S. Sadat-Ebrahimi

发表

An efficient, four-component reaction for the synthesis of novel carbamodithioates

A. Shafiee, A. Foroumadi, M. Mahdavi, 2017 .

Design, Synthesis, and Biological Evaluation of New Indole-Acrylamide-1,2,3-Triazole Derivatives as Potential α-Glucosidase Inhibitors

B. Larijani, M. Faramarzi, A. Foroumadi, 2020, Polycyclic Aromatic Compounds.

New phthalimide-benzamide-1,2,3-triazole hybrids; design, synthesis, α-glucosidase inhibition assay, and docking study

B. Larijani, M. Mahdavi, M. Mohammadi‐Khanaposhtani, 2020, Medicinal Chemistry Research.

Synthesis and bioactivities evaluation of quinazolin-4(3H)-one derivatives as α-glucosidase inhibitors

M. Faramarzi, A. Iraji, K. Zomorodian, 2022, BMC Chemistry.

As an Infection Imaging Agent

M. Talebi, M. Erfani, S. F. Mirshojaei, 2011 .

A Highly Efficient Method for the Synthesis of Novel 1′H-spiro[indene-2,2′-quinazoline]-1,3,4′(3′H)-trione Derivatives

A. Shafiee, A. Foroumadi, M. Mahdavi, 2015 .

Cu(II)-β-cyclodextrin-catalyzed synthesis of spiro[indoline-3,4′-pyrano[3,2-c]chromene]-3′-carbonitrile derivatives

S. Bahadorikhalili, M. Mahdavi, Mina Saeedi, 2017 .

Straightforward Approach Toward Dihydrothiazoles via Intramolecular Bromocyclization

A. Shafiee, A. Foroumadi, M. Mahdavi, 2015 .

Three-component one-pot synthesis of dihydrochromeno[4,3-b]pyrazolo[4,3-e]pyridines

A. Shafiee, A. Foroumadi, M. Mahdavi, 2016 .

Novel 5-(nitrothiophene-2-yl)-1,3,4-Thiadiazole Derivatives: Synthesis and Antileishmanial Activity against promastigote stage of Leishmania major

A. Foroumadi, S. Moghimi, M. Hashemian, 2019, Iranian journal of pharmaceutical research : IJPR.

Strong, Specific, Reversible Binding Ligands for Transfer RNA: Comparison by Fluoresence and NMR Spectroscopies with Distamycin Binding for a New Structural Class of Ligand

D. Marks, K. Douglas, E. Bichenkova, 1998 .

Novel phenylurea-pyridinium derivatives as potent urease inhibitors: Synthesis, in vitro, and in silico studies

B. Larijani, A. Iraji, K. Zomorodian, 2022, Journal of Molecular Structure.

Increased stability and lifetime of the complex formed between DNA and meta-phenyl-substituted Hoechst dyes as studied by fluorescence titrations and stopped-flow kinetics.

R. Clegg, K. Douglas, F. Loontiens, 2001, Journal of molecular biology.

Synthesis and Evaluation of Chroman‐4‐One Linked to N‐Benzyl Pyridinium Derivatives as New Acetylcholinesterase Inhibitors

A. Shafiee, A. Foroumadi, H. Nadri, 2015, Archiv der Pharmazie.

Rational Design of a New Class of DNA Cleaver Based on Prediction of Minor Groove Binding Interactions and NMR Structural Studies

J. Parkinson, J. Andrews, A. Wilton, 1996 .

Synthetic inhibitors of the processing of pretransfer RNA by the ribonuclease P ribozyme: enzyme inhibitors which act by binding to substrate.

K. Douglas, Y. Sugiura, Y. Kikuchi, 2001, Biochemistry.

Synthesis, in vitro inhibitor screening, structure–activity relationship, and molecular dynamic simulation studies of novel thioquinoline derivatives as potent α-glucosidase inhibitors

M. Faramarzi, A. Iraji, Shahrzad Javanshir, 2023, Scientific reports.