EventsMOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed.
Published
This submission belongs to the session 05. NICEXSM-02: North-Ibero-American Congress on Exp. and Simul. Methods, Valencia, Spain-Miami, USA, 2016 of the event MOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed.
Published date
17 Nov, 2016
Citation
Luciana Scotti, Francisco Mendonça Jr, Frederico F Ribeiro, Josean F Tavares, Marcelo S Da Silva, José Maria Barbosa Filho, Marcus T Scotti, Natural Product Inhibitors of Topoisomerases against cancer, in Proceedings of MOL2NET'16, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 2nd ed., 15 October–20 October 2022, MDPI: Basel, Switzerland, doi: 10.3390/mol2net-02-14002
Share
Email
Facebook
Twitter
LinkedIn

Natural Product Inhibitors of Topoisomerases against cancer

image
image
image
1. Federal University of Paraiba, Brazil
2. State University of Paraíba, Biological Science Department, Laboratory of Synthesis and Drug Delivery, 58070-450, João Pessoa-PB, Brazil
3. Federal University of Pernambuco, Campus I, Recife-PE, Brazil
4. Federal University of Paraiba
Abstract

Since ancient times, natural products have been used in treating various diseases effectively and safely. Nowadays, these natural compounds are submitted to sophisticated methodologies from isolation, computing, analytical, and even serving as pharmacophore suggestions for synthesis. The substances extracted from marine species, plants, and microorganisms present activities beneficial to our health, including protection against malignant tumors. The topoisomerase enzymes play an important role in DNA metabolism, and searching for enzyme inhibitors is an important target in the search for new anticancer drugs. We performed a docking study with our Brazilian diterpenes in topoisomerases I and II. The better compound, the trachylobane 1, forms one hydrogen bond when submitted to docking with Topo I (with the ASP533 residue) and two with residues in Topo II (THR213 and TYR188). The difference observed in the energy of formation can be attributed to hydrogen-bond interactions.

Keywords
cancer
docking
terpenes
topoisomerases
Poster
ppt.pdf
Editorial: MOL2NET 2016, International Conference Series on Multidisciplinary Sciences.
Food sources and emerging methods to obtain Ellagic Acid