| Name | GR 89696 fumarate,4-[(3,4-Dichlorophenyl)acetyl]-3-(1-pyrrolidinylmethyl)-1-piperazinecarboxylicacidmethylesterfumarate |
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| Description | GR 89696 is a highly selective κ2 opioid receptor agonist with potential to prevent pruritus[1]. |
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| Related Catalog | |
| In Vivo | GR 89696 (intramuscular injection, 0.01-0.1 μg/kg) 可以以一种剂量依赖的方式减轻鞘内注射吗啡(0.03mg)诱导的抓挠反应而不影响吗啡镇痛作用[1]。 GR-896960(subcutaneous injection, 1 mg/kg) 在大鼠永久性局灶性缺血模型中,使大脑动脉梗塞体积减少了 38%[2]。 |
| References |
| Boiling Point | 559.2ºC at 760 mmHg |
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| Molecular Formula | C23H29Cl2N3O7 |
| Molecular Weight | 530.39800 |
| Flash Point | 292ºC |
| Exact Mass | 529.13800 |
| PSA | 127.69000 |
| LogP | 2.43640 |
| Vapour Pressure | 1.55E-12mmHg at 25°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| RIDADR | NONH for all modes of transport |