LY 225910

Pricing Availability   Qty
说明: Potent CCK2 antagonist
化学名: 2-[2-(5-Bromo-1H-indol-3-yl)ethyl]-3-[3-(1-methylethoxy)phenyl]-4-(3H)-quinazoline
说明书
引用文献 (3)
评论
文献 (1)

生物活性 for LY 225910

LY 225910 is a potent CCK2 receptor antagonist (IC50 = 9.3 nM for inhibition of 125I-labeled CCK-8 sulfate binding at mouse brain membranes).

许可信息

Sold with the permission of Eli Lilly and Company.

技术数据 for LY 225910

分子量 502.41
公式 C27H24BrN3O2
储存 Desiccate at -20°C
CAS Number 133040-77-4
PubChem ID 4355450
InChI Key KUECXUACQOYKNB-UHFFFAOYSA-N
Smiles CC(C)OC1=CC=CC(=C1)N1C(CCC2=CNC3=CC=C(Br)C=C23)=NC2=C(C=CC=C2)C1=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 LY 225910

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 100

制备储备液 for LY 225910

以下数据基于产品分子量 502.41。 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 1.99 mL 9.95 mL 19.9 mL
5 mM 0.4 mL 1.99 mL 3.98 mL
10 mM 0.2 mL 1 mL 1.99 mL
50 mM 0.04 mL 0.2 mL 0.4 mL

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产品说明书 for LY 225910

分析证书/产品说明书
选择另一批次:

参考文献 for LY 225910

参考文献是支持产品生物活性的出版物。

Suman-Chauhan et al (1996) The influence of guanyl nucleotide on agonist and antagonist affinity at guinea-pig CCK-B / gastrin receptors: binding studies using [3H]PD140376. Regul.Pept. 65 37 PMID: 8876034

Yu et al (1991) Quinazolinone cholecystokinin receptor ligands. J.Med.Chem. 34 1505 PMID: 2016728


If you know of a relevant reference for LY 225910, please let us know.

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关键词: LY 225910, LY 225910 supplier, Potent, CCK2, antagonists, Cholecystokinin2, Receptors, LY225910, Receptor, 1018, Tocris Bioscience

3 篇 LY 225910 的引用文献

引用文献是使用了 Tocris 产品的出版物。 LY 225910 的部分引用包括:

Seillier et al (2013) Phencyclidine-induced social withdrawal results from deficient stimulation of cannabinoid CB1 receptors: implications for schizophrenia. Neuropharmacology 38 1816 PMID: 23563893

Karson et al (2008) Cholecystokinin inhibits endocannabinoid-sensitive hippocampal IPSPs and stimulates others. J Card Fail 54 117 PMID: 17689570

Gallopin et al (2006) Cortical sources of CRF, NKB, and CCK and their effects on pyramidal cells in the neocortex. Neuropsychopharmacology 16 1440 PMID: 16339088


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