Thapsigargin: a promising natural product with diverse medicinal potential - a review of synthetic approaches and total syntheses

被引:0
|
作者
Suresh, Anisha [1 ]
Bagchi, Dibyojeet [1 ]
Kaliappan, Krishna P. [1 ]
机构
[1] Indian Inst Technol IIT, Dept Chem, Mumbai 400076, India
关键词
RING-CLOSING METATHESIS; PAUSON-KHAND REACTION; MECHANISTIC ORGANIC-PHOTOCHEMISTRY; LIBERATING SESQUITERPENE LACTONES; PROSTATE-SPECIFIC ANTIGEN; BOND-FORMING REACTIONS; THAPSIA-GARGANICA; ENANTIOSELECTIVE SYNTHESIS; MANGANESE(III) ACETATE; ROUTE;
D O I
10.1039/d4ob01239a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Thapsigargin, a sesquiterpene lactone, naturally occurring in the roots and fruits of the Mediterranean shrub Thapsia garganica L, is known to the practitioners of traditional medicines since the medieval ages as a cure for rheumatic pain, lung diseases, and female infertility. This naturally occurring guaianolide has shown remarkable activity for Sarco endoplasmic reticulum Ca2+ ATPase inhibition, which eventually renders it fit as a potential candidate for anti-cancer drugs. Mipsagargin, a prodrug derived from thapsigargin, is under clinical trials for the treatment of glioblastoma. Recently, thapsigargin has shown promise as an antiviral against SARS-CoV-2. Limited natural availability and challenging synthesis have prompted research into new synthetic pathways. This review discusses significant synthetic approaches and total syntheses of thapsigargin reported to date. Thapsigargin, a sesquiterpene lactone, has been known to the practitioners of traditional medicines as a cure for rheumatic pain and female infertility. This review discusses synthetic approaches and total syntheses of thapsigargin reported to date.
引用
收藏
页码:8551 / 8569
页数:19
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