AZ PFKFB3 26

Pricing Availability   Qty
说明: Potent and selective PFKFB3 inhibitor
化学名: (2S)-N-[4-[[3-Cyano-1-(2-methylpropyl)-1H-indol-5-yl]oxy]phenyl]-2-pyrrolidinecarboxamide
纯度: ≥98% (HPLC)
说明书
引用文献
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文献 (3)

生物活性 for AZ PFKFB3 26

AZ PFKFB3 26 is a potent and selective PFKFB3 inhibitor (IC50 = 0.023 μM). Selective for PFKFB3 over PFKFB2 and PFKFB1 isoforms (IC50 values are 0.382 μM and 2.06 μM, respectively). Reduces levels of fructose-1,6-bisphosphate in A549 cells (IC50 = 0.343 μM). Exhibits no significant inhibition of other kinases.

化合物库 for AZ PFKFB3 26

AZ PFKFB3 26 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 AZ PFKFB3 26

分子量 402.49
公式 C24H26N4O2
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 1704740-52-2
PubChem ID 118735769
InChI Key OOGHGWKBJXQNEJ-QFIPXVFZSA-N
Smiles N#CC1=CN(CC(C)C)C2=C1C=C(OC3=CC=C(NC([C@H]4NCCC4)=O)C=C3)C=C2

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 AZ PFKFB3 26

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 40.25 100
ethanol 40.25 100

制备储备液 for AZ PFKFB3 26

以下数据基于产品分子量 402.49。 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 2.48 mL 12.42 mL 24.85 mL
5 mM 0.5 mL 2.48 mL 4.97 mL
10 mM 0.25 mL 1.24 mL 2.48 mL
50 mM 0.05 mL 0.25 mL 0.5 mL

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参考文献 for AZ PFKFB3 26

参考文献是支持产品生物活性的出版物。

Boyd et al (2015) Structure-based design of potent and selective inhibitors of the metabolic kinase PFKFB3. J.Med.Chem. 58 3611 PMID: 25849762


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关键词: AZ PFKFB3 26, AZ PFKFB3 26 supplier, AZPFKFB326, phosphofructokinase2, PFKFB3, inhibitors, inhibits, fructose-1,6-bisphosphate, kinase, cancer, 5675, Tocris Bioscience

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