Cargando…
Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation
Curcumin is a medicinal agent that exhibits anti-cancer properties and bioactive pigment in Turmeric has a huge therapeutic value. It has a keto-enol moiety that gives rise to many of its chemical properties. A recent study has shown that keto-enol tautomerisation at this moiety is implicated the ef...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109441/ https://www.ncbi.nlm.nih.gov/pubmed/29934731 http://dx.doi.org/10.1007/s13659-018-0170-1 |
_version_ | 1783350322463244288 |
---|---|
author | Manimaran, S. SambathKumar, K. Gayathri, R. Raja, K. Rajkamal, N. Venkatachalapathy, M. Ravichandran, G. Lourdu EdisonRaj, C. |
author_facet | Manimaran, S. SambathKumar, K. Gayathri, R. Raja, K. Rajkamal, N. Venkatachalapathy, M. Ravichandran, G. Lourdu EdisonRaj, C. |
author_sort | Manimaran, S. |
collection | PubMed |
description | Curcumin is a medicinal agent that exhibits anti-cancer properties and bioactive pigment in Turmeric has a huge therapeutic value. It has a keto-enol moiety that gives rise to many of its chemical properties. A recent study has shown that keto-enol tautomerisation at this moiety is implicated the effect of curcumin. The tautomerisation of curcumin in methanol, acetone and acetonitrile are used in nuclear magnetic resonance ((1)H, (13)C) spectroscopy. It was characterized using UV, IR and Raman spectral values. The molecular electrostatic potential surface of the Curcumin has been visualized in electropositive potential in the region of the CH(3+) group and most electronegative potential in the two oxygen atom has very strong binding group. In the following, the modality of structural and thermo dynamical parameters, electrophilicity (ω), chemical potential (μ), chemical hardness (η) and electronic charge transfer confirms the local reactivity. The rate constant of tautomerisation of curcumin shows strong temperature dependence. Molecular electrostatic potential and Temperature dependence of various thermodynamic properties like [Formula: see text] is increase with increase in temperature for monomer and dimer of various electrical fields. |
format | Online Article Text |
id | pubmed-6109441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-61094412018-09-05 Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation Manimaran, S. SambathKumar, K. Gayathri, R. Raja, K. Rajkamal, N. Venkatachalapathy, M. Ravichandran, G. Lourdu EdisonRaj, C. Nat Prod Bioprospect Original Article Curcumin is a medicinal agent that exhibits anti-cancer properties and bioactive pigment in Turmeric has a huge therapeutic value. It has a keto-enol moiety that gives rise to many of its chemical properties. A recent study has shown that keto-enol tautomerisation at this moiety is implicated the effect of curcumin. The tautomerisation of curcumin in methanol, acetone and acetonitrile are used in nuclear magnetic resonance ((1)H, (13)C) spectroscopy. It was characterized using UV, IR and Raman spectral values. The molecular electrostatic potential surface of the Curcumin has been visualized in electropositive potential in the region of the CH(3+) group and most electronegative potential in the two oxygen atom has very strong binding group. In the following, the modality of structural and thermo dynamical parameters, electrophilicity (ω), chemical potential (μ), chemical hardness (η) and electronic charge transfer confirms the local reactivity. The rate constant of tautomerisation of curcumin shows strong temperature dependence. Molecular electrostatic potential and Temperature dependence of various thermodynamic properties like [Formula: see text] is increase with increase in temperature for monomer and dimer of various electrical fields. Springer Singapore 2018-06-22 /pmc/articles/PMC6109441/ /pubmed/29934731 http://dx.doi.org/10.1007/s13659-018-0170-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Manimaran, S. SambathKumar, K. Gayathri, R. Raja, K. Rajkamal, N. Venkatachalapathy, M. Ravichandran, G. Lourdu EdisonRaj, C. Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation |
title | Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation |
title_full | Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation |
title_fullStr | Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation |
title_full_unstemmed | Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation |
title_short | Medicinal Plant Using Ground State Stabilization of Natural Antioxidant Curcumin by Keto-Enol Tautomerisation |
title_sort | medicinal plant using ground state stabilization of natural antioxidant curcumin by keto-enol tautomerisation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109441/ https://www.ncbi.nlm.nih.gov/pubmed/29934731 http://dx.doi.org/10.1007/s13659-018-0170-1 |
work_keys_str_mv | AT manimarans medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT sambathkumark medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT gayathrir medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT rajak medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT rajkamaln medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT venkatachalapathym medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT ravichandrang medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation AT lourduedisonrajc medicinalplantusinggroundstatestabilizationofnaturalantioxidantcurcuminbyketoenoltautomerisation |