92156-97-3

Upstream product

• 797754-03-1 5-hexyl-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 797754-02-0 (E)-5-(hex-1-en-1-yl)-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 164014-40-8 2,2-dimethyl-5-trifluoromethylsulfonyloxy-4H-(1,3)benzodioxin-4-one 
• 154714-19-9 5-hydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 303-07-1 2,6-Dihydroxybenzoic acid 

Relevant academic research and scientific papers

Synthesis and Evaluation of Ginkgolic Acid Derivatives as SUMOylation Inhibitors

SUMOylation has emerged as an important post-translational modification that has been shown to modulate protein activity associated with various signaling pathways, and consequently, it has emerged as an important therapeutic target. While several natural products have been shown to inhibit enzymes involved in the SUMOylation process, there has been little progress toward the development of more selective and potent SUMOylation inhibitors. Ginkgolic acid was one of the first natural products discovered to inhibit the SUMO E1 enzyme. Despite its use to mechanistically investigate the SUMOylation process, ginkgolic acid also modulates other pathways as well. In this Letter, preliminary structure-activity relationships for ginkgolic acid as a SUMOylation inhibitor are presented.

Direct magnesiation of polyfunctionalized arenes and heteroarenes using (tmp)2Mg·2 LiCl

(Chemical Equation Presented) Outstripping lithium bases: A wide range of polyfunctional aryl and heteroaryl magnesium reagents were efficiently prepared in THF by direct magnesiation with (tmp)2Mg·2 LiCl, an exceptionally active base. These co