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. Author manuscript; available in PMC: 2023 Aug 1.
Published in final edited form as: Pain. 2022 Feb 2;163(8):e899–e916. doi: 10.1097/j.pain.0000000000002604

Table 1. Specifications and concentrations of the estrogen receptor (ER) agonists and antagonists applied to trigeminal ganglia neuron primary cultures.

E2-BSA: β-Estradiol 6-(O-carboxymethyl)oxime conjugated to bovine serum albumin (BSA); G-1: rel-1-[4-(6-bromo-1,3-benzodioxol-5-yl)-3aR,4S,5,9bS-tetrahydro-3H-cyclopenta[c]quinolin-8-yl]-ethanone; ICI 182,780: 7α,17β-[9-[(4,4,5,5,5 Pentafluoropentyl)sulfinyl]nonyl]estra-1,3,5(10)-triene-3,17-diol; PPT: 1,3,5-Tris(4-hydroxyphenyl)-4-propyl-1H-pyrazole; DPN: 2,3-Bis(4-hydroxyphenyl)propionitrile; MPP: MPP Dihydrochloride; PHTPP: 4-[2-Phenyl-5,7-bis(trifluoromethyl)pyrazolo[1,5-a]-pyrimidin-3-yl]phenol.

Pharmacologic Target Company Cat. # Concentration Ref.
E2-BSA Membrane-impermeable E2 Sigma–Aldrich E5630 50 nM [95]
G-1 GPER agonist Cayman Chemical 10008933 10 nM [15; 93]
ICI 182,780 ER antagonist; GPER agonist Sigma–Aldrich 5310420001 1 μM [96]
PPT ERα agonist Sigma–Aldrich H6036 100 nM [21; 62; 96]
DPN ERβ agonist Sigma–Aldrich H5915 15 nM [21; 78; 96; 116]
MPP ERα antagonist Sigma–Aldrich M7068 300 nM [96; 107]
PHTPP ERβ antagonist Sigma–Aldrich SML1355 1 μM [21; 60]