Bioorganic & Medicinal Chemistry 2008-01-01

Structure–activity correlations for β-phenethylamines at human trace amine receptor 1

Anita H. Lewin, Hernán A. Navarro, S. Wayne Mascarella, Anita H. Lewin, Hernán A. Navarro, S. Wayne Mascarella

Index: Bioorg. Med. Chem. 16 , 7415-23, (2008)

Full Text: HTML

Abstract

CoMFA 3D-QSAR studies on the potency of 68 β-phenethylamine analogs to activate hTAAR 1 (61% steric, 39% electrostatic) indicates that bulk both at nitrogen and 4-aryl leads to lower potency.


Related Compounds

Related Articles:

Oxidation of phenethylamine derivatives by cytochrome P450 2D6: the issue of substrate protonation in binding and catalysis.

2001-11-27

[Biochemistry 40 , 14215, (2001)]

A microdialysis study on striatal dopamine, 5-HT and metabolites in conscious rats after various treatments: evidence for extravesicular release of dopamine.

1993-10-25

[Neuroreport 5(1) , 53-6, (1993)]

[Tetrahedron 62 , 9002, (2006)]

[Tetrahedron Lett. 48 , 835, (2007)]

More Articles...