نتایج جستجو برای: glucosidase inhibitor

تعداد نتایج: 217557  

Journal: :The Journal of biological chemistry 2001
U G Danilczyk D B Williams

Calnexin and calreticulin are molecular chaperones of the endoplasmic reticulum that bind to newly synthesized glycoproteins in part through a lectin site specific for monoglucosylated (Glc(1)Man(7-9)GlcNAc(2)) oligosaccharides. In addition to this lectin-oligosaccharide interaction, in vitro studies have demonstrated that calnexin and calreticulin can bind to polypeptide segments of both glyco...

Journal: :Phytochemistry 2016
Yasodha Sivasothy Kong Yong Loo Kok Hoong Leong Marc Litaudon Khalijah Awang

A dimeric acylphenol and a potent α-glucosidase inhibitor, giganteone D (IC50 5.05μM), was isolated and characterized from the bark of Myristica cinnamomea King. The bark also yielded an acylphenol with an unprecedented skeleton for which the name cinnamomeone A (IC50 358.80μM) was proposed. Their structures were established by means of NMR and MS spectrometric analyses. The Lineweaver-Burk plo...

Journal: :International Journal of Pharmacology 2009

Journal: :Molecules 2014
Zhanwu Sheng Haofu Dai Siyi Pan Hui Wang Yingying Hu Weihong Ma

The use of α-glucosidase inhibitors is considered to be an effective strategy in the treatment of diabetes. Using a bioassay-guided fractionation technique, five Bacillus stearothermophilus α-glucosidase inhibitors were isolated from the flowers of Musa spp. (Baxijiao). Using NMR spectroscopy analysis they were identified as vanillic acid (1), ferulic acid (2), β-sitosterol (3), daucosterol (4)...

Journal: :Journal of Analytical & Pharmaceutical Research 2018

2012
Kathirvel Alagesan Prabhakar Thennarasu Vinoth Kumar Sadasivam Sankarnarayanan

We screened for α-glucosidase inhibitors from 12 traditional medicinal plants used for the treatment of diabetes. Potent α-glucosidase inhibitory activity was found in aqueous extract of Psidium guajava leaves and Syzygium cumini Linn seed extract. Active principles inhibiting α-glucosidase were isolated and identified as apigenin 7O-glucoside in the S.cumini Linn seed extract and Dihydro-3,3’,...

Journal: :Gut 1987
B Lembcke C Löser U R Fölsch J Wöhler W Creutzfeldt

Intestinal adaptation (small intestinal weight and length, weight of the caecum and of the residual colon) to feeding different doses (0-5-50-500 mg/kg bw) of the absorbable, competitive alpha-glucosidase inhibitors BAY m 1099 and BAY o 1248 for three, seven, or 28 days was studied in rats. With the highest dose of either inhibitor, a significant and time dependent growth of the caecum was obse...

2015
Lang Wu Jingjing Zhu Larry J. Prokop Mohammad Hassan Murad

Different anti-diabetic medications (ADMs) may modify cancer risk and mortality in patients with diabetes. We conducted a systematic review and meta-analysis to estimate the magnitude of association and quality of supporting evidence for each ADM. A total of 265 studies (44 cohort studies, 39 case-control studies, and 182 randomized controlled trials (RCT)) were identified, involving approximat...

Journal: :American journal of physiology. Endocrinology and metabolism 2001
A Salehi B G Fan M Ekelund G Nordin I Lundquist

We examined the relation between nutrient-stimulated insulin secretion and the islet lysosome acid glucan-1,4-alpha-glucosidase system in rats undergoing total parenteral nutrition (TPN). During TPN treatment, serum glucose was normal, but free fatty acids, triglycerides, and cholesterol were elevated. Islets from TPN-infused rats showed increased basal insulin release, a normal insulin respons...

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