Results 111 to 120 of about 1,117 (151)
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ESKAPE Pathogens: Structure-Activity Relationships of 24-Diarylquinolines
2021Drug resistance by persisters is a global issue that requires urgent attention. Quinolines and quinolones have proven to be important cores in several bioactive organic chemotypes, based on this, the antimicrobial activity of six derivatives of 2,4-diarylquinolines was evaluated using the disc diffusion method at 5-20 µM/mL.
K. A. Oluwafemi
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Diarylquinolines target subunit c of mycobacterial ATP synthase
Nature Chemical Biology, 2007The diarylquinoline R207910 (TMC207) is a promising candidate in clinical development for the treatment of tuberculosis. Though R207910-resistant mycobacteria bear mutations in ATP synthase, the compound's precise target is not known. Here we establish by genetic, biochemical and binding assays that the oligomeric subunit c (AtpE) of ATP synthase is ...
Koul, Anil +11 more
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Tetrahedron Letters, 2018
MeOTf-induced one-pot method for the synthesis of a series of 4-methoxylquinolones has been descripted. This route provides a practical and convenient method for the synthesis of 4-methoxylquinolones from readily available starting materials under metal ...
Chanjuan Xi
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MeOTf-induced one-pot method for the synthesis of a series of 4-methoxylquinolones has been descripted. This route provides a practical and convenient method for the synthesis of 4-methoxylquinolones from readily available starting materials under metal ...
Chanjuan Xi
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Synthesis of 2,3-Diarylquinolines via Trapping of the Vinyl Metal Intermediate
Synfacts, 2018P. Knochel, Dorothée S. Ziegler
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SmI2-mediated facile one-pot preparation of 2,4-diarylquinolines from 3-aryl-2,1-benzisoxazoles
Tetrahedron Letters, 2002Xuesen Fan, Yongmin Zhang
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Journal of the Chemical Society Perkin Transactions 1, 1983
Takehiko Nishio, Yoshimori Omote
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Takehiko Nishio, Yoshimori Omote
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Synthesis and antiproliferative evaluation of 2,3-diarylquinoline derivatives
Organic & Biomolecular Chemistry, 2011A number of 2,3-diarylquinoline derivatives were synthesized and evaluated for antiproliferative activities against the growth of six cancer cell lines including human hepatocellular carcinoma (Hep G2 and Hep 3B), non-small cell lung cancer (A549 and H1299), and breast cancer (MCF-7 and MDA-MB-231) cell lines.
Chih-Hua, Tseng +6 more
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