Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maedeh, Sherafati"'
Autor:
Behnam, Tahmasebi, Aida, Iraji, Maedeh, Sherafati, Ali, Moazzam, Seyed Alireza, Akhlagh, Mehdi, Adib, Mohammad, Mahdavi
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-10
A new series of ciprofloxacin-derived Ugi adducts were rationally designed and synthesized. The synthesized molecules were explored for their potential antimicrobial activities against four pathogenic microorganisms. Among these derivatives, compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea6ed4db45ed008284e5a593cbd9cb58
https://doi.org/10.1080/07391102.2022.2130985
https://doi.org/10.1080/07391102.2022.2130985
Autor:
Haleh Hamedifar, Maryam Mohammadi‐Khanaposhtani, Maedeh Sherafati, Milad Noori, Ali Moazam, Samanesadat Hosseini, Bagher Larijani, Mir H. Hajimiri, Mohammad Mahdavi, Mehmet K. Erdogan, Ramazan Gundogdu, Mahinur Kirici, Parham Taslimi, İlhami Gülçin
Publikováno v:
Archiv der Pharmazie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::040f7c062cf4e5db86406dfcf4aaa6df
https://doi.org/10.1002/ardp.202200571
https://doi.org/10.1002/ardp.202200571
Autor:
Mir Hamed Hajimiri, Mohammad Mahdavi, Haleh Hamedifar, Mohammad Ali Faramarzi, Maedeh Sherafati, Shahram Moradi, Nadia Najafabadipour, Mohammad Sadegh Asgari, Mahmood Biglar, Bagher Larijani, Maryam Mohammadi-Khanaposhtani
Publikováno v:
Chemical Papers. 74:4379-4388
We have designed and synthesized phthalimide-Schiff base-coumarin hybrids 8a–b, 9a–d, 10a–b, and 11a–d and evaluated them for α-glucosidase inhibitory potential against yeast form of this enzyme. For the synthesis of title compounds 4-hydrox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::039cece2827ea55d9dbdd64bd618eb30
https://doi.org/10.1007/s11696-020-01246-7
https://doi.org/10.1007/s11696-020-01246-7
Autor:
Maryam Mohammadi-Khanaposhtani, Hossein Rastegar, İlhami Gülçin, Parham Taslimi, Maedeh Sherafati, Keyvan Pedrood, Ebrahim Barzegari, Bagher Larijani, Roghieh Mirzazadeh, Hojjat Rahmani, Mohammad Sadegh Asgari, Mohammad Mahdavi, Eda M. Üç
Publikováno v:
ARCHIV DER PHARMAZIE
A new series of quinoxalin-1,3,4-oxadiazole (10a-l) derivatives was synthesized and evaluated against some metabolic enzymes including human carbonic anhydrase (hCA) isoenzymes I and II (carbonic anhydrases I and II), cholinesterase (acetylcholineste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::450b2f71b31186dfe570d183f88ac0b8
https://pubmed.ncbi.nlm.nih.gov/33999440
https://pubmed.ncbi.nlm.nih.gov/33999440
Autor:
Somayeh Mojtabavi, Homa Azizian, Ebrahim Barzegari, Hossein Rastegar, Roghieh Mirzazadeh, Mohammad Sadegh Asgari, Samanesadat Hosseini, Maedeh Sherafati, Mohammad Mahdavi, Ebrahim Zabihi, Mohammad Ali Faramarzi, Bagher Larijani, Maryam Mohammadi-Khanaposhtani, Mir Hamed Hajimiri, Haleh Hamedifar
Publikováno v:
Bioorganic chemistry. 109
A series of new quinazolinone-dihydropyrano[3,2-b]pyran derivatives 10A-L were synthesized by simple chemical reactions and were investigated for inhibitory activities against α-glucosidase and α-amylase. New synthesized compounds showed high α-gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df5e581649122da5ae6b37792cfca2b1
https://pubmed.ncbi.nlm.nih.gov/33609917
https://pubmed.ncbi.nlm.nih.gov/33609917