SULFOSUCCINIMIDYL OLEATE

SULFOSUCCINIMIDYL OLEATE

中文名称SULFOSUCCINIMIDYL OLEATE
中文同义词化合物 T13036;化合物SULFOSUCCINIMIDYL OLEATE SODIUM;磺基琥珀酰亚胺基油酸酯;化合物SULFOSUCCINIMIDYL OLEATE;磺基琥珀酰亚胺油酸钠
英文名称Sulfosuccinimidyl Oleate Sodium
英文同义词(Z)-2,5-Dioxo-1-[(1-oxo-9-octadecenyl)oxy]-3-pyrrolidinesulfonic Acid Sodium;Sulfosuccinimidyl Oleate;Sulphosuccinimyl oleate sodium salt;2,5-Dioxo-1-[[(9Z)-1-oxo-9-octadecenyl]oxy]pyrrolidine-3-sulphonic acid sodium salt;2,5-Dioxo-1-[[(9Z)-1-oxo-9-octadecenyl]oxy]-3-pyrrolidinesulfonic Acid Sodium;Sulfosuccinimidyl Oleate Sodium;3-Pyrrolidinesulfonic acid, 2,5-dioxo-1-[[(9Z)-1-oxo-9-octadecenyl]oxy]-;Sulfo-N-succinimidyl Oleate sodium
CAS号135661-44-8
分子式C22H37NO7S
分子量459.6
EINECS号
相关类别Heterocyclic Compounds;Fatty Acid Derivatives & Lipids;Glycerols;Heterocycles;Sulfur & Selenium Compounds
Mol文件135661-44-8.mol
结构式SULFOSUCCINIMIDYL OLEATE 结构式

SULFOSUCCINIMIDYL OLEATE 性质

熔点220-2220C
密度1.19±0.1 g/cm3(Predicted)
储存条件-20°C Freezer
溶解度可溶于DMSO(轻微)、甲醇(轻微、加热)
形态固体
酸度系数(pKa)-0.04±0.20(Predicted)
颜色白色至类白色
稳定性吸湿性

SULFOSUCCINIMIDYL OLEATE 用途与合成方法

Sulfosuccinimidyl oleate (Sulfo-N-succinimidyl oleate) 是一种长链脂肪酸,抑制脂肪酸向细胞转运。Sulfosuccinimidyl oleate 是一种有效且不可逆的线粒体呼吸链抑制剂。Sulfosuccinimidyl oleate 结合小胶质细胞表面上的 CD36 受体。具有抗炎作用。

Sulfosuccinimidyl oleate (20 μM and 50 μM, 24 hours) alone does not alter the cellular viability. Exposure to 100 ng/ml LPS+5 ng/mL IFNγ modestly, yet significantly reduces the viability of the BV2 cells. Co-treatment with Sulfosuccinimidyl oleate prevents the LPS+IFNγ-induced reduction in the cell viability.
Sulfosuccinimidyl oleate (50 μM, 24 hours) co-treatment significantly reduces the LPS+IFNγ-induced expression of NOS2 and COX-2 in BV2 cells. Western blot analysis reveals a significant LPS/IFNγ-induced upregulation in the phosphorylated form of the p38, which is prevented by co-treatment with Sulfosuccinimidyl oleate (50 μM, 24 hours).

Cell Viability Assay

Cell Line: BV2 cells
Concentration: 20 μM and 50 μM
Incubation Time: 24 hours
Result: Did not alter the viability of BV2 cells alone. Exposure of BV2 cells to 100 ng/mL LPS and 5 ng/mL IFNγ significantly reduced the viability of BV2 cells while simultaneous treatment with Sulfosuccinimidyl oleate prevented it.

Western Blot Analysis

Cell Line: BV2 cells
Concentration: 50 μM
Incubation Time: 24 hours
Result: Drastically increased the levels of NOS2, COX-2, and P-p38/T-p38.

Sulfosuccinimidyl oleate (50 mg/kg; administered once by single oral gavage) significantly reduces the cortical ischemic infarct size compared to vehicle-treated controls in male BALB/cABom mice with pMCAo model. In addition, Sulfosuccinimidyl oleate at 50 mg/kg is suitable to see a beneficial effect after stroke.

Animal Model: 4-month-old male BALB/cABom mice with pMCAo model
Dosage: 50 mg/kg
Administration: Administered once by single oral gavage
Result: Reduced brain damage following ischemia. Attenuated infarct size.

安全信息

海关编码2928009090

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-112847ASULFOSUCCINIMIDYL OLEATE
Sulfosuccinimidyl oleate sodium
135661-44-85mg1900元
2024/04/30HY-112847ASULFOSUCCINIMIDYL OLEATE
Sulfosuccinimidyl oleate sodium
135661-44-810mM * 1mLin DMSO2090元

SULFOSUCCINIMIDYL OLEATE 上下游产品信息

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