中文名 | SN 6 |
英文名 | SN 6 |
别名 | 化合物SN6 2-(4-((4-硝基苄基)氧基)苄基)噻唑烷-4-羧酸乙酯 |
英文别名 | SN6 SN-6 SN 6 Ethyl 2-(4-((4-nitrobenzyl)oxy)benzyl)thiazolidine-4-carboxylate 2-[[4-[(4-NITROPHENYL)METHOXY]PHENYL]METHYL]-4-THIAZOLIDINECARBOXYLIC ACID ETHYL ESTER 4-Thiazolidinecarboxylic acid, 2-[[4-[(4-nitrophenyl)methoxy]phenyl]methyl]-, ethyl ester |
CAS | 415697-08-4 |
化学式 | C20H22N2O5S |
分子量 | 402.46 |
密度 | 1.285±0.06 g/cm3(Predicted) |
沸点 | 581.2±50.0 °C(Predicted) |
酸度系数 | 6.63±0.60(Predicted) |
存储条件 | Keep in dark place,Sealed in dry,2-8°C |
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. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.485 ml | 12.424 ml | 24.847 ml |
5 mM | 0.497 ml | 2.485 ml | 4.969 ml |
10 mM | 0.248 ml | 1.242 ml | 2.485 ml |
5 mM | 0.05 ml | 0.248 ml | 0.497 ml |
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