| 1, 2, 3‐Triazole‐linked 5‐benzylidene (thio) barbiturates as novel tyrosinase inhibitors and free‐radical scavengers S Ranjbar, P Shahvaran, N Edraki, M Khoshneviszadeh, M Darroudi, ... Archiv der Pharmazie 353 (10), 2000058, 2020 | 26 | 2020 |
| 2-alkylthio-5-(nitroaryl)-1, 3, 4-thiadiazole derivatives as anti-Helicobacter pylori agents: investigation of structure-activity relationship A Asadipour, N Edraki, M Nakhjiri, A Meymandi, E Alipour, P Saniee, ... Research in Pharmaceutical Sciences 7 (5), 506, 2012 | | 2012 |
| 2-Imino 2H-chromene and 2-(phenylimino) 2H-chromene 3-aryl carboxamide derivatives as novel cytotoxic agents: synthesis, biological assay, and molecular … N Edraki, A Iraji, O Firuzi, Y Fattahi, M Mahdavi, A Foroumadi, ... Journal of the Iranian Chemical Society 13, 2163-2171, 2016 | 29 | 2016 |
| 5-Oxo-hexahydroquinoline and 5-oxo-tetrahydrocyclopentapyridine derivatives as promising antiproliferative agents with potential apoptosis-inducing capacity S Ranjbar, M Khoshneviszadeh, M Tavakkoli, R Miri, N Edraki, O Firuzi Molecular Diversity, 1-20, 2022 | 6 | 2022 |
| 5-Oxo-hexahydroquinoline derivatives and their tetrahydroquinoline counterparts as multidrug resistance reversal agents O Shahraki, M Khoshneviszadeh, M Dehghani, M Mohabbati, M Tavakkoli, ... Molecules 25 (8), 1839, 2020 | 7 | 2020 |
| 5-Oxo-hexahydroquinoline derivatives as modulators of P-gp, MRP1 and BCRP transporters to overcome multidrug resistance in cancer cells S Ranjbar, R Khonkarn, A Moreno, H Baubichon-Cortay, R Miri, ... Toxicology and Applied Pharmacology 362, 136-149, 2019 | 40 | 2019 |
| 5-Oxo-hexahydroquinoline: An attractive scaffold with diverse biological activities S Ranjbar, N Edraki, O Firuzi, M Khoshneviszadeh, R Miri Molecular Diversity 23, 471-508, 2019 | 40 | 2019 |
| 5-Oxohexahydroquinolines bearing 4-pyridyl methyl carboxylate as P-glycoprotein inhibitors and multidrug resistance reversal agents in cancer cells S Ranjbar, FF Lashkarian, M Khoshneviszadeh, F Moosavi, A Sakhteman, ... Journal of Molecular Structure 1285, 135427, 2023 | 1 | 2023 |
| 5, 6-Diphenyl triazine-thio methyl triazole hybrid as a new Alzheimer’s disease modifying agents M Yazdani, N Edraki, R Badri, M Khoshneviszadeh, A Iraji, O Firuzi Molecular diversity 24, 641-654, 2020 | 36 | 2020 |
| 6-Methoxy-3, 4-dihydronaphthalenone chalcone-like derivatives as potent tyrosinase inhibitors and radical scavengers S Ranjbar, A Akbari, N Edraki, M Khoshneviszadeh, H Hemmatian, ... Letters in Drug Design & Discovery 15 (11), 1170-1179, 2018 | 21 | 2018 |
| A Series of Benzylidenes Linked to Hydrazine‐1‐carbothioamide as Tyrosinase Inhibitors: Synthesis, Biological Evaluation and Structure− Activity Relationship H Hosseinpoor, A Iraji, N Edraki, S Pirhadi, M Attarroshan, ... Chemistry & Biodiversity 17 (8), e2000285, 2020 | 25 | 2020 |
| Ab initio modeling of a potent isophthalamide-based BACE-1 inhibitor: amino acid decomposition analysis N Razzaghi-Asl, A Ebadi, N Edraki, S Shahabipour, R Miri Medicinal Chemistry Research 22, 3259-3269, 2013 | 16 | 2013 |
| Acenaphthotriazine Thio-triazole Derivatives as Anti-cancer Agents Triggering Cell Cycle Arrest in Breast Cancer Cells A Iraji, N Shahrokh, O Firuzi, M Mohabbati, R Miri, H Sadeghpour, ... Letters in Drug Design & Discovery 20 (6), 639-648, 2023 | 2 | 2023 |
| Advanced catalyst-free pseudo-six-component synthesis of tetrahydrodipyrazolopyridines in water by using ammonium carbonate as an ecofriendly source of nitrogen F Tamaddon, A Khorram Synlett 31 (07), 691-694, 2020 | 8 | 2020 |
| Aminoimidazo [1, 2-a] pyridine Bearing Different Pyrazole Moieties as the Structural Scaffold for the Development of BACE1 Inhibitor; Synthesis, Structural Characterization, in … SES Ebrahimi, A Iraji, K Jelveh, A Moazzam, S Bahadorikhalili, ... Current Organic Synthesis 19 (6), 685-692, 2022 | 1 | 2022 |
| Anti-Helicobacter pylori activity and Structure-Activity Relationship study of 2-Alkylthio-5-(nitroaryl)-1, 3, 4-thiadiazole Derivatives A Asadipour, N Edraki, M Nakhjiri, A Yahya-Meymandi, E Alipour, ... Iranian journal of pharmaceutical research: IJPR 12 (3), 281, 2013 | 27 | 2013 |
| Anti-Helicobacter pylori activity evaluation and docking study F Alvandifar, A Tahghighi, R Sabourian, L Firoozpour, M Mahdavi, ... Journal of Chemical and Pharmaceutical Research 7 (3), 2512-2519, 2015 | 4 | 2015 |
| 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 | 32 | 2021 |
| Anticholinesterase activity of cinnamic acids derivatives: in vitro, in vivo biological evaluation, and docking study S Ghafary, H Nadri, M Mahdavi, A Moradi, T Akbarzadeh, M Sharifzadeh, ... Letters in Drug Design & Discovery 17 (8), 965-982, 2020 | 1 | 2020 |
| Benzyl‐Triazole Derivatives of Hydrazinecarbothiamide Derivatives as Potent Tyrosinase Inhibitors: Synthesis, Biological Evaluation, Structure‐Activity Relationship and Docking … M Divar, S Tadayyon, M Khoshneviszadeh, S Pirhadi, M Attarroshan, ... ChemistrySelect 8 (8), e202203382, 2023 | 4 | 2023 |
