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Total synthesis of luminacin D, isopanepoxydone, panepoxydone, and an isopanepoxydone derived biotinylated affinity reagent.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Total synthesis of luminacin D, isopanepoxydone, panepoxydone, and an isopanepoxydone derived biotinylated affinity reagent.
作者:
Shotwell, John Bradford.
面頁冊數:
550 p.
附註:
Directors: Craig M. Crews; John L. Wood.
附註:
Source: Dissertation Abstracts International, Volume: 64-10, Section: B, page: 4950.
Contained By:
Dissertation Abstracts International64-10B.
標題:
Chemistry, Organic.
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3109462
ISBN:
0496570048
Total synthesis of luminacin D, isopanepoxydone, panepoxydone, and an isopanepoxydone derived biotinylated affinity reagent.
Shotwell, John Bradford.
Total synthesis of luminacin D, isopanepoxydone, panepoxydone, and an isopanepoxydone derived biotinylated affinity reagent.
[electronic resource] - 550 p.
Directors: Craig M. Crews; John L. Wood.
Thesis (Ph.D.)--Yale University, 2003.
Bioactive natural products and their derivatives serve essential roles (i) as lead compounds in the development of new treatments for disease and (ii) as indispensable biochemical probes in the elucidation of new intracellular signaling pathways. Described herein are efficient total syntheses of the novel inhibitors of NF-kappaB signaling isopanepoxydone (91 ) and panepoxydone (2), in addition to the potent inhibitor of angiogenesis, luminacin D (180). These successful synthetic endeavors afforded not only usable quantities of these bioactive small molecules for subsequent biological investigations, but also served as a platform from which derivatization and molecular mode of action studies were launched.
ISBN: 0496570048Subjects--Topical Terms:
193634
Chemistry, Organic.
Total synthesis of luminacin D, isopanepoxydone, panepoxydone, and an isopanepoxydone derived biotinylated affinity reagent.
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Bioactive natural products and their derivatives serve essential roles (i) as lead compounds in the development of new treatments for disease and (ii) as indispensable biochemical probes in the elucidation of new intracellular signaling pathways. Described herein are efficient total syntheses of the novel inhibitors of NF-kappaB signaling isopanepoxydone (91 ) and panepoxydone (2), in addition to the potent inhibitor of angiogenesis, luminacin D (180). These successful synthetic endeavors afforded not only usable quantities of these bioactive small molecules for subsequent biological investigations, but also served as a platform from which derivatization and molecular mode of action studies were launched.
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