Ursolic acid derivatives for pharmaceutical use: a patent review (2012-2016)

被引:105
作者
Hussain, Hidayat [1 ,2 ]
Green, Ivan R. [3 ]
Ali, Iftikhar [4 ]
Khan, Ikhlas A. [5 ]
Ali, Zulfiqar [5 ]
Al-Sadi, Abdullah M. [6 ]
Ahmed, Ishtiaq [7 ]
机构
[1] Univ Nizwa, UoN Chair Omans Med Plants & Marine Nat Prod, Nizwa, Oman
[2] Univ Calif San Diego, Ctr Marine Biotechnol & Biomed, Scripps Inst Oceanog, San Diego, CA 92103 USA
[3] Univ Stellenbosch, Dept Chem & Polymer Sci, Stellenbosch, South Africa
[4] Karakoram Int Univ, Dept Chem, Gilgit Baltistan, Pakistan
[5] Univ Mississippi, Natl Ctr Nat Prod Res, Oxford, MS USA
[6] Sultan Qaboos Univ, Dept Crop Sci, Coll Agr & Marine Sci, Al Khoud, Oman
[7] KIT, DFG Ctr Funct Nanostruct, Karlsruhe, Germany
关键词
Ursolic acid; anticancer; anti-inflammatory; diabetes; in vitro; in vivo; ADVANCED SOLID TUMORS; HIGH-FAT DIET; PENTACYCLIC TRITERPENOIDS; INCREASES CERAMIDES; BOSWELLIC ACIDS; MOUSE MODEL; HUMAN SKIN; LIVER; MICE; PATHWAY;
D O I
10.1080/13543776.2017.1344219
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Ursolic acid (UA), belongs to a group of pentacyclic triterpenoids and is known to possess some very interesting biological properties. Protocols have been developed in order to synthesize bioactive UA analogs which have resulted in numerous ursolic acid analogs being synthesized during the period 2012-2016. Ursolic acid and its analogues can be employed to treat various cancers, inflammatory diseases, diabetes, Parkinson's disease, Alzheimer's disease, hepatitis B, hepatitis C and AIDS to mention but a few. Areas covered: This review covers patents on therapeutic activities of ursolic acid (UA) and its synthetic derivatives published during the four year period 2012-2016. A discussion about structure-activity relationships (SAR) of these analogs is also included. Expert opinion: Ursolic acid and its synthetic derivatives demonstrated excellent anticancer, antidiabetic, antiarrhythmic, anti-hyperlipidemic, antimicrobial, anti-hypercholesterolemic, and anti-cardiovascular properties. Additionally, various ursolic acid analogues have been synthesized through modification at positions C-2-OH, C-3-OH and C17-CO2H. It is noteworthy that the C-17 amide and amino analogs of UA possessed better anticancer activity compared to the parent compound (UA). Most importantly, UA has the potential to conjugate with other anticancer drugs or be transformed into its halo derivatives since this will greatly facilitate scientists to get lead compounds in cancer drug discovery.
引用
收藏
页码:1061 / 1072
页数:12
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