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Anticancer Activity of Region B Capsaicin Analogs

[Image: see text] The heterocyclic vanilloid compound capsaicin is responsible for the spicy and pungent flavor of chili peppers. Several convergent studies have shown that capsaicin suppresses the growth of multiple human cancers. Apart from capsaicin, natural and synthetic capsaicin-like compounds...

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Autores principales: Brown, Kathleen C., Modi, Kushal J., Light, Reagan S., Cox, Ashley J., Long, Timothy E., Gadepalli, Rama S., Rimoldi, John M., Miles, Sarah L., Rankin, Gary, Valentovic, Monica, Denning, Krista L., Tirona, Maria T., Finch, Paul T., Hess, Joshua A., Dasgupta, Piyali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108357/
https://www.ncbi.nlm.nih.gov/pubmed/37000154
http://dx.doi.org/10.1021/acs.jmedchem.2c01594
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author Brown, Kathleen C.
Modi, Kushal J.
Light, Reagan S.
Cox, Ashley J.
Long, Timothy E.
Gadepalli, Rama S.
Rimoldi, John M.
Miles, Sarah L.
Rankin, Gary
Valentovic, Monica
Denning, Krista L.
Tirona, Maria T.
Finch, Paul T.
Hess, Joshua A.
Dasgupta, Piyali
author_facet Brown, Kathleen C.
Modi, Kushal J.
Light, Reagan S.
Cox, Ashley J.
Long, Timothy E.
Gadepalli, Rama S.
Rimoldi, John M.
Miles, Sarah L.
Rankin, Gary
Valentovic, Monica
Denning, Krista L.
Tirona, Maria T.
Finch, Paul T.
Hess, Joshua A.
Dasgupta, Piyali
author_sort Brown, Kathleen C.
collection PubMed
description [Image: see text] The heterocyclic vanilloid compound capsaicin is responsible for the spicy and pungent flavor of chili peppers. Several convergent studies have shown that capsaicin suppresses the growth of multiple human cancers. Apart from capsaicin, natural and synthetic capsaicin-like compounds display growth suppressive activity in human cancers. The pharmacophore of capsaicin is comprised of three regions, namely region A (the aromatic ring), region B (the amide bond), and region C (the side chain). The present manuscript describes the isolation and synthesis of capsaicin analogs which have structural modifications in region B of the molecule. Furthermore, the pharmacokinetic properties, anticancer activity of region B capsaicin analogs, as well as the signaling pathways (underlying the growth-inhibitory effects of region B capsaicin analogs) have also been described. The discovery of novel, second-generation region B capsaicin analogs may foster the hope of innovative nutrition-based combination therapies in human cancers.
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spelling pubmed-101083572023-04-18 Anticancer Activity of Region B Capsaicin Analogs Brown, Kathleen C. Modi, Kushal J. Light, Reagan S. Cox, Ashley J. Long, Timothy E. Gadepalli, Rama S. Rimoldi, John M. Miles, Sarah L. Rankin, Gary Valentovic, Monica Denning, Krista L. Tirona, Maria T. Finch, Paul T. Hess, Joshua A. Dasgupta, Piyali J Med Chem [Image: see text] The heterocyclic vanilloid compound capsaicin is responsible for the spicy and pungent flavor of chili peppers. Several convergent studies have shown that capsaicin suppresses the growth of multiple human cancers. Apart from capsaicin, natural and synthetic capsaicin-like compounds display growth suppressive activity in human cancers. The pharmacophore of capsaicin is comprised of three regions, namely region A (the aromatic ring), region B (the amide bond), and region C (the side chain). The present manuscript describes the isolation and synthesis of capsaicin analogs which have structural modifications in region B of the molecule. Furthermore, the pharmacokinetic properties, anticancer activity of region B capsaicin analogs, as well as the signaling pathways (underlying the growth-inhibitory effects of region B capsaicin analogs) have also been described. The discovery of novel, second-generation region B capsaicin analogs may foster the hope of innovative nutrition-based combination therapies in human cancers. American Chemical Society 2023-03-31 /pmc/articles/PMC10108357/ /pubmed/37000154 http://dx.doi.org/10.1021/acs.jmedchem.2c01594 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brown, Kathleen C.
Modi, Kushal J.
Light, Reagan S.
Cox, Ashley J.
Long, Timothy E.
Gadepalli, Rama S.
Rimoldi, John M.
Miles, Sarah L.
Rankin, Gary
Valentovic, Monica
Denning, Krista L.
Tirona, Maria T.
Finch, Paul T.
Hess, Joshua A.
Dasgupta, Piyali
Anticancer Activity of Region B Capsaicin Analogs
title Anticancer Activity of Region B Capsaicin Analogs
title_full Anticancer Activity of Region B Capsaicin Analogs
title_fullStr Anticancer Activity of Region B Capsaicin Analogs
title_full_unstemmed Anticancer Activity of Region B Capsaicin Analogs
title_short Anticancer Activity of Region B Capsaicin Analogs
title_sort anticancer activity of region b capsaicin analogs
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108357/
https://www.ncbi.nlm.nih.gov/pubmed/37000154
http://dx.doi.org/10.1021/acs.jmedchem.2c01594
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