Asimadoline-HCl
| 中文名称 | Asimadoline-HCl |
|---|---|
| 中文同义词 | 阿西马朵林盐酸盐;化合物ASIMADOLINE HYDROCHLORIDE;N-((S)-2-((S)-3-羟基吡咯烷-1-基)-1-苯乙基)-N-甲基-2,2-二苯基乙酰胺盐酸盐;PERFEMIKER]ASIMADOLINE HYDROCHLORIDE,98%;阿西马朵林盐酸盐,10 MM DMSO 溶液;【进口原装】Asimadoline hydrochloride/185951-07-9;Asimadoline hydrochloride :阿西马朵林盐酸盐;【进口原装】Asimadoline hydrochloride/185951-07-9 |
| 英文名称 | Asimadoline-HCl |
| 英文同义词 | Asimadoline-HCl;Asimadoline hydrochloride;Asimadoline Hydrochlorine;N-[(1S)-2-[(3S)-3-hydroxypyrrolidin-1-yl]-1-phenylethyl]-N-methyl-2,2-diphenylacetamide;EMD-61753 hydrochloride;syndrome,bowel,diabetic,EMD61753,Asimadoline,irritable,κ-opioid,δ-opioid,EMD 61753,inhibit,Asimadoline hydrochloride,EMD-61753,μ-opioid,Opioid Receptor,allodynia,Inhibitor;Asimadoline hydrochloride, 10 mM in DMSO;N-((S)-2-((S)-3-Hydroxypyrrolidin-1-yl)-1-phenylethyl)-N-methyl-2,2-diphenylacetamide hydrochloride |
| CAS号 | 185951-07-9 |
| 分子式 | C27H31ClN2O2 |
| 分子量 | 451.01 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 185951-07-9.mol |
| 结构式 |  |
Asimadoline-HCl 性质
| 储存条件 | Store at -20°C |
|---|---|
| 溶解度 | 二甲基亚砜：240 mg/mL（532.15 mM） |
| 形态 | 固体 |
| 颜色 | 米白色至浅黄色 |
| InChIKey | GMJSLABTEURMBF-CLSOAGJSSA-N |
| SMILES | CN([C@H](CN1C[C@@H](O)CC1)C2=CC=CC=C2)C(C(C3=CC=CC=C3)C4=CC=CC=C4)=O.Cl |
IC50: 5.6 nM (guinea pig κ opioid), 1.2 nM (human recombinant κ opioid)
Asimadoline (EMD-61753) hydrochloride has high selectively in κ: μ: δ opioid binding ratios of 1:501:498 in human recombinant receptors. The IC
50
for Asimadoline hydrochloride binding to μ-opioid receptors is 3 µM and to δ-opioid receptors is 0.7 µM. The IC
50
values for D1, D2, kainate, σ, PCP/NMDA, H1, α1, α2, M1/M2, glycine, 5HT1A, 5HT1C, 5HT1D, 5HT2, 5HT3, AMPA and kainate/AMPA receptors are all >10 µM.
Asimadoline hydrochloride has affinity to sodium and L type Ca
2+
ion channels at IC
50
concentrations 150 to 800 fold the IC
50
for the κ receptors.
At high concentrations, Asimadoline hydrochloride demonstrates spasmolytic action against 400 µM barium chloride in the rat duodenum (IC
50
=4.2 µM), suggesting that Asimadoline hydrochloride may block the direct stimulant effects of barium on smooth muscle through mechanisms that are not identified.
Asimadoline (EMD-61753 hydrochloride; 1, 5, 15 mg/kg; s.c.) acutely ameliorates both formalin-evoked hyperalgesia and tactile allodynia in diabetic rats.
The absorption rate following oral administration is 80% in rats and >90% in dogs and monkeys. The metabolism of Asimadoline hydrochloride is rapid and appears similar in animals and man. Asimadoline hydrochloride has peripheral anti-inflammatory actions that are partly mediated through increase in joint fluid substance P levels.
Treatment with Asimadoline hydrochloride (5 mg/kg/day; i.p.) produces marked (and sustained) attenuation of the disease with all three time regimes.
| Animal Model: | Adult female Sprague-Dawley rats |
| Dosage: | 1, 5, 15 mg/kg |
| Administration: | SC; single dose |
| Result: | Acutely ameliorated both formalin-evoked hyperalgesia and tactile allodynia in diabetic rats. |
安全信息
| WGK Germany | WGK 3 |
|---|---|
| 存储类别 | 11 - 可燃固体 |
| 危险性类别 | 急性毒性 类别4 经口 |
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026/03/03 | S0009 | Asimadoline-HCl Asimadoline hydrochloride | 185951-07-9 | 5mg | 5053.23元 |
| 2026/03/03 | S0009 | Asimadoline-HCl Asimadoline hydrochloride | 185951-07-9 | 25mg | 15225.2元 |