A Focused Library of NO-Donor Compounds with Potent Antiproliferative Activity Based on Green Multicomponent Reactions
Cancer is the second leading cause of death worldwide. Herein, a strategy to quickly and efficiently identify novel lead compounds to develop anticancer agents, using green multicomponent reactions followed by antiproliferative activity and structure–activity relationship studies, is described. A second-generation focused library of nitric oxide-releasing compounds was prepared by microwave-assisted Passerini and Ugi reactions. Nearly all compounds displayed potent antiproliferative activities against a panel of human solid tumor cell lines, with 1-phenyl-1-[(tert-butylamino)carbonyl]methyl 3-[(3-phenylsulfonyl-[1,2,5]oxadiazol-4-yl N-oxide)oxy]benzoate (4 k) and N-[1-(tert-butylaminocarbonyl)-1-phenylmethyl]-N-(4-methylphenyl)-3-(3-phenylsulfonyl-[1,2,5]oxadiazol-4-yl N-oxide)oxyphenyl carboxamide (6 d) exhibiting the strongest activity on SW1573 lung cell line (GI=110 and 21 nm) with selectivity indices of 70 and 470, respectively. Preliminary mechanistic studies suggest a relationship between NO release and antiproliferative activity. Our strategy allowed the rapid identification of at least two molecules as future candidates for the development of potent antitumor drugs.
Main Authors: | Ingold, Marina, Colella, Lucía, Hernández, Paola, Batthyány, Carlos, Tejedor, David, Puerta, Adrian, García-Tellado, Fernando, Padrón, José M., Porcal, Williams, López, Gloria V. |
---|---|
Other Authors: | Agencia Nacional de Investigación e Innovación (Uruguay) |
Format: | artículo biblioteca |
Published: |
Wiley-VCH
2019-09-18
|
Subjects: | Green chemistry, Solvent-free, Multicomponent reactions, Microwave-assisted synthesis, Antiproliferative agents, |
Online Access: | http://hdl.handle.net/10261/193160 http://dx.doi.org/10.13039/100008725 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A green multicomponent synthesis of tocopherol analogues with antiproliferative activities
by: Ingold, Mariana, et al.
Published: (2018-01-01) -
A substrate-based folding process incorporating chemodifferentiating ABB' three-component reactions of terminal alkynoates and 1,2-dicarbonyl compounds: a skeletal-diversity-oriented synthetic manifold
by: Tejedor, David, et al.
Published: (2007-01-22) -
Combined Ugi-4CR/CuAAC approach to triazole-based neoglycolipids
by: Pérez-Labrada, Karell, et al.
Published: (2014-06) -
Multicomponent Ligation of Steroids: Creating Diversity at the Linkage Moiety of Bis-spirostanic Conjugates by Ugi Reactions
by: Pérez-Labrada, Karell, et al.
Published: (2013-04-10) -
Fluoride-Triggered Domino Reactions Involving Ammonium Acetylides and Carbonyl Compounds
by: Tejedor, David, et al.
Published: (2010-01)