Zobrazeno 1 - 10
of 44
pro vyhledávání: '"ESKANDAR ALIPOUR"'
Autor:
Mina Saeedi, Mohammad Jeiroudi, Leila Ma’mani, Mohammad Mahdavi, Eskandar Alipour, Abbas Shafiee, Ali Reza Foroumadi
Publikováno v:
Iranian Journal of Chemistry & Chemical Engineering, Vol 34, Iss 4, Pp 39-45 (2015)
The surface of SBA-15 was modified by diphenylphosphine; then, it was treated with butane sultone and sulfuric acid to obtain Brønsted acid HO3S-phosphonium based ionic liquid functionalized SBA-15 with HSO4- as a counteranion. It efficiently cataly
Externí odkaz:
https://doaj.org/article/42742c7d6a5b4df4aa6796b147b8ffe6
Autor:
ABBAS SHAFIEE, ESKANDAR ALIPOUR, MARYAM OMRANI, MOHSEN VOSOOGHI, FARIDEH SIAVOSHI, MARYAM NAKHJIRI, SAEED EMAMI, SEYED ESMAEIL SADAT-EBRAHIMI, AZADEH YAHYA-MEYMANDI, MOHAMMAD HASSAN MOSHAFI, ALIREZA FOROUMADI
Publikováno v:
Journal of the Serbian Chemical Society, Vol 76, Iss 2, Pp 201-210 (2011)
In order to find new and potent drug candidates for the treatment of Helicobacter pylori infections‚ in this study attention was focused on the synthesis and anti-H. pylori activity of a series of 5-(5-nitrofuran-2-yl)-1,3,4-thiadiazoles containing
Externí odkaz:
https://doaj.org/article/a859d3673bda4b89b417596b5e80459e
Autor:
Eskandar Alipour, Negar Mohammad Hosseini, Fatemeh Panah, Sussan K. Ardestani, Maliheh Safavi, Abbas Shafiee, Alireza Foroumadi
Publikováno v:
E-Journal of Chemistry, Vol 8, Iss 3, Pp 1226-1231 (2011)
Quinolone are a class of potent broad-spectrum antibacterial drugs that target the bacterial type II DNA topoisomerases (DNA gyrase) and topoisomerase IV. In the present study, the synthesis and evaluation of cytotoxicity activity of a new series of
Externí odkaz:
https://doaj.org/article/60e8f8f999d24bdb828e5191de5d884b
Publikováno v:
Clinical Laboratory. 69
Autor:
Farzad Kobarfard, Mohammad Reza Shoushizadeh, Eskandar Alipour, Neda Adibpour, Zahra Ghiasifar, Hafezeh Salehabadi
Publikováno v:
Bulletin of the Korean Chemical Society. 42:48-59
Autor:
Eskandar Alipour, Iman Gholamali
Publikováno v:
Regenerative Engineering and Translational Medicine. 6:398-406
The drug delivery approach was developed through effective preparation of nanocomposite hydrogels in situ while CuO nanoparticles were being formed within swollen CMCS/starch hydrogels. Nanocomposite hydrogel have obtained significant attention in re
Publikováno v:
Polymer Science, Series A. 62:502-514
The CsMe/PVA/ZnO nanocomposite hydrogels have been introduced as a new object to deliver drugs, which is dependent on pH. They were prepared successfully in situ by forming of ZnO nanoparticles within swollen CsMe/PVA hydrogels. The resulting hydroge
Publikováno v:
International Journal of Polymeric Materials and Polymeric Biomaterials. 70:967-980
In this paper, the bio-nanocomposites were used as a potential candidate for controlled release of anticancer drug doxorubicin. Formation of CuO nanoparticles in hydrogels was confirmed using FT-IR...
Publikováno v:
Journal of Polymers and the Environment. 28:906-917
In the present study, we introduce the formation of Starch/PEG-poly (acrylic acid) hydrogel (St-PEG-AcAH) and nanocomposite of AgNPs-base St-PEG-AcAH (AgNPs-St-PEG-AcANCH) free radical method, and their characterization using analytical techniques of
Publikováno v:
Organic Preparations and Procedures International. 52:37-47
In recent years, organofluorine compounds have achieved a significant place in life sciences.1 Fluorinated compounds are prized because of their wide applications in medicinal chemistry and use in ...