106392-48-7
106392-48-7
Chemical Structure
ST271
- CAS No.: 106392-48-7
- Formula:C16H20N2O2
- Molecular Weight:272.34
IUPAC Name: (E)-2-cyano-3-(4-hydroxy-3,5-diisopropylphenyl)acrylamide
InChIKey: HMLQHJRJKQDTKW-LFYBBSHMSA-N
SMILES: O=C(N)/C(C#N)=C/C1=CC(C(C)C)=C(O)C(C(C)C)=C1
Biological Activity: ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
ST271 | 98.00% | ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
ST271 (Standard) | ≥98% | ST271 (Standard) is the analytical standard of ST271 (HY-103097). This product is intended for research and analytical applications. ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
