| 中文名 | 莫那可林J |
|---|---|
| 英文名 | monacolin J |
| 中文别名 |
洛伐他汀二醇内酯
辛伐他汀内酯二醇,10 MM DMSO 溶液 辛伐他汀杂质H 洛伐他汀酮内酯 洛伐他汀二醇内酯 ((4R,6R)-6-[2-[(1S,2S,6R,8S,8-1,2,6,7,8,8A-六氢-8-羟基-2,6-二甲基-1-萘基]乙基]四氢-4-羟基-2H-吡喃-2-酮) 洛伐他汀杂质14 6(R)-[2-(8(S)-羟基]-2(S),6(R)-二甲基-1,2,6,7,8,8A(R)-六氢-1(S)-萘基]乙基-4(R)-羟基-3,4,5,6-四氢-2H-吡喃-2-酮 辛伐他汀杂质10 洛伐他汀杂质8 辛伐他汀杂质H(4R-异构体) 洛伐他汀内酯二醇 辛伐他汀杂质08 辛伐他汀杂质 |
| 英文别名 |
SiMvastatin Lactone Diol
Simvastatin Impurity H Monacolin J Simvastatin Impurity H (4R)-Diastereomer SimvastatinimpH Simvastatin Impurity H (Simvastatin Lactone Diol/ Lovastatin Lactone Diol) Lovastatin Lactone Diol (4RS,6R)-4-Hydroxy-6-[2-[(1S,2S,6R,8S,8-8-hydroxy-2,6-dimethyl-1,2,6,7,8,8ahexahydronaphthalen-1-yl]ethyl]tetrahydro-2H-pyran-2-one Lovastatin Diol Lactone ((4R,6R)-6-[2-[(1S,2S,6R,8S,8-1,2,6,7,8,8a-Hexahydro-8-hydroxy-2,6-dimeth Simvastatin Impurity H (4R-Isomer) Lovastatin diol lactone Simvastatin Impurity 8 Lovastatin Diol Lactone ((4R,6R)-6-[2-[(1S,2S,6R,8S,8-1,2,6,7,8,8a-Hexahydro-8-hydroxy-2,6-dimethyl-1-naphthalenyl]ethyl]tetrahydro-4-hydroxy-2H-pyran-2-one) Lovastatin Lactone Diol (Simvastatin Impurity H/ Simvastatin Lactone Diol) Antibiotic MB 530A Autophagy,inhibit,Inhibitor,Monacolin J,HMG-CoA Reductase (HMR) (4R,6R)-4-Hydroxy-6-{2-[(1S,2S,6R,8S,8aR)-8-hydroxy-2,6-dimethyl-1,2,6,7,8,8a-hexahydro-1-naphthalenyl]ethyl}tetrahydro-2H-pyran-2-one (4R,6R) 6(R)-[2-(8(S)-Hydroxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydro-1(S)-naphthyl]ethyl-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one Monacolin J, 10 mM in DMSO 2H-Pyran-2-one, 6-[2-[(1S,2S,6R,8S,8-1,2,6,7,8,8a-hexahydro-8-hydroxy-2,6-dimethyl-1-naphthalenyl]ethyl]tetrahydro-4-hydroxy-, (4R,6R) (4R,6R)-4-Hydroxy-6-(2-((1S,2S,6R,8S,8-8-hydroxy-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl)ethyl)tetrahydro-2H-pyran-2-one Lovastatin Impurity 8 (4R,6R)-6-[2-[(1S,2S,6R,8S,8aR)-8-hydroxy-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl]-4-hydroxyoxan-2-one Simvastatin EP Impurity H |
| 描述 | Monacolin J 是胆固醇合成抑制剂,能够抑制 HMG-CoA reductase 的活性。 |
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| 相关类别 | |
| 靶点 |
HMG-CoA reductase[1] |
| 体外研究 | Monacolin J是胆固醇生物合成的抑制剂,并抑制HMG-CoA还原酶的活性。 Monacolin J的Na盐在1.2μg/ mL时对还原酶产生50%的抑制[1]。 |
| 参考文献 |
| 密度 | 1.2±0.1 g/cm3 |
|---|---|
| 沸点 | 535.7±50.0 °C at 760 mmHg |
| 熔点 | 104-114 °C |
| 分子式 | C19H28O4 |
| 分子量 | 320.423 |
| 闪点 | 191.2±23.6 °C |
| 精确质量 | 320.198761 |
| PSA | 66.76000 |
| LogP | 1.81 |
| 蒸汽压 | 0.0±3.2 mmHg at 25°C |
| 折射率 | 1.558 |
| 储存条件 | -20°C,干燥,密封 |
| 危害码 (欧洲) | Xi |
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