Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shima H. M. E. Ketabforoosh"'
Autor:
Mahsa Toolabi, Fatemeh Safari, Adileh Ayati, Parnian Fathi, Setareh Moghimi, Somayeh Salarinejad, Roham Foroumadi, Shima H. M. E. Ketabforoosh, Alireza Foroumadi
Publikováno v:
Archiv der PharmazieREFERENCES. 355(3)
A novel series of 2-acetamide-5-phenylthio-1,3,4-thiadiazol derivatives containing a phenyl urea warhead were synthesized and evaluated as antiproliferative agents. The cytotoxic activities of the newly synthesized compounds were evaluated toward thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e76601f61e1380f13716a0cc0460e031
https://pubmed.ncbi.nlm.nih.gov/35014090
https://pubmed.ncbi.nlm.nih.gov/35014090
Autor:
Siavash Salek Soltani, Alireza Foroumadi, S. Morteza F. Farnia, Mostafa Golshani, Shima H. M. E. Ketabforoosh, Setareh Moghimi, Tahmineh Akbarzadeh
Publikováno v:
ChemistrySelect. 4:13695-13697
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9343fb3c75f7618a496b0ecf1413e4dd
https://doi.org/10.1002/slct.201902872
https://doi.org/10.1002/slct.201902872
Autor:
Shima H. M. E. Ketabforoosh, Loghman Firoozpour, Mohammad Amin Boshagh, Aram Faraji, Rasoul Motahari, Zaman Hasanvand, Mahsa Toolabi, Setareh Moghimi, Hamid Reza Bijanzadeh, Rezvan Esmaeili, Alireza Foroumadi, Roya Rahmani, Tayebeh Oghabi Bakhshaiesh
Publikováno v:
Bioorganic Chemistry. 108:104553
A series of quinazolin-4(3H)-one based agents containing thiadiazole-urea were designed, synthesized, and biologically evaluated. The proliferation rate of PC3 cells was moderately reduced by compound 9f (IC50 = 17.7 μ M ) which was comparable with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcd46e59d44efe2d6c6734cc67670f6c
https://doi.org/10.1016/j.bioorg.2020.104553
https://doi.org/10.1016/j.bioorg.2020.104553
Autor:
Abbas Shafiee, Saeed Emami, Alireza Foroumadi, Shima H. M. E. Ketabforoosh, Maliheh Safavi, Loghman Firoozpour, Asma Kheirollahi, Nasim Esmati, Sussan K. Ardestani
Publikováno v:
Archiv der Pharmazie. 347:853-860
A novel series of chalcones and flavanones discriminated by the presence of a 3,4-dimethoxyphenyl moiety in their structures were synthesized as anti-cancer agents. The cytotoxicity evaluation of the analogs against the MCF-7, MDA-MB-231 (human breas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdee7f4beb610cf4405e698fa15389b8
https://doi.org/10.1002/ardp.201400215
https://doi.org/10.1002/ardp.201400215
Autor:
Shima H M E, Ketabforoosh, Asma, Kheirollahi, Maliheh, Safavi, Nasim, Esmati, Sussan K, Ardestani, Saeed, Emami, Loghman, Firoozpour, Abbas, Shafiee, Alireza, Foroumadi
Publikováno v:
Archiv der Pharmazie. 347(11)
A novel series of chalcones and flavanones discriminated by the presence of a 3,4-dimethoxyphenyl moiety in their structures were synthesized as anti-cancer agents. The cytotoxicity evaluation of the analogs against the MCF-7, MDA-MB-231 (human breas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d668f18344b3e46aef137820d05f91fc
https://pubmed.ncbi.nlm.nih.gov/25201534
https://pubmed.ncbi.nlm.nih.gov/25201534