Novel Hybrids from Lamellarin D and Combretastatin A 4 As Cytotoxic Agents
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A new series of hybrids of lamellarin D and combretastatin A 4, 1,2-diphenyl-5,6-dihydropyrrolo [2,1-a] isoquinolines, were designed as cytotoxic agents based on principles of combination in medicinal chemistry and taking the parent compounds' different anti-proliferative mechanisms into consideration. Twenty-two novel hybrids were synthesized through a convenient route, with a key step of core pyrrole formation and evaluated for their anti-proliferative activities in vitro against K-562, A-549, SMMC-7721, SGC-7901 and HCT-116 cancer cell lines. The results showed that some hybrids had good anti-proliferative activities in low IC50 ranges.
Hybrid -stilbene Molecules: Novel Anticancer Agents.
Piekus-Slomka N, Mikstacka R, Ronowicz J, Sobiak S Int J Mol Sci. 2019; 20(6).
PMID: 30875859 PMC: 6471163. DOI: 10.3390/ijms20061300.
Design and Synthesis of Pyrrolo[2,1-a]Isoquinoline-Based Derivatives as New Cytotoxic Agents.
Kakhki S, Shahosseini S, Zarghi A Iran J Pharm Res. 2017; 15(4):743-751.
PMID: 28243270 PMC: 5316252.
Anticancer properties of lamellarins.
Bailly C Mar Drugs. 2015; 13(3):1105-23.
PMID: 25706633 PMC: 4377975. DOI: 10.3390/md13031105.
Synthesis of pyrrolo[2,1-a]isoquinolines by multicomponent 1,3-dipolar cycloaddition.
Dumitrascu F, Georgescu E, Georgescu F, Popa M, Dumitrescu D Molecules. 2013; 18(3):2635-45.
PMID: 23446920 PMC: 6270538. DOI: 10.3390/molecules18032635.
Chernyak D, Gevorgyan V Org Lett. 2010; 12(23):5558-60.
PMID: 21058673 PMC: 3131228. DOI: 10.1021/ol102447s.