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 …

Design, synthesis, computational study and cytotoxic evaluation of some new quinazoline derivatives containing pyrimidine moiety

S Zare, L Emami, Z Faghih, F Zargari, Z Faghih… - Scientific reports, 2023 - nature.com
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 …

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 …

1, 2, 4-Triazole derivatives as novel and potent antifungal agents: Design, synthesis and biological evaluation

S Sadeghian, L Emami, A Mojaddami, Z Faghih… - Journal of Molecular …, 2023 - Elsevier
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 …

Synthesis, biological evaluation, and computational studies of some novel quinazoline derivatives as anticancer agents

L Emami, S Khabnadideh, Z Faghih, F Farahvasi… - BMC chemistry, 2022 - Springer
A series of quinazolinone derivatives (7a–7h) were synthesized as antiproliferative agents.
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

M Rashedinia, Z Rasti Arbabi, R Sabet… - Biochemistry …, 2023 - Wiley Online Library
Several diabetic complications are associated with forming advanced glycation end
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 …

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 …

Novel quinazolinone derivatives as anticancer agents: Design, synthesis, biological evaluation and computational studies

E Ataollahi, M Behrouz, P Mardaneh, M Emami… - Journal of Molecular …, 2024 - Elsevier
A novel series of quinazoline-pyrimidine derivatives (3a-3i) linked to different aryl
substitutions were designed and synthesized as promising anti-cancer candidates. The …

Two new cytotoxic ursane triterpenoids from the aerial parts of Salvia urmiensis Bunge

S Hashemi, AR Jassbi, N Erfani, R Kiani, H Seradj - Fitoterapia, 2021 - Elsevier
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 …