Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Murat Bingül"'
Autor:
Zehra Arslan, Murat Bingül
Publikováno v:
Journal of Ata-Chem, Vol 1, Iss 1, Pp 38-51 (2021)
Kumarinler (2H-1-benzopiran-2-on) ve izokumarinler (1H-2-benzopiran-1-on), çoğunlukla bitkilerde ve mikroorganizmalarda bulunan doğal olarak oluşan biyolojik aktif bileşiklerdir. Çok sayıda kumarin ve izokumarin türevi, farklı mekanizmalar y
Externí odkaz:
https://doaj.org/article/b19e04adf0d34c38bb0ccb86cf10e4cd
Autor:
Murat Bingul, Greg M. Arndt, Glenn M. Marshall, David StC. Black, Belamy B. Cheung, Naresh Kumar
Publikováno v:
Molecules, Vol 26, Iss 19, p 5745 (2021)
The dihydropyranoindole structures were previously identified as promising scaffolds for improving the anti-cancer activity of histone deacetylase inhibitors. This work describes the synthesis of related furoindoles and their ability to synergize wit
Externí odkaz:
https://doaj.org/article/5ac922c7d9514cd0856e8892e2cfc186
Autor:
Salih Pasa, Safa Aydın, Sadık Kalaycı, Mehmet Boğa, Metin Atlan, Murat Bingul, Fikrettin Şahin, Hamdi Temel
Publikováno v:
Journal of Pharmaceutical Analysis, Vol 6, Iss 1, Pp 39-48 (2016)
Boronic acid compounds with different substituted groups were handled to synthesize various ligands encoded as B1, B2, B3, B4, B5, B6, B7 and B8. B5 and B7 were tested for the cytotoxic activity against the prostate cancer cells and it was found that
Externí odkaz:
https://doaj.org/article/905c4b6f94c64d26b32085112c94b838
Autor:
Murat Bingul, Greg M. Arndt, Glenn M. Marshall, Belamy B. Cheung, Naresh Kumar, David StC. Black
Publikováno v:
Molecules, Vol 25, Iss 6, p 1377 (2020)
The dihydropyranoindole scaffold was identified as a promising target for improving the anti-cancer activity of HDAC inhibitors from the preliminary screening of a library of compounds. A suitable methodology has been developed for the preparation of
Externí odkaz:
https://doaj.org/article/b37062249de3454b8a469b8df3be0707
Autor:
Murat Bingul, Owen Tan, Christopher R. Gardner, Selina K. Sutton, Greg M. Arndt, Glenn M. Marshall, Belamy B. Cheung, Naresh Kumar, David StC. Black
Publikováno v:
Molecules, Vol 21, Iss 7, p 916 (2016)
Identification of the novel (E)-N′-((2-chloro-7-methoxyquinolin-3-yl)methylene)-3-(phenylthio)propanehydrazide scaffold 18 has led to the development of a new series of biologically active hydrazide compounds. The parent compound 18 and new quinoli
Externí odkaz:
https://doaj.org/article/333f7a73b761430e8ecd8b6a2dc991e6