Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Adileh Ayati"'
Autor:
Zaman Hasanvand, Rasoul Motahari, Hamid Nadri, Setareh Moghimi, Roham Foroumadi, Adileh Ayati, Tahmineh Akbarzadeh, Syed Nasir Abbas Bukhari, Alireza Foroumadi
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
A novel multifunctional series of 3-aminobenzofuran derivatives 5a-p were designed and synthesized as potent inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). The target compounds 5a-p were prepared via a three-step reactio
Externí odkaz:
https://doaj.org/article/49ac214d9db24ab097e14bbceb7415f2
Autor:
Behjat Pouramiri, Seyed Reza Seyedhosseini, Mohammad Hadi Nematollahi, Sanaz Faramarz, Fatemeh Seyedi, Adileh Ayati
Publikováno v:
Polycyclic Aromatic Compounds. 43:176-189
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67694d36d9ee2108e40f0672138d24d6
https://doi.org/10.1080/10406638.2021.2011753
https://doi.org/10.1080/10406638.2021.2011753
Autor:
Behjat Pouramiri, Ali akbar Mariki, Mahboobeh Zahedifar, Safa Lotfi, Adileh Ayati, Akbar Anaeigoudari
Publikováno v:
Polycyclic Aromatic Compounds. 42:5231-5241
A series of novel tetrahydropyrimidin-4-yl)pyridine derivatives 6(a–h) have been designed and synthesized as inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). The chemical...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfccae09eef1f2f78bdb6117fd1e5a06
https://doi.org/10.1080/10406638.2021.1933102
https://doi.org/10.1080/10406638.2021.1933102
Autor:
Adileh Ayati, Tayebeh Oghabi Bakhshaiesh, Mahsa Toolabi, Rezvan Esmaeili, Elahe Nazeri, Loghman Firoozpour, Alireza Foroumadi, Ayoub Aghcheli, Maryam Norouzbahari, Setareh Moghimi
Publikováno v:
Medicinal Chemistry Research. 29:2000-2010
A novel series of 1-(5-(benzylthio)-1,3,4-thiadiazol-2-yl)-3-phenylurea derivatives (5a–l) were designed and synthesized as sorafenib analogs. The in vitro cytotoxicity effects of synthesized compounds were evaluated against four different human ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84bfec1c3526e0d5780f813bac51c82c
https://doi.org/10.1007/s00044-020-02616-2
https://doi.org/10.1007/s00044-020-02616-2
Publikováno v:
Journal of the Serbian Chemical Society, Vol 85, Iss 11, Pp 1405-1415 (2020)
A series of biologically active disubstituted benzofuran derivatives (3a?d) have been designed and synthesized via C?H bond activation reaction. The chemical structures of all final compounds were confirmed by spectroscopic methods. In vitro anti ace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c16021fe491a5b57c7c9edf5e4fa33d
https://doi.org/10.2298/jsc191231039p
https://doi.org/10.2298/jsc191231039p
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
Publikováno v:
Future Medicinal Chemistry. 11:1929-1952
Cancer is known as one of the main causes of death in the world; and many compounds have been synthesized to date with potential use in cancer therapy. Thiazole is a versatile heterocycle, found in the structure of many drugs in use as well as antica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb739c7896d6f660b432c97e51d93bf
https://doi.org/10.4155/fmc-2018-0416
https://doi.org/10.4155/fmc-2018-0416
Autor:
Saeed Emami, Tayebeh Oghabi Bakhshaiesh, Loghman Firoozpour, Adileh Ayati, Keivan Majidzadeh-A, Rezvan Esmaeili, Setareh Moghimi, Maliheh Safavi, Alireza Foroumadi
Publikováno v:
European Journal of Medicinal Chemistry. 155:483-491
A series of new coumarin-containing compounds 3a-l and 4a-c was designed and synthesized based on the chalcone-type 4-amino-5-cinnamoylthiazole scaffold 2, and screened for their in vitro anticancer and antioxidant activities. Representatively, the 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f169470e894fea4e7ab97a3efb59303
https://doi.org/10.1016/j.ejmech.2018.06.015
https://doi.org/10.1016/j.ejmech.2018.06.015
Autor:
Tayebeh Oghabi Bakhshaiesh, Keivan Majidzadeh-A, Saeed Emami, Setareh Moghimi, Rezvan Esmaeili, Zahra Eslami-S, Alireza Foroumadi, Adileh Ayati, Maliheh Safavi
Publikováno v:
European Journal of Medicinal Chemistry. 145:404-412
A series of 4-amino-5-cinnamoylthiazoles 3a-p were designed and synthesized as chalcone-like anticancer agents. The synthesized derivatives 3a-p were evaluated for their in vitro antiproliferative activities against three different human cancer cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9003f63187f61afdedc9d970e751c6e1
https://doi.org/10.1016/j.ejmech.2018.01.015
https://doi.org/10.1016/j.ejmech.2018.01.015
Publikováno v:
European Journal of Medicinal Chemistry. 221:113523
Despite significant improvements of new treatment options, cancer continues to represent as one of the most common and fatal disease. The EGFR signaling pathway is considered as a significant approach in targeted therapy of cancers. Blocking the EGFR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c10eed6f7f7886a826d634baadb9da04
https://doi.org/10.1016/j.ejmech.2021.113523
https://doi.org/10.1016/j.ejmech.2021.113523