[Phe1_(CH2-NH)Gly2]Nociceptin(1-13)NH2 TP1988
Specifications
| 1mg/5mg/10mg/25mg/50mg/100mg |
Bioactivity:
Potent agonist of the nociceptin (ORL1) receptor, demonstrated both in vitro and in vivo. Selective, competitive antagonism at the nociceptin receptor has also been reported (pA2 = 7.02 and 6.75 in the guinea pig ileum and mouse vas deferens respectively)
CAS nr:
213130-17-7
Purity:
98%
Molecular Weight:
1367,6
SMILES:
Formula:
C61H102N22O14
Pathway:
Target:
