Natural diterpene pyrones: chemistry and biology

被引:15
|
作者
Al-Khdhairawi, Amjad Ayad Qatran [1 ,2 ]
Cordell, Geoffrey A. [3 ,4 ]
Thomas, Noel F. [5 ]
Nagojappa, Narendra Babu Shivanagere [1 ]
Weber, Jean-Frederic F. [2 ]
机构
[1] Taylors Univ, Sch Pharm, Fac Hlth & Med Sci, Lakeside Campus, Subang Jaya 47500, Selangor, Malaysia
[2] Univ Teknol MARA UiTM, Selangor Branch, Atta ur Rahman Inst Nat Prod Discovery AuRIns, Bandar Puncak Alam 42300, Selangor, Malaysia
[3] Nat Prod Inc, Evanston, IL 60203 USA
[4] Univ Florida, Coll Pharm, Dept Pharmaceut, Gainesville, FL 32601 USA
[5] Methodist Coll Kuala Lumpur, Kuala Lumpur 50470, Malaysia
关键词
ENANTIOSELECTIVE TOTAL-SYNTHESIS; CANDELALIDES A-C; FUNGUS; SPIRODITERPENOIDS; SESQUICILLIN; BIOSYNTHESIS; SUBGLUTINOLS; KV1.3; MEROTERPENOIDS; DERIVATIVES;
D O I
10.1039/c9ob01501a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Diterpene pyrones (DTPs) are a group of well-known, mainly fungal, natural products, first isolated in 1966. As the name indicates, they are composed of two main structural features: a diterpenyl moiety and a pyrone ring. Various names have been given to this class of metabolites; however, biogenetic evidence indicates that they originate through the same metabolic pathway. Based on their biosynthesis, which leads to differences in their structural architecture, the DTPs can be classified into three main types. In addition to their intriguing chemistry, these compounds demonstrate a wide range of biological activities rendering them a desirable target for total synthesis. To date, sixty-seven DTPs have been isolated from various fungal species, with one example originating from the plant kingdom. This review aims at unifying the classification of these compounds, in addition to presenting a detailed description of their isolation, bioactivities, biosynthesis, and total synthesis.
引用
收藏
页码:8943 / 8957
页数:15
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