D8040
反式 -U-50488 甲磺酸盐
别名:
反 -(±)-3,4-二氯-N-甲基-N- [2-（1-吡咯烷基）环己基] 苯乙酰胺 甲磺酸盐, U-50488H
表单
powder
质量水平
溶解性
H2O: 50 mg/mL
储存温度
2-8°C
SMILES字符串
CS(O)(=O)=O.CN([C@@H]1CCCC[C@H]1N2CCCC2)C(=O)Cc3ccc(Cl)c(Cl)c3
InChI
1S/C19H26Cl2N2O.CH4O3S/c1-22(19(24)13-14-8-9-15(20)16(21)12-14)17-6-2-3-7-18(17)23-10-4-5-11-23;1-5(2,3)4/h8-9,12,17-18H,2-7,10-11,13H2,1H3;1H3,(H,2,3,4)/t17-,18-;/m1./s1
InChI key
OJPHNZCUXUUVKU-JAXOOIEVSA-N
基因信息
human ... OPRK1(4986)
应用
(±)-反式-U-50488 甲磺酸盐已被用作 κ -阿片受体的对照激动剂。
生化/生理作用
选择性 κ-已知阿片受体激动剂 (±)-反式-U-50488 甲磺酸盐可诱导利尿。研究发现 U-50488H 与其联合给药时可预防吗啡耐受。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Opioid receptor delta as a global modulator of skin differentiation and barrier function repair
Chajra H, et al.
International Journal of Cosmetic Science, 37(4), 386-394 (2015)
Guang-Jie Gao et al.
Evidence-based complementary and alternative medicine : eCAM, 2022, 2868135-2868135 (2022-08-30)
Acute lung injury (ALI) is one of the common and severe complications of cardiopulmonary bypass (CPB), which is the primary cause of death in intensive care units. Nevertheless, there is a lack of effective treatment for ALI secondary to CPB.
Differential effects of the novel kappa opioid receptor antagonist, JDTic, on reinstatement of cocaine-seeking induced by footshock stressors vs cocaine primes and its antidepressant-like effects in rats
Beardsley PM, et al.
Psychopharmacology, 183(1), 118-118 (2005)
Alena Karnošová et al.
International journal of molecular sciences, 22(16) (2021-08-28)
The anorexigenic neuropeptide prolactin-releasing peptide (PrRP) is involved in the regulation of food intake and energy expenditure. Lipidization of PrRP stabilizes the peptide, facilitates central effect after peripheral administration and increases its affinity for its receptor, GPR10, and for the
Characterization of the antinociceptive actions of bicifadine in models of acute, persistent, and chronic pain
Basile AS, et al.
Journal of Pharmacology and Experimental Therapeutics, 321(3), 1208-1225 (2007)
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