Biscoumarin-1, 2, 3-triazole hybrids as novel anti-diabetic agents: Design, synthesis, in vitro α-glucosidase inhibition, kinetic, and docking studies MS Asgari, M Mohammadi-Khanaposhtani, M Kiani, PR Ranjbar, E Zabihi, ... Bioorganic chemistry 92, 103206, 2019 | 97 | 2019 |
Design, synthesis, characterization, enzymatic inhibition evaluations, and docking study of novel quinazolinone derivatives K Pedrood, M Sherafati, M Mohammadi-Khanaposhtani, MS Asgari, ... International Journal of Biological Macromolecules 170, 1-12, 2021 | 54 | 2021 |
The natural-based optimization of kojic acid conjugated to different thio-quinazolinones as potential anti-melanogenesis agents with tyrosinase inhibitory activity N Sepehri, A Iraji, A Yavari, MS Asgari, S Zamani, S Hosseini, ... Bioorganic & Medicinal Chemistry 36, 116044, 2021 | 53 | 2021 |
Design, synthesis, in vitro, and in silico studies of novel diarylimidazole-1, 2, 3-triazole hybrids as potent α-glucosidase inhibitors M Saeedi, M Mohammadi-Khanaposhtani, MS Asgari, N Eghbalnejad, ... Bioorganic & medicinal chemistry 27 (23), 115148, 2019 | 46 | 2019 |
Anti-melanogenesis and anti-tyrosinase properties of aryl-substituted acetamides of phenoxy methyl triazole conjugated with thiosemicarbazide: Design, synthesis and biological … H Hosseinpoor, SM Farid, A Iraji, MS Asgari, N Edraki, S Hosseini, ... Bioorganic Chemistry 114, 104979, 2021 | 43 | 2021 |
New 1, 2, 3‐triazole–(thio) barbituric acid hybrids as urease inhibitors: design, synthesis, in vitro urease inhibition, docking study, and molecular dynamic simulation MS Asgari, H Azizian, M Nazari Montazer, M Mohammadi‐Khanaposhtani, ... Archiv der Pharmazie 353 (9), 2000023, 2020 | 38 | 2020 |
Design and synthesis of 4,5-diphenyl-imidazol-1,2,3-triazole hybrids as new anti-diabetic agents: in vitro α-glucosidase inhibition, kinetic and docking studies MS Asgari, M Mohammadi-Khanaposhtani, Z Sharafi, MA Faramarzi, ... Molecular Diversity 25, 877-888, 2021 | 33 | 2021 |
Arylmethylene hydrazine derivatives containing 1, 3-dimethylbarbituric moiety as novel urease inhibitors K Pedrood, H Azizian, MN Montazer, M Mohammadi‐Khanaposhtani, ... Scientific reports 11 (1), 10607, 2021 | 25 | 2021 |
Design, synthesis and biological evaluation of novel phthalimide-Schiff base-coumarin hybrids as potent α-glucosidase inhibitors M Sherafati, M Mohammadi-Khanaposhtani, S Moradi, MS Asgari, ... Chemical Papers 74, 4379-4388, 2020 | 24 | 2020 |
Novel (thio)barbituric-phenoxy-N-phenylacetamide derivatives as potent urease inhibitors: synthesis, in vitro urease inhibition, and in silico evaluations S Sedaghati, H Azizian, MN Montazer, M Mohammadi-Khanaposhtani, ... Structural Chemistry 32, 37-48, 2021 | 23 | 2021 |
Design and synthesis of phenoxymethybenzoimidazole incorporating different aryl thiazole-triazole acetamide derivatives as α-glycosidase inhibitors A Nasli Esfahani, A Iraji, A Alamir, S Moradi, MS Asgari, S Hosseini, ... Molecular Diversity, 1-15, 2021 | 22 | 2021 |
Quinazolinone-dihydropyrano [3, 2-b] pyran hybrids as new α-glucosidase inhibitors: Design, synthesis, enzymatic inhibition, docking study and prediction of pharmacokinetic M Sherafati, R Mirzazadeh, E Barzegari, M Mohammadi-Khanaposhtani, ... Bioorganic chemistry 109, 104703, 2021 | 19 | 2021 |
Magnetic silica nanoparticle-supported copper complex as an efficient catalyst for the synthesis of novel triazolopyrazinylacetamides with improved antibacterial activity MS Asgari, S Sepehri, S Bahadorikhalili, PR Ranjbar, R Rahimi, ... Chemistry of Heterocyclic Compounds 56, 488-494, 2020 | 18 | 2020 |
New quinoxalin‐1, 3, 4‐oxadiazole derivatives: Synthesis, characterization, in vitro biological evaluations, and molecular modeling studies R Mirzazadeh, MS Asgari, E Barzegari, K Pedrood, ... Archiv der Pharmazie 354 (9), 2000471, 2021 | 17 | 2021 |
Application of porphyrin modified sba-15 in adsorption of lead ions from aqueous media MS Asgari, A Zonouzi, R Rahimi, M Rabbani Orient. J. Chem 31 (3), 1537-1544, 2015 | 17 | 2015 |
Novel and efficient synthesis of triazolobenzodiazepine analogues through the sequential Ugi 4CR-click-N-arylation reactions MS Asgari, M Soheilizad, PR Ranjbar, B Larijani, R Rahimi, M Mahdavi Tetrahedron Letters 60 (8), 583-585, 2019 | 16 | 2019 |
Design, synthesis, biological evaluation, and molecular docking study of thioxo-2, 3-dihydroquinazolinone derivative as tyrosinase inhibitors N Sepehri, M Khoshneviszadeh, SM Farid, SS Moayedi, MS Asgari, ... Journal of Molecular Structure 1253, 132283, 2022 | 13 | 2022 |
Design, synthesis, in vitro and in silico biological assays of new quinazolinone-2-thio-metronidazole derivatives S Ansari, M Mohammadi-Khanaposhtani, MS Asgari, EN Esfahani, ... Journal of Molecular Structure 1244, 130889, 2021 | 11 | 2021 |
Synthesis, in vitro and in silico enzymatic inhibition assays, and toxicity evaluations of new 4, 5-diphenylimidazole-N-phenylacetamide derivatives as potent α-glucosidase … M Mohammadi-Khanaposhtani, A Nikraftar, MS Asgari, M Emadi, ... Medicinal Chemistry Research 30 (6), 1273-1283, 2021 | 11 | 2021 |
Design, synthesis, and biological evaluation of new indole-acrylamide-1, 2, 3-triazole derivatives as potential α-glucosidase inhibitors SE Sadat-Ebrahimi, H Babania, M Mohammadi-Khanaposhtani, ... Polycyclic Aromatic Compounds 42 (6), 3157-3165, 2022 | 10 | 2022 |