产品
编 号：F252923
分子式：C18H18Cl2N2O
分子量：349.25
分子式：C18H18Cl2N2O
分子量：349.25
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
询价
询价
1mg
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5mg
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10mg
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25mg
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结构图
CAS No: 2059904-66-2
产品详情
生物活性：
BPR1M97 is a dual-acting mu opioid receptor (MOP) and nociceptin-orphanin FQ peptide (NOP) receptor agonist with Ki values of 1.8 and 4.2 nM, respectively. BPR1M97 shows high potency and blood-brain barrier penetration, and produces potent antinociceptive effects.
体内研究：
BPR1M97 (1.8 mg/kg; s.c.; once) demonstrates antinociception in a murine model of cancer pain.Animal Model:Male wild-type C57BL/6 mice (25-30?g)
Dosage:1.8 mg/kg
Administration:Subcutaneous injection (s.c.); once
Result:Demonstrated antinociception in a murine model of cancer pain.
BPR1M97 is a dual-acting mu opioid receptor (MOP) and nociceptin-orphanin FQ peptide (NOP) receptor agonist with Ki values of 1.8 and 4.2 nM, respectively. BPR1M97 shows high potency and blood-brain barrier penetration, and produces potent antinociceptive effects.
体内研究：
BPR1M97 (1.8 mg/kg; s.c.; once) demonstrates antinociception in a murine model of cancer pain.Animal Model:Male wild-type C57BL/6 mice (25-30?g)
Dosage:1.8 mg/kg
Administration:Subcutaneous injection (s.c.); once
Result:Demonstrated antinociception in a murine model of cancer pain.
产品资料
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