60229-56-3Relevant academic research and scientific papers
New aporphinoid 5-HT2A and α1A antagonists via structural manipulations of nantenine
Chaudhary, Sandeep,Ponnala, Shashikanth,Legendre, Onica,Gonzales, Junior A.,Navarro, Hernán A.,Harding, Wayne W.
experimental part, p. 5861 - 5868 (2011/11/04)
A series of C1, C2, C3 and N6 analogs of nantenine (2) was synthesized and evaluated in 5-HT2A and α1A receptor functional assays. Alkyl substitution of the C1 and N6 methyl groups of nantenine provided selective 5-HT2A an
