Abstract
SummaryA method was described for synthesis of 1-benzyl-2-methyl-5-hydroxytryptamine involving cleavage of the methyl ether of 1-benzyl − 2-methyl − 5-methoxytryptamine (BAS) by heating with pyridine hydrochloride. The phenol so produced exhibited powerful antiserotonin action either orally or intravenously in dogs. In the intravenous test it was the most potent antiserotonin thus far encountered. It also had considerable serotoninlike activity.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
