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Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review
Carbazoles represent an important class of heterocycles. These have been reported to exhibit diverse biological activities such as antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidative, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective and pancreatic lipase inhibition pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332089/ https://www.ncbi.nlm.nih.gov/pubmed/26213906 http://dx.doi.org/10.3390/molecules200813496 |
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author | Bashir, Maryam Bano, Afifa Ijaz, Abdul Subhan Chaudhary, Bashir Ahmad |
author_facet | Bashir, Maryam Bano, Afifa Ijaz, Abdul Subhan Chaudhary, Bashir Ahmad |
author_sort | Bashir, Maryam |
collection | PubMed |
description | Carbazoles represent an important class of heterocycles. These have been reported to exhibit diverse biological activities such as antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidative, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective and pancreatic lipase inhibition properties. A series of carbazole derivatives such as N-substituted carbazoles, benzocarbazoles, furocarbazoles, pyrrolocarbazoles, indolocarbazoles, imidazocarbazoles, etc. have been synthesized. The N-substituted derivatives have gained the attention of researchers due to their therapeutic potential against neurological disorders and cell proliferation. Herein an attempt is made to review the medicinal importance of recently synthesized N-substituted carbazoles. |
format | Online Article Text |
id | pubmed-6332089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63320892019-01-24 Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review Bashir, Maryam Bano, Afifa Ijaz, Abdul Subhan Chaudhary, Bashir Ahmad Molecules Review Carbazoles represent an important class of heterocycles. These have been reported to exhibit diverse biological activities such as antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidative, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective and pancreatic lipase inhibition properties. A series of carbazole derivatives such as N-substituted carbazoles, benzocarbazoles, furocarbazoles, pyrrolocarbazoles, indolocarbazoles, imidazocarbazoles, etc. have been synthesized. The N-substituted derivatives have gained the attention of researchers due to their therapeutic potential against neurological disorders and cell proliferation. Herein an attempt is made to review the medicinal importance of recently synthesized N-substituted carbazoles. MDPI 2015-07-23 /pmc/articles/PMC6332089/ /pubmed/26213906 http://dx.doi.org/10.3390/molecules200813496 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bashir, Maryam Bano, Afifa Ijaz, Abdul Subhan Chaudhary, Bashir Ahmad Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review |
title | Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review |
title_full | Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review |
title_fullStr | Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review |
title_full_unstemmed | Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review |
title_short | Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review |
title_sort | recent developments and biological activities of n-substituted carbazole derivatives: a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332089/ https://www.ncbi.nlm.nih.gov/pubmed/26213906 http://dx.doi.org/10.3390/molecules200813496 |
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