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pro vyhledávání: '"M. Abdullah Alagoz"'
Autor:
Derya Aktas Anil, M. Fatih Polat, Ruya Saglamtas, Ayse H. Tarikogullari, M. Abdullah Alagoz, Ilhami Gulcin, Oztekin Algul, Serdar Burmaoglu
Enzyme inhibition is a very active area of research in drug design and development. Chalcone derivatives have a broad enzyme inhibitory activity and function as potential molecules in the development of new drugs. In this study, the synthesized novel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36c5aba484208c0a9195d9e91e6614ab
https://hdl.handle.net/11454/76484
https://hdl.handle.net/11454/76484
Akademický článek
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Autor:
Erhan Tek, M. Abdullah Alagoz, Funda Cimen, Baris Anil, Derya Aktaş, Oztekin Algul, Serdar Burmaoglu, Emrah Ay, M. Fatih Polat, Nizami Duran
Publikováno v:
International Journal of Clinical Practice
Aims Flavonoids and related compounds, such as quercetin‐based antiviral drug Gene‐Eden‐VIR/Novirin, inhibit the protease of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). The alkylated chalcones isolated from Angelica keiske
Autor:
Nizami Duran, M. Fatih Polat, Derya Anil Aktas, M. Abdullah Alagoz, Emrah Ay, Funda Cimen, Erhan Tek, Baris Anil, Serdar Burmaoglu, Oztekin Algul
Flavonoids and related compounds, such as quercetin-based antiviral drug Gene-Eden-VIR/Novirin, inhibit the protease of severe acute respiratory syndrome coronavirus (SARS-CoV-2). The alkylated chalcones isolated from Angelica keiskei inhibit SARS-Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::354e88ea4974e96daf8a7b670c21af2c
https://doi.org/10.21203/rs.3.rs-515050/v1
https://doi.org/10.21203/rs.3.rs-515050/v1