Current anti-diabetic agents and their molecular targets: A review

N Kerru, A Singh-Pillay, P Awolade, P Singh - European Journal of …, 2018 - Elsevier
Diabetes mellitus is a medical condition characterized by the body's loss of control over
blood sugar. The frequency of diagnosed cases and consequential increases in medical …

Biological activity of dihydropyrimidinone (DHPM) derivatives: A systematic review

LHS Matos, FT Masson, LA Simeoni… - European journal of …, 2018 - Elsevier
Dihydropyrimidinones are heterocycles with a pyrimidine moiety in the ring nucleus, which,
in recent decades, have aroused interest in medicinal chemistry due to alleged versatile …

Synthesis of novel flavone hydrazones: In-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies

S Imran, M Taha, NH Ismail, SM Kashif, F Rahim… - European journal of …, 2015 - Elsevier
Thirty derivatives of flavone hydrazone (5–34) had been synthesized through a five-step
reaction and screened for their α-glucosidase inhibition activity. Chalcone 1 was …

Natural prenylchalconaringenins and prenylnaringenins as antidiabetic agents: α-glucosidase and α-amylase inhibition and in vivo antihyperglycemic and …

H Sun, D Wang, X Song, Y Zhang, W Ding… - Journal of agricultural …, 2017 - ACS Publications
Inhibition of α-glucosidase and α-amylase decreases postprandial blood glucose levels and
delays glucose absorption, making it a treatment strategy for type 2 diabetes. This study …

Design and synthesis of 2-amino-4,6-diarylpyrimidine derivatives as potent α-glucosidase and α-amylase inhibitors: structure–activity relationship, in vitro, QSAR …

EU Mughal, S Amjid, A Sadiq, N Naeem… - Journal of …, 2024 - Taylor & Francis
In the present study, a series of 2-amino-4, 6-diarylpyrimidine derivatives was designed,
synthesized, characterized and evaluated for their in vitro α-glucosidase and α-amylase …

Design, synthesis, molecular docking, and in vitro α-glucosidase inhibitory activities of novel 3-amino-2, 4-diarylbenzo [4, 5] imidazo [1, 2-a] pyrimidines against yeast …

F Peytam, G Takalloobanafshi, T Saadattalab… - Scientific reports, 2021 - nature.com
In an attempt to find novel, potent α-glucosidase inhibitors, a library of poly-substituted 3-
amino-2, 4-diarylbenzo [4, 5] imidazo [1, 2-a] pyrimidines 3a–ag have been synthesized …

Synthesis, In vitro and Docking Studies of New Flavone Ethers as α‐Glucosidase Inhibitors

S Imran, M Taha, NH Ismail, SM Kashif… - Chemical biology & …, 2016 - Wiley Online Library
We report herein the synthesis, α‐glucosidase inhibition and docking studies for a series of
3–15 new flavones. A simple nucleophilic substitution reaction takes place between 3 …

The Chemistry of Aldehydes and Ketones in the Synthesis of Heterocycles-Historical Reactions with a New and Green Perspective

F Martins da Silva, JJ Junior… - Current Organic …, 2024 - benthamdirect.com
The reactivity of aldehydes and ketones carries great potential for multicomponent
heterocyclizations. These reactions are convergent and highly versatile in the development …

Pyridine sulfonamide as a small key organic molecule for the potential treatment of type-II diabetes mellitus and Alzheimer's disease: in vitro studies against yeast α …

S Riaz, IU Khan, M Bajda, M Ashraf, A Shaukat… - Bioorganic …, 2015 - Elsevier
This paper presents the efficient high yield synthesis of novel pyridine 2, 4, 6-
tricarbohydrazide derivatives (4a–4i) along with their α-glucosidase, acetylcholinesterase …

An efficient and targeted synthetic approach towards new highly substituted 6-amino-pyrazolo[1,5-a]pyrimidines with α-glucosidase inhibitory activity

F Peytam, M Adib, R Shourgeshty, L Firoozpour… - Scientific Reports, 2020 - nature.com
In an attempt to find novel α-glucosidase inhibitors, an efficient, straightforward reaction to
synthesize a library of fully substituted 6-amino-pyrazolo [1, 5-a] pyrimidines 3 has been …