Name | [Nphe1]Nociceptin(1-13)NH2 |
---|---|
Synonyms | BzlGlyGGFTGARKSARK-NH2 |
Description | [Nphe1]Nociceptin(1-13)NH2, a novel nociceptin/orphanin FQ (NC) endogenous ligand, is a selective and competitive ociceptin receptor antagonist without any residual agonist activity. [Nphe1]nociceptin(1-13)NH2 binds selectively to recombinant nociceptin receptors (pKi=8.4) and antagonizes the inhibitory effects of nociceptin on cyclic AMP accumulation in CHO cells (pA2=6.0). [Nphe1]Nociceptin(1-13)NH2 has the potential to act as an analgesic agent[1]. |
---|---|
Related Catalog | |
In Vitro | [Nphe1]nociceptin(1-13)NH2 binds selectively to recombinant nociceptin receptors expressed in Chinese hamster ovary (CHO) cells (pKi=8.4) and competitively antagonizes the inhibitory effects of nociceptin on cyclic AMP accumulation in CHO cells (pA2=6.0). |
References |
Molecular Formula | C61H100N22O15 |
---|---|
Molecular Weight | 1381.59000 |
Exact Mass | 1380.77000 |
PSA | 620.62000 |
LogP | 0.97790 |
WGK Germany | 3 |
---|