875271-85-5Relevant academic research and scientific papers
Increasing synthetic efficiency via direct C-H functionalization: Formal synthesis of an inhibitor of botulinum neurotoxin
Potavathri, Shathaverdhan,Kantak, Abhishek,DeBoef, Brenton
, p. 4679 - 4681 (2011/06/20)
A new and efficient scheme for the synthesis of one of the best known inhibitors of botulinum neurotoxin serotype A (BoNTA) is reported herein. The synthetic route involves two palladium-catalyzed C-H functionalization reactions, formally activating three C-H bonds. The Royal Society of Chemistry 2011.
SMALL-MOLECULE BOTULINUM TOXIN INHIBITORS
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Page/Page column 16, (2010/11/03)
Small-molecule inhibitors of Botulinum toxin, including BoNTA, BoNTD and BoNTE are provided, as well as methods of using the inhibitors.
Serotype-selective, small-molecule inhibitors of the zinc endopeptidase of botulinum neurotoxin serotype A
Park, Jewn Giew,Sill, Peter C.,Makiyi, Edward F.,Garcia-Sosa, Alfonso T.,Millard, Charles B.,Schmidt, James J.,Pang, Yuan-Ping
, p. 395 - 408 (2007/10/03)
Botulinum neurotoxin serotype A (BoNTA) is one of the most toxic substances known. Currently, there is no antidote to BoNTA. Small molecules identified from high-throughput screening reportedly inhibit the endopeptidase-the zinc-bound, catalytic domain of
