ST638
Synonym(s):α-Cyano-(3-ethoxy-4-hydroxy-5-phenylthiomethyl)cinnamide
- CAS NO.:107761-24-0
- Empirical Formula: C19H18N2O3S
- Molecular Weight: 354.42
- MDL number: MFCD00236446
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-01-13 11:16:10
What is ST638?
The Uses of ST638
ST638 is a protein tyrosine kinase inhibitor and PLD inhibitor.
What are the applications of Application
ST638 is a protein tyrosine kinase inhibitor and PLD inhibitor
Biological Activity
st638 is a tyrosine kinase inhibitor [1].tyrosine kinases are a family of protein kinases that phosphorylate the serine and threonine on other proteins. phosphorylation of proteins by kinases has been involved in signal transduction and regulating cellular activity, such as cell division. tyrosine kinases function in a variety of processes, such as mitogenesis, induction of mitosis, and transmembrane signaling [2].in human platelets, preincubation with 50 μm of st638 completely blocked the platelet aggregation induced with 0.05 unit/ml of thrombin. st638 inhibited the increase of protein-tyrosine phosphorylation bands induced with thrombin in a dose-dependent manner. st638 blocked the platelet aggregation and protein-tyrosine phosphorylation induced with thrombin in aspirin-treated platelets [1]. in terminal erythroid differentiation of mouse erythroleukemia (mel) cells, st638 effectively induced differentiation in a synergistic manner [3]. in rat and rabbit pulmonary artery cells, st 638 (0.5 to 40 μmol/l) blocked ik in a dose-dependent manner [4].
References
[1] asahi m, yanagi s, ohta s, et al. thrombin-induced human platelet aggregation is inhibited by protein-tyrosine kinase inhibitors, st638 and genistein[j]. febs letters, 1992, 309(1): 10-14.
[2] levitzki a, gazit a. tyrosine kinase inhibition: an approach to drug development[j]. science, 1995, 267(5205): 1782.
[3] watanabe t, shiraishi t, sasaki h, et al. inhibitors for protein-tyrosine kinases, st638 and genistein, induce differentiation of mouse erythroleukemia cells in a synergistic manner[j]. experimental cell research, 1989, 183(2): 335-342.
[4] smirnov s v, aaronson p i. inhibition of vascular smooth muscle cell k+ currents by tyrosine kinase inhibitors genistein and st 638[j]. circulation research, 1995, 76(2): 310-316.
Properties of ST638
| Melting point: | 134-135.5 °C |
| Boiling point: | 611.2±55.0 °C(Predicted) |
| Density | 1.32±0.1 g/cm3(Predicted) |
| storage temp. | −20°C |
| solubility | DMSO: 19 mg/mL |
| pka | 8.79±0.50(Predicted) |
| form | solid |
| color | yellow |
Safety information for ST638
Computed Descriptors for ST638
New Products
DL-beta-(3-Bromophenyl)alanine Tetrabutylammonium perchlorate N,O-Dimethylhydroxylamine hydrochloride (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid 2-Amino-5-bromo-4-(trifluoromethyl)pyridine(RM for Indian lab) N,N CARBONYL DIIMIDAZOLE Levothyroxine Impurity-F Montelukast EP Impurity-D/Montelukast USP Related Compound C Atorvastatin FXA Impurity/Atorvastatin Cyclic 6-Hydroxy Impurity Sodium Salt Isosulfan blue Keto N-Oxide Impurity Ivermectin Impurity F N-Nitroso des Methyl Tramadol/N-Nitroso-N-Desmethyl-Tramadol (R)-BoroLeu-(+)-Pinanediol-CF3COOH 1,4-bis(methylsulfonyl)butane 4-(5-amino-1-methyl-1h-benzoimidazol-2-yl)-butyric acid isopropyl ester. 5-Methyl-1,3-benzenediacetonitrile 4-Fluorothiophenol 1-methyl amino-2,4-dinitro benzene CSA (DL-10-Camphorsulfonic Acid) 2-Hydroxy-4-methylnicotinic acid 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2S)-1-((2S,3S)-3-(2-methylbutyl)-4-oxooxetan-2-yl)pentadecan-2-yl formylleucinate 1-(3,5-dichlorophenyl)-2,2,2-trifluoroethane-1-sulfonyl chloride S-(1-(3,5-dichlorophenyl)-2,2,2-trifluoroethyl) ethanethioateRelated products of tetrahydrofuran
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