AM 4113

Pricing Availability   Qty
说明: High affinity and selective CB1 antagonist
化学名: 5-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide
纯度: ≥98% (HPLC)
说明书
引用文献
评论
文献 (2)

生物活性 for AM 4113

AM 4113 is a high affinity and selective CB1 antagonist (Kd = 0.89 nM). Exhibits 100-fold selectivity for CB1 over CB2. Attenuates CB1 agonist AM 411-induced locomotor suppression and reduces food intake in vivo, but does not induce signs of nausea.

化合物库 for AM 4113

AM 4113 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for AM 4113

分子量 380.66
公式 C17H12Cl3N3O
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 614726-85-1
PubChem ID 66844170
InChI Key BBUKVPCUOHFAQN-UHFFFAOYSA-N
Smiles CC1=C(C2=CC=C(C=C2)Cl)N(C3=C(C=C(C=C3)Cl)Cl)N=C1C(N)=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.

溶解性数据 for AM 4113

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 7.61 20
ethanol 7.61 20

制备储备液 for AM 4113

以下数据基于产品分子量 380.66。 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.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.2 mM 13.14 mL 65.68 mL 131.35 mL
1 mM 2.63 mL 13.14 mL 26.27 mL
2 mM 1.31 mL 6.57 mL 13.14 mL
10 mM 0.26 mL 1.31 mL 2.63 mL

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参考文献 for AM 4113

参考文献是支持产品生物活性的出版物。

Sink et al (2008) The novel cannabinoid CB1 receptor neutral antagonist AM4113 suppresses food intake and food-reinforced behavior but does not induce signs of nausea in rats. Neuropsychopharmacology 33 946 PMID: 17581535

Hodge et al (2008) The cannabinoid CB1 receptor inverse agonist AM 251 and antagonist AM 4113 produce similar effects on the behavioral satiety sequence in rats Behav. Brain Res. 193 298 PMID: 18602425


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关键词: AM 4113, AM 4113 supplier, AM4113, high, affinity, selective, CB1, antagonists, Cannabinoids, Receptors, cb1r, 6193, Tocris Bioscience

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