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Submit ReviewSCH 336 is a highly potent and selective CB2 receptor inverse agonist (Ki = 1.8 nM, EC50 = 2 nM). Displays 100-fold selectivity for CB2 receptors over CB1. Increases Forskolin stimulated cAMP accumulation in CHO cells expressing human CB2 receptors. Inhibits leukocyte migration in a murine model of delayed-type hypersensitivity and inhibits antigen-induced lung eosinophilia in a mouse allergy model.
SCH 336 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。
分子量 | 539.64 |
公式 | C23H25NO8S3 |
储存 | Store at RT |
纯度 | ≥98% (HPLC) |
CAS Number | 447459-51-0 |
PubChem ID | 10324989 |
InChI Key | NXODIUKWAVUFGF-INIZCTEOSA-N |
Smiles | CS(N[C@@H](C)C1=CC=C(S(C2=C(S(=O)(C3=CC=C(OC)C=C3)=O)C=C(OC)C=C2)(=O)=O)C=C1)(=O)=O |
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 | 53.96 | 100 |
以下数据基于产品分子量 539.64。 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 | 1.85 mL | 9.27 mL | 18.53 mL |
5 mM | 0.37 mL | 1.85 mL | 3.71 mL |
10 mM | 0.19 mL | 0.93 mL | 1.85 mL |
50 mM | 0.04 mL | 0.19 mL | 0.37 mL |
参考文献是支持产品生物活性的出版物。
Lunn et al (2006) A novel cannabinoid peripheral cannabinoid receptor-selective inverse agonist blocks leukocyte recruitment in vivo. J.Pharmacol.Exp.Ther. 316 780 PMID: 16258021
If you know of a relevant reference for SCH 336, please let us know.
关键词: SCH 336, SCH 336 supplier, SCH336, potent, selective, cannabinoid, 2, receptor, CB2, inverse, agonists, Receptors, 5815, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 SCH 336 的部分引用包括:
Dos-Santos-Pereira et al (2020) Cannabidiol prevents LPS-induced microglial inflammation by inhibiting ROS/NF-κB-dependent signaling and glucose consumption. Glia 68 561 PMID: 31647138
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