Chemical Structure : PFK15
CAS No.: 4382-63-2
货号: PC-42915Not For Human Use, Lab Use Only.
PFK15 (PFK 015) is a potent, selective 6-phosphofructo-2-kinase (PFKFB3) inhibitor with IC50 of 207 nM against recombinant human PFKFB3, displays 100-fold more activity than 3PO.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
25 mg | ¥1280 | In stock | |
50 mg | ¥1980 | In stock | |
100 mg | ¥2980 | In stock | |
200 mg | Get quote | ||
1 g | Get quote |
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PFK15 (PFK 015) is a potent, selective 6-phosphofructo-2-kinase (PFKFB3) inhibitor with IC50 of 207 nM against recombinant human PFKFB3, displays 100-fold more activity than 3PO.
PFK15 (PFK 015) does not inhibit PFK-1, hexokinase, phosphoglucose isomerase and PFKFB4, and has no activity against a panel of 96 kinases.
PFK15 (PFK 015) inhibits cancer cell viability (H522 cell IC50=0.72 uM) and induces apoptosis.
PFK15 (PFK 015) suppresses the glucose uptake and exhibits antitumor effects in human xenograft models.
分子量 | 260.29 | |
分子式 | C17H12N2O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: 25.2 mg/mL |
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Chemical Name/SMILES |
2-Propen-1-one, 1-(4-pyridinyl)-3-(2-quinolinyl)- |
1. Clem BF, et al. Mol Cancer Ther. 2013 Aug;12(8):1461-70.
2. Lea MA, et al. Anticancer Res. 2016 Apr;36(4):1479-88.
3. Zhu W, et al. PLoS One. 2016 Sep 26;11(9):e0163768.
4. Li HM, et al. J Exp Clin Cancer Res. 2017 Jan 7;36(1):7.
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