[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a selective agonist for the nociceptin receptor (ORL1). This compound has been demonstrated to significantly inhibit the nociceptive flexor reflex in rodent models, highlighting its potential utility in analgesia studies. [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a valuable tool for investigating pain mechanisms and developing therapeutic strategies for pain management.
[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a selective agonist for the nociceptin receptor (ORL1). This compound has been demonstrated to significantly inhibit the nociceptive flexor reflex in rodent models, highlighting its potential utility in analgesia studies. [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a valuable tool for investigating pain mechanisms and developing therapeutic strategies for pain management.
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