Novel synthesis of dihydropyrimidines for α-glucosidase inhibition to treat type 2 diabetes: in vitro biological evaluation and in silico docking.
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Crystal structure of ethyl (2S)-9-meth-oxy-2-methyl-4-oxo-3,4,5,6-tetra-hydro-2H- 2,6-methano-benzo[g][1,3,5]oxa-diazocine-11-carboxyl-ate.Synthesis, Biological Evaluation and Molecular Docking Study of 2-Substituted-4,6-Diarylpyrimidines as α-Glucosidase Inhibitors.Novel pyridine-2,4,6-tricarbohydrazide thiourea compounds as small key organic molecules for the potential treatment of type-2 diabetes mellitus: In vitro studies against yeast α- and β-glucosidase and in silico molecular modeling.Probing the influence of carboxyalkyl groups on the molecular flexibility and the charge density of apigenin derivatives.Organocatalyzed Novel Synthetic Methodology for Highly Functionalized Piperidines as Potent α-Glucosidase Inhibitors.
P2860
Novel synthesis of dihydropyrimidines for α-glucosidase inhibition to treat type 2 diabetes: in vitro biological evaluation and in silico docking.
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2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
Novel synthesis of dihydropyri ...... luation and in silico docking.
@en
Novel synthesis of dihydropyri ...... luation and in silico docking.
@nl
type
label
Novel synthesis of dihydropyri ...... luation and in silico docking.
@en
Novel synthesis of dihydropyri ...... luation and in silico docking.
@nl
prefLabel
Novel synthesis of dihydropyri ...... luation and in silico docking.
@en
Novel synthesis of dihydropyri ...... luation and in silico docking.
@nl
P2093
P1433
P1476
Novel synthesis of dihydropyri ...... aluation and in silico docking
@en
P2093
Ather Farooq Khan
Islam Ullah Khan
Lubna Shahzadi
Maqsood Ahmed
Muhammad Ashraf
Muhammad Yar
Umber Alam
P304
P356
10.1016/J.BIOORG.2014.05.003
P577
2014-05-15T00:00:00Z