Fariba Peytam

发表

A new synthetic strategy towards 2,4,5-trisubstituted 1H-imidazoles and highly substituted pyrrolo[1,2-c]imidazoles by use of α-azidochalcones via Michael addition-cyclization followed by Wittig reaction

M. Adib, H. Bijanzadeh, M. Amanlou, 2017 .

An efficient synthesis of fully substituted pyrazolo[3,4-b]pyridin-5-amines from α-azidochalcones

M. Adib, Fariba Peytam, 2018 .

Design, Synthesis, Molecular Docking, and Kinetic Study of 3-Amino-2,4-Diarylbenzo[4,5]Imidazo[1,2-a]Pyrimidines as Novel, Potent Α-Glucosidase Inhibitor

M. Faramarzi, A. Foroumadi, H. Bijanzadeh, 2021 .

Synthesis and biological evaluation of new dihydroindolizino[8,7-b]indole derivatives as novel α-glucosidase inhibitors

B. Larijani, A. Moghadamnia, M. Faramarzi, 2021 .

The possible effect of microRNA-155 (miR-155) and BACE1 inhibitors in the memory of patients with down syndrome and Alzheimer's disease: Design, synthesis, virtual screening, molecular modeling and biological evaluations

A. Iraji, N. Edraki, M. Adib, 2021, Journal of biomolecular structure & dynamics.

Design, synthesis and evaluation of novel tetrahydropyridothienopyrimidin-ureas as cytotoxic and anti-angiogenic agents

R. Esmaeili, A. Foroumadi, A. Khalaj, 2022, Scientific Reports.

Design and synthesis of new imidazo[1,2-b]pyrazole derivatives, in vitro α-glucosidase inhibition, kinetic and docking studies

B. Larijani, H. Rastegar, A. Moghadamnia, 2019, Molecular Diversity.

Mono- and bis-pyrazolophthalazines: Design, synthesis, cytotoxic activity, DNA/HSA binding and molecular docking studies.

R. Esmaeili, M. Khoobi, H. Forootanfar, 2020, Bioorganic & medicinal chemistry.

A one-pot, three-component and solvent-free synthesis of 2,3-disubstituted isoindolin-1-ones

M. Adib, Long‐Guan Zhu, Fariba Peytam, 2015 .

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 and rat α-glucosidase

M. Faramarzi, A. Foroumadi, H. Bijanzadeh, 2021, Scientific Reports.

Isoindolin-1-one derivatives as urease inhibitors: Design, synthesis, biological evaluation, molecular docking and in-silico ADME evaluation.

M. Adib, M. Mahdavi, M. Jahani, 2019, Bioorganic chemistry.

A One‐Pot, Three‐Component and Solvent‐Free Synthesis of 2,3‐Disubstituted Isoindolin‐1‐ones.

M. Adib, Longguan Zhu, Fariba Peytam, 2015 .

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

F. Safari, M. Faramarzi, A. Foroumadi, 2020, Scientific Reports.

Design, synthesis and in vitro α-glucosidase inhibition of novel coumarin-pyridines as potent antidiabetic agents

B. Larijani, M. Faramarzi, M. Adib, 2018 .

New 6-amino-pyrido[2,3-d]pyrimidine-2,4-diones as novel agents to treat type 2 diabetes: A simple and efficient synthesis, α-glucosidase inhibition, molecular modeling and kinetic study.

B. Larijani, M. Faramarzi, M. Adib, 2018, European journal of medicinal chemistry.

A one-pot and three-component synthetic approach for the preparation of asymmetric and multi-substituted 1,4-dihydropyrazines

B. Larijani, M. Adib, M. Mahdavi, 2019, Tetrahedron Letters.

Design and synthesis of new fused carbazole-imidazole derivatives as anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and in silico studies.

B. Larijani, A. Moghadamnia, M. Faramarzi, 2019, Bioorganic & medicinal chemistry letters.

Imidazo[1,2-a]quinazolines as novel, potent EGFR-TK inhibitors: Design, synthesis, bioactivity evaluation, and in silico studies.

B. Baratte, R. Esmaeili, A. Foroumadi, 2023, Bioorganic chemistry.

Quinazoline-based VEGFR-2 inhibitors as potential anti-angiogenic agents: A contemporary perspective of SAR and molecular docking studies.

A. Foroumadi, S. Moghimi, S. Bach, 2023, European journal of medicinal chemistry.

Novel fluoroquinolones analogues bearing 4-(arylcarbamoyl)benzyl: design, synthesis, and antibacterial evaluation.

A. Foroumadi, M. B. Tehrani, Loghman Firoozpour, 2023, Molecular diversity.

Imidazopyridine-based kinase inhibitors as potential anticancer agents: A review.

M. Safavi, Loghman Firoozpour, Roham Foroumadi, 2023, Bioorganic chemistry.

Design and synthesis of new imidazo[1,2-b]pyrazole derivatives, in vitro α-glucosidase inhibition, kinetic and docking studies

B. Larijani, H. Rastegar, A. Moghadamnia, 2019, Molecular Diversity.