Abstract
A series of compounds having the pyranopyrazole pharmacophore were synthesised by the traditional method and then by an unreported rapid four-component microwave assisted method. The microwave strategy required substantially shorter reaction times as compared to the traditional method. The prepared molecules were tested in-vitro for their cytotoxic activity against the Hep3B cancer cell lines. The activity results were subsequently rationalized for a quick structure-activity relationship leading to the conclusion that the presence of certain heteroatom substituents at a 3-position of the pharmacophore may be crucial for anticancer potency.
Keywords: Anticancer, green chemistry, heterocycles, microwave assisted synthesis, pyranopyrazole.
Graphical Abstract
Current Microwave Chemistry
Title:Fast Microwave Assisted Synthesis of Pyranopyrazole Derivatives as New Anticancer Agents
Volume: 3 Issue: 1
Author(s): Ashok Sharma, Rajdeep Chowdhury, Subhra Dash, Badvel Pallavi and Paritosh Shukla
Affiliation:
Keywords: Anticancer, green chemistry, heterocycles, microwave assisted synthesis, pyranopyrazole.
Abstract: A series of compounds having the pyranopyrazole pharmacophore were synthesised by the traditional method and then by an unreported rapid four-component microwave assisted method. The microwave strategy required substantially shorter reaction times as compared to the traditional method. The prepared molecules were tested in-vitro for their cytotoxic activity against the Hep3B cancer cell lines. The activity results were subsequently rationalized for a quick structure-activity relationship leading to the conclusion that the presence of certain heteroatom substituents at a 3-position of the pharmacophore may be crucial for anticancer potency.
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Cite this article as:
Sharma Ashok, Chowdhury Rajdeep, Dash Subhra, Pallavi Badvel and Shukla Paritosh, Fast Microwave Assisted Synthesis of Pyranopyrazole Derivatives as New Anticancer Agents, Current Microwave Chemistry 2016; 3 (1) . https://dx.doi.org/10.2174/2213335602666150116233238
DOI https://dx.doi.org/10.2174/2213335602666150116233238 |
Print ISSN 2213-3356 |
Publisher Name Bentham Science Publisher |
Online ISSN 2213-3364 |
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