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. Author manuscript; available in PMC: 2011 Apr 1.
Published in final edited form as: Steroids. 2010 Jan 22;75(4-5):314–322. doi: 10.1016/j.steroids.2010.01.010

Table 2.

Rank order of binding affinities of natural and synthetic steroids to CHO and MCF-7 cells transfected with human nPR

Compounds pIC50 (mean) logRBA
Promegestone 8.90 2.18
16α-ethyl-21-hydoxy-19-norpregn-4-ene-3,20-dione (Org 2058) 8.72 2.00
19-Norprogesterone 8.53 1.81
Mifepristone 8.26 1.54
17-Hydroxy-19-nor-17α-pregn-4-en-3-one 8.24 1.52
Progesterone 7.87 1.15
Desogestrel 7.80 1.08
17β-Hydroxy-16α-isopropylestr-4-en-3-one 7.72 1.00
17β-Hydroxy-17α-methylestr-4-en-3-one 7.66 0.94
Ethylestrenol 7.21 0.49
Nandrolone 7.20 0.48
Allylestrenol 7.04 0.32
Ethisterone 6.99 0.27
Lynestrenol 6.95 0.23
5α-Dihydronandrolone 6.50 −0.22
5α-Dihydrotestosterone (DHT) 6.16 −0.56
Androst-4-ene-3,17-dione (androstenedione) 6.02 −0.70
Testosterone 6.02 −0.70

Each value is the mean of at least three separate competitive binding assays. IC50 is the competitor concentration (nM) that causes 50% displacement of [3H] Org 2058. RBA (Relative Binding Affinity), RBA (%) compared with that of Org 2058.