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Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study

ABSTRACT: Phytochemical investigations of the ethanolic extract of leaves of Clutia lanceolata (Family: Euphorbiaceae) resulted in the isolation of four compounds viz. 3,4-dihydroxy-2-methylbenzoic acid (1), 2,2′-dihydroxy-1,1′-binaphthyl (2), 1,3,8-trihydroxy-6-methylanthracene-9,10-dione (3) and 5...

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Autores principales: Parveen, Mehtab, Ahmad, Faheem, Malla, Ali Mohammed, Azaz, Shaista, Alam, Mahboob, Basudan, Omer A., Silva, Manuela Ramos, Pereira Silva, Pedro S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136371/
https://www.ncbi.nlm.nih.gov/pubmed/27757926
http://dx.doi.org/10.1007/s13659-016-0110-x
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author Parveen, Mehtab
Ahmad, Faheem
Malla, Ali Mohammed
Azaz, Shaista
Alam, Mahboob
Basudan, Omer A.
Silva, Manuela Ramos
Pereira Silva, Pedro S.
author_facet Parveen, Mehtab
Ahmad, Faheem
Malla, Ali Mohammed
Azaz, Shaista
Alam, Mahboob
Basudan, Omer A.
Silva, Manuela Ramos
Pereira Silva, Pedro S.
author_sort Parveen, Mehtab
collection PubMed
description ABSTRACT: Phytochemical investigations of the ethanolic extract of leaves of Clutia lanceolata (Family: Euphorbiaceae) resulted in the isolation of four compounds viz. 3,4-dihydroxy-2-methylbenzoic acid (1), 2,2′-dihydroxy-1,1′-binaphthyl (2), 1,3,8-trihydroxy-6-methylanthracene-9,10-dione (3) and 5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trien-3-one (4). Although all the isolated compounds were known but this was the first report from this plant source. Their structures were established on the basis of chemical and physical evidences viz. elemental analysis, FT-IR, (1)H-NMR, (13)C-NMR and mass spectral analysis. Structure of compound 2 and 4 was further authenticated by single-crystal X-ray analysis and density functional theory calculations. The isolated compounds (1–4) were screened for AChE enzyme inhibition assay in which compound 3 and 4 were found to be more potent AChE inhibitor. Molecular docking study of potent AChE inhibitor was performed to find the probable binding mode of the compounds into the active site of receptor. Moreover, the isolated compounds were also screened for in vivo cytotoxicity by brine shrimp lethality assay. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13659-016-0110-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-51363712016-12-19 Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study Parveen, Mehtab Ahmad, Faheem Malla, Ali Mohammed Azaz, Shaista Alam, Mahboob Basudan, Omer A. Silva, Manuela Ramos Pereira Silva, Pedro S. Nat Prod Bioprospect Original Article ABSTRACT: Phytochemical investigations of the ethanolic extract of leaves of Clutia lanceolata (Family: Euphorbiaceae) resulted in the isolation of four compounds viz. 3,4-dihydroxy-2-methylbenzoic acid (1), 2,2′-dihydroxy-1,1′-binaphthyl (2), 1,3,8-trihydroxy-6-methylanthracene-9,10-dione (3) and 5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)hepta-1,4,6-trien-3-one (4). Although all the isolated compounds were known but this was the first report from this plant source. Their structures were established on the basis of chemical and physical evidences viz. elemental analysis, FT-IR, (1)H-NMR, (13)C-NMR and mass spectral analysis. Structure of compound 2 and 4 was further authenticated by single-crystal X-ray analysis and density functional theory calculations. The isolated compounds (1–4) were screened for AChE enzyme inhibition assay in which compound 3 and 4 were found to be more potent AChE inhibitor. Molecular docking study of potent AChE inhibitor was performed to find the probable binding mode of the compounds into the active site of receptor. Moreover, the isolated compounds were also screened for in vivo cytotoxicity by brine shrimp lethality assay. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13659-016-0110-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-10-18 /pmc/articles/PMC5136371/ /pubmed/27757926 http://dx.doi.org/10.1007/s13659-016-0110-x Text en © The Author(s) 2016 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
Parveen, Mehtab
Ahmad, Faheem
Malla, Ali Mohammed
Azaz, Shaista
Alam, Mahboob
Basudan, Omer A.
Silva, Manuela Ramos
Pereira Silva, Pedro S.
Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study
title Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study
title_full Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study
title_fullStr Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study
title_full_unstemmed Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study
title_short Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study
title_sort acetylcholinesterase and cytotoxic activity of chemical constituents of clutia lanceolata leaves and its molecular docking study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136371/
https://www.ncbi.nlm.nih.gov/pubmed/27757926
http://dx.doi.org/10.1007/s13659-016-0110-x
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