Title : Synthesis and biological activity of a 2-bromoethylamine (mustard) derivative of hemicholinium-3 and hemicholinium-15.

Pub. Date : 1983 Jan

PMID : 6827521






1 Functional Relationships(s)
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1 When compared on an equivalent concentration basis, HC3-BrM effected substantially greater inhibition of SDHACU than HC-3 and is, thus, at present the most potent known synthetic inhibitor of this uptake system. Hemicholinium 3 CYCS pseudogene 24 Homo sapiens