L-365,260

Pricing Availability   Qty
说明: Selective CCK2 antagonist
化学名: N-[(3R)-2,3-Dihydro-1-methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl]-N'-(3-methylphenyl)urea
纯度: ≥99% (HPLC)
说明书
引用文献 (1)
评论
文献 (1)

生物活性 for L-365,260

L-365,260 is a selective cholecystokinin receptor 2 (CCK2) antagonist (IC50 values are 2 and 280 nM at CCK2 and CCK1 receptors respectively) that is inactive at a range of other receptors including opiate, muscarinic acetylcholine, α- and β adrenergic, histamine, angiotensin and bradykinin receptors.

技术数据 for L-365,260

分子量 398.46
公式 C24H22N4O2
储存 Store at +4°C
纯度 ≥99% (HPLC)
CAS Number 118101-09-0
PubChem ID 5311201
InChI Key KDFQABSFVYLGPM-QFIPXVFZSA-N
Smiles O=C1[C@H](NC(NC4=CC=CC(C)=C4)=O)N=C(C3=CC=CC=C3)C2=C(C=CC=C2)N1C

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 L-365,260

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 39.85 100
ethanol 39.85 100

制备储备液 for L-365,260

以下数据基于产品分子量 398.46。 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 2.51 mL 12.55 mL 25.1 mL
5 mM 0.5 mL 2.51 mL 5.02 mL
10 mM 0.25 mL 1.25 mL 2.51 mL
50 mM 0.05 mL 0.25 mL 0.5 mL

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产品说明书 for L-365,260

分析证书/产品说明书
选择另一批次:

参考文献 for L-365,260

参考文献是支持产品生物活性的出版物。

Kees et al (1989) Benzodiazepine gastrin and brain cholecystokinin receptor ligands: L-365,260. J.Med.Chem. 32 13 PMID: 2909725

Lotti and Chang (1989) A new potent and selective non-peptide gastrin antagonist and brain cholecystokinin receptor (CCK-B) ligand: L-365,260. Eur.J.Pharmacol. 162 273 PMID: 2721567

Chung et al (2009) Cholecystokinin action on layer 6b neurons in somatosensory cortex. Brain Res. 1282 10 PMID: 19497313


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关键词: L-365,260, L-365,260 supplier, Selective, CCK2, antagonists, Cholecystokinin2, Receptors, L365260, Receptor, 2767, Tocris Bioscience

1 篇 L-365,260 的引用文献

引用文献是使用了 Tocris 产品的出版物。 L-365,260 的部分引用包括:

Wu et al (2014) Role of cholecystokinin in anorexia induction following oral exposure to the 8-ketotrichothecenes deoxynivalenol, 15-acetyldeoxynivalenol, 3-acetyldeoxynivalenol, fusarenon X, and nivalenol. Toxicol Sci 138 278 PMID: 24385417


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