2019
DOI: 10.1002/slct.201900114
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Regioselective Synthesis, Molecular Descriptors of (1,5‐Disubstituted 1,2,3‐Triazolyl)Coumarin/Quinolone Derivatives and Their Docking Studies against Cancer Targets

Abstract: A series of (1,5‐disubstituted 1,2,3‐triazolyl)coumarin/quinolone derivatives (tcd and tqd) have been synthesized in good to excellent yields via Ag2O NPs catalyzed azide‐alkyne cycloaddition reactions. We then tested the drug‐likeness of tcd and tqd by analyzing molecular descriptors. Rational drug design showed that these derivatives indeed are potential anticancer agents against tankyrases.

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Cited by 9 publications
(2 citation statements)
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References 74 publications
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“…Some other coumarin fused 1,2,3-triazole macrocycles were also developed and found to be active against cancer cells. 47–50 The most active hybrid 17 (Fig. 12) with IC 50 = 49 μM only showed moderate activity against the MCF-7 cancer cell line.…”
Section: Coumarin Hybridsmentioning
confidence: 99%
“…Some other coumarin fused 1,2,3-triazole macrocycles were also developed and found to be active against cancer cells. 47–50 The most active hybrid 17 (Fig. 12) with IC 50 = 49 μM only showed moderate activity against the MCF-7 cancer cell line.…”
Section: Coumarin Hybridsmentioning
confidence: 99%
“…Although various methods have been reported for preparing 1,2,3‐triazoles, 1,3‐dipolar Huisgen cycloaddition of azide‐alkyne, known as “click reaction”, in the presence of transition metal catalysts is the most effective and popular method for production of this class of materials. Various homogeneous and heterogeneous catalytic systems based on transition metal ions like Pd, Zn, Ru, Ag, etc . have been employed for production of 1,2,3‐triazoles.…”
Section: Introductionmentioning
confidence: 99%