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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
CID 1261822
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
713121-80-3
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥696.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥300.0 |
| 规格: | 5 mg | 产品价格: | ¥600.0 |
| 规格: | 10 mg | 产品价格: | ¥960.0 |
| 规格: | 25 mg | 产品价格: | ¥1920.0 |
| 规格: | 50 mg | 产品价格: | ¥3072.0 |
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ML-193
CAS No. : 713121-80-3
MCE 国际站:ML-193
产品活性:ML-193 (CID 1261822) 是一种有效和选择性的 GPR55 拮抗剂,IC50 值为 221 nM。ML-193 对 GPR55 的选择性是 GPR35,CB1 和 CB2 的 27 倍以上。ML-193 可以改善帕金森氏病 (PD) 大鼠的运动和感觉运动缺陷。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:GPR55
In Vitro: ML-193 (0.01-100 μM; pretreated for 15 min) inhibits β-arrestin trafficking induced by L-α-lysophophosphatidylinositol (LPI, 10 μM) and ML186 (1 μM) with IC50s of 0.22 μM and 0.12 μM, respectively.
ML-193 (0.01-10 μM; pretreated for 30 min) decreases the LPI-mediated ERK1/2 phosphorylation, with an IC50 of 0.2 μM in U2OS cells.
ML-193 (5 μM; pretreated for 30 min) attenuates the GPR55 agonists induced increases in hNSCs proliferation rates.
ML-193 (5 μM; 10 d) attenuates the ML184-induced increases in hNSCs differentiation.
In Vivo: ML193 (1 and 5 µg/rat; intra-striatal at a rate of 1 μL/min) attenuates sensorimotor deficits and slip steps, increases motor coordination in PD rats.
相关产品:Bioactive Compound Library Plus | GPCR/G Protein Compound Library | Neuronal Signaling Compound Library | Anti-Parkinson's Disease Compound Library | Neurodegenerative Disease-related Compound Library | Targeted Diversity Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | Highly Selective Inhibitors Library | Anandamide | CID 16020046 | O-1602 | ML-184 | ML192 | Tetrahydromagnolol | ML191 | Anandamide-d11 | GPR55 agonist 3 | GPR55 agonist 4 | L-α-lysophosphatidylinositol (Soy) (sodium) | PSB-SB-487 | Tocrifluor 1117
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