S. Emami

发表

Design of Conformationally Constrained Azole Antifungals: Efficient Synthesis and Antifungal Activity of trans‐3‐Imidazolylflavanones

A. Foroumadi, M. Falahati, S. Emami, 2009, Chemical biology & drug design.

Synthesis and biological evaluation of new coumarins bearing 2,4-diaminothiazole-5-carbonyl moiety.

K. Majidzadeh-A, R. Esmaeili, A. Foroumadi, 2018, European journal of medicinal chemistry.

New racemic annulated pyrazolo[1,2-b]phthalazines as tacrine-like AChE inhibitors with potential use in Alzheimer's disease.

Hamid Nadri, Alireza Moradi, Ali Asadipour, 2017, European journal of medicinal chemistry.

Polyoxygenated cinnamoylcoumarins as conformationally constrained analogs of cytotoxic diarylpentanoids: synthesis and biological activity.

O. Firuzi, A. Shafiee, M. Khoobi, 2013, European journal of medicinal chemistry.

Synthesis and biological evaluation of quinazolinone-based hydrazones with potential use in Alzheimer's disease.

O. Firuzi, B. Hemmateenejad, R. Miri, 2017, Bioorganic chemistry.

Cytotoxic activity evaluation and QSAR study of chromene-based chalcones

A. Shafiee, A. Foroumadi, N. Edraki, 2012, Archives of Pharmacal Research.

New potent antifungal triazole alcohols containing N-benzylpiperazine carbodithioate moiety: Synthesis, in vitro evaluation and in silico study.

H. Badali, H. Fakhim, S. Emami, 2019, Bioorganic chemistry.

The effect of edelfosine on GRA1 and MIC3 expressions in acute toxoplasmosis

A. Daryani, S. Sarvi, M. Sharif, 2020, Parasitology Research.

Heterocycle-bridged and Conformationally Constrained Retinoids: Synthesis of 4-(7,8,9,10-Tetrahydro-7,7,10,10-tetramethyl-4H-benzo[6,7]chromeno- [4,3-d]thiazole-2-yl)benzoic Acid

A. Shafiee, A. Foroumadi, M. Amini, 2010 .

Synthesis and Biological Evaluation of 99mTc-Labeled Phenylpiperazine Derivatives as Selective Serotonin-7 Receptor Ligands for Brain Tumor Imaging.

S. Hosseinimehr, S. Emami, F. Amiri, 2021, Molecular pharmaceutics.

Thiazole in the targeted anticancer drug discovery.

A. Foroumadi, S. Emami, Adile Ayati, 2019, Future medicinal chemistry.

Complexes of 2-hydroxyacetophenone semicarbazones: A novel series of superoxide dismutase mimetics.

M. Ganjali, M. Abdollahi, S. Hosseinimehr, 2010, Bioorganic & medicinal chemistry letters.

Mannich bases of 7-piperazinylquinolones and kojic acid derivatives: synthesis, in vitro antibacterial activity and in silico study.

M. Faramarzi, A. Foroumadi, S. Emami, 2013, European journal of medicinal chemistry.

Synthesis and antibacterial activity of nitroaryl thiadiazole-gatifloxacin hybrids.

A. Shafiee, A. Foroumadi, S. Emami, 2009, European journal of medicinal chemistry.

Induction of apoptosis through tubulin inhibition in human cancer cells by new chromene-based chalcones

A. Foroumadi, Hassan Aryapour, S. Emami, 2012, Pharmaceutical biology.

Imidazolylchromanones containing alkyl side chain as lanosterol 14α-demethylase inhibitors: synthesis, antifungal activity and docking study

A. Foroumadi, M. Falahati, S. Emami, 2014, Journal of enzyme inhibition and medicinal chemistry.

Synthesis, in vitro antifungal activity and in silico study of 3-(1,2,4-triazol-1-yl)flavanones.

M. Faramarzi, S. Emami, H. Irannejad, 2013, European journal of medicinal chemistry.

Development of an Economical, Single Step Synthesis of FAZA, a Clinical Hypoxia Marker, and Potential Synthons to Prepare its Positional Analogs

A. McEwan, Piyush Kumar, S. Emami, 2009 .

Synthesis and Free Radical Scavenging Activity of Coumarin Derivatives Containing a 2‐Methylbenzothiazoline Motif

A. Ramazani, A. Shafiee, M. Khoobi, 2011, Archiv der Pharmazie.

99mTc-radiolabeled imidazo[2,1-b]benzothiazole derivatives as potential radiotracers for glioblastoma

S. Hosseinimehr, S. Emami, S. M. Abedi, 2019, Journal of Radioanalytical and Nuclear Chemistry.

Synthesis and biological evaluation of fluconazole analogs with triazole-modified scaffold as potent antifungal agents.

H. Badali, S. Emami, M. Shokrzadeh, 2015, Bioorganic & medicinal chemistry.

Removal of congo red from aqueous solution by its sorption onto the metal organic framework MIL-100(Fe): equilibrium, kinetic and thermodynamic studies

S. Dadfarnia, A. Shabani, S. Emami, 2015 .

Recent advances of chroman-4-one derivatives: synthetic approaches and bioactivities.

S. Emami, Zahra Ghanbarimasir, 2015, European journal of medicinal chemistry.

Benzofuran-derived benzylpyridinium bromides as potent acetylcholinesterase inhibitors.

A. Shafiee, A. Foroumadi, H. Nadri, 2015, European journal of medicinal chemistry.

Indolinone-based acetylcholinesterase inhibitors: synthesis, biological activity and molecular modeling.

A. Shafiee, M. Khoobi, A. Foroumadi, 2014, European journal of medicinal chemistry.

Biological evaluation of synthetic analogues of curcumin: chloro-substituted-2′-hydroxychalcones as potential inhibitors of tubulin polymerization and cell proliferation

A. Shafiee, A. Foroumadi, M. Sorkhi, 2011, Medicinal Chemistry Research.

Synthesis and antioxidant properties of substituted 3-benzylidene-7-alkoxychroman-4-ones.

M. Heidari, M. Abdollahi, A. Shafiee, 2007, Bioorganic & medicinal chemistry letters.

Chemical and biological aspects of posaconazole as a classic antifungal agent with non-classical properties: highlighting a tetrahydrofuran-based drug toward generation of new drugs

S. Emami, Sakineh Dadashpour, E. Ghobadi, 2022, Medicinal Chemistry Research.

Synthesis and anti-leishmanial activity of 5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-amines containing N-[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl] moieties.

A. Shafiee, F. Kobarfard, A. Foroumadi, 2012, European journal of medicinal chemistry.

Acetophenone benzoylhydrazones as antioxidant agents: Synthesis, in vitro evaluation and structure-activity relationship studies.

G. Dehghan, S. Emami, Z. Esmaili, 2018, Food chemistry.

Highly cis-Diastereoselective Synthesis of Coumarin-Based 2,3-Disubstituted Dihydrobenzothiazines by Organocatalysis

A. Ramazani, A. Shafiee, M. Khoobi, 2012 .

An Overview on Anticancer Drugs with Antileishmanial Activity

M. Keighobadi, M. Fakhar, J. Akhtari, 2018 .

In Vitro Activities of Novel Azole Compounds ATTAF-1 and ATTAF-2 against Fluconazole-Susceptible and -Resistant Isolates of Candida Species

H. Badali, H. Fakhim, A. Vaezi, 2016, Antimicrobial Agents and Chemotherapy.

Imidazolylchromanones containing non-benzylic oxime ethers: synthesis and molecular modeling study of new azole antifungals selective against Cryptococcus gattii.

H. Badali, S. Emami, M. H. Afsarian, 2014, European journal of medicinal chemistry.

Benzo[d]imidazo[2,1-b]thiazole-based fluorescent sensor for Zn2+ ion detection

S. Hosseinimehr, S. Emami, Sajjad Molavipordanjani, 2020 .

Application of emetine in SARS-CoV-2 treatment: regulation of p38 MAPK signaling pathway for preventing emetine-induced cardiac complications

S. Emami, H. Irannejad, Mehdi Valipour, 2022, Cell cycle.

Effective removal of ciprofloxacin from aqueous solutions using magnetic metal–organic framework sorbents: mechanisms, isotherms and kinetics

S. Dadfarnia, S. Emami, A. M. Haji Shabani, 2016, Journal of the Iranian Chemical Society.

Papaverine, a promising therapeutic agent for the treatment of COVID‐19 patients with underlying cardiovascular diseases (CVDs)

S. Emami, H. Irannejad, Mehdi Valipour, 2022, Drug development research.

New tacrine-derived AChE/BuChE inhibitors: Synthesis and biological evaluation of 5-amino-2-phenyl-4H-pyrano[2,3-b]quinoline-3-carboxylates.

A. Foroumadi, O. Sabzevari, H. Nadri, 2017, European journal of medicinal chemistry.

Design, synthesis, in vivo and in silico evaluation of phenacyl triazole hydrazones as new anticonvulsant agents.

S. Emami, N. Ahangar, H. Irannejad, 2018, Bioorganic chemistry.

Synthesis and anti-cholinesterase activity of new 7-hydroxycoumarin derivatives.

A. Shafiee, M. Khoobi, M. Alipour, 2014, European journal of medicinal chemistry.

Discovery of benzylthio analogs of fluconazole as potent antifungal agents.

H. Badali, H. Fakhim, A. Vaezi, 2018, Future medicinal chemistry.

New thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety as anticancer agents.

S. Emami, M. Shokrzadeh, M. Fallah, 2019, European journal of medicinal chemistry.

Evaluation of anti-parasitic activities of new quinolones containing nitrofuran moiety against Toxoplasma gondii.

A. Daryani, S. Sarvi, A. Khalilian, 2022, Experimental parasitology.

New tetracyclic tacrine analogs containing pyrano[2,3-c]pyrazole: efficient synthesis, biological assessment and docking simulation study.

A. Shafiee, M. Khoobi, A. Foroumadi, 2015, European journal of medicinal chemistry.

An Overview of Anticancer Chalcones with ApoptosisInducing Activity

M. Keighobadi, S. Emami, Hassan Mirzaei, 2017 .

N-Substituted piperazinyl quinolones as potential cytotoxic agents: structure-activity relationships study.

A. Shafiee, A. Foroumadi, S. Emami, 2009, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Synthesis and antibacterial activity of new N-[2-(thiophen-3-yl)ethyl] piperazinyl quinolones.

M. Faramarzi, A. Shafiee, A. Foroumadi, 2007, Chemical & pharmaceutical bulletin.

Antinociceptive properties of new coumarin derivatives bearing substituted 3,4-dihydro-2H-benzothiazines

M. Abdollahi, A. Shafiee, M. Khoobi, 2014, DARU Journal of Pharmaceutical Sciences.

Synthesis and evaluation of 4-substituted coumarins as novel acetylcholinesterase inhibitors.

A. Shafiee, M. Khoobi, A. Foroumadi, 2013, European journal of medicinal chemistry.

2-Hydroxyphenacyl azoles and related azolium derivatives as antifungal agents.

A. Shafiee, A. Foroumadi, M. Falahati, 2008, Bioorganic & medicinal chemistry letters.

Coumarin‐Based Bioactive Compounds: Facile Synthesis and Biological Evaluation of Coumarin‐Fused 1,4‐Thiazepines

A. Ramazani, A. Shafiee, M. Khoobi, 2011, Chemical biology & drug design.

Synthesis and anticancer activity of N-substituted 2-arylquinazolinones bearing trans-stilbene scaffold.

A. Shafiee, A. Foroumadi, M. Adib, 2015, European journal of medicinal chemistry.

Sulfonated metal organic framework loaded on iron oxide nanoparticles as a new sorbent for the magnetic solid phase extraction of cadmium from environmental water samples

S. Dadfarnia, A. Shabani, S. Emami, 2016 .

Synthesis and antibacterial activity of N-(5-benzylthio-1,3,4-thiadiazol-2-yl) and N-(5-benzylsulfonyl-1,3,4-thiadiazol-2-yl)piperazinyl quinolone derivatives.

A. Shafiee, A. Foroumadi, S. Emami, 2005, Bioorganic & medicinal chemistry letters.

Quinoline-based imidazole-fused heterocycles as new inhibitors of 15-lipoxygenase

A. Shafiee, A. Foroumadi, H. Nadri, 2016, Journal of enzyme inhibition and medicinal chemistry.

New 7-piperazinylquinolones containing (benzo[d]imidazol-2-yl)methyl moiety as potent antibacterial agents

M. Faramarzi, A. Foroumadi, S. Emami, 2018, Molecular Diversity.

Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1-$$c$$c][1,2,4]triazin-6-amines

A. Shafiee, A. Foroumadi, K. Divsalar, 2015, Molecular Diversity.

Tropolone alkaloids from Colchicum kurdicum (Bornm.) Stef. (Colchicaceae) as the potent novel antileishmanial compounds; purification, structure elucidation, antileishmanial activities and molecular docking studies.

Adel R. Bakhtiyari, M. Keighobadi, M. Fakhar, 2020, Experimental parasitology.

Synthesis of Ciprofloxacin-Isatin Conjugates as Potential Cytotoxic Agents

S. Emami, M. Raeesi, 2016 .

Asymmetrical 2,6-bis(benzylidene)cyclohexanones: Synthesis, cytotoxic activity and QSAR study.

A. Shafiee, A. Foroumadi, S. Emami, 2012, European journal of medicinal chemistry.

Isochaihulactone analogues: synthesis and anti-proliferative activity of novel dibenzylbutyrolactones.

A. Shafiee, M. Khoobi, A. Foroumadi, 2010, European journal of medicinal chemistry.

Synthesis and biological evaluation of 2-phenylthiazole-4-carboxamide derivatives as anticancer agents.

J. Davoodi, S. Ostad, A. Shafiee, 2010, European journal of medicinal chemistry.

Synthesis and in‐vitro Cytotoxicity of Poly‐functionalized 4‐(2‐Arylthiazol‐4‐yl)‐4H‐chromenes

A. Shafiee, A. Foroumadi, M. Mohagheghi, 2010, Archiv der Pharmazie.

Synthesis, computational study and cytotoxicity of 4-hydroxycoumarin-derived imines/enamines

M. Yousefi, S. Vaseghi, S. Emami, 2020, Molecular Diversity.

Stereoselective synthesis and antifungal activity of (Z)-trans-3-azolyl-2-methylchromanone oxime ethers.

A. Shafiee, M. Falahati, S. Emami, 2004, Bioorganic & medicinal chemistry.

Synthetic approaches and structural diversity of triazolylbutanols derived from voriconazole in the antifungal drug development.

S. Emami, Shahnaz Saednia, E. Ghobadi, 2022, European journal of medicinal chemistry.

Current advances of triazole alcohols derived from fluconazole: Design, in vitro and in silico studies.

S. Emami, Seyedeh Mahdieh Hashemi, Shahnaz Saednia, 2019, European journal of medicinal chemistry.

Design, synthesis, pharmacological evaluation, and docking study of new acridone-based 1,2,4-oxadiazoles as potential anticonvulsant agents.

A. Shafiee, A. Foroumadi, M. Shabani, 2016, European journal of medicinal chemistry.

Microwave-assisted synthesis and anticonvulsant activity of 5,6-bisaryl-1,2,4-triazine-3-thiol derivatives

A. Foroumadi, S. Emami, N. Naderi, 2014, Medicinal Chemistry Research.

Microwave-assisted synthesis and anticonvulsant activity of 5,6-bisaryl-1,2,4-triazine-3-thiol derivatives

A. Foroumadi, S. Emami, N. Naderi, 2013, Medicinal Chemistry Research.

Cytotoxic Activity and DNA Binding Property of New Aminopyrimidine Derivatives

O. Firuzi, A. Saboury, M. Khoobi, 2020 .

Facile synthesis and antiproliferative activity of 7H-benzo[7,8]chromeno[2,3-d]pyrimidin-8-amines.

M. Khoobi, F. Salehi, A. Foroumadi, 2017, European journal of medicinal chemistry.

2-Amino-4-(nitroalkyl)-4H-chromene-3-carbonitriles as New Cytotoxic Agents

A. Foroumadi, S. Emami, M. Safavi, 2013, Iranian journal of pharmaceutical research : IJPR.

Green and Catalyst-Free One-Pot Synthesis of Anthranilamide Schiff Bases: An Approach Toward Sirtinol

A. Shafiee, M. Khoobi, A. Foroumadi, 2014 .

Current developments of coumarin-based anti-cancer agents in medicinal chemistry.

S. Emami, Sakineh Dadashpour, 2015, European journal of medicinal chemistry.

5-Nitro-heteroarylidene analogs of 2-thiazolylimino-4-thiazolidinones as a novel series of antibacterial agents

M. Faramarzi, A. Shafiee, A. Foroumadi, 2013, Medicinal Chemistry Research.

Recent advances of cytotoxic chalconoids targeting tubulin polymerization: Synthesis and biological activity.

S. Emami, Hassan Mirzaei, 2016, European journal of medicinal chemistry.

Hetero-annulated coumarins as new AChE/BuChE inhibitors: synthesis and biological evaluation

A. Shafiee, A. Foroumadi, H. Nadri, 2016, Medicinal Chemistry Research.

Synthesis, in vitro cytotoxicity and apoptosis inducing study of 2-aryl-3-nitro-2H-chromene derivatives as potent anti-breast cancer agents.

A. Shafiee, A. Foroumadi, M. Mahdavi, 2014, European journal of medicinal chemistry.

2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents.

Ramin Miri, Abbas Shafiee, Saeed Emami, 2013, European journal of medicinal chemistry.

Chromene‐Based Synthetic Chalcones as Potent Antileishmanial Agents: Synthesis and Biological Activity

Samaneh Heydari, A. Shafiee, A. Foroumadi, 2010, Chemical biology & drug design.

Novel triazole alcohol antifungals derived from fluconazole: design, synthesis, and biological activity

H. Badali, M. Faramarzi, S. Emami, 2014, Molecular diversity.

Quinolones: Recent Structural and Clinical Developments

A. Shafiee, A. Foroumadi, S. Emami, 2005 .

One-pot, four-component synthesis of novel cytotoxic agents 1-(5-aryl-1,3,4-oxadiazol-2-yl)-1-(1H-pyrrol-2-yl)methanamines.

A. Ramazani, M. Faramarzi, A. Shafiee, 2014, European journal of medicinal chemistry.

Design, synthesis, biological evaluation and docking study of 5-oxo-4,5-dihydropyrano[3,2-c]chromene derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors.

A. Shafiee, M. Khoobi, M. Alipour, 2013, European journal of medicinal chemistry.

Synthesis and antileishmanial activity of novel 5-(5-nitrofuran-2-y1)-1,3,4-thiadiazoles with piperazinyl-linked benzamidine substituents.

A. Shafiee, F. Kobarfard, A. Foroumadi, 2011, European journal of medicinal chemistry.

The importance of triazole scaffold in the development of anticonvulsant agents.

A. Foroumadi, S. Emami, Adile Ayati, 2016, European journal of medicinal chemistry.

Recent applications of 1,3-thiazole core structure in the identification of new lead compounds and drug discovery.

A. Shafiee, A. Foroumadi, A. Asadipour, 2015, European journal of medicinal chemistry.

Synthesis and in vitro anti-Toxoplasma gondii activity of a new series of aryloxyacetophenone thiosemicarbazones

A. Daryani, S. Emami, M. Ansari, 2020, Molecular Diversity.

Synthesis and in vitro anti-Toxoplasma gondii activity of a new series of aryloxyacetophenone thiosemicarbazones

A. Daryani, S. Emami, M. Ansari, 2019, Molecular Diversity.

Synthesis and biological evaluation of novel imidazopyrimidin‐3‐amines as anticancer agents

M. Abdollahi, A. Shafiee, A. Foroumadi, 2017, Chemical biology & drug design.

Synthesis and Antibacterial Activity of Nitroaryl Thiadiazole‐Levofloxacin Hybrids

A. Shafiee, J. Mirzaei, A. Foroumadi, 2006, Archiv der Pharmazie.

Synthesis and antibacterial activity of new fluoroquinolones containing a substituted N-(phenethyl)piperazine moiety.

M. Faramarzi, A. Shafiee, A. Foroumadi, 2006, Bioorganic & medicinal chemistry letters.

Structural features of new quinolones and relationship to antibacterial activity against Gram-positive bacteria.

A. Shafiee, A. Foroumadi, S. Emami, 2006, Mini reviews in medicinal chemistry.

Synthesis and antibacterial activity of N-[2-(5-bromothiophen-2-yl)-2-oxoethyl] and N-[(2-5-bromothiophen-2-yl)-2-oximinoethyl] derivatives of piperazinyl quinolones.

A. Shafiee, A. Foroumadi, S. Emami, 2005, Bioorganic & medicinal chemistry letters.

Synthesis and in vitro antibacterial activity of N-[5-(5-nitro-2-furyl)-1,3,4-thiadiazole-2-yl] piperazinyl quinolone derivatives.

A. Foroumadi, S. Emami, A. Zeynali, 2003, Die Pharmazie.

Therapeutic potential of quinazoline derivatives for Alzheimer's disease: A comprehensive review.

S. Emami, Z. Haghighijoo, Leila Zamani, 2021, European journal of medicinal chemistry.

Design, synthesis and evaluation of novel multi-target-directed ligands for treatment of Alzheimer's disease based on coumarin and lipoic acid scaffolds.

M. Ganjali, M. Abdollahi, M. Khoobi, 2018, European journal of medicinal chemistry.

Synthesis and biological evaluation of 3-(trimethoxyphenyl)-2(3H)-thiazole thiones as combretastatin analogs.

A. Foroumadi, Hassan Aryapour, S. Emami, 2013, European journal of medicinal chemistry.

Synthesis and Evaluation of 2(3H)‐Thiazole Thiones as Tyrosinase Inhibitors

A. Enayati, S. Hosseinimehr, S. Emami, 2012, Archiv der Pharmazie.

Synthesis of 4-(4-Methylsulfonylphenyl)-3-phenyl-2(3H)-thiazole Thione Derivatives as New Potential COX-2 Inhibitors

A. Foroumadi, S. Emami, 2006 .

9H‐Carbazole Derivatives Containing the N‐Benzyl‐1,2,3‐triazole Moiety as New Acetylcholinesterase Inhibitors

A. Shafiee, M. Khoobi, A. Foroumadi, 2015, Archiv der Pharmazie.

Indole in the target-based design of anticancer agents: A versatile scaffold with diverse mechanisms.

Saeed Emami, S. Emami, Sakineh Dadashpour, 2018, European journal of medicinal chemistry.

Synthesis and structure-activity relationship study of tacrine-based pyrano[2,3-c]pyrazoles targeting AChE/BuChE and 15-LOX.

I. Haririan, A. Shafiee, M. Khoobi, 2016, European journal of medicinal chemistry.

Design, synthesis and anticholinesterase activity of novel benzylidenechroman-4-ones bearing cyclic amine side chain.

A. Shafiee, A. Foroumadi, H. Nadri, 2015, European journal of medicinal chemistry.

Synthesis and antibacterial activity of N-[2-[5-(methylthio)thiophen-2-yl]-2-oxoethyl] and N-[2-[5-(methylthio)thiophen-2-yl]-2-(oxyimino)ethyl]piperazinylquinolone derivatives.

A. Shafiee, A. Foroumadi, S. Emami, 2006, Bioorganic & medicinal chemistry.

Halogenated flavanones as potential apoptosis-inducing agents: synthesis and biological activity evaluation.

J. Davoodi, A. Shafiee, A. Foroumadi, 2012, European journal of medicinal chemistry.

Synthesis and anticholinesterase activity of coumarin-3-carboxamides bearing tryptamine moiety.

A. Shafiee, M. Khoobi, A. Marjani, 2016, European journal of medicinal chemistry.

Synthesis and neuroprotective activity of novel 1,2,4-triazine derivatives with ethyl acetate moiety against H2O2 and Aβ-induced neurotoxicity

M. Amini, Alireza Moradi, S. Emami, 2017, Medicinal Chemistry Research.

Synthesis and in vitro anti-Helicobacter pylori activity of N-[5-(5-nitro-2-heteroaryl)-1,3,4-thiadiazol-2-yl]thiomorpholines and related compounds.

M. Khoshayand, F. Safari, A. Shafiee, 2008, European journal of medicinal chemistry.

Synthesis and biological evaluation of 4-amino-5-cinnamoylthiazoles as chalcone-like anticancer agents.

K. Majidzadeh-A, R. Esmaeili, A. Foroumadi, 2018, European journal of medicinal chemistry.

Synthesis and cytotoxic properties of novel (E)-3-benzylidene-7-methoxychroman-4-one derivatives

A. Shafiee, A. Foroumadi, S. Emami, 2013, DARU Journal of Pharmaceutical Sciences.

Novel antileishmanial chalconoids: synthesis and biological activity of 1- or 3-(6-chloro-2H-chromen-3-yl)propen-1-ones.

Samaneh Heydari, A. Shafiee, A. Foroumadi, 2010, European journal of medicinal chemistry.

2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents.

O. Firuzi, A. Ramazani, A. Shafiee, 2013, European journal of medicinal chemistry.

Synthesis and Antibacterial Activity of Quinolone‐Based Compounds Containing a Coumarin Moiety

M. Faramarzi, A. Foroumadi, S. Emami, 2008, Archiv der Pharmazie.

Efficient Solvent-Free Synthesis of Benzothiazine-Fused Pyrrolo[3,4-c]coumarins: Cycloaddition Reactions between Coumarin-Based Dihydrobenzothiazoles and Isocyanides

A. Ramazani, A. Shafiee, M. Khoobi, 2014 .

Synthesis and biological evaluation of 5-benzylidenerhodanine-3-acetic acid derivatives as AChE and 15-LOX inhibitors

A. Shafiee, M. Khoobi, A. Foroumadi, 2015, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of 4‐Hydroxycoumarin‐Based Triazoles/Oxadiazoles as Novel Anticancer Agents

S. Emami, Z. Hosseini-Khah, Seyedeh Mahdieh Hashemi, 2022, Chemistry & biodiversity.

Modification of 7-piperazinylquinolone antibacterials to promising anticancer lead compounds: Synthesis and in vitro studies.

S. Emami, Hamideh Ahadi, 2019, European journal of medicinal chemistry.

Functionalized N(2-oxyiminoethyl) piperazinyl quinolones as new cytotoxic agents.

A. Shafiee, A. Foroumadi, S. Emami, 2007, Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques.

Kojic acid and its manganese and zinc complexes as potential radioprotective agents.

S. M. Taghdisi, S. Akhlaghpoor, S. Hosseinimehr, 2007, Bioorganic & medicinal chemistry letters.

Kojic acid-derived tyrosinase inhibitors: synthesis and bioactivity

S. Emami, Seyedeh Mahdieh Hashemi, 2015 .

Application of kojic acid scaffold in the design of non‐tyrosinase enzyme inhibitors

R. Ahmadi, S. Emami, Hamideh Ahadi, 2022, Chemical biology & drug design.

In vitro and in vivo evaluation of kojic acid against Toxoplasma gondii in experimental models of acute toxoplasmosis.

A. Daryani, S. Sarvi, M. Sharif, 2019, Experimental parasitology.

Synthesis and Antifungal Activity of 1‐[(2‐Benzyloxy)Phenyl]‐2‐(Azol‐1‐yl)Ethanone Derivatives: Exploring the Scaffold Flexibility

M. Faramarzi, A. Foroumadi, M. Falahati, 2011, Chemical biology & drug design.

2-Substituted-5-nitroheterocycles: in vitro anti-Helicobacter pylori activity and structure-activity relationship study.

A. Shafiee, A. Foroumadi, M. Sorkhi, 2009, Medicinal chemistry (Shariqah (United Arab Emirates)).

Selective leishmanicidal effect of 1,3,4-thiadiazole derivatives and possible mechanism of action against Leishmania species.

A. Kariminia, A. Shafiee, A. Foroumadi, 2009, Experimental parasitology.

Synthesis and in vitro anti-leishmanial activity of 1-[5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-yl]- and 1-[5-(5-nitrothiophen-2-yl)-1,3,4-thiadiazol-2-yl]-4-aroylpiperazines.

A. Shafiee, S. Ardestani, A. Foroumadi, 2008, Bioorganic & medicinal chemistry.

Antituberculosis agents. V. Synthesis, evaluation of in vitro antituberculosis activity and cytotoxicity of some 2-(5-nitro-2-furyl)-1,3,4-thiadiazole derivatives.

M. Mirzaei, A. Foroumadi, A. Asadipour, 2002, Farmaco.

Synthesis of Cytotoxic Isodeoxypodophyllotoxin Analogs

A. Shafiee, A. Foroumadi, G. Dehghan, 2017 .

β-Ionone and its analogs as promising anticancer agents.

S. Emami, M. Ansari, 2016, European journal of medicinal chemistry.

Replacement of the Methylene of Dihydrochalcones with Oxygen: Synthesis and Biological Evaluation of 2‐Phenoxyacetophenones

M. Faramarzi, A. Foroumadi, M. Maghsoodlou, 2012, Chemical biology & drug design.

Synthesis and in vitro leishmanicidal activity of 2-(1-methyl-5-nitro-1H-imidazol-2-yl)-5-substituted-1,3,4-thiadiazole derivatives.

A. Kharazmi, A. Shafiee, A. Foroumadi, 2005, European journal of medicinal chemistry.

New 5-(nitroheteroaryl)-1,3,4-thiadiazols containing acyclic amines at C-2: synthesis and SAR study for their antileishmanial activity

A. Shafiee, F. Kobarfard, A. Foroumadi, 2013, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and antibacterial activity of some novel N-substituted piperazinyl-quinolones.

M. Mirzaei, A. Foroumadi, S. Emami, 2001, Bollettino chimico farmaceutico.

5‐Nitroimidazole‐based 1,3,4‐Thiadiazoles: Heterocyclic Analogs of Metronidazole as Anti‐Helicobacter pylori Agents

A. Shafiee, A. Foroumadi, M. Sorkhi, 2011, Archiv der Pharmazie.

Synthesis and anti-Helicobacter pylori activity of 5-(nitroaryl)-1,3,4-thiadiazoles with certain sulfur containing alkyl side chain.

F. Safari, A. Shafiee, A. Foroumadi, 2008, Bioorganic & medicinal chemistry letters.

Indole-derived chalcones as anti-dermatophyte agents: In vitro evaluation and in silico study

Hassan Mirzaei, Mahdi Abastabar, Saeed Emami, 2019, Comput. Biol. Chem..

Design, synthesis and biological evaluation of flexible and rigid analogs of 4H-1,2,4-triazoles bearing 3,4,5-trimethoxyphenyl moiety as new antiproliferative agents.

S. Emami, M. Shokrzadeh, M. Fallah, 2019, Bioorganic chemistry.

(E)- and (Z)-1,2,4-triazolylchromanone oxime ethers as conformationally constrained antifungals.

A. Shafiee, M. Amanlou, M. Falahati, 2004, Bioorganic & medicinal chemistry.

Synthesis and in vitro anti-Helicobacter pylori activity of 2-[(chlorobenzyl)thio]-5-(5-nitro-2-furyl)-1,3,4-thiadiazoles

F. Safari, A. Shafiee, A. Foroumadi, 2008, Medicinal Chemistry Research.

Synthesis and antibacterial activity of levofloxacin derivatives with certain bulky residues on piperazine ring.

A. Shafiee, A. Foroumadi, F. Shirazi, 2007, European journal of medicinal chemistry.

Synthesis and antibacterial activity of novel levofloxacin derivatives containing a substituted thienylethyl moiety

M. Faramarzi, A. Shafiee, A. Foroumadi, 2012, DARU Journal of Pharmaceutical Sciences.

Conformationally Constrained Analogs of N‐Substituted Piperazinylquinolones: Synthesis and Antibacterial Activity of N‐(2,3‐Dihydro‐4‐hydroxyimino‐4H‐1‐benzopyran‐3‐yl)‐piperazinylquinolones

M. Faramarzi, A. Foroumadi, S. Emami, 2009, Archiv der Pharmazie.

Design, Synthesis and In Vitro Study of 5,6‐Diaryl‐1,2,4‐triazine‐3‐ylthioacetate Derivatives as COX‐2 and β‐Amyloid Aggregation Inhibitors

Saeed Emami, S. Emami, Sakineh Dadashpour, 2015, Archiv der Pharmazie.

Synthesis and In Vitro Cytotoxic Activity of Novel Chalcone-Like Agents

A. Foroumadi, S. Emami, M. Safavi, 2013, Iranian journal of basic medical sciences.

7-Piperazinylquinolones with methylene-bridged nitrofuran scaffold as new antibacterial agents

M. Faramarzi, A. Foroumadi, S. Emami, 2013, Medicinal Chemistry Research.

Synthesis and In‐vitro Antibacterial Activity of New N‐Substituted Piperazinyl Quinolones

A. Foroumadi, S. Emami, M. Moshafi, 1999 .

Synthesis and In‐vitro Antibacterial Activities of N‐substituted Piperazinyl Quinolones

A. Shafiee, A. Foroumadi, G. Sepehri, 1997 .

Imidazolylchromanone oxime ethers as potential anticonvulsant agents: Anticonvulsive evaluation in PTZ-kindling model of epilepsy and SAR study.

A. Kebriaeezadeh, S. Emami, R. Khorasani, 2011, Bioorganic & medicinal chemistry letters.

Synthesis, characterization, crystal structure, anti-cancer activities, and computational study of a novel thiophenylchromane

S. Vaseghi, S. Emami, Zinatossadat Hossaini, 2021, Journal of Molecular Structure.

A new boronic acid fluorescent sensor based on fluorene for monosaccharides at physiological pH.

R. Hosseinzadeh, S. Emami, Abbas Eslami, 2015, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

Synthesis and Free Radical Scavenging Activity of Coumarin Derivatives Containing a 2-Methylbenzothiazoline Motif.

A. Ramazani, A. Shafiee, M. Khoobi, 2012 .

Structure-activity relationship study of a series of N-substituted piperazinyl-fluoroquinolones as anti-Helicobacter pylori agents.

F. Safari, A. Shafiee, A. Foroumadi, 2008, Medicinal chemistry (Shariqah (United Arab Emirates)).

Synthesis and antibacterial activity of N-[5-chlorobenzylthio-1,3,4-thiadiazol-2-yl] piperazinyl quinolone derivatives

A. Shafiee, A. Foroumadi, M. Amini, 2007, Archives of pharmacal research.

Phytochemical Profiles, Physicochemical Analysis, and Biological Activity of Three Colchicum Species

S. Hosseinimehr, A. Davoodi, M. Azadbakht, 2021, Jundishapur Journal of Natural Pharmaceutical Products.

Phytochemical, physicochemical and biological evaluation of Colchicum kurdicum (Bornm.) Stef.: a study on materia medica of Persian medicine

S. Hosseinimehr, A. Davoodi, M. Azadbakht, 2020, Journal of Medicinal Plants.

Effectiveness of Fluconazole for Suppressive Maintenance Therapy in Patients with RVVC: a Randomized Placebo-Controlled Study

A. Shafiee, A. Foroumadi, M. Falahati, 2010 .

Promising antileishmanial activity of novel imidazole antifungal drug luliconazole against Leishmania major: In vitro and in silico studies.

M. Keighobadi, M. Fakhar, S. Teshnizi, 2018, Journal of global antimicrobial resistance.

Design, synthesis and biological activity of hybrid antifungals derived from fluconazole and mebendazole.

H. Badali, H. Fakhim, S. Emami, 2023, European journal of medicinal chemistry.

An overview of azoles targeting sterol 14α-demethylase for antileishmanial therapy.

M. Keighobadi, S. Emami, Pegah Tavangar, 2017, European journal of medicinal chemistry.

Synthesis, in vitro antifungal evaluation and in silico study of 3-azolyl-4-chromanone phenylhydrazones

M. Falahati, S. Emami, Adile Ayati, 2012, DARU Journal of Pharmaceutical Sciences.

Stereoselective Synthesis and in Vitro Antifungal Evaluation of (E)‐ and (Z)‐Imidazolylchromanone Oxime Ethers

A. Shafiee, M. Falahati, S. Emami, 2002, Archiv der Pharmazie.

9H-Carbazole Derivatives Containing the N-Benzyl-1,2,3-triazole Moiety as New Acetylcholinesterase Inhibitors.

A. Shafiee, M. Khoobi, A. Foroumadi, 2015 .

Repurposing azole antifungals into antileishmanials: Novel 3-triazolylflavanones with promising in vitro antileishmanial activity against Leishmania major.

M. Keighobadi, M. Fakhar, S. Emami, 2019, Parasitology international.

Current application of arylazoles and annulated azoles in the design of new antileishmanial agents

M. Keighobadi, M. Fakhar, S. Emami, 2017 .

Synthesis and antibacterial activity of N-[2-(2-naphthyl)ethyl]piperazinyl quinolones

M. Faramarzi, A. Shafiee, A. Foroumadi, 2009 .

Synthesis of 2-aryl-3-triazolyl-indoles from phenacyltriazole-derived hydrazones: exploring new scaffolds for anticonvulsant activity

S. Emami, N. Ahangar, Seyedeh Mahdieh Hashemi, 2022, Journal of Molecular Structure.

Anticonvulsant Activity of 3-imidazolylflavanones and Their Flexible Analogs: 1-[(2-benzyloxy)phenyl]-2-(azol-1-yl)ethanones as New Lead Compounds

S. Emami, N. Ahangar, H. Irannejad, 2017, Pharmaceutical Chemistry Journal.

1‐[(2‐Arylthiazol‐4‐yl)methyl]azoles as a New Class of Anticonvulsants: Design, Synthesis, In vivo Screening, and In silico Drug‐like Properties

A. Foroumadi, S. Emami, E. Alipour, 2011, Chemical biology & drug design.

Anticonvulsant and antiepileptogenic effects of azolylchromanones on lithium-pilocarpine induced seizures and pentylenetetrazole-kindling model of epilepsy.

A. Shafiee, M. Sharifzadeh, A. Kebriaeezadeh, 2008, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Azolylchromans as a novel scaffold for anticonvulsant activity.

A. Shafiee, A. Kebriaeezadeh, S. Emami, 2006, Bioorganic & medicinal chemistry letters.

In silico prediction of ATTAF-1 and ATTAF-2 selectivity towards human/fungal lanosterol 14α-demethylase using molecular dynamic simulation and docking approaches

S. Emami, H. Irannejad, Seyedeh Mahdieh Hashemi, 2020 .

Novel triazole alcohol antifungals derived from fluconazole: design, synthesis, and biological activity

H. Badali, M. Faramarzi, S. Emami, 2015, Molecular Diversity.

Synthesis and biological assessment of ciprofloxacin-derived 1,3,4-thiadiazoles as anticancer agents.

N. Razzaghi-Asl, S. Emami, M. Shokrzadeh, 2020, Bioorganic chemistry.

Activity, Stability, and Structure of Native and Modified by Woodward Reagent K Mushroom Tyrosinase

S. Emami, H. Piri, N. Gheibi, 2018 .

Kinetic, Thermodynamic and Structural Studies of Native and N-Bromosuccinimide-Modified Mushroom Tyrosinase

S. Emami, N. Gheibi, 2016 .

Kojic acid-natural product conjugates as mushroom tyrosinase inhibitors.

Rezvan Yazdian-Robati, S. Emami, A. Rafiei, 2020, European journal of medicinal chemistry.

1,2,3-Triazole-based kojic acid analogs as potent tyrosinase inhibitors: Design, synthesis and biological evaluation.

S. Emami, A. Rafiei, M. Khoshneviszadeh, 2019, Bioorganic chemistry.

Diverse therapeutic potential of 3-hydroxy-4-pyranones and related compounds as kojic acid analogs

R. Ahmadi, S. Emami, Hamideh Ahadi, 2022, Medicinal Chemistry Research.

Recent applications of vinyl sulfone motif in drug design and discovery.

R. Ahmadi, S. Emami, 2022, European journal of medicinal chemistry.

New indole-based chalconoids as tubulin-targeting antiproliferative agents.

S. Emami, M. Shokrzadeh, G. Riazi, 2017, Bioorganic chemistry.

N‐(2‐(Piperazin‐1‐yl)phenyl)arylamide Derivatives as β‐Secretase (BACE1) Inhibitors: Simple Synthesis by Ugi Four‐Component Reaction and Biological Evaluation

O. Firuzi, A. Shafiee, A. Foroumadi, 2015, Archiv der Pharmazie.

Mannich Bases of 7‐Piperazinylquinolones and Kojic Acid Derivatives: Synthesis, in vitro Antibacterial Activity and in silico Study.

M. Faramarzi, A. Foroumadi, S. Emami, 2014 .

Radioprotective effects of kojic acid against mortality induced by gamma irradiation in mice.

S. Hosseinimehr, A. Ahmadi, S. Emami, 2009, Saudi medical journal.

Imidazo[2,1-b]thiazole derivatives as new inhibitors of 15-lipoxygenase.

A. Shafiee, A. Foroumadi, H. Nadri, 2014, European journal of medicinal chemistry.

Synthesis and antileishmanial activity of 5-(5-nitroaryl)-2-substituted-thio-1,3,4-thiadiazoles

A. Shafiee, A. Foroumadi, S. Emami, 2011, Journal of enzyme inhibition and medicinal chemistry.

Current Developments of Coumarin-Based Anticancer Agents in Medicinal Chemistry

S. Emami, Sakineh Dadashpour, 2015 .

Synthesis and Biological Evaluation of 3-(Trimethoxyphenyl)-2(3H)-thiazole Thiones as Combretastatin Analogues.

A. Foroumadi, Hassan Aryapour, S. Emami, 2014 .

Anti-inflammatory Properties of 4-(4-Methylsulfonylphenyl)-3-phenyl-2(3H)-thiazole thione Derivatives by Carrageenan Method in Mice

S. Emami, N. Ahangar, D. Jafari, 2015 .

1,2‐Diaryl‐2‐hydroxyiminoethanones as Dual COX‐1 and β‐Amyloid Aggregation Inhibitors: Biological Evaluation and In Silico Study

S. Emami, N. Ahangar, H. Irannejad, 2015, Chemical biology & drug design.

Synthesis, biological evaluation and docking study of 3-aroyl-1-(4-sulfamoylphenyl)thiourea derivatives as 15-lipoxygenase inhibitors.

A. Shafiee, A. Foroumadi, H. Nadri, 2014, European journal of medicinal chemistry.

Synthesis and structure-activity relationship study of benzofuran-based chalconoids bearing benzylpyridinium moiety as potent acetylcholinesterase inhibitors.

A. Shafiee, A. Foroumadi, H. Nadri, 2015, European journal of medicinal chemistry.

Methyl red removal from water by iron based metal-organic frameworks loaded onto iron oxide nanoparticle adsorbent

S. Dadfarnia, A. Shabani, S. Emami, 2015 .

Synthesis and Hypoxia Selective Radiosensitization Potential of β-2-FAZA and β-3-FAZL: Fluorinated Azomycin β-Nucleosides

A. McEwan, Piyush Kumar, S. Emami, 2009 .

Hypothesis: The potential application of doxorubicin against cutaneous leishmaniasis

M. Keighobadi, M. Fakhar, S. Emami, 2015, Tropical parasitology.

In vitro antileishmanial activity of novel azoles (3-imidazolylflavanones) against promastigote and amastigote stages of Leishmania major.

M. Keighobadi, M. Fakhar, S. Teshnizi, 2017, Acta tropica.

Synthesis and biological evaluation of new N-benzylpyridinium-based benzoheterocycles as potential anti-Alzheimer's agents.

I. Haririan, M. Khoobi, H. Forootanfar, 2019, Bioorganic chemistry.

Phthalimide‐Derived N‐Benzylpyridinium Halides Targeting Cholinesterases: Synthesis and Bioactivity of New Potential Anti‐Alzheimer's Disease Agents

A. Shafiee, A. Foroumadi, H. Nadri, 2016, Archiv der Pharmazie.

Novel coumarin-3-carboxamides bearing N-benzylpiperidine moiety as potent acetylcholinesterase inhibitors.

A. Shafiee, M. Khoobi, M. Alipour, 2013, European journal of medicinal chemistry.

Synthesis, antileishmanial activity and QSAR study of (1,3,4-thiadiazol-2-ylthio) acetamides derived from 5-nitrofuran

A. Shafiee, A. Foroumadi, N. Edraki, 2014, Medicinal Chemistry Research.

Nitroimidazolyl-1,3,4-thiadiazole-based anti-leishmanial agents: synthesis and in vitro biological evaluation.

A. Shafiee, A. Foroumadi, S. Emami, 2009, European journal of medicinal chemistry.

Synthesis, in silico, in vitro and in vivo evaluations of isatin aroylhydrazones as highly potent anticonvulsant agents.

M. Tajbakhsh, S. Emami, N. Ahangar, 2021, Bioorganic chemistry.

Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1-c\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}

A. Shafiee, A. Foroumadi, K. Divsalar, 2015, Molecular Diversity.

A review on the structures and biological activities of anti-Helicobacter pylori agents.

S. Emami, Zahra Ghanbarimasir, E. Ghobadi, 2021, European journal of medicinal chemistry.

Novel 3-phenylcoumarin-lipoic acid conjugates as multi-functional agents for potential treatment of Alzheimer's disease.

M. Ganjali, M. Abdollahi, S. N. Bukhari, 2018, Bioorganic chemistry.

Synthesis, computational study and cytotoxicity of 4-hydroxycoumarin-derived imines/enamines

M. Yousefi, S. Vaseghi, S. Emami, 2020, Molecular Diversity.

Synthesis and Anticholinergic Activity of 4‐hydroxycoumarin Derivatives Containing Substituted Benzyl‐1,2,3‐triazole Moiety

A. Shafiee, M. Khoobi, A. Foroumadi, 2015, Chemical biology & drug design.

99mTc-labeled small molecules for diagnosis of Alzheimer's disease: Past, recent and future perspectives.

S. Hosseinimehr, S. Emami, Sajjad Molavipordanjani, 2018, Current medicinal chemistry.

Multi-structure docking analysis of BACE1 crystal structures and non-peptidic ligands.

Bahram Hemmateenejad, Ramin Miri, Saeed Emami, 2017, Journal of molecular graphics & modelling.

Microwave-enhanced Fenton-like degradation by surface-modified metal-organic frameworks as a promising method for removal of dye from aqueous samples

S. Dadfarnia, A. Shabani, S. Emami, 2017 .

Synthesis, Cytotoxic Activity and Docking Study of Two Indole-Chalcone Derivatives

S. Emami, M. Shokrzadeh, Hassan Mirzaei, 2017 .

Recent Advances of Cytotoxic Chalconoids Targeting Tubulin Polymerization: Synthesis and Biological Activity

S. Emami, Hassan Mirzaei, 2016 .

Cytotoxic activity evaluation and QSAR study of chromene-based chalcones

A. Shafiee, A. Foroumadi, N. Edraki, 2012, Archives of pharmacal research.

Novel 99mTc-2-arylimidazo[2,1-b]benzothiazole derivatives as SPECT imaging agents for amyloid-β plaques.

S. Hosseinimehr, S. Emami, Zohreh Noaparast, 2019, European journal of medicinal chemistry.

Down-regulation of peroxin synthesis by silencing RNA (siRNA): A novel hypothesis for treatment of leishmaniasis

M. Keighobadi, M. Fakhar, S. Emami, 2016, Indian journal of dermatology, venereology and leprology.

Synthesis and biological activity of 5-nitrofuran-containing (1,3,4-thiadiazol-2-yl)piperazine moieties as a new type of anti-Helicobacter pylori heterocycles

A. Shafiee, A. Foroumadi, S. Emami, 2011 .

An Overview of the Effects of polyphenols on Cardiac Mitochondrial Function

M. Keighobadi, S. Emami, Hassan Mirzaei, 2019 .

Molecular Modeling and Structural Stability of Wild-Type and Mutant CYP51 from Leishmania major: In Vitro and In Silico Analysis of a Laboratory Strain

M. Keighobadi, M. Fakhar, S. Emami, 2018, Molecules.

Selective hydrogenation of 4-carboxybenzaldehyde over palladium catalysts supported with different structural organization

A. Rashidi, N. Izadi, S. Emami, 2017 .

Synthesis, transport and hypoxia- selective binding of 1-β-D-(5-deoxy- 5-fluororibofuranosyl)-2-nitroimid- azole (β-5-FAZR), a configurational isomer of the clinical hypoxia marker, FAZA

Jennifer Yang, R. Paproski, A. McEwan, 2007 .

Stereospecific deuteration of alpha-furanosyl azomycin nucleosides: a model reaction for tritium radiolabeling.

A. McEwan, Piyush Kumar, S. Emami, 2008, Bioorganic & Medicinal Chemistry Letters.

Stereospecific Deuteration of α-Furanosyl Azomycin Nucleosides: A Model Reaction for Tritium Radiolabeling.

A. McEwan, Piyush Kumar, S. Emami, 2008 .

Data on molecular docking of tautomers and enantiomers of ATTAF-1 and ATTAF-2 selectivty to the human/fungal lanosterol-14α-demethylase

S. Emami, H. Irannejad, Seyedeh Mahdieh Hashemi, 2020, Data in brief.

Current development of sigma-2 receptor radioligands as potential tumor imaging agents.

M. Alvandi, Z. Shaghaghi, S. Emami, 2021, Bioorganic chemistry (Print).

Promising antileishmanial effectiveness of doxorubicin and Doxil against Leishmania major: An in vitro assay.

M. Keighobadi, M. Fakhar, S. Teshnizi, 2017, Asian Pacific journal of tropical medicine.

Quinolones: Recent Structural and Clinical Developments

A. Shafiee, A. Foroumadi, S. Emami, 2005 .

Synthesis and Antibacterial Activity of New N-[2-(Thiophen-3-yl)ethyl]piperazinyl Quinolones.

M. Faramarzi, A. Shafiee, A. Foroumadi, 2007 .

Design, synthesis and biological evaluation of naphthalene-derived (arylalkyl)azoles containing heterocyclic linkers as new anticonvulsants: a comprehensive in silico, in vitro, and in vivo study.

S. Emami, N. Naderi, F. Amiri, 2021, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Synthesis and biological evaluation of quinazolinone-based hydrazones with potential use in Alzheimer's disease.

O. Firuzi, B. Hemmateenejad, R. Miri, 2017, Bioorganic chemistry.

Synthesis and antileishmanial activity of novel 5-(5-nitrofuran-2-y1)-1,3,4-thiadiazoles with piperazinyl-linked benzamidine substituents.

A. Shafiee, F. Kobarfard, A. Foroumadi, 2011, European journal of medicinal chemistry.

Selective leishmanicidal effect of 1,3,4-thiadiazole derivatives and possible mechanism of action against Leishmania species.

A. Kariminia, A. Shafiee, A. Foroumadi, 2009, Experimental parasitology.

Nitroimidazolyl-1,3,4-thiadiazole-based anti-leishmanial agents: synthesis and in vitro biological evaluation.

A. Shafiee, A. Foroumadi, S. Emami, 2009, European journal of medicinal chemistry.

New 7-piperazinylquinolones containing (benzo[d]imidazol-2-yl)methyl moiety as potent antibacterial agents

M. Faramarzi, A. Foroumadi, S. Emami, 2018, Molecular Diversity.

New 5-(nitroheteroaryl)-1,3,4-thiadiazols containing acyclic amines at C-2: synthesis and SAR study for their antileishmanial activity

A. Shafiee, F. Kobarfard, A. Foroumadi, 2013, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and anti-leishmanial activity of 5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-amines containing N-[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl] moieties.

A. Shafiee, F. Kobarfard, A. Foroumadi, 2012, European journal of medicinal chemistry.

One-pot, four-component synthesis of novel cytotoxic agents 1-(5-aryl-1,3,4-oxadiazol-2-yl)-1-(1H-pyrrol-2-yl)methanamines.

A. Ramazani, M. Faramarzi, A. Shafiee, 2014, European journal of medicinal chemistry.

Novel coumarin-3-carboxamides bearing N-benzylpiperidine moiety as potent acetylcholinesterase inhibitors.

A. Shafiee, M. Khoobi, M. Alipour, 2013, European journal of medicinal chemistry.

Synthesis and anti-cholinesterase activity of new 7-hydroxycoumarin derivatives.

A. Shafiee, M. Khoobi, M. Alipour, 2014, European journal of medicinal chemistry.

Inhibition by dicyclohexylcarbodiimide of ATP synthesis in isolated rat hepatocytes

S. Emami, A. Lodola, D. Sanadi, 1984, Bioscience reports.

Recent advances of cytotoxic chalconoids targeting tubulin polymerization: Synthesis and biological activity.

S. Emami, Hassan Mirzaei, 2016, European journal of medicinal chemistry.

Benzofuran-derived benzylpyridinium bromides as potent acetylcholinesterase inhibitors.

A. Shafiee, A. Foroumadi, H. Nadri, 2015, European journal of medicinal chemistry.

Recent applications of 1,3-thiazole core structure in the identification of new lead compounds and drug discovery.

A. Shafiee, A. Foroumadi, A. Asadipour, 2015, European journal of medicinal chemistry.

Induction of apoptosis through tubulin inhibition in human cancer cells by new chromene-based chalcones

A. Foroumadi, Hassan Aryapour, S. Emami, 2012, Pharmaceutical biology.