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Ловастатин

Ловастатин структура
75330-75-5
CAS №
75330-75-5
Химическое название:
Ловастатин
английское имя:
Lovastatin
Синонимы:
MONACOLIN K;MEVINOLIN;LOVASTATION;Lovastatin,Monacolin K;mevlor;msd803;MK-803;Sivlor;LOVALIP;MEVACOR
CBNumber:
CB7169342
Формула:
C24H36O5
молекулярный вес:
404.54
MOL File:
75330-75-5.mol

Ловастатин атрибут

Температура плавления: 175°C
альфа: D25 +323° (c = 0.5 g in 100 ml acetonitrile)
Температура кипения: 559.2±50.0 °C(Predicted)
плотность: 1.12±0.1 g/cm3(Predicted)
давление пара: 0Pa at 25℃
показатель преломления: 320 ° (C=0.5, CH3CN)
температура хранения: -20°C
растворимость: этанол: растворим 9,80-10,20 мг/мл, прозрачный, от бесцветного до бледно-желтого
форма: белого до почти белого цвета
пка: 13.49±0.40(Predicted)
цвет: белый
Растворимость в воде: 0,0004 мг/мл при 25 °C
Мерк: 14,5586
BCS Class: 2
Стабильность:: Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 2 months.
LogP: 4.260
Справочник по базе данных CAS: 75330-75-5(CAS DataBase Reference)
FDA UNII: 9LHU78OQFD
Словарь онкологических терминов NCI: lovastatin; Mevacor
Словарь наркотиков NCI: lovastatin
Код УВД: C10AA02
Предложение 65 Список: Lovastatin
Система регистрации веществ EPA: Lovastatin (75330-75-5)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xi
Заявления о рисках 36/37/38
Заявления о безопасности 22-24/25-36/37/39-26
РИДАДР 3077
WGK Германия 3
RTECS EK7907000
Класс опасности 9
Группа упаковки III
кода HS 29322090
Банк данных об опасных веществах 75330-75-5(Hazardous Substances Data)
Токсичность LD50 orally in mice: >1000 mg/kg (Endo)
символ(GHS) GHS hazard pictograms
сигнальное слово Warning
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H351 Предполагается, что данное вещество вызывает раковые заболевания. Канцерогенность Категория 2 Предупреждение P201, P202, P281, P308+P313, P405,P501
H361f Предполагается, что данное вещество может отрицательно повлиять на способность к деторождению.
Внимание
P201 Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.
P202 Перед использованием ознакомиться с инструкциями по технике безопасности.
P280 Использовать перчатки/ средства защиты глаз/ лица.
P308+P313 ПРИ подозрении на возможность воздействия обратиться за медицинской помощью.
P405 Хранить в недоступном для посторонних месте.
P501 Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.

Ловастатин химические свойства, назначение, производство

Описание

Lovastatin is an orally-active hypocholesterolemic useful in the treatment of familial hypercholesterolemia. The drug acts by inhibiting the HMG-CoA reductase-catalyzed rate limiting step of cholesterol biosynthesis. While treatment with lovastatin leads to significant reductions in total and LDL cholesterol, its effect on atherosclerosis or coronary heart disease has not been established.

Химические свойства

White Solid

Физические свойства

Appearance: White, nonhygroscopic crystalline powder. Solubility: Insoluble in water (0.0004?mg/mL); sparingly soluble in ethanol, methanol, isobutanol, isopropanol, acetonitrile, n-propanol; soluble in acetone, N-dimethylformamide; freely soluble in chloroform. Melting point: 174.5?°C. Specific optical rotation: 25?°C for D (sodium) line, +323° (concentration 0.5? g in 100? ml acetonitrile). Stability: Lovastatin is sensitive to light. Following exposure to extreme light conditions, the drug is stable for 24?h or 1?month when exposed to UV (approximately 3230 lux) or fluorescent (approximately 10,764 lux) light, respectively, at 28?°C in air.

История

Statins are the most extensively used class of lipid-lowering medication. Lovastatin is the second statin discovered by scientists.
Later, the official name lovastatin was established. The activity of lovastatin is much better than compactin.
In July 1982, lovastatin showed dramatic effects on lowering LDL cholesterol in patients with severe hypercholesterolemia who were unresponsive to the existedmedicines, with very few adverse reactions .

Использование

Lovastatin (mevinolin) is a metabolite first isolated from Monascus ruber and later found in several other fungal species. Lovastatin is a potent inhibitor of HMG-CoA. HMG-CoA reductase is the rate-controlling enzyme of the mevalonate pathway, responsible for the biosynthesis of cholesterol. Lovastatin was developed as a drug as a hypolipemic agent.

Показания

Hypercholesterolemia, combined hyperlipidemia.

Общее описание

Lovastatin, 2-methylbutanoic acid 1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-(tetrahydro-4-hydroxy6-oxo-2H-pyran-2-yl)ethyl]-1-naphthalenyl ester, mevinolin,MK-803 (Mevacor) (formerly called mevinolin), is a potentinhibitor of HMG-CoA. The drug was obtained originallyfrom the fermentation products of the fungi Aspergillus terreusand Monascus ruber. Lovastatin was one of two originalHMG-CoA reductase inhibitors. The other drug, mevastatin(formerly called compactin), was isolated from cultures ofPenicillium cillium citrum. Mevastatin was withdrawn fromclinical trials because it altered intestinal morphology in dogs.This effect was not observed with lovastatin. For inhibitoryeffects on HMG-CoA reductase, the lactone ring must be hydrolyzedto the open-ring heptanoic acid.

Биологическая активность

Potent, competitive inhibitor of HMG-CoA reductase (K i = 0.6 nM) therefore decreases cholesterol biosynthesis, in vitro and in vivo . Decreases CDK2, 4, 6 and cyclin E levels and induces G1 arrest and apoptosis in tumor cell lines in vitro .

Фармаколо?гия

Lovastatin is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), an enzyme that catalyzes the conversion of HMG-CoA to mevalonate , a rate-determining step of cholesterol biosynthesis. Lovastatin is metabolized as a prodrug into an active form, lovastatin acid. Lovastatin acid is a reversible competitive inhibitor for HMG-CoA.
However, the reduction in plasma cholesterol by statins is not only due to reduction in cholesterol biosynthesis. .
In addition to their lipid-lowering properties, statins produce several nonlipidrelated properties, include decreasing levels of high-sensitivity C-reactive protein (hsCRP), improving endothelial function, reducing inflammation at the site of the atherosclerotic plaque, inhibiting platelet aggregation, anticoagulant, etc. .

Клиническое использование

The primary uses of lovastatin are the treatment of dyslipidemia and the prevention of cardiovascular disease. It is recommended to be used only when other approaches such as diet, exercise, and weight reduction have not improved the cholesterol profile (“Lovastatin”. The American Society of Health-System Pharmacists. Retrieved 3 April 2011.). Lovastatin is useful in treating hypercholesterolemia and combined hyperlipidemia. However, lovastatin is not effective in treatment of receptornegative homozygous familial hypercholesterolemia .

Побочные эффекты

Lovastatin's common side effects are listed in approximately descending order of occurrence frequency: creatine phosphokinase elevation, flatulence, abdominal pain, constipation, diarrhea, muscle aches or pains, nausea, indigestion, weakness, blurred vision, rash, dizziness, and muscle cramps. As with all statin drugs, it can rarely cause myopathy, hepatotoxicity (liver damage), dermatomyositis, or rhabdomyolysis.

Ловастатин препаратная продукция и сырье

сырьё

препарат


Ловастатин поставщик

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