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Farzad Kobarfard

Researcher at Shahid Beheshti University of Medical Sciences and Health Services

Publications -  279
Citations -  5141

Farzad Kobarfard is an academic researcher from Shahid Beheshti University of Medical Sciences and Health Services. The author has contributed to research in topics: Chemistry & Detection limit. The author has an hindex of 29, co-authored 260 publications receiving 3669 citations. Previous affiliations of Farzad Kobarfard include Shahid Beheshti University & University of Tehran.

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Journal ArticleDOI

One Pot Synthesis and Biological Activity Evaluation of Novel Schiff Bases Derived from 2‐Hydrazinyl‐1,3,4‐thiadiazole.

Kamaleddin Haj Mohammad Ebrahim Tehrani, +5 more
- 16 Jul 2013 - 
TL;DR: In this article, the antiplatelet aggregation activity comparable to that of indomethacin was demonstrated for four compounds (IVa,b, d, e, f).
Journal Article

Fatty Acid Composition of Echium amoenum Fisch et. Mey. Seeds (Boraginaceae)

Faraz Mojab, +4 more
- 15 Mar 2009 - 
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Development of an Analytical Method for Dibutyl Phthalate Determination Using Surrogate Analyte Approach.

Vahid Farzanehfar, +3 more
- 01 Mar 2017 - 
TL;DR: A surrogate analyte approach that is based on using deuterium labeled analyte (DBP-d4) to construct the calibration line was applied to determine DBP in hexane samples.
Journal Article

Short Communication - Synthesis of drug metal complexes and their influence on human platelet aggregation.

Mansoor Ahmed, +7 more
- 01 Mar 2018 - 
TL;DR: In this study, transition metal complexes of pyrazinamide (PZ), isoniazid (INH), fluconazole (FCZ), metformin (dimethylbiguanide, DMBG) and losartan potassium (LS-K) were selected to evaluate for their possible anti-platelets aggregation in the light of reports on divalent and trivalent cations.
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The Photothermal Effect of Targeted Methotrexate-Functionalized Multi-Walled Carbon Nanotubes on MCF7 Cells.

Ali Karimi, +6 more
- 01 Jan 2019 - 
TL;DR: Carboxylated multi-walled carbon nanotubes were functionalized with MTX as a cytotoxic agent, FA as a targeting moiety and polyethylene amine (PEI) as a hydrophilic agent to reduce the release rate of methotrexate and increase cell death efficiency.