ST638是一种蛋白质酪氨酸激酶抑制剂(IC | 50 | = 370 nM),也可以抑制HGF诱导的肝细胞中MAP激酶激活。ST638还显示出抑制人类嗜中性粒细胞中PC-PLD(磷脂酶D)的活性。该产品减少了中性粒细胞中过钒酸盐诱导的O2⋅产生。 ST638 is a protein tyrosine kinase inhibitor (IC|50|= 370 nM) that also inhibits HGF-induced MAP kinase activation in hepatocytes. ST638 has also shown to inhibit PC-PLD (phospholipase D) activity in human neutrophils. This product decreases the O2? production induced by pervanadate in neutrophils.
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2-cyano-3-[3-ethoxy-4-hydroxy-5-(phenylsulfanylmethyl)phenyl]prop-2-enamide
Dangerous GoodsCAS number:107761-24-0 molecular formula:C19H18N2O3S
overview
compound introduction
Specs
| Chinese alias | - | ||
| English alias | Q27164644 | (Z)-2-cyano-3-(3-ethoxy-4-hydroxy-5-(phenylthiomethyl)phenyl)acrylamide | DTXSID701147014 | 2-Propenamide, 2-cyano-3-[3-ethoxy-4-hydroxy-5-[(phenylthio)methyl]phenyl]- | alpha-Cyano-(3-ethoxy-4-hydroxy-5-phenylthiomethyl)cinnamide | 2-cyano-3- | ||
| CAS number | 107761-24-0 | molecular formula | C19H18N2O3S |
| molecular weight | 354.4 | Exact mass | - |
| PSA | 122 | logp | 3.1 |
numbering system
| CAS | 107761-24-0 |
| HMDB ID | HMDB0248195 |
| Wikidata | Q27164644 |
| PubChem CID | 5276 |
| DSSTox Substance ID | DTXSID701147014 |
| European Community (EC) Number | 634-605-1 |
physicochemical properties
| XLogP3 | XLogP3-AA: 3.1 |
| 复杂性 | 522 |
| Exact Mass | 354.10381361 |
| 形式电荷 | 0 |
| 重原子计数 | 25 |
| Molecular Weight | 354.4 |
| Monoisotopic Mass | 354.10381361 |
| 可旋转键计数 | 7 |
| 氢键供体计数 | 2 |
| 氢键受体计数 | 5 |
| 共价键单元计数 | 1 |
| 同位素原子计数 | 0 |
| 拓扑极性表面积 | 122 Ų |
| 定义键立体中心计数 | 0 |
| 定义原子立体中心计数 | 0 |
| 未定义键立体中心计数 | 1 |
| 未定义原子手性中心计数 | 0 |
Safety information
危害类别和分类:
急性毒性 4 (100%)
Production methods and uses
purpose
工业应用参考:
工业分类参考:化学纤维制造业。
应用场景参考:适合对材料精细度、设备条件和应用环境要求较高的场景,通常需要结合工艺目标做进一步筛选 。
作用参考:在科研材料体系中具备较强的组合应用潜力,价值往往取决于具体配方、纯度等级和工艺设计 。
选型提示:面向研发或检测用途时,建议同步评估品牌一致性、批次稳定性和后续技术支持能力 。
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MSDS
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