| Literature DB >> 30308112 |
Muhammad T Islam1,2, Abul B R Khalipha3, Rajat Bagchi3, Milon Mondal3, Shanita Z Smrity3, Shaikh J Uddin4, Jamil A Shilpi4, Razina Rouf3.
Abstract
This review aims to summarize the anticancer effects of the natural monoterpene phenol derivative of cymenethymol and its derivatives as well as further molecular docking study to correlate the interaction of thymol and biomacromolecules that involved in cancer cell growth. For this, an up-to-date (till July 2018) literature study were made through using PubMed, Science Direct, Web of Science, Scopus, The American Chemical Society, Clinicaltrials.gov, and Google Scholar databases. Literature study demonstrated that thymol, melasolv (3,4,5-Trimethoxycinnamate thymol ester), and Mannich bases of thymol have potential anticancer effects in various test systems, including mice, rats and cultured cancer cells through various anticancer pathways such as antioxidant/oxidative stress induction, apoptosis, anti-inflammatory/immunomodulatory, anti-genotoxicity, chemo-, and radiopreventive ways. A few earlier scientific evidences showed that thymol is less toxic to mammalian systems. In silico study of thymol and its derivatives against 17 essential proteins revealed that 6BVH (PARP-1) and 5LIH (protein kinase C) are the most efficient receptor protein for interaction and binding of thymol and melaslov for the cancer prevention and initiation. On the basis of the summary of this review and docking study, it is evident that thymol may be one of promising plant-derived cancer chemotherapeutic agents.Entities:
Keywords: anticancer; molecular docking; monoterpene phenol; thymol
Year: 2018 PMID: 30308112 DOI: 10.1002/iub.1935
Source DB: PubMed Journal: IUBMB Life ISSN: 1521-6543 Impact factor: 3.885