Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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P129814-10mg | 10mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $86.90 | |
P129814-50mg | 50mg | In stock | $271.90 |
Potent and selective FAK inhibitor
Synonyms | P4N | PF-573228, >=95% (HPLC) | 4-(4-nitrophenyl)-1-acetylpiperazine | MLS006011194 | PF-228 | FT-0719732 | NCGC00263133-11 | 6-[[4-[(3-methylsulfonylphenyl)methylamino]-5-(trifluoromethyl)pyrimidin-2-yl]amino]-3,4-dihydro-1H-quinolin-2-one | 6-[4-(3-Meth |
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Specifications & Purity | ≥98% |
Biochemical and Physiological Mechanisms | PF 573228 is a potent and selective FAK (focal adhesion kinase) inhibitor (IC50 = 4 nM). PF 573228 displays 50-250-fold selectivity over other protein kinases. PF 573228 decreases focal adhesion kinase (FAK) turnover in vitro. PF 573228 also blocks serum |
Legal Information | Sold for only research purposes |
Storage Temp | Store at 2-8°C |
Shipped In | Wet ice |
Note | Toxic, refer to SDS for further information Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | PF-573228 is an ATP-competitive inhibitor of FAK with IC50 of 4 nM in a cell-free assay, ~50- to 250-fold selective for FAK than Pyk2, CDK1/7 and GSK-3β. |
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IUPAC Name | 6-[[4-[(3-methylsulfonylphenyl)methylamino]-5-(trifluoromethyl)pyrimidin-2-yl]amino]-3,4-dihydro-1H-quinolin-2-one |
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INCHI | InChI=1S/C22H20F3N5O3S/c1-34(32,33)16-4-2-3-13(9-16)11-26-20-17(22(23,24)25)12-27-21(30-20)28-15-6-7-18-14(10-15)5-8-19(31)29-18/h2-4,6-7,9-10,12H,5,8,11H2,1H3,(H,29,31)(H2,26,27,28,30) |
InChi Key | HESLKTSGTIBHJU-UHFFFAOYSA-N |
Canonical SMILES | CS(=O)(=O)C1=CC=CC(=C1)CNC2=NC(=NC=C2C(F)(F)F)NC3=CC4=C(C=C3)NC(=O)CC4 |
Isomeric SMILES | CS(=O)(=O)C1=CC=CC(=C1)CNC2=NC(=NC=C2C(F)(F)F)NC3=CC4=C(C=C3)NC(=O)CC4 |
WGK Germany | 3 |
PubChem CID | 11612883 |
Molecular Weight | 491.49 |
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Solubility | Soluble in DMSO (≥20 mg/ml), water (<1 mg/ml at 25 °C), and ethanol (<1 mg/ml at 25 °C). |
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Pictogram(s) | GHS06, GHS07 |
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Signal | Danger |
Hazard Statements | H319:Causes serious eye irritation H301:Toxic if swallowed |
Precautionary Statements | P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P301+P316:IF SWALLOWED: Get emergency medical help immediately. P337+P317:If eye irritation persists: Get medical help. |
WGK Germany | 3 |
1. Jianghong Wu, Ziwen Long, Hong Cai, Shengjia Yu, Xiaowen Liu. (2019) Homeobox B7 accelerates the cancer progression of gastric carcinoma cells by promoting epithelial–mesenchymal transition (EMT) and activating Src–FAK pathway. OncoTargets and Therapy, 12 ( 3743–3751). [PMID:31190875] [10.2147/OTT.S198115] |
1. Jianghong Wu, Ziwen Long, Hong Cai, Shengjia Yu, Xiaowen Liu. (2019) Homeobox B7 accelerates the cancer progression of gastric carcinoma cells by promoting epithelial–mesenchymal transition (EMT) and activating Src–FAK pathway. OncoTargets and Therapy, 12 ( 3743–3751). [PMID:31190875] [10.2147/OTT.S198115] |