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Submit ReviewCyprodime hydrochloride is a selective μ-opioid receptor antagonist (Ki values are 5.4, 244.6 and 2187 nM for μ-, δ- and κ-opioid receptors respectively). Reduces levodopa-induced dyskinesia in the MPTP-lesioned primate model of Parkinson's disease.
分子量 | 391.93 |
公式 | C22H29NO3.HCl |
储存 | Desiccate at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 2387505-50-0 |
PubChem ID | 71628324 |
InChI Key | MMOBYZBXXHEAAX-NCBCLDNOSA-N |
Smiles | O=C3C[C@]24C1=C(OC)C=CC=C1C[C@@H](N(CC5CC5)CC4)[C@@](OC)2CC3.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 39.19 | 100 | |
ethanol | 39.19 | 100 |
以下数据基于产品分子量 391.93。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.55 mL | 12.76 mL | 25.51 mL |
5 mM | 0.51 mL | 2.55 mL | 5.1 mL |
10 mM | 0.26 mL | 1.28 mL | 2.55 mL |
50 mM | 0.05 mL | 0.26 mL | 0.51 mL |
参考文献是支持产品生物活性的出版物。
Schmidhammer et al (1995) Synthesis and biological evaluation of 14-alkoxymorphinans. 11. 3-hydroxycyprodime and analogues: opioid antagonist profile in comparison to cyprodime. J.Med.Chem. 38 3071 PMID: 7636870
Marki et al (1999) μ-opioid receptor specific antagonist cyprodime: characterization by in vitro radioligand and [35S]GTPγs binding assays. Eur.J.Pharmacol. 383 209 PMID: 10585536
Henry et al (2001) μ- and δ-opioid receptor antagonists reduce levodopa-induced dyskinesia in the MPTP-lesioned primate model of Parkinson's disease. Exp.Neurol. 171 139 PMID: 11520128
If you know of a relevant reference for Cyprodime hydrochloride, please let us know.
关键词: Cyprodime hydrochloride, Cyprodime hydrochloride supplier, Selective, μ-opioid, mu-opioid, antagonists, MOP, Receptors, OP3, 118111-54-9, Mu, Opioid, 2601, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Cyprodime hydrochloride 的部分引用包括:
Norris et al (2019) The Bivalent Rewarding and Aversive properties of δ9-tetrahydrocannabinol are Mediated Through Dissociable Opioid Receptor Substrates and Neuronal Modulation Mechanisms in Distinct Striatal Sub-Regions. Sci Rep 9 9760 PMID: 31278333
Lee et al (2012) Prostatic relaxation induced by loperamide is reduced in spontaneously hypertensive rats. J Neurosci 2012 941685 PMID: 22645476
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