Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sedighe Sadeghi"'
Autor:
Sedighe Sadeghi, Mojtaba Jokar, Seyed Mostafa Seyed Hossieni Tezerjani, Hasan Haghaninejad, Elahe Zare, Mahmood Emami Meybodi, Mohammadtaghi Sareban hassanabadi, Masoud Mirzaei, Hamidreza Mohammadi, Forough Sadat Tabatabaei
Publikováno v:
Health Science Reports, Vol 7, Iss 4, Pp n/a-n/a (2024)
Abstract Background and Aims Electrocardiography (ECG) is a widely accessible, noninvasive, and cost‐effective diagnostic instrument used to evaluate patients with suspected heart failure (HF). The aim of this study is to investigate electrocardiog
Externí odkaz:
https://doaj.org/article/70212ee336c64239902426f032369a73
Recently, Babaie-Kafaki et al. \cite{Babaie-Kafaki,Babaie-Kafakinew} have suggested a model for the fuzzy bus terminal location problem. Here, we propose a new optimization model by improving Babaie-Kafaki et al.'s model. In our model, we define new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0968d05884f7cca704c5c67c71d57f54
https://doi.org/10.21203/rs.3.rs-1978446/v1
https://doi.org/10.21203/rs.3.rs-1978446/v1
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2ca25b23c59f26e15880a641bda1a77
https://doi.org/10.2139/ssrn.4276481
https://doi.org/10.2139/ssrn.4276481
Akademický článek
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Publikováno v:
Research in Pharmaceutical Sciences, Vol 13, Iss 2, Pp 168-176 (2018)
A series of novel sorafenib analogues containing a quinoxalinedione ring and amide linker were synthesized. A total of 9 novel compounds in 6 synthetic steps were synthesized. Briefly, the amino group of p-aminophenol was first protected which then f
Externí odkaz:
https://doaj.org/article/4a93a176926c4954a7c016431af6c542
Autor:
Sedighe Sadeghian-Rizi, Ghadamali Khodarahmi, Amirhossein Sakhteman, Ali Jahanian-Najafabadi, Mahboubeh Rostami, Mahmoud Mirzaei, Farshid Hassanzadeh
Publikováno v:
Research in Pharmaceutical Sciences, Vol 13, Iss 1, Pp 82-92 (2018)
Diaryl urea derivatives have exhibited a broad spectrum of biochemical effects and pharmaceutical applications. Several diaryl urea derivatives such as sorafenib, regorafenib, linifanib, and tivozanib and lenvatinib are in clinical trial or clinical
Externí odkaz:
https://doaj.org/article/1a616a658a984cc0b3cbf7310b9f4c4c
Synthesis and cytotoxic evaluation of novel quinazolinone derivatives as potential anticancer agents
Autor:
Safoora Poorirani, Sedighe Sadeghian-Rizi, Ghadamali Khodarahmi, Marzieh Rahmani Khajouei, Farshid Hassanzadeh
Publikováno v:
Research in Pharmaceutical Sciences, Vol 13, Iss 5, Pp 450-459 (2018)
Nitrogen-rich heterocyclic compounds represent a unique class of chemicals with especial properties and have been modified to design novel pharmaceutically active compounds. In this study, a series of novel quinazolinone derivatives with substituted
Externí odkaz:
https://doaj.org/article/4faa5471857549a8940794c6ab2a6fc8
Autor:
Sedighe Sadeghian-Rizi, Ghadamali Ali Khodarahmi, Amirhossein Sakhteman, Ali Jahanian-Najafabadi, Mahboubeh Rostami, Mahmoud Mirzaei, Farshid Hassanzadeh
Publikováno v:
Research in Pharmaceutical Sciences, Vol 12, Iss 6, Pp 500-509 (2017)
In this study a series of diarylurea derivatives containing quinoxalindione group were biologically evaluated for their cytotoxic activities using MTT assay against MCF-7 and HepG2 cell lines. Antibacterial activities of these compounds were also eva
Externí odkaz:
https://doaj.org/article/317dfa96e87f4719b67a882c3f9476c7
Autor:
Elham Jafari, Najmeh Taghi jarah-Najafabadi, Ali Jahanian-Najafabadi, Safoora Poorirani, Farshid Hassanzadeh, Sedighe Sadeghian-Rizi
Publikováno v:
Research in Pharmaceutical Sciences, Vol 12, Iss 6, Pp 526-534 (2017)
Cyclic imides are a group of compounds which have valuable biological properties including cytotoxic, anti-inflammatory, antibacterial and antifungal activities. In this study, succinic and phthalic anhydrides were treated with glycinamide in pyridin
Externí odkaz:
https://doaj.org/article/918c70a929724772bf185974a3ad2342
Publikováno v:
Research in Pharmaceutical Sciences, Vol 11, Iss 6, Pp 445-453 (2016)
In the current study, both ligand-based molecular docking and receptor-based quantitative structure activity relationships (QSAR) modeling were performed on 35 diaryl urea derivative inhibitors of V600E B-RAF. In this QSAR study, a linear (multiple l
Externí odkaz:
https://doaj.org/article/2c4a25513d3a46beb7c000632b78136e