Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ali Rafinejad"'
Autor:
M. Hashemi, Seyedeh Sara Mirfazli, Zahra Najafi, R. Mohammadian, Mina Saeedi, Mohammad Mahdavi, Malihe Safavi, Tahmineh Akbarzadeh, Elahe Karimpour-Razkenari, S. Kabudanian Ardestani, Ali Rafinejad
Publikováno v:
Polycyclic Aromatic Compounds. 40:1568-1580
In this study, a new series of N-(di or trimethoxyaryl)-5-arylisoxazole-3-carboxamide derivatives were synthesized and evaluated against human breast cancer cell lines including MCF-7, MDA-MB-231, ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f45ecfcce2349608601157966a69eb3
https://doi.org/10.1080/10406638.2018.1564677
https://doi.org/10.1080/10406638.2018.1564677
Autor:
Abbas Shafiee, Marzieh Omidi, Mina Saeedi, Farhad Sarrafzadeh, Tahmineh Akbarzadeh, Ghasem Rezanejade Bardajee, Fereshteh Goli-Garmroodi, Mohammad Mahdavi, Alireza Foroumadi, Loghman Firoozpour, Ali Rafinejad
Publikováno v:
Tetrahedron Letters. 56:743-746
A novel series of benzo[4,5]imidazo[1,2- a ]pyridine derivatives is synthesized through the reaction of 2-(1 H -benzo[ d ]imidazol-2-yl)acetonitrile and different ethyl 2,4-dioxo-4-arylbutanoate derivatives in the presence of piperidine in refluxing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46ff5943014dff150458357889995bcd
https://doi.org/10.1016/j.tetlet.2014.12.099
https://doi.org/10.1016/j.tetlet.2014.12.099
Autor:
Elahe Karimpour-Razkenari, Mahnaz Khanavi, Tahmineh Akbarzadeh, Ali Rafinejad, Bilqees Sameem, Fahimeh Vafadarnejad, Mohammad Mahdavi, Mina Saeedi
Publikováno v:
Letters in Drug Design & Discovery. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d7c6ac87e11be2609c09ba8f022786f
https://doi.org/10.2174/1570180813666161018124726
https://doi.org/10.2174/1570180813666161018124726
Autor:
Morteza Rafiee-Tehrani, Taraneh Naghibi, Shahnaz Rafiei, Mohammad Taghikhani, Soheila Ajdary, Faramarz Dobakhti, Ali Rafinejad, Khosrow Bayati
Publikováno v:
Microbes and Infection. 11:296-301
Bacillus Calmette-Guerin (BCG) is the only available vaccine against tuberculosis. The research for an improved vaccine is currently a very active field of investigation. In the present study, adjuvanticity effect of sterile sodium alginate on subcut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd371654845f1bca7b47bf642f8b82a7
https://doi.org/10.1016/j.micinf.2008.12.003
https://doi.org/10.1016/j.micinf.2008.12.003
Autor:
Mahboobeh Pordeli, Sussan Kabudanian Ardestani, Maliheh Safavi, Abbas Shafiee, Tahmineh Akbarzadeh, Javad Malekian Mollaghasem, Asal Fallah-Tafti, Ali Rafinejad, Alireza Foroumadi
Publikováno v:
ChemInform. 43
A new series of 4-aryl-4H-chromenes bearing a 5-arylisoxazol-3-yl moiety at the C-4 position were prepared as potential anticancer agents. The in vitro cytotoxic activity of the synthesized compounds was investigated against a panel of tumor cell lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::679f3c9e267ba3aea0d5cc7e182f0779
https://doi.org/10.1002/chin.201237135
https://doi.org/10.1002/chin.201237135
Autor:
Abbas Shafiee, Rakesh Tiwari, Deendayal Mandal, Ali Rafinejad, Tahmineh Akbarzadeh, Keykavous Parang, Asal Fallah-Tafti, Alireza Foroumadi, Amir Nasrolahi Shirazi
Publikováno v:
DARU Journal of Pharmaceutical Sciences
Background A series of 2-amino-4-aryl-4H-benzo[h or f]chromene-3-carbonitrile derivatives were synthesized and evaluated for inhibition of Src kinase and cell proliferation in breast carcinoma (BT-20) cell lines. Methods The one-pot, three-component
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d29c8c9eaa636b18c144ed35d51adba3
https://pubmed.ncbi.nlm.nih.gov/23351304
https://pubmed.ncbi.nlm.nih.gov/23351304
Autor:
Abbas Shafiee, Maliheh Safavi, Tahmineh Akbarzadeh, Ali Rafinejad, Mahboobeh Pordeli, Asal Fallah-Tafti, Sussan Kabudanian Ardestani, Javad Malekian Mollaghasem, Alireza Foroumadi
Publikováno v:
Archiv der Pharmazie. 345(5)
A new series of 4-aryl-4H-chromenes bearing a 5-arylisoxazol-3-yl moiety at the C-4 position were prepared as potential anticancer agents. The in vitro cytotoxic activity of the synthesized compounds was investigated against a panel of tumor cell lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a89251b077f89b9da16f0dc94425129
https://pubmed.ncbi.nlm.nih.gov/22266847
https://pubmed.ncbi.nlm.nih.gov/22266847