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. Author manuscript; available in PMC: 2011 Jan 1.
Published in final edited form as: Neuropharmacology. 2009 Jun 21;58(1):117–125. doi: 10.1016/j.neuropharm.2009.06.009

Table 1.

A representative list of affinities (Kd or Ki) for the dopamine (DA) agonists employed in this study at rat or human DA receptor subtypes. Lower values represent higher affinities. Much variation in affinity values is present in the literature, largely depending on experimental parameters, whether both high- and low-affinity receptors are considered, and cell line within which cloned receptors are expressed.

Drug target
receptor
source
species
Kd or Ki
(nM)
reference
SKF38393
SKF38393
D1
D1
rat
human
26.6
45.6
Neumeyer et al, 2003
Yanagawa et al., 1997
SKF38393 D2 rat 9560 Sokoloff et al., 1990
SKF38393 D3 rat 5000 Sokoloff et al., 1990
Quinpirole D1 rat >1000 Mottola et al., 2002
Quinpirole
Quinpirole
D2
D2A
rat
human
4
3.7
Malmberg and Mohell, 1995
Malmberg and Mohell, 1995
Quinpirole D3 rat 47 Boundy et al., 1993
Quinpirole D3 human 0.6 Malmberg and Mohell, 1995
Quinpirole D4.2 human 140-250 Tallman et al., 1997
7-OH-DPAT
7-OH-DPAT
D2
D2
rat
human
3.6
125
Gonzalez and Sibley, 1995
Damsma et al., 1993
7-OH-DPAT D3 rat 0.5 Gonzalez and Sibley, 1995
7-OH-DPAT D3 human 0.1 Damsma et al., 1993
7-OH-DPAT D4.2 human 520-1469 Tallman et al., 1997
PD168077 D1 human 4600 Moreland et al., 2004
PD168077 D2 human 1280 Moreland et al., 2004
PD168077 D3 human 2300 Moreland et al., 2004
PD168077 D4 human 11.9 Moreland et al., 2004