LY 288513

Pricing Availability   Qty
说明: Selective CCK2 antagonist
化学名: (4S,5R)-N-(4-Bromophenyl)-3-oxo-4,5-diphenyl-1-pyrazolidinecarboxamide
纯度: ≥98% (HPLC)
说明书
引用文献 (1)
评论
文献 (1)

生物活性 for LY 288513

LY 288513 is a selective CCK2 receptor antagonist (IC50 values are 16 and > 30,000 nM for CCK2 and CCK1 respectively). Displays anxiolytic and antipsychotic properties in vivo.

许可信息

Sold with the permission of Eli Lilly and Company

技术数据 for LY 288513

分子量 436.3
公式 C22H18BrN3O2
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 147523-65-7
PubChem ID 2802894
InChI Key LMUQHXHWJWQXSD-PMACEKPBSA-N
Smiles BrC1=CC=C(NC(=O)N2NC(=O)[C@H]([C@@H]2C2=CC=CC=C2)C2=CC=CC=C2)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.

溶解性数据 for LY 288513

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 43.63 100

制备储备液 for LY 288513

以下数据基于产品分子量 436.3。 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
1 mM 2.29 mL 11.46 mL 22.92 mL
5 mM 0.46 mL 2.29 mL 4.58 mL
10 mM 0.23 mL 1.15 mL 2.29 mL
50 mM 0.05 mL 0.23 mL 0.46 mL

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产品说明书 for LY 288513

分析证书/产品说明书
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参考文献 for LY 288513

参考文献是支持产品生物活性的出版物。

Rasmussen (1994) CCK, schizophrenia, and anxiety. CCK-B antagonists inhibit the activity of brain DA neurons. Ann.N.Y.Acad.Sci. 713 300 PMID: 8185172

Helton et al (1996) Central nervous system characterization of the new cholecystokininB antagonist LY288513. Pharmacol.Biochem.Behav. 53 493 PMID: 8866946

Rasmussen et al (1992) Electrophysiological effects of diphenylpyrazolidinone cholecystokinin-B and cholecystokinin-A antagonists on midbrain DA neurons. J.Pharmacol.Exp.Ther. 264 480


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查看全部 CCK2 Receptor Antagonists

关键词: LY 288513, LY 288513 supplier, Selective, CCK2, antagonists, Cholecystokinin2, Receptors, LY288513, Receptor, 1524, Tocris Bioscience

1 篇 LY 288513 的引用文献

引用文献是使用了 Tocris 产品的出版物。 LY 288513 的部分引用包括:

Wen et al (2012) Cholecystokinin receptor-1 mediates the inhibitory effects of exogenous cholecystokinin octapeptide on cellular mor. dependence. Front Endocrinol (Lausanne) 13 63 PMID: 22682150


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