Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/90921
Title: Spiro-Lactams as Novel Antimicrobial Agents
Authors: Alves, Américo J S
Alves, Nuno G
Caratão, Cátia C
Esteves, Margarida I M
Fontinha, Diana
Bártolo, Inês
Soares, Maria I L 
Lopes, Susana M M 
Prudêncio, Miguel 
Taveira, Nuno
Melo, Teresa M V D Pinho e 
Keywords: 5-Oxohexahydropyrrolo[2,1-b]thiazoles; Anti-HIV Agents; Antiplasmodial Agents; Diazo Compounds; Dipolar Cycloaddition; Spiro-penicillanate; Spiro-γ-lactams
Issue Date: 2020
Publisher: Bentham Science
Project: UID/QUI/00313/2019 
SFRH/BD/128910/2017 
PD/BD/135287/2017 
PTDC-SAU-INF-29550-2017 
Serial title, monograph or event: Current Topics in Medicinal Chemistry
Volume: 20
Issue: 2
Abstract: Introduction: Structural modulation of previously identified lead spiro-β-lactams with antimicrobial activity was carried out. Objective: The main objective of this work was to synthesize and evaluate the biological activity of novel spiro-lactams based on previously identified lead compounds with antimicrobial activity. Methods: The target chiral spiro-γ-lactams were synthesized through 1,3-dipolar cycloaddition reaction of a diazo-γ-lactam with electron-deficient dipolarophiles. In vitro activity against HIV and Plasmodium of a wide range of spiro-β-lactams and spiro-γ-lactams was evaluated. Among these compounds, one derivative with good anti-HIV activity and two with promising antiplasmodial activity (IC50 < 3.5 µM) were identified. Results: A novel synthetic route to chiral spiro-γ-lactams has been established. The studied β- and γ- lactams were not cytotoxic, and three compounds with promising antimicrobial activity were identified, whose structural modulation may lead to new and more potent drugs. Conclusion: The designed structural modulation of biologically active spiro-β-lactams involved the replacement of the four-membered β-lactam ring by a five-membered γ-lactam ring. Although conformational and superimposition computational studies revealed no significant differences between β- and γ- lactam pharmacophoric features, the studied structural modulation did not lead to compounds with a similar biological profile. The observed results suggest that the β-lactamic core is a requirement for the activity against both HIV and Plasmodium.
URI: http://hdl.handle.net/10316/90921
ISSN: 15680266
DOI: 10.2174/1568026619666191105110049
Rights: embargoedAccess
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais

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