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. Author manuscript; available in PMC: 2018 Jan 5.
Published in final edited form as: Eur J Pharmacol. 2016 Nov 19;794:115–126. doi: 10.1016/j.ejphar.2016.11.026

Table 3.

Effects of [Dmt1]N/OFQ(1-13)-NH2 and PWT2-[Dmt1] at NOP and classical opioid receptors coupled with calcium signaling via chimeric G proteins.

NOP mu kappa delta
pEC50
(CL95%)
α±
S.E.M.
pEC50
(CL95%)
α±
S.E.M.
pEC50
(CL95%)
α±
S.E.M.
pEC50
(CL95%)
α±
S.E.M.
[Dmt1]N/OFQ(1-
13)-NH2
9.18
(8.71-
9.64)
0.99 ±
0.04
7.78
(7.14-
8.42)
0.85 ±
0.04
7.66
(7.37-
7.95)
0.92 ±
0.03
7.24
(6.92-
7.57)
0.83 ±
0.07
PWT2-[Dmt1] 7.83
(7.62-
8.03)
0.98 ±
0.08
6.82
(6.20-
7.43)
0.87 ±
0.04
6.40
(6.20-
6.60)
0.86 ±
0.03
6.79
(6.42-
7.16)
0.80 ±
0.08

N/OFQ, dermorphin, dynorphin A and DPDPE were used as standard agonists for calculating intrinsic activity at NOP, mu, kappa, and delta receptor respectively.