Medicinal chemistry of non-peptidomimetic dipeptidyl peptidase IV (DPP IV) inhibitors for treatment of Type-2 diabetes mellitus: Insights on recent development
JP Ambhore, PR Laddha, A Nandedkar… - Journal of Molecular …, 2023 - Elsevier
Nowadays, dipeptidyl peptidase-IV (DPP-IV) is emerging as a hopeful drug target for treating
Type 2 diabetic mellitus (T2DM). Currently marketed DPP-IV inhibitors work by lowering the …
Type 2 diabetic mellitus (T2DM). Currently marketed DPP-IV inhibitors work by lowering the …
Design, synthesis, computational study and cytotoxic evaluation of some new quinazoline derivatives containing pyrimidine moiety
Quinazoline derivatives, as an important category of heterocyclic compounds, have received
much attention for the design and development of new drugs due to their various …
much attention for the design and development of new drugs due to their various …
Anticancer Biological Profile of Some Heterocylic Moieties-Thiadiazole, Benzimidazole, Quinazoline, and Pyrimidine
PS Sidat, TMK Jaber, SR Vekariya… - …, 2022 - pharmacophorejournal.com
Cancer is a disease characterized by genetic or epigenetic alterations in somatic cells that
result in uncontrolled cell growth and spread to other regions of the body. They are one type …
result in uncontrolled cell growth and spread to other regions of the body. They are one type …
1, 2, 4-Triazole derivatives as novel and potent antifungal agents: Design, synthesis and biological evaluation
Fungal infections are still threatening human health due to resistance to existing drugs,
therefore, the design and development of novel antifungal agents is to be necessary and …
therefore, the design and development of novel antifungal agents is to be necessary and …
Synthesis, biological evaluation, and computational studies of some novel quinazoline derivatives as anticancer agents
A series of quinazolinone derivatives (7a–7h) were synthesized as antiproliferative agents.
All compounds, were synthesized through three steps method and structurally evaluated by …
All compounds, were synthesized through three steps method and structurally evaluated by …
Comparison of protective effects of phenolic acids on protein glycation of BSA supported by in vitro and docking studies
Several diabetic complications are associated with forming advanced glycation end
products (AGEs). Different chemical and natural compounds are able to prevent the …
products (AGEs). Different chemical and natural compounds are able to prevent the …
Design, synthesis, biological evaluation and computational studies of 4-Aminopiperidine-3, 4-dihyroquinazoline-2-uracil derivatives as promising antidiabetic agents
L Baziar, L Emami, Z Rezaei, A Solhjoo… - Scientific Reports, 2024 - nature.com
A novel series of 4-aminopiperidin-3, 4-dihyroquinazoline-2-uracil derivatives (9a-9 L) were
logically designed and synthesized as potent DPP4 inhibitors as antidiabetic agents …
logically designed and synthesized as potent DPP4 inhibitors as antidiabetic agents …
6-Bromo quinazoline derivatives as cytotoxic agents: design, synthesis, molecular docking and MD simulation
L Emami, M Hassani, P Mardaneh, F Zare, M Saeedi… - BMC chemistry, 2024 - Springer
Based on unselectively, several side effects and drug resistance of available anticancer
agents, the development and research for novel anticancer agents is necessary. In this …
agents, the development and research for novel anticancer agents is necessary. In this …
Novel quinazolinone derivatives as anticancer agents: Design, synthesis, biological evaluation and computational studies
A novel series of quinazoline-pyrimidine derivatives (3a-3i) linked to different aryl
substitutions were designed and synthesized as promising anti-cancer candidates. The …
substitutions were designed and synthesized as promising anti-cancer candidates. The …
Two new cytotoxic ursane triterpenoids from the aerial parts of Salvia urmiensis Bunge
Bioassay-guided fractionation of a dichloromethane extract of the aerial parts of Salvia
urmiensis, an endemic plant species of Iran, led to the isolation of two new cytotoxic ursane …
urmiensis, an endemic plant species of Iran, led to the isolation of two new cytotoxic ursane …