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Submit ReviewLinifanib is a potent receptor tyrosine kinase (RTK) inhibitor. It inhibits PDGFRβ, KDR, FLT3, CSF-1R (IC50 values are 2, 4, 4 and 7 nM, respectively). Linifanib inhibits angiogenesis in vascularized micro-organs and potently inhibits VEGF-stimulated endothelial cell proliferation (IC50 = 0.2 nM). Linifanib also promotes the generation and reprogramming of iPSCs from somatic cells.
分子量 | 375.4 |
公式 | C21H18FN5O |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 796967-16-3 |
PubChem ID | 11485656 |
InChI Key | MPVGZUGXCQEXTM-UHFFFAOYSA-N |
Smiles | O=C(NC=1C=CC(=CC1)C=2C=CC=C3NN=C(N)C32)NC4=CC(=CC=C4F)C |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
ethanol | 7.51 | 20 | |
DMSO | 37.54 | 100 |
以下数据基于产品分子量 375.4。 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.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.66 mL | 13.32 mL | 26.64 mL |
5 mM | 0.53 mL | 2.66 mL | 5.33 mL |
10 mM | 0.27 mL | 1.33 mL | 2.66 mL |
50 mM | 0.05 mL | 0.27 mL | 0.53 mL |
参考文献是支持产品生物活性的出版物。
Albert et al (2006) Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor. Mol.Cancer Ther. 5 995 PMID: 16648571
Guan et al (2022) Chemical reprogramming of human somatic cells to pluripotent stem cells. Nature 605 325 PMID: 35418683
Jahid et al (2022) Structure-based design of CDC42 effector interaction inhibitors for the treatment of cancer. Cell Rep. 39 110641 PMID: 35385746
If you know of a relevant reference for Linifanib, please let us know.
关键词: Linifanib, Linifanib supplier, receptor, tyrosine, kinases, inhibitors, potent, vegfr, pdgfr, angiogeneis, stem, cells, reprogramming, iPSC, PDGFR, VEGFR, Stem, Cell, Reprogramming, 7743, Tocris Bioscience
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