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415697-08-4

中文名称 415697-08-4
英文名称 2-[[4-[(4-NITROPHENYL)METHOXY]PHENYL]METHYL]-4-THIAZOLIDINECARBOXYLIC ACID ETHYL ESTER
CAS 415697-08-4
分子式 C20H22N2O5S
分子量 402.46
MOL 文件 415697-08-4.mol
更新日期 2024/03/06 11:25:45
415697-08-4 结构式 415697-08-4 结构式

基本信息

中文别名
化合物SN6
英文别名
SN-6
SN-6
SN6
SN 6
2-[[4-[(4-NITROPHENYL)METHOXY]PHENYL]METHYL]-4-THIAZOLIDINECARBOXYLIC ACID ETHYL ESTER
4-Thiazolidinecarboxylic acid, 2-[[4-[(4-nitrophenyl)methoxy]phenyl]methyl]-, ethyl ester

物理化学性质

沸点581.2±50.0 °C(Predicted)
密度1.285±0.06 g/cm3(Predicted)
储存条件Keep in dark place,Sealed in dry,2-8°C
溶解度DMSO : 62.5 mg/mL (155.29 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
酸度系数(pKa)6.63±0.60(Predicted)
形态粉末
颜色White to light yellow

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335
SN 6价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-107658SN 6
SN 6
415697-08-45mg840元
2024/04/30HY-107658SN 6
SN 6
415697-08-410mM * 1mLin DMSO924元
2024/04/30HY-107658SN 6
SN 6
415697-08-410mg1300元

常见问题列表

生物活性
SN-6 是一种选择性的 Na+/Ca2+ exchanger (NCX) 抑制剂。SN-6 可抑制NCX1、NCX2和NCX3,对应的IC50值分别为2.9 μM、16 μM和8.6 μM。SN-6 可消除 acetylcholine (ACh) 诱导的血管舒张。
靶点
TargetValue
NCX1
(Cell-free assay)
2.9 μM
NCX3
(Cell-free assay)
8.6 μM
NCX2
(Cell-free assay)
16 μM
体外研究

SN 6 is a selective Na + /Ca 2+ exchanger inhibitor, which inhibits the initial rate of 45 Ca 2+ uptake into NCX1, NCX2, and NCX3 transfectants with IC 50 values of 2.9 ± 0.12, 16 ± 1.1, and 8.6 ± 0.27 μM. SN 6 (up to 30 μM) also less potently inhibits muscarinic acetylcholine receptor, with a higher IC 50 of 18 μM. SN 6 (0.3-30 μM) completely inhibits the initial rate of Na + i -dependent 45 Ca 2+ uptake into Na + -loaded sarcolemmal vesicles in a dose dependent manner (IC 50 , 5.3 ± 0.37 μM). SN 6 (0.3-10 μM) dose-dependently protects against the hypoxia/reoxygenation-induced LDH release in parental LLC-PK1 cells and NCX1 transfectants but not in K229Q transfectants. SN 6 (1-30 μM) suppresses the bidirectional outward and inward I NCX in a concentration-dependent manner, with IC 50 values of 2.3 μM and 1.9 μM, respectively. SN 6 also inhibits bidirectional current (I NCX ) in a [Na + ]i concentration-dependent manner, with IC 50 values of 3.4 μM, 2.3 μM, and 1.1 μM at 10 mM, 20 mM, and 30 mM [Na + ]i, respectively. SN 6 inhibits hypoxia/reoxygenation-induced LDH release with an IC 50 value of 0.63 ± 0.15 μM in NCX1 transfectants.

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