中文名称: SN6
英文名称: SN6
CAS No: 415697-08-4
分子式: C20H22N2O5S
分子量: 402.46
S10966 SN6 ≥98% (psaitong)
包装规格:
5mg 25mg 100mg in glass bottle
溶解性:
溶于DMSO(60mg/ml 超声)
产品描述:

基本信息

产品编号:

S10966

产品名称:

SN6

CAS:

415697-08-4

 

储存条件

粉末

-20℃

四年

 

 

分子式:

C20H22N2O5S

溶于液体

-80℃

6个月

分子量:

402.46

-20℃

1个月

化学名: 

2-[[4-[(4-NITROPHENYL)METHOXY]PHENYL]METHYL]-4-THIAZOLIDINECARBOXYLIC ACID ETHYL ESTER

Solubility (25°C):

 

体外:

 

DMSO

80mg/mL (198.77mM)

Ethanol

Insoluble

Water

Insoluble

体内(现配现用):

 

1mg/ml表示微溶或不溶。

普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。

 

制备储备液

 

浓度

 

溶液体积

质量

 

1mg

 

5mg

 

10mg

1mM

2.4847mL

12.4236mL

24.8472mL

5mM

0.4969mL

2.4847mL

4.9694mL

10mM

0.2485mL

1.2424mL

2.4847mL

 

生物活性

产品描述

一种选择性的NCX抑制剂

靶点

IC502.9μM (NCX1),16μM (NCX2),8.6μM (NCX3)

 

体外研究

SN 6 is a selective Na+/Ca2+ exchanger inhibitor,which inhibits the initial rate of 45Ca2+ uptake into NCX1,NCX2,and NCX3 transfectants with IC50 values of 2.9±0.12,16±1.1,and 8.6±0.27μM.SN 6 (up to 30μM) also less potently inhibits muscarinic acetylcholine receptor,with a higher IC50 of 18μM.SN 6 (0.3-30μM) completely inhibits the initial rate of Na+i-dependent 45Ca2+ uptake into Na+loaded sarcolemmal vesicles in a dose dependent manner (IC50,5.3±0.37μM).SN 6 (0.3-10μM) 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 (1-30μM) suppresses the bidirectional outward and inward INCX in a concentration-dependent manner,with IC50 values of 2.3μM and 1.9μM,respectively.SN 6 also inhibits bidirectional current (INCX) in a [Na+]i concentration-dependent manner,with IC50 values of 3.4μM,2.3μM,and 1.1μM at 10mM,20mM,and 30mM [Na+]i,respectively.SN 6 inhibits hypoxia/reoxygenation-induced LDH release with an IC50 value of 0.63±0.15μM in NCX1 transfectants.

 

推荐实验方法(仅供参考)

细胞实验:

 

Na+i-dependent 45Ca2+ uptake into cells expressing the wild-type or mutated exchangers are assayed.In brief,confluent transfectants in 24-well dishes are loaded with Na+ by incubation at 37℃ for 40 min in 0.5mL of balanced salt solution (BSS) (10mM HEPES/Tris,pH 7.4,146mM NaCl,4mM KCl,2mM MgCl2,0.1mM CaCl2,10mM glucose,and 0.1% bovine serum albumin) containing 1mM ouabain and 10μM monensin.45Ca2+ uptake is then initiated by switching the medium to Na+-free BSS (replacing NaCl with equimolar choline chloride) or to normal BSS,both of which contain 0.1mM 45CaCl2 (370 kBq/mL) and 1mM ouabain.After a 30-s incubation,45Ca2+ uptake is terminated by washing cells four times with an ice-cold solution containing 10mM HEPES/Tris,pH 7.4,120mM choline chloride,and 10mM LaCl3.Cells are then solubilized with 0.1 N NaOH,and aliquots are taken for determination of radioactivity and protein.When present, SN 6 and KB-R7943 are included in the medium 15 min before the start of 45Ca2+ uptake.

保存条件:
-20℃
UN码:
HazardClass:
危害声明:
安全说明:
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参考文献 & 客户发表文献

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摩尔浓度计算公式

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稀释公式

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  • 稀释倍数:
  • 计算结果

  • C1=C0/X C1: LOG(C1):
    C2=C1/X C2: LOG(C2):
    C3=C2/X C3: LOG(C3):
    C4=C3/X C4: LOG(C4):
    C5=C4/X C5: LOG(C5):
    C6=C5/X C6: LOG(C6):
    C7=C6/X C7: LOG(C7):
    C8=C7/X C8: LOG(C8):