Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mostafa Golshani"'
Autor:
Ebrahim Kianmehr, Bahareh Bari, Mahdi Jafarzadeh, Ali Rostami, Mostafa Golshani, Alireza Foroumadi
Publikováno v:
New Journal of Chemistry. 46:19455-19459
A palladium-catalyzed decarboxylative domino reaction of imidazo[1,2-a]pyridines and coumarin-3-carboxylic acids has been developed, which provides access to dibenzoisochromenoimidazo[1,2-a]pyridin-6-ones possessing six fused rings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75abbb7a4e3db21162e536545b6a56af
https://doi.org/10.1039/d2nj02706b
https://doi.org/10.1039/d2nj02706b
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:
Hamid Nadri, Alireza Moradi, Farshad Homayouni Moghadam, Loghman Firoozpour, Bahar Pakseresht, Ali Ramazani, Alireza Foroumadi, Laleh Faraji, Setareh Moghimi, Zeinab Hasanpour, Mostafa Golshani, Mehdi Khoobi
Publikováno v:
Medicinal Chemistry Research. 27:1741-1747
A novel hybrid series of umbellipherone and benzyl amine scaffolds, linked via triazole ring, was synthesized and evaluated as both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitors. Most of the synthesized compounds showed mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96fcadfd9b7da01338f3e99fe0e16608
https://doi.org/10.1007/s00044-018-2187-8
https://doi.org/10.1007/s00044-018-2187-8
Publikováno v:
Chemical communications (Cambridge, England). 53(77)
A highly regioselective and transition-metal free one-pot arylation of chromenones with arylboronic acids has been achieved employing K2S2O8. The procedure consists of a sequence of some reactions including an arylation/decarboxylation cascade and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fab0a28b923647407611fe688f3a29e
https://pubmed.ncbi.nlm.nih.gov/28905058
https://pubmed.ncbi.nlm.nih.gov/28905058
Autor:
Mojtaba Shakibaie, Hamid Nadri, Alireza Moradi, Ali Asadipour, Loghman Firoozpour, Alireza Foroumadi, Syed Nasir Abbas Bukhari, Mehdi Khoobi, Saeed Emami, Leili Jalili-Baleh, Mostafa Golshani, Mandana Jafari, Farshad Homayouni Moghadam
Publikováno v:
European journal of medicinal chemistry. 139
A novel series of tacrine-like compounds 7a-u possessing a fused pyrazolo[1,2-b]phthalazine structure were designed and synthesized as potent and selective inhibitors of AChE. The in-vitro biological assessments demonstrated that several compounds ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c5dffe2d63ba5b028db731003d5c19b
https://pubmed.ncbi.nlm.nih.gov/28803044
https://pubmed.ncbi.nlm.nih.gov/28803044
Autor:
Leili Jalili-Baleh, Mehdi Khoobi, Tuba Tüylü Küçükkılınç, Mostafa Golshani, Alireza Foroumadi, Alireza Moradi, Alieh Ameri, Niloufar Choubdar, Zahra Abdolahi, Beyza Ayazgök, Fatemeh Salehian, Hamid Nadri, Farshad Homayouni Moghadam
Publikováno v:
Bioorganic Chemistry. 91:103164
Multi-Target approach is particularly promising way to drug discovery against Alzheimer's disease. In the present study, we synthesized a series of compounds comprising the carbazole backbone linked to the benzyl piperazine, benzyl piperidine, pyridi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55eb1f5355dcd4898c194ac5042d346a
https://doi.org/10.1016/j.bioorg.2019.103164
https://doi.org/10.1016/j.bioorg.2019.103164
Autor:
Seyed Esmaeil Sadat Ebrahimi, Alireza Foroumadi, Zahra Abdolahi, Beyza Ayazgök, Leili Jalili-Baleh, Tuba Tüylü Küçükkılınç, Helia Abdshahzadeh, Mehdi Khoobi, Setareh Moghimi, Mostafa Golshani, Hamid Forootanfar, Ismaeil Haririan, Hamid Nadri, Alieh Ameri, Iraj Saberi Kia
Publikováno v:
Chemistry & Biodiversity. 16:e1800436
Two series of novel coumarin derivatives, substituted at 3 and 7 positions with aminoalkoxy groups, are synthesized, characterized, and screened. The effect of amine substituents and the length of cross-linker are investigated in acetyl- and butyrylc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90ed14d1e6f6c7c40ebccc0a8174417e
https://doi.org/10.1002/cbdv.201800436
https://doi.org/10.1002/cbdv.201800436