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79952-42-4生产厂家

79952-42-4价格

79952-42-4

79952-42-4结构式
79952-42-4结构式

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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。
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

[1]. Endo A, et al. Monacolins J and L, new inhibitors of cholesterol biosynthesis produced by Monascus ruber. J Antibiot (Tokyo). 1985 Mar;38(3):420-2.

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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