Heterocyclic scaffolds: centrality in anticancer drug development

Cancer has been cursed for human beings for long time. Millions people lost their lives due to cancer. Despite of the several anticancer drugs available, cancer cannot be cured; especially at the late stages without showing any side effect. Heterocyclic compounds exhibit exciting medicinal propertie...

Full description

Bibliographic Details
Main Authors: Ali, Imran, Lone, Mohammad Nadeem, Al-Othman, Zeid Abdullah, Al-Warthan, Abdulrahman, Sanagi, Mohd. Marsin
Format: Article
Published: Bentham Science Publishers 2015
Subjects:
_version_ 1796860177049190400
author Ali, Imran
Lone, Mohammad Nadeem
Al-Othman, Zeid Abdullah
Al-Warthan, Abdulrahman
Sanagi, Mohd. Marsin
author_facet Ali, Imran
Lone, Mohammad Nadeem
Al-Othman, Zeid Abdullah
Al-Warthan, Abdulrahman
Sanagi, Mohd. Marsin
author_sort Ali, Imran
collection ePrints
description Cancer has been cursed for human beings for long time. Millions people lost their lives due to cancer. Despite of the several anticancer drugs available, cancer cannot be cured; especially at the late stages without showing any side effect. Heterocyclic compounds exhibit exciting medicinal properties including anticancer. Some market selling heterocyclic anticancer drugs include 5-flourouracil, methortrexate, doxorubicin, daunorubicin, etc. Besides, some natural products such as vinblastine and vincristine are also used as anticancer drugs. Overall, heterocyclic moeities have always been core parts in the expansion of anticancer drugs. This article describes the importance of heterocyclic nuclei in the development of anticancer drugs. Besides, the attempts have been made to discuss both naturally occurring and synthetic heterocyclic compounds as anticancer agents. In addition, some market selling anticancer heterocyclic compounds have been described. Moreover, the efforts have been made to discuss the mechanisms of actions and recent advances in heterocyclic compounds as anticancer agents. The current challenges and future prospectives of heterocyclic compounds have also been discussed. Finally, the suggestions for syntheses of effective, selective, fast and human friendly anticancer agents are discussed into the different sections
first_indexed 2024-03-05T19:38:03Z
format Article
id utm.eprints-55564
institution Universiti Teknologi Malaysia - ePrints
last_indexed 2024-03-05T19:38:03Z
publishDate 2015
publisher Bentham Science Publishers
record_format dspace
spelling utm.eprints-555642017-02-15T04:36:33Z http://eprints.utm.my/55564/ Heterocyclic scaffolds: centrality in anticancer drug development Ali, Imran Lone, Mohammad Nadeem Al-Othman, Zeid Abdullah Al-Warthan, Abdulrahman Sanagi, Mohd. Marsin QD Chemistry Cancer has been cursed for human beings for long time. Millions people lost their lives due to cancer. Despite of the several anticancer drugs available, cancer cannot be cured; especially at the late stages without showing any side effect. Heterocyclic compounds exhibit exciting medicinal properties including anticancer. Some market selling heterocyclic anticancer drugs include 5-flourouracil, methortrexate, doxorubicin, daunorubicin, etc. Besides, some natural products such as vinblastine and vincristine are also used as anticancer drugs. Overall, heterocyclic moeities have always been core parts in the expansion of anticancer drugs. This article describes the importance of heterocyclic nuclei in the development of anticancer drugs. Besides, the attempts have been made to discuss both naturally occurring and synthetic heterocyclic compounds as anticancer agents. In addition, some market selling anticancer heterocyclic compounds have been described. Moreover, the efforts have been made to discuss the mechanisms of actions and recent advances in heterocyclic compounds as anticancer agents. The current challenges and future prospectives of heterocyclic compounds have also been discussed. Finally, the suggestions for syntheses of effective, selective, fast and human friendly anticancer agents are discussed into the different sections Bentham Science Publishers 2015-08 Article PeerReviewed Ali, Imran and Lone, Mohammad Nadeem and Al-Othman, Zeid Abdullah and Al-Warthan, Abdulrahman and Sanagi, Mohd. Marsin (2015) Heterocyclic scaffolds: centrality in anticancer drug development. Current Drug Targets, 6 (7). pp. 711-734. ISSN 1389-4501
spellingShingle QD Chemistry
Ali, Imran
Lone, Mohammad Nadeem
Al-Othman, Zeid Abdullah
Al-Warthan, Abdulrahman
Sanagi, Mohd. Marsin
Heterocyclic scaffolds: centrality in anticancer drug development
title Heterocyclic scaffolds: centrality in anticancer drug development
title_full Heterocyclic scaffolds: centrality in anticancer drug development
title_fullStr Heterocyclic scaffolds: centrality in anticancer drug development
title_full_unstemmed Heterocyclic scaffolds: centrality in anticancer drug development
title_short Heterocyclic scaffolds: centrality in anticancer drug development
title_sort heterocyclic scaffolds centrality in anticancer drug development
topic QD Chemistry
work_keys_str_mv AT aliimran heterocyclicscaffoldscentralityinanticancerdrugdevelopment
AT lonemohammadnadeem heterocyclicscaffoldscentralityinanticancerdrugdevelopment
AT alothmanzeidabdullah heterocyclicscaffoldscentralityinanticancerdrugdevelopment
AT alwarthanabdulrahman heterocyclicscaffoldscentralityinanticancerdrugdevelopment
AT sanagimohdmarsin heterocyclicscaffoldscentralityinanticancerdrugdevelopment