16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
a-Glucosidase anda-Amylase Inhibitors from Arcytophyllum thymifolium.
University of Basilicata
From carbohydrates to drug-like fragments: Rational development of novela-amylase inhibitors.
Freie Universit£T Berlin
Synthesis, crystal structure and antidiabetic activity of substituted (E)-3-(Benzo [d]thiazol-2-ylamino) phenylprop-2-en-1-one.
North Maharashtra University
Synthesis and glycosidase inhibitory activity of novel (2-phenyl-4H-benzopyrimedo[2,1-b]-thiazol-4-yliden)acetonitrile derivatives.
North Maharashtra University
Kinetic characterisation of ene-diol-based inhibitors of alpha-amylase.
University of Canterbury
Development of thiazole-appended novel hydrazones as a new class of α-amylase inhibitors with anticancer assets: an
Ccs Haryana Agricultural University
Metronidazole-conjugates: A comprehensive review of recent developments towards synthesis and medicinal perspective.
North-West University
Phenolic group on A-ring is key for dracoflavan B as a selective noncompetitive inhibitor of α-amylase.
National University of Singapore
Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid.
Ep Cnrs 51
Synthesis of piperazine sulfonamide analogs as diabetic-II inhibitors and their molecular docking study.
University of Dammam
Antidiabetic potential of phytochemicals isolated from the stem bark of Myristica fatua Houtt. var. magnifica (Bedd.) Sinclair.
Csir-National Institute For Interdisciplinary Science and Technology
Pentacyclic triterpenes asα-glucosidase andα-amylase inhibitors: Structure-activity relationships and the synergism with acarbose.
Dalian University of Technology
Muscarinic receptor subtype specificity of (N,N-dialkylamino)alkyl 2-cyclohexyl-2-phenylpropionates: cylexphenes (cyclohexyl-substituted aprophen analogues).
Institute of Research
Microwave-assisted synthesis and tyrosinase inhibitory activity of chalcone derivatives.
Shaoyang University