Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Murat Bingul"'
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
Publikováno v:
Polycyclic Aromatic Compounds. :1-22
Chemically and biologically important -C = N-N = C- diimine linkage was used to build unsymmetrical azine systems with indole heterocyclic backbone and substituted aromatic carbaldehydes. Ten novel compounds 7a-j were synthesized by the Schiff base r
Autor:
Şebnem Abadan, Mehmet F. Saglam, Mehmet Serdar Koca, Murat Bingul, Hasan Sahin, Yunus Zorlu, Ibrahim F. Sengul
Publikováno v:
Journal of Molecular Structure. 1278:134954
Autor:
Murat Bingul
Publikováno v:
Journal of Chemical Research. 43:399-406
Two sets of novel indole-based thiosemicarbazone systems 8a–d and 9a–d are prepared by the Schiff base condensation reaction of indole carbaldehydes 4 and 6 with a range of thiosemicarbazides 7a–d in high yields and purity. The antioxidant prop
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 150:1553-1560
A range of novel 4,6-dimethoxy-1H-indole-2-carbohydrazides was prepared starting from methyl 4,6-dimethoxy-1H-indole-2-carboxylate which underwent cyclodehydration to generate the corresponding 2-(indol-2-yl)-1,3,4-oxadiazole scaffolds in the presenc
Autor:
Murat Bingul, Elif Şenkuytu, Ibrahim F. Sengul, Hakan Kandemir, Mehmet F. Saglam, Mehmet Boga
Publikováno v:
Research on Chemical Intermediates. 45:4487-4499
Utilizing Schiff base condensation of the 9-ethylcarbazole-3,6-dicarbaldehyde and thiosemicarbazides, four new N-ethylcarbazole-based bis-thiosemicarbazone compounds 4a–d were successfully synthesized in high yields. The photophysical properties of
Autor:
Glenn M. Marshall, Naresh Kumar, David StC. Black, Murat Bingul, Greg M. Arndt, Belamy B. Cheung
Publikováno v:
Molecules, Vol 26, Iss 5745, p 5745 (2021)
Molecules
Volume 26
Issue 19
Molecules
Volume 26
Issue 19
PMID: 34641289 WOS:000708237400001 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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e24071947b04112551d7786538c175f
https://hdl.handle.net/11468/9387
https://hdl.handle.net/11468/9387