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Novel Adamantane-Linked Isothiourea Derivatives as Potential Chemotherapeutic Agents: Synthesis, Structural Insights, and Antimicrobial/Anti-Proliferative Profiles
[Image: see text] In this study, two adamantane-linked isothiourea derivatives containing a common 4-chlorophenyl substituent coupled with 4-nitrobenzyl or 4-bromobenzyl moieties were synthesized. Both derivatives were characterized, in the solid state and in solution, through a synergistic combinat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099428/ https://www.ncbi.nlm.nih.gov/pubmed/37065023 http://dx.doi.org/10.1021/acsomega.3c01469 |
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author | Al-Omary, Fatmah A. M. Alvarez, Natalia Al-Rasheed, Lamees S. Veiga, Nicolás Hassan, Hanan M. El-Emam, Ali A. |
author_facet | Al-Omary, Fatmah A. M. Alvarez, Natalia Al-Rasheed, Lamees S. Veiga, Nicolás Hassan, Hanan M. El-Emam, Ali A. |
author_sort | Al-Omary, Fatmah A. M. |
collection | PubMed |
description | [Image: see text] In this study, two adamantane-linked isothiourea derivatives containing a common 4-chlorophenyl substituent coupled with 4-nitrobenzyl or 4-bromobenzyl moieties were synthesized. Both derivatives were characterized, in the solid state and in solution, through a synergistic combination of experimental and in silico techniques, and the results are of great value for the chemical and structural characterization of related compounds. The crystal structures of both derivatives were analyzed in depth, including Hirshfeld surface analysis and lattice energy calculations, revealing a predominant dispersive component of the total energy that stabilizes crystal packing. Both compounds showed potent broad-spectrum antibacterial activity and moderate activity against the pathogenic fungus Candida albicans. In addition, in vitro anti-proliferative activity assays showed that the 4-bromobenzyl analogue displays higher activity than the 4-nitrobenzyl one, with IC(50) values under 30 μM against five human cancer cell lines. Our results give evidence of the potential of the adamantane/isothiourea combination to render auspicious scaffolds for new potential chemotherapeutic agents. |
format | Online Article Text |
id | pubmed-10099428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100994282023-04-14 Novel Adamantane-Linked Isothiourea Derivatives as Potential Chemotherapeutic Agents: Synthesis, Structural Insights, and Antimicrobial/Anti-Proliferative Profiles Al-Omary, Fatmah A. M. Alvarez, Natalia Al-Rasheed, Lamees S. Veiga, Nicolás Hassan, Hanan M. El-Emam, Ali A. ACS Omega [Image: see text] In this study, two adamantane-linked isothiourea derivatives containing a common 4-chlorophenyl substituent coupled with 4-nitrobenzyl or 4-bromobenzyl moieties were synthesized. Both derivatives were characterized, in the solid state and in solution, through a synergistic combination of experimental and in silico techniques, and the results are of great value for the chemical and structural characterization of related compounds. The crystal structures of both derivatives were analyzed in depth, including Hirshfeld surface analysis and lattice energy calculations, revealing a predominant dispersive component of the total energy that stabilizes crystal packing. Both compounds showed potent broad-spectrum antibacterial activity and moderate activity against the pathogenic fungus Candida albicans. In addition, in vitro anti-proliferative activity assays showed that the 4-bromobenzyl analogue displays higher activity than the 4-nitrobenzyl one, with IC(50) values under 30 μM against five human cancer cell lines. Our results give evidence of the potential of the adamantane/isothiourea combination to render auspicious scaffolds for new potential chemotherapeutic agents. American Chemical Society 2023-03-30 /pmc/articles/PMC10099428/ /pubmed/37065023 http://dx.doi.org/10.1021/acsomega.3c01469 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Al-Omary, Fatmah A. M. Alvarez, Natalia Al-Rasheed, Lamees S. Veiga, Nicolás Hassan, Hanan M. El-Emam, Ali A. Novel Adamantane-Linked Isothiourea Derivatives as Potential Chemotherapeutic Agents: Synthesis, Structural Insights, and Antimicrobial/Anti-Proliferative Profiles |
title | Novel Adamantane-Linked Isothiourea Derivatives as
Potential Chemotherapeutic Agents: Synthesis, Structural Insights,
and Antimicrobial/Anti-Proliferative Profiles |
title_full | Novel Adamantane-Linked Isothiourea Derivatives as
Potential Chemotherapeutic Agents: Synthesis, Structural Insights,
and Antimicrobial/Anti-Proliferative Profiles |
title_fullStr | Novel Adamantane-Linked Isothiourea Derivatives as
Potential Chemotherapeutic Agents: Synthesis, Structural Insights,
and Antimicrobial/Anti-Proliferative Profiles |
title_full_unstemmed | Novel Adamantane-Linked Isothiourea Derivatives as
Potential Chemotherapeutic Agents: Synthesis, Structural Insights,
and Antimicrobial/Anti-Proliferative Profiles |
title_short | Novel Adamantane-Linked Isothiourea Derivatives as
Potential Chemotherapeutic Agents: Synthesis, Structural Insights,
and Antimicrobial/Anti-Proliferative Profiles |
title_sort | novel adamantane-linked isothiourea derivatives as
potential chemotherapeutic agents: synthesis, structural insights,
and antimicrobial/anti-proliferative profiles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099428/ https://www.ncbi.nlm.nih.gov/pubmed/37065023 http://dx.doi.org/10.1021/acsomega.3c01469 |
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