Cargando…
Plumbagin analogs-synthesis, characterization, and antitubercular activity
Considering the emerging problem of drug resistance in tuberculosis, there is an urgent need of development of new analogs that are useful in curing drug resistant tuberculosis. In India, tuberculosis continues to remain one of the most pressing health problems. India is the highest tuberculosis bur...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960791/ https://www.ncbi.nlm.nih.gov/pubmed/24696815 http://dx.doi.org/10.4103/2231-4040.126984 |
_version_ | 1782308198292652032 |
---|---|
author | Nayak, Nishi Bajpai, Meenakshi Razdan, Balkishen |
author_facet | Nayak, Nishi Bajpai, Meenakshi Razdan, Balkishen |
author_sort | Nayak, Nishi |
collection | PubMed |
description | Considering the emerging problem of drug resistance in tuberculosis, there is an urgent need of development of new analogs that are useful in curing drug resistant tuberculosis. In India, tuberculosis continues to remain one of the most pressing health problems. India is the highest tuberculosis burden country in the world, accounting one fifth of global incidence - estimated 2.0-2.5 million cases annually. In 2011, approximately 8.7 million new cases of tuberculosis and 1.4 million people die from tuberculosis each year worldwide. Current antitubercular therapies are successful against normal tuberculosis but it is not suitable for drug resistant tuberculosis. In this study Plumbagin analogs, obtained from Plumbago zeylanica (Family-Plumbaginaceae), have been synthesized. Out of the various synthesized analogs, the antitubercular activity of compound a and b was evaluated using standard H(37)Rv and S, H, R, and E sensitive M tuberculosis strains using LRF assay method. Compound a showed strong activity against both standard H(37)Rv and S, H, R and E sensitive M. tuberculosis strains as compared to standard Rifampicin. The other compounds are proved to be more active against standard H(37)Rv and S, H, R and E sensitive M. tuberculosis strain as compared to Rifampicin. |
format | Online Article Text |
id | pubmed-3960791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39607912014-04-02 Plumbagin analogs-synthesis, characterization, and antitubercular activity Nayak, Nishi Bajpai, Meenakshi Razdan, Balkishen J Adv Pharm Technol Res Original Article Considering the emerging problem of drug resistance in tuberculosis, there is an urgent need of development of new analogs that are useful in curing drug resistant tuberculosis. In India, tuberculosis continues to remain one of the most pressing health problems. India is the highest tuberculosis burden country in the world, accounting one fifth of global incidence - estimated 2.0-2.5 million cases annually. In 2011, approximately 8.7 million new cases of tuberculosis and 1.4 million people die from tuberculosis each year worldwide. Current antitubercular therapies are successful against normal tuberculosis but it is not suitable for drug resistant tuberculosis. In this study Plumbagin analogs, obtained from Plumbago zeylanica (Family-Plumbaginaceae), have been synthesized. Out of the various synthesized analogs, the antitubercular activity of compound a and b was evaluated using standard H(37)Rv and S, H, R, and E sensitive M tuberculosis strains using LRF assay method. Compound a showed strong activity against both standard H(37)Rv and S, H, R and E sensitive M. tuberculosis strains as compared to standard Rifampicin. The other compounds are proved to be more active against standard H(37)Rv and S, H, R and E sensitive M. tuberculosis strain as compared to Rifampicin. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3960791/ /pubmed/24696815 http://dx.doi.org/10.4103/2231-4040.126984 Text en Copyright: © Journal of Advanced Pharmaceutical Technology & Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nayak, Nishi Bajpai, Meenakshi Razdan, Balkishen Plumbagin analogs-synthesis, characterization, and antitubercular activity |
title | Plumbagin analogs-synthesis, characterization, and antitubercular activity |
title_full | Plumbagin analogs-synthesis, characterization, and antitubercular activity |
title_fullStr | Plumbagin analogs-synthesis, characterization, and antitubercular activity |
title_full_unstemmed | Plumbagin analogs-synthesis, characterization, and antitubercular activity |
title_short | Plumbagin analogs-synthesis, characterization, and antitubercular activity |
title_sort | plumbagin analogs-synthesis, characterization, and antitubercular activity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960791/ https://www.ncbi.nlm.nih.gov/pubmed/24696815 http://dx.doi.org/10.4103/2231-4040.126984 |
work_keys_str_mv | AT nayaknishi plumbaginanalogssynthesischaracterizationandantitubercularactivity AT bajpaimeenakshi plumbaginanalogssynthesischaracterizationandantitubercularactivity AT razdanbalkishen plumbaginanalogssynthesischaracterizationandantitubercularactivity |