Chemical Synthesis of the Cardiotonic Steroid Glycosides and Related Natural Products

被引:81
作者
Heasley, Brian [1 ]
机构
[1] Scynexis Inc, Res Triangle Pk, NC 27709 USA
关键词
digitoxin; medicinal chemistry; ouabain; semisynthesis; steroids; total synthesis; ENANTIOSELECTIVE TOTAL-SYNTHESIS; ABC RING-SYSTEM; CARDIOACTIVE STEROIDS; DIELS-ALDER; SEX-HORMONES; STEREOSELECTIVE SYNTHESIS; REDUCTIVE ALKYLATION; ASYMMETRIC-SYNTHESIS; CONVERGENT SYNTHESIS; DEFENSIVE STEROIDS;
D O I
10.1002/chem.201103733
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The active components from the extracts of Digitalis, cardiotonic steroid glycosides, have been ingested by humans for more than 200 years as a medicinal therapy for heart failure and abnormal heart rhythms. The positive inotropic activity of the cardiotonic steroids that mediates clinically useful physiological effects in patients has been attributed largely to a high affinity inhibitory interaction with the extracellular surface of the membrane-bound sodium pump (Na+/K+-ATPase). However, previously unrecognized intracellular signaling pathways continue to be uncovered. This Review examines both partial and de novo synthetic approaches to the medicinally important and structurally captivating cardenolide and bufadienolide steroid families, with an emphasis on the stereocontrolled construction of the pharmacophoric aglycone (genin) framework.
引用
收藏
页码:3092 / 3120
页数:29
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