Abstract |
The global pandemic of drug-sensitive cancers and the increasing threat from drug-resistant cancers make an urgent need to develop more effective anti- cancer candidates. Quinolone derivatives possess promising anti- cancer activity, and some of them have already been approved to treat cancers or under clinical trials. Hybridization of quinolone with other anti- cancer pharmacophores may provide more efficient anti- cancer candidates, so quinolone hybrids worth to be investigated. In this review, the recent advances in the development of novel quinolone hybrids as potential anti- cancer agents are highlighted, and the structure-activity relationship is also discussed to provide an insight for further development of more active quinolone hybrids.
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Authors | Feng Gao, Xia Zhang, Tengfei Wang, Jiaqi Xiao |
Journal | European journal of medicinal chemistry
(Eur J Med Chem)
Vol. 165
Pg. 59-79
(Mar 01 2019)
ISSN: 1768-3254 [Electronic] France |
PMID | 30660827
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2019 Elsevier Masson SAS. All rights reserved. |
Chemical References |
- Antineoplastic Agents
- Quinolones
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Topics |
- Animals
- Antineoplastic Agents
(chemistry, pharmacology)
- Humans
- Neoplasms
(drug therapy)
- Quinolones
(chemistry, pharmacology, therapeutic use)
- Structure-Activity Relationship
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