Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity.

作者: Vladimir V. Poroikov , Valery M. Dembitsky , Tatyana A. Gloriozova , Ekaterina Ermolenko , Nick Savidov

DOI: 10.3390/MOLECULES26030686

关键词:

摘要: Polycyclic endoperoxides are rare natural metabolites found and isolated in plants, fungi, marine invertebrates. The purpose of this review is a comparative analysis the pharmacological potential these products. According to PASS (Prediction Activity Spectra for Substances) estimates, they more likely exhibit antiprotozoal antitumor properties. Some them now widely used clinical medicine. All polycyclic presented article demonstrate activity can be divided into three groups. third group includes endoperoxides, which show weak with reliability up 70%, only 1.1% metabolites. second largest number 65% average confidence level 70 90%. Lastly, 33.9% strong 90 99.6%. Interestingly, artemisinin its analogs 79 99.6% against obligate intracellular parasites belong genera Plasmodium, Toxoplasma, Leishmania, Coccidia. In addition activities, proportion: 4.6% 65.6% an 90%, 29.8% 98.3%. It should also noted that some properties, other activities 97%. These include antifungal Aspergillus, Candida, Cryptococcus, as well anti-inflammatory activity. This provides insights on further utilization by medicinal chemists, pharmacologists, pharmaceutical industry.

参考文章(242)
Luis A. Loyola, Glauco Morales, María C. De La Torre, Samuel Pedreros, Benjamin Rodríguez, 17-Acetoxymulinic acid, a rearranged diterpenoid from Mulinum crassifolium Phytochemistry. ,vol. 29, pp. 3950- 3951 ,(1990) , 10.1016/0031-9422(90)85372-M
Luis A. Loyola, Glauco Morales, Benjamin Rodriguez, Jesús Jiménez-Barbero, Maria C.de la Torre, Aurea Perales, Maria R. Torres, Mulinic and isomulinic acids. Rearranged diterpenes with a new carbon skeleton from mulinum crassifolium Tetrahedron. ,vol. 46, pp. 5413- 5420 ,(1990) , 10.1016/S0040-4020(01)87848-0
Geneive E Henry, Helen Jacobs, C.M.Sean Carrington, Stewart McLean, William F Reynolds, Prenylated benzophenone derivatives from Caribbean Clusia species (Guttiferae). Plukenetiones B-G and xerophenone A Tetrahedron. ,vol. 55, pp. 1581- 1596 ,(1999) , 10.1016/S0040-4020(98)01203-4
Jian-Min Yue, Shao-Nong Chen, Zhong-Wen Lin, Han-Dong Sun, Sterols from the fungus Lactarium volemus Phytochemistry. ,vol. 56, pp. 801- 806 ,(2001) , 10.1016/S0031-9422(00)00490-8
Dong-Ze Liu, Ze-Jun Dong, Fang Wang, Ji-Kai Liu, Two novel norsesquiterpene peroxides from basidiomycete Steccherinum ochraceum Tetrahedron Letters. ,vol. 51, pp. 3152- 3153 ,(2010) , 10.1016/J.TETLET.2010.04.048
R. Caniato, L. Puricelli, Review: Natural Antimalarial Agents (1995-2001) Critical Reviews in Plant Sciences. ,vol. 22, pp. 79- 105 ,(2003) , 10.1080/713610851
Bora Mun, Weihong Wang, Hiyoung Kim, Dongyup Hahn, Inho Yang, Dong Hwan Won, Eun-hee Kim, Jihye Lee, Chulkyeong Han, Hyunji Kim, Merrick Ekins, Sang-Jip Nam, Hyukjae Choi, Heonjoong Kang, Cytotoxic 5α,8α-epidioxy sterols from the marine sponge Monanchora sp. Archives of Pharmacal Research. ,vol. 38, pp. 18- 25 ,(2015) , 10.1007/S12272-014-0480-8
Jian-Yong Dong, Xi-Yan Ma, Xiao-Qin Cai, Peng-Cheng Yan, Lei Yue, Chen Lin, Wei-Wei Shao, Sesquiterpenoids from Curcuma wenyujin with anti-influenza viral activities. Phytochemistry. ,vol. 85, pp. 122- 128 ,(2013) , 10.1016/J.PHYTOCHEM.2012.09.008
Ce-Ming Tan, Jian-Cheng He, Peng-Shan Duan, Lu-Ping Qin, Wen-Hui Ma, A novel eudesmene sesquiterpenoid from Schisandra sphenanthera stems Chemistry of Natural Compounds. ,vol. 47, pp. 713- 715 ,(2011) , 10.1007/S10600-011-0042-Y
Quan-Xiang Wu, Xia Liu, Yan-Ping Shi, Chemical components from Gentiana aristata. Chemistry & Biodiversity. ,vol. 4, pp. 175- 182 ,(2007) , 10.1002/CBDV.200790022