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PF-562271是一种有效的，ATP竞争性的，可逆的FAK抑制剂，作用于FAK比作用于Pyk2选择性高10倍左右，比作用于其他蛋白激酶（除了一些CDKs）选择性高100倍以上。
Targets
| Target | Value |
|---|---|
| FAK | IC50: 1.5nM |
| PYK2 | IC50: 13nM |
| CDK2/CyclinE | IC50: 30nM |
| CDK3/CyclinE | IC50: 47nM |
| CDK1/CyclinB | IC50: 58nM |
| CDK7/CyclinH/MAT1 | IC50: 97nM |
| FLT3 | IC50: 97nM |
| GSK-3α | IC50: 101nM |
| CDK5/p35 | IC50: 120nM |
| GSK-3β | IC50: 133nM |
| AuroraA | IC50: 145nM |
| CDK2/CyclinA | IC50: 227nM |
| YES | IC50: 294nM |
| MAPK1 | IC50: 340nM |
| Fyn | IC50: 377nM |
| LCK | IC50: 408nM |
| IGF-1R | IC50: >500nM |
| PKA | IC50: 620nM |
| c-Src | IC50: 797nM |
| CDK4 | IC50: >1μM |
| CDK6/CyclinD2 | IC50: >1μM |
| Chk1 | IC50: >1μM |
| Chk2 | IC50: >1μM |
| EGFR | IC50: >1μM |
| EphB2 | IC50: >1μM |
| FGFR3 | IC50: >1μM |
| Abl | IC50: >1μM |
| Fms | IC50: >1μM |
| IKKα | IC50: >1μM |
| IKKβ | IC50: >1μM |
| JNK1α1 | IC50: >1μM |
| MEK1 | IC50: >1μM |
| p70S6K | IC50: >1μM |
| PKBα | IC50: >1μM |
| PKBβ | IC50: >1μM |
| PKBγ | IC50: >1μM |
| PKCα | IC50: >1μM |
| PKCβ2 | IC50: >1μM |
| PKCδ | IC50: >1μM |
| TrkB | IC50: >2.5μM |
| PDGFRβ | IC50: >3μM |
| In vitro (25°C) | DMSO | Warmed: 91 mg/mL (179.31 mM) | |
| Water | Insoluble | ||
| Ethanol | Insoluble | ||
| In vivo | 5% DMSO+40% PEG 300+5% Tween 80+50% ddH2O | 4 mg/mL | |
|
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
|||
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 19.7 mL | 98.52 mL | 197.05 mL |
| 0.5 mM | 3.94 mL | 19.7 mL | 39.41 mL |
| 1 mM | 1.97 mL | 9.85 mL | 19.7 mL |
| 5 mM | 0.39 mL | 1.97 mL | 3.94 mL |
*The above data is based on the productmolecular weight 507.49. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| 目录号 | A11192 |
|---|---|
| 作用机制 | Inhibitor (抑制剂) |
| M. Wt | 507.49 |
| Formula | C21H20F3N7O3S |
| Purity | >99% |
| Storage | Store lyophilized at -20ºC, keep desiccated. |
| CAS No. | 717907-75-0 |
| Synonyms | PF562271 |
| SMILES | CN(C1=C(C=CC=N1)CNC2=NC(=NC=C2C(F)(F)F)NC3=CC4=C(C=C3)NC(=O)C4)S(=O)(=O)C |
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