journal of medicinal chemistry 2016
Yeong Hun Song Dae Wook Kim Marcus J Curtis-Long Chanin Park Minky Son Jeong Yoon Kim Heung Joo Yuk Keun Woo Lee Ki Hun Park

The α-glucosidase inhibitory potential of Tribulus terrestris extracts has been reported but as yet the active ingredients are unknown. This study attempted to isolate the responsible metabolites and elucidate their inhibition mechanism of α-glucosidase. By fractionating T. terristris extracts, three cinnamic acid amide derivatives (1-3) were ascertained to be active components against α-glucos...

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