Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Negar, Mohammadhosseini"'
Autor:
Roshanak Hariri, Maryam Baeeri, Negar Mohammadhosseini, Saeed Emami, Alireza Foroumadi, Maliheh Barazandeh Tehrani
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 33, Iss 227, Pp 13-23 (2023)
Background and purpose: The spread of cancer, coupled with the challenges posed by complex treatments, stands as one of the foremost medical issues in today's world. Researchers consistently strive to identify novel compounds with enhanced efficacy a
Externí odkaz:
https://doaj.org/article/91268b01d50240b3896bf7871671a769
Autor:
Bahram letafat, Raheleh Shakeri, Saeed Emami, Saeedeh Noushini, Negar Mohammadhosseini, Nayyereh Shirkavand, Sussan Kabudanian Ardestani, Maliheh Safavi, Marjaneh Samadizadeh, Aida Letafat, Abbas Shafiee, Alireza Foroumadi
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 16, Iss 11, Pp 1155-1162 (2013)
Objective(s): Chalcones and their rigid analogues represent an important class of small molecules having anticancer activities. Therefore, in this study the synthesis and cytotoxic activity of new 3-benzylidenchroman-4-ones were described as rigid ch
Externí odkaz:
https://doaj.org/article/905d2b038f6d4703bc8020bc3083490c
Publikováno v:
E-Journal of Chemistry, Vol 8, Iss 3, Pp 1120-1123 (2011)
In the present study we report the synthesis and antibacterial activity of a new series 2-(1-methyl-4-nitro-1H-imidazol-5-ylsulfonyl)-1,3,4-thiadiazoles (6a-c). Compounds 6a-c were tested in vitro by the conventional agar dilution method against a pa
Externí odkaz:
https://doaj.org/article/84a13e11299c4b2fb2edb08c767abbb6
Publikováno v:
Acta Scientiarum Polonorum Technologia Alimentaria. 17:219-226
BACKGROUND A. ursinum is found to contain high levels of some beneficial phenolic and poly phenolic compounds were found to be effective in scavenging DPPH radicals and tyroinase inhibition. The aim of this study was to evaluate the anti-tyrosinase a
Publikováno v:
Energy Conversion and Management. 158:327-345
The objective of this research is a comparative analysis of various kinds of heat and mass exchangers of dew point indirect evaporative cooler. Considering three key performance parameters of an evaporative cooler, namely life-cycle cost, annual wate
Autor:
Mina Saeedi, Negar Mohammadhosseini, Abbas Shafiee, Mohammad Mahdavi, Alireza Foroumadi, Shahram Moradi, Omidreza Firuzi
Publikováno v:
Volume: 41, Issue: 1 125-134
Turkish Journal of Chemistry
Turkish Journal of Chemistry
Various thioxo-quinazolino[3,4-$a$]quinazolinones were prepared and evaluated for their cytotoxicity in MOLT-4 (lymphoblastic leukemia) and MCF-7 (breast adenocarcinoma) cell lines. Synthesis of the target compounds was started from isatoic anhydride
Publikováno v:
Journal of Heterocyclic Chemistry. 53:1595-1602
Novel 6-mercapto-12-phenethyl-quinazolino[3,4-a]quinazolinone derivatives were synthesized through a user-friendly five-step reaction starting from isatoic anhydride. All products were characterized by IR, 1H-NMR, 13C-NMR spectroscopy, and chemical a
Autor:
Negar, Mohammadhosseini, Mahboobeh, Pordeli, Maliheh, Safavi, Loghman, Firoozpour, Fatame, Amin, Sussan, Kabudanian Ardestani, Najmeh, Edraki, Abbas, Shafiee, Alireza, Foroumadi
Publikováno v:
Iranian Journal of Pharmaceutical Research : IJPR
Quinolone antibacterials are one of the most important classes of pharmacological agents known as potent inhibitors of bacterial DNA gyrase and topoisomerase IV that efficiently inhibit DNA replication and transcription by generating several double-s
Publikováno v:
E-Journal of Chemistry, Vol 8, Iss 3, Pp 1120-1123 (2011)
In the present study we report the synthesis and antibacterial activity of a new series 2-(1-methyl-4-nitro-1H-imidazol-5-ylsulfonyl)-1,3,4-thiadiazoles (6a-c). Compounds6a-cwere testedin vitroby the conventional agar dilution method against a panel
Autor:
Marziyeh Badinloo, Abbas Shafiee, Saeed Emami, Saeed Rajabalian, Negar Mohammadhosseini, Alireza Foroumadi
Publikováno v:
Biomedicine & Pharmacotherapy. 63:216-220
As part of a continuing search for new potential anticancer candidates in the piperazinyl quinolone series, the cytotoxicity evaluation of new N-substituted piperazinyl quinolones was of our interest. The growth inhibitory activities of 12 new compou