辛伐他汀钠盐结构式
|
常用名 | 辛伐他汀钠盐 | 英文名 | Simvastatin Hydroxy Acid Sodium Salt |
|---|---|---|---|---|
| CAS号 | 101314-97-0 | 分子量 | 458.563 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C25H39NaO6 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
辛伐他汀钠盐用途Simvastatin sodium 是内酯的前药,可通过非特异性羧酯酶或非酶促过程水解为活性羟基酸。Simvastatin sodium 对 HMG-CoA 还原酶的抑制作用,其 Ki 值为 0.12 nM。 |
| 中文名 | 辛伐他汀钠盐 |
|---|---|
| 英文名 | sodium,(3R,5S)-7-[(1R,2R,6S,8S)-8-(2,2-dimethylbutanoyloxy)-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate |
| 中文别名 | 辛伐他汀杂质A |
| 英文别名 | 更多 |
| 描述 | Simvastatin sodium 是内酯的前药,可通过非特异性羧酯酶或非酶促过程水解为活性羟基酸。Simvastatin sodium 对 HMG-CoA 还原酶的抑制作用,其 Ki 值为 0.12 nM。 |
|---|---|
| 相关类别 | |
| 体外研究 | 辛伐他汀钠对人淋巴母细胞和SV40转化的MRC成纤维细胞中HMG-CoA还原酶有抑制作用[1]。辛伐他汀钠(100μM)可抑制Na~+H~+antiport活性,导致细胞内pH值下降,细胞增殖减少,而甲羟戊酸盐(mevalonate)可阻止这种抑制作用,而不是多利醇(dolichol)或角鲨烯[1]。 |
| 体内研究 | 辛伐他汀钠(口服;8 mg/kg;18天)可降低血浆胆固醇水平33%,辛伐他汀可与依西替米联合治疗血脂异常[1]。 |
| 参考文献 |
| 分子式 | C25H39NaO6 |
|---|---|
| 分子量 | 458.563 |
| 精确质量 | 458.264435 |
| PSA | 106.89000 |
| LogP | 2.77100 |
| InChIKey | SVIXZYADIXSPPP-OKDJMAGBSA-N |
| SMILES | CCC(C)(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC(O)CC(O)CC(=O)O)C21.[Na] |
| 储存条件 | 2-8°C,密封,干燥 |
|
~80%
辛伐他汀钠盐 101314-97-0 |
| 文献:Griffin, John; Lanza, Guido; Yu, Jessen Patent: US2005/261354 A1, 2005 ; Location in patent: Page/Page column 53 ; US 20050261354 A1 |
| 辛伐他汀钠盐上游产品 1 | |
|---|---|
| 辛伐他汀钠盐下游产品 0 | |
|
实验名称:Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum Bre1
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL960525
|
|
实验名称:Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum FCR3
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL960526
|
|
实验名称:Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum IMT031
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL960523
|
|
实验名称:Antiplasmodial activity against chloroquine-resistant Plasmodium falciparum W2
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL960524
|
|
实验名称:Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D6
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL960521
|
|
实验名称:Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum 3D7
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL960522
|
| Sodium (3R,5R)-7-{(1S,2S,6R,8S,8aR)-8-[(2,2-dimethylbutanoyl)oxy]-2,6-dimethyl-1,2,6,7,8,8a-hexahydro-1-naphthalenyl}-3,5-dihydroxyheptanoate |
| Simvastatin Hydroxy Acid Sodium Salt |
| simvastatin sodium |
| Si-Methyl-N,N'N''-triphenyl-silantriyltriamin |
| 1-Naphthaleneheptanoic acid, 8-(2,2-dimethyl-1-oxobutoxy)-1,2,6,7,8,8a-hexahydro-β,δ-dihydroxy-2,6-dimethyl-, sodium salt, (βR,δR,1S,2S,6R,8S,8aR)- (1:1) |
| trianilino-methyl-silane |
| simvastatin sodium salt |
| Silanetriamine,1-methyl-N,N',N''-triphenyl |
| Methyl-tris-anilino-silan |
| simivastin sodium salt |
| Simvastatin EP Impurity A Sodium Salt |
| Simvastatin Impurity 1 |