Synthesis of novel 6,7-dimethoxy-4-anilinoquinolines as potent c-Met inhibitors
HGF/c-Met signalling pathway plays an important role in the development of cancers. A series of 6,7-dimethoxy-4-anilinoquinolines possessing benzimidazole moiety were synthesised and identified as potent inhibitors of the tyrosine kinase c-Met. Their in vitro biological activities against three canc...
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| Main Authors: | , , , , , |
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| Format: | Book |
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Taylor & Francis Group,
2019-01-01T00:00:00Z.
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| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | doaj_e8f8ac4c13f44fe3b1297cbbd50bae5c | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Qing-Wen Zhang |e author |
| 700 | 1 | 0 | |a Zi-Dan Ye |e author |
| 700 | 1 | 0 | |a Chang Shen |e author |
| 700 | 1 | 0 | |a Hong-Xia Tie |e author |
| 700 | 1 | 0 | |a Lei Wang |e author |
| 700 | 1 | 0 | |a Lei Shi |e author |
| 245 | 0 | 0 | |a Synthesis of novel 6,7-dimethoxy-4-anilinoquinolines as potent c-Met inhibitors |
| 260 | |b Taylor & Francis Group, |c 2019-01-01T00:00:00Z. | ||
| 500 | |a 1475-6366 | ||
| 500 | |a 1475-6374 | ||
| 500 | |a 10.1080/14756366.2018.1533822 | ||
| 520 | |a HGF/c-Met signalling pathway plays an important role in the development of cancers. A series of 6,7-dimethoxy-4-anilinoquinolines possessing benzimidazole moiety were synthesised and identified as potent inhibitors of the tyrosine kinase c-Met. Their in vitro biological activities against three cancer cell lines (A549, MCF-7, and MKN-45) were also evaluated. Most of these compounds exhibited moderate to remarkable potency. Among them, compound 12n showed the most potent inhibitory activity against c-Met with IC50 value of 0.030 ± 0.008 µM and it also showed excellent anticancer activity against the tested cancer cell lines at low micromolar concentration. Molecular docking verified the results and revealed the possible binding mode of the most promising compound 12n into the ATP-binding site of c-Met kinase. | ||
| 546 | |a EN | ||
| 690 | |a c-met | ||
| 690 | |a inhibitor | ||
| 690 | |a 6,7-dimethoxy-4-anilinoquinoline | ||
| 690 | |a synthesis | ||
| 690 | |a antitumour | ||
| 690 | |a Therapeutics. Pharmacology | ||
| 690 | |a RM1-950 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 124-133 (2019) | |
| 787 | 0 | |n http://dx.doi.org/10.1080/14756366.2018.1533822 | |
| 787 | 0 | |n https://doaj.org/toc/1475-6366 | |
| 787 | 0 | |n https://doaj.org/toc/1475-6374 | |
| 856 | 4 | 1 | |u https://doaj.org/article/e8f8ac4c13f44fe3b1297cbbd50bae5c |z Connect to this object online. |