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Submit ReviewPSNCBAM-1 is a CB1 receptor negative allosteric modulator (IC50 values are 45 and 209 nM for the inhibition of CP 55,940 and WIN 55,212-2 respectively). Has no effect at the CB2 receptor. Decreases food intake and body weight in rats.
PSNCBAM-1 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 | 392.88 |
公式 | C22H21ClN4O |
储存 | Store at +4°C |
纯度 | ≥99% (HPLC) |
CAS Number | 877202-74-9 |
PubChem ID | 11560249 |
InChI Key | HDAYFSFWIPRJSO-UHFFFAOYSA-N |
Smiles | ClC1=CC=C(NC(NC2=CC(C3=CC=CC(N4CCCC4)=N3)=CC=C2)=O)C=C1 |
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 | 39.29 | 100 |
以下数据基于产品分子量 392.88。 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 | 12.73 mL | 25.45 mL |
5 mM | 0.51 mL | 2.55 mL | 5.09 mL |
10 mM | 0.25 mL | 1.27 mL | 2.55 mL |
50 mM | 0.05 mL | 0.25 mL | 0.51 mL |
参考文献是支持产品生物活性的出版物。
Horswill et al (2007) PSNCBAM-1, a novel allosteric antagonist at cannabinoid CB1 receptors with hypophagic effects in rats. Br.J.Pharmacol. 152 805 PMID: 17592509
German et al (2014) Diarylureas as allosteric modulators of the cannabinoid CB1 receptor: structure-activity relationship studies on 1-(4-chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea (PSNCBAM-1). J.Med.Chem. 57 7758 PMID: 25162172
If you know of a relevant reference for PSNCBAM-1, please let us know.
关键词: PSNCBAM-1, PSNCBAM-1 supplier, subtype, selective, cb1, cannabinoids, receptors, negative, allosteric, modulators, antagonists, hypophagic, NAM, CB1, Receptors, 5321, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。
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Allosteric enhancement of radiolabeled agonist binding.
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The key feature of drug addiction is the inability to stop using a drug despite clear evidence of harm. This poster describes the brain circuits associated with addiction, and provides an overview of the main classes of addictive drugs and the neurotransmitter systems that they target.