化合物 TP1988 TP1988
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Product IntroductionBioactivity英文名: [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2描述: Potent agonist of the nociceptin (ORL1) rec
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Product Introduction
Bioactivity
英文名: [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
描述: 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).
存储条件: keep away from moisturePowder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: H2O : 0.70 mg/mL
关键字: [Phe1Ψ(CH2-NH)Gly2]NociceptinNH2 | [Phe1Ψ(CH2 NH)Gly2]Nociceptin(1 13)NH2 | [Phe1psi(CH2-NH)Gly2]NociceptinNH2 | [Phe1Ψ(CH2NH)Gly2]Nociceptin(113)NH2 | [Phe-1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
Bioactivity
英文名: [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
描述: 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).
存储条件: keep away from moisturePowder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: H2O : 0.70 mg/mL
关键字: [Phe1Ψ(CH2-NH)Gly2]NociceptinNH2 | [Phe1Ψ(CH2 NH)Gly2]Nociceptin(1 13)NH2 | [Phe1psi(CH2-NH)Gly2]NociceptinNH2 | [Phe1Ψ(CH2NH)Gly2]Nociceptin(113)NH2 | [Phe-1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
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