Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Somayeh Salarinejad"'
Autor:
Loghman Firoozpour, Setareh Moghimi, Somayeh Salarinejad, Mahsa Toolabi, Mahdi Rafsanjani, Roya Pakrad, Farzaneh Salmani, Seyed Mohammad Shokrolahi, Seyed Esmail Sadat Ebrahimi, Saeed Karima, Alireza Foroumadi
Publikováno v:
BMC Chemistry, Vol 17, Iss 1, Pp 1-10 (2023)
Abstract In this work, a novel series of pyridazine-triazole hybrid molecules were prepared and evaluated as inhibitors of rat intestinal α-glucosidase enzyme. Amongst all newly synthesized compounds, 10k showed good inhibition in the series with IC
Externí odkaz:
https://doaj.org/article/c30599aa34a441b394c7777d3e7aeaf9
Autor:
Loghman Firoozpour, Setareh Moghimi, Mohammad Hossein Fallah Barzegar, Mahsa Toolabi, Somayeh Salarinejad, Hamid Reza Bijanzadeh, Seyed Esmaeil Sadat Ebrahimi, Fatemeh Safari, Alireza Foroumadi
Publikováno v:
Polycyclic Aromatic Compounds. :1-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3711fd3bfeadee5e65636c1a70c17f54
https://doi.org/10.1080/10406638.2023.2212101
https://doi.org/10.1080/10406638.2023.2212101
Autor:
Behjat Pouramiri, Razieh Kooshki, Mohammad Reza Islami, Fatemeh Zigheimat, Faezeh Sadat Hosseini, Mehdi Abbasnejad, Somayeh Salarinejad
Publikováno v:
ChemistrySelect. 5:14190-14197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feb9001cce971e2b1e3810ff29e61b94
https://doi.org/10.1002/slct.202003119
https://doi.org/10.1002/slct.202003119
Publikováno v:
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV
Comprehensive Heterocyclic Chemistry IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d482f910b5180b8428dd7f32bf6ebeb
https://doi.org/10.1016/b978-0-12-409547-2.14826-7
https://doi.org/10.1016/b978-0-12-409547-2.14826-7
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:
Gizem Şanlıtürk, Mahsa Toolabi, Mümtaz Güran, Maryam Norouzbahari, Somayeh Salarinejad, Hamid Reza Bijanzadeh, Zahra Emamgholipour, Alireza Foroumadi
Publikováno v:
Daru
BACKGROUND: Increasing bacterial resistance to quinolones is concerning. Hence, the development of novel quinolones by chemical modifications to overcome quinolone resistance is an attractive perspective in this context. OBJECTIVE: In this study, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851543f14ff2c7582ba758a5b23eb2ea
https://europepmc.org/articles/PMC7704824/
https://europepmc.org/articles/PMC7704824/
Autor:
Adileh Ayati, Maliheh Safavi, Setareh Moghimi, Somayeh Salarinejad, Alireza Foroumadi, Behjat Pouramiri
Publikováno v:
Bioorganic chemistry. 99
The identification of molecular agents inhibiting specific functions in cancer cells progression is considered as one of the most successful plans in cancer treatment. The epidermal growth factor receptor (EGFR) over-activation is observed in a vast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa20dcabd4932552bf49e01c904f0cd0
https://pubmed.ncbi.nlm.nih.gov/32278207
https://pubmed.ncbi.nlm.nih.gov/32278207
Autor:
Tayebeh Oghabi Bakhshaiesh, Zaman Hasanvand, Rezvan Esmaeili, Ali Khalaj, Mahsa Toolabi, Ayoub Aghcheli, Setareh Moghimi, Somayeh Salarinejad, Elahe Nazeri, Alireza Foroumadi
Publikováno v:
European journal of medicinal chemistry. 185
In this paper, we described the synthesis and cytotoxic activities of two new series of thieno[2,3-d]pyrimidine and thieno[3,2-d] pyrimidine derivatives. Most of the synthesized compounds had significant antiproliferative activities against PC3, MDA-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b34742bf2376a16e667702e18019cda
https://pubmed.ncbi.nlm.nih.gov/31671308
https://pubmed.ncbi.nlm.nih.gov/31671308
Autor:
Loghman Firoozpour, Fatemeh Madani-Qamsari, Roya Pakrad, Somayeh Mojtabavi, Somayeh Salarinejad, Mohammad Ali Faramarzi, Mahsa Toolabi, Saeed Karima, Fatemeh Safari, Setareh Moghimi, Seyed Esmaeil Sadat Ebrahimi, Alireza Foroumadi
Publikováno v:
Bioorganic Chemistry. 109:104670
In this study, we reported the discovery of pyridazine based 1,2,3-triazole derivatives as inhibitors of α-glucosidase. All target compounds exhibited significant inhibitory activities against yeast and rat α-glucosidase enzymes compared to positiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa140fa0cc1e008bbbce2d99faae179
https://doi.org/10.1016/j.bioorg.2021.104670
https://doi.org/10.1016/j.bioorg.2021.104670
Autor:
Somayeh Mojtabavi, Loghman Firoozpour, Mohammad Ali Faramarzi, Mahsa Toolabi, Seyed Esmaeil Sadat Ebrahimi, Fatemeh Safari, Alireza Foroumadi, Setareh Moghimi, Somayeh Salarinejad
Publikováno v:
Bioorganic Chemistry. 102:104071
We herein applied the four step-synthetic route to prepare the pyridazine core attached to the various N-aryl acetamides. By this approach, a new series of pyridazine-based compounds were synthesized, characterized and evaluated for their activities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3745f2d3107797a04a5b9f1d8b170e69
https://doi.org/10.1016/j.bioorg.2020.104071
https://doi.org/10.1016/j.bioorg.2020.104071