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≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product description:
A potent, cell-permeable, reversible, substrate competitive, and specific inhibitor of Bruton’s Tyrosine Kinase (BTK; IC50 = 17.2 µM for human BTK in vitro and IC50 = 2.5 µM for recombinant BTK). Also inhibits Polo-like kinase in an ATP-competitive manner (IC50 = 10 µM and 61 µM for Plx1 and Plk3, respectively), and displays antitumor properties. Does not affect the enzymatic activity of other protein tyrosine kinases, including EGFR, HCK, IRK JAK1, and JAK3 even at concentrations of 278 µM. Enhances the chemosensitivity of BTK-positive B-lineage leukemia cells to ceramide- and vincristine-induced apoptosis.
A potent, cell-permeable, reversible, substrate competitive, and specific inhibitor of Bruton′s tyrosine kinase (BTK; IC50 = 17.2 µM for human BTK in vitro and IC50 = 2.5 µM for recombinant BTK). Also inhibits Polo-like kinase in an ATP-competitive manner (IC50 = 10 µM and 61 µM for Plx1 and Plk3, respectively), and displays antitumor properties. Does not affect the enzymatic activity of other protein tyrosine kinases, including EGFR, HCK, IRK JAK1, and JAK3 even at concentrations of 278 µM. Enhances the chemosensitivity of BTK-positive B-lineage leukemia cells to ceramide- and vincristine-induced apoptosis.
| Pubchem Sid | 488201704 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488201704 |
| Canonical Smiles | CC(=C(C#N)C(=O)NC1=C(C=CC(=C1)Br)Br)O |
| IUPAC Name | 2-cyano-N-(2,5-dibromophenyl)-3-hydroxybut-2-enamide |
| InChIKey | UVSVTDVJQAJIFG-UHFFFAOYSA-N |
| INCHI | 1S/C11H8Br2N2O2/c1-6(16)8(5-14)11(17)15-10-4-7(12)2-3-9(10)13/h2-4,16H,1H3,(H,15,17) |
| Isomeric SMILES | CC(=C(C#N)C(=O)NC1=C(C=CC(=C1)Br)Br)O |
| Molecular Weight | 360 |
| Reaxy-Rn | 10678941 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10678941&ln= |
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| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Sep 16, 2025 | L286934 | |
| Certificate of Analysis | Aug 15, 2022 | L286934 |
| Solubility | Solvent:DMSO, Max Conc. mg/mL: 36, Max Conc. mM: 100 |
|---|---|
| Sensitivity | light & heat sensitive |
| Molecular Weight | 360.000 g/mol |
| XLogP3 | 3.800 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 359.893 Da |
| Monoisotopic Mass | 357.895 Da |
| Topological Polar Surface Area | 73.100 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 386.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 1 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |