F
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
Exposure Assessment for Some Pesticides through Rice Consumption in Iran Using a Multiresidue Analysis by GC-MS
Maryam Amirahmadi,Hassan Yazdanpanah,Farzad Kobarfard,Shahram Shoeibi,Morteza Pirali-Hamedani,Hossein Rastegar +5 more
TL;DR: An attempt for monitoring of 56 pesticides from different chemical groups in rice samples collected from local markets in Tehran and estimation of daily intake of interested pesticides through this monitoring and a valid method based on spiked calibration curves and QuEChERS sample preparation was developed.
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Synthesis of aminoquinoline-based aminoalcohols and oxazolidinones and their antiplasmodial activity.
TL;DR: The potency of these derivatives decreased against chloroquine‐resistant species in all cases and the resistance indices for these compounds improved significantly in comparison with those of β‐aminoalcohols, suggesting the absence of cross‐resistance between these new derivatives and chlorquine.
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Synthesis, dihydrofolate reductase inhibition, anti-proliferative testing, and saturation transfer difference ¹H-NMR study of some new 2-substituted-4,6-diaminopyrimidine derivatives.
Shohreh Mohebbi,Juan M. Falcón-Pérez,Esperanza Gonzalez,Oscar Millet,José M. Mato,Farzad Kobarfard +5 more
TL;DR: A series of 2-substituted-4,6-diaminipyrimidine derivatives were synthesized and evaluated for their dihydrofolate reductase (DHFR) inhibitory activity and compounds 16, 17, and 22 demonstrated the most potent in vitro anti-proliferative activity among the others.
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Synthesis and evaluation of in vitro anti-tuberculosis activity of N-substituted glycolamides.
TL;DR: Among the synthesized compounds, all those with disubstituted amide structure accompanied by one or two heteroatom with loan pair of electrons atom(s) beta to the amide nitrogen demonstrated moderate anti-tuberculosis activity and all the monosubstitute amides showed no activity at all.
Journal Article
Diterpenoids of Otostegia persica (Burm.) Boiss
S A Ayat Elahi,Farzad Kobarfard,Jinous Asgarpanah,M Rahmati Roudsari,G H Fanai,M. Iqbal Choudhary +5 more
TL;DR: Four known diterpenoids belonging to the clerodane and tetracyclic diterpene types were isolated for the first time from Otostegia persica (Burm.) Boiss.