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Эноксолон структурированное изображение

Эноксолон

  • английское имя18β-Glycyrrhetinic Acid
  • CAS №471-53-4
  • CBNumberCB8474793
  • ФормулаC30H46O4
  • мольный вес470.69
  • EINECS207-444-6
  • номер MDLMFCD00003706
  • файл Mol471-53-4.mol
химическое свойство
Температура плавления 292-295 °C(lit.)
альфа 165 º (c=1, CHCl3,on dry ba)
Температура кипения 492.11°C (rough estimate)
плотность 0.9967 (rough estimate)
давление пара 10-220Pa at 20-50℃
показатель преломления 162 ° (C=1, MeOH)
температура хранения 2-8°C
растворимость Practically insoluble in water, soluble in ethanol, sparingly soluble in methylene chloride.
пка pKa 5.56±0.1 (Uncertain)
форма Crystalline Powder
цвет White to off-white
оптическая активность [α]22/D +170.0°, c = 1 in chloroform
Растворимость в воде SOLUBLE IN ACETIC ACID
Мерк 14,3590
БРН 2229654
LogP 4.5 at 20℃
Справочник по базе данных CAS 471-53-4(CAS DataBase Reference)
Рейтинг продуктов питания EWG 1
FDA UNII P540XA09DR
Код УВД D03AX10
Система регистрации веществ EPA Enoxolone (471-53-4)
UNSPSC Code 41116107
NACRES NA.24
больше
Заявления об опасности и безопасности
Коды опасности Xn
Заявления о рисках 22-36
Заявления о безопасности 22-24/25
WGK Германия 3
RTECS RK0180000
кода HS 29189900
Токсичность mouse,LD50,intraperitoneal,308mg/kg (308mg/kg),Drugs in Japan Vol. -, Pg. 319, 1990.
NFPA 704:
0
1 0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    предупреждение

  • вредная бумага

    H319:При попадании в глаза вызывает выраженное раздражение.

    H302:Вредно при проглатывании.

  • оператор предупредительных мер

    P264:После работы тщательно вымыть кожу.

    P270:При использовании продукции не курить, не пить, не принимать пищу.

    P280:Использовать перчатки/ средства защиты глаз/ лица.

    P301+P312:ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.

    P305+P351+P338:ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.

    P501:Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.

Эноксолон MSDS

Эноксолон химические свойства, назначение, производство

Описание

Extracting from liquorice (Glycyrrhiza uralensis Fisch, Gan Cao), glycyrrhetic acid also can be detected in other plants, such as Abrus cantoniensis Hance and Herba Abri fruticulosi. As one of traditional Chinese medicines, liquorice has been applied clinically for a long period. Due to its extensive usage, it plays an extremely important role in traditional Chinese medicine formula mainly as “guide” drug. As is recorded in Shen Nong’s Herbal Classic and later in pharmaceutical monographs, liquorice is able to strengthen bones and muscles and enhance metabolism and detoxification. Also, abnormal symptoms of the body and wound can be improved. Glycyrrhetic acid, the most important and potent ingredient of liquorice, has been recorded in Pharmacopoeia of the People’s Republic of China.

Химические свойства

white or greyish-white crystalline powder

Физические свойства

Solubility: insoluble in water; it exists in crystal with methanol and chloroform. Melting point: the compound melts at 292–295?°C. Specific optical rotation: under the condition of 20?°C, 589.3?nm, and 1?dm, polarized light rotates at 68° when it passes through the chloroform with a concentration of 64? mol/L.? Both 18α-glycyrrhetic acid and 18β-glycyrrhetic acid are chiral isomers of glycyrrhetic acid.

История

Glycyrrhetic acid originates from hydrolysis of glycyrrhizin, which has a therapeutic effect on disease. Dating back to the 1930s, the chemical structure of glycyrrhetic acid was demonstrated . Subsequently, the discovery of antiulcer activity promotes following research . The ramification of glycyrrhetic acid, carbenoxolone sodium, has a therapeutic effect on ulcer. In 2010, followed by the approval of raw materials, batches of tablets and capsules were approved in 2009, respectively. In foreign countries, 18β-glycyrrhetic acid was studied for anti-inflammatory effect on arthritis, rheumatoid disease, and periodontitis in BioNetWorks. The company applied for the patent of 18β-glycyrrhetic acid in 1999. Also, after joining the leading worldwide market in 2006, phase III clinical trials would be carried out in 2007. However, the progress was hindered in 2008. To detecting more indications, its carbenoxolone sodium was studied by other three companies: after conducting phase III clinical trials in the UK, the project of RB intending to improve nonspecific inflammatory bowel disease was given up in 1992. York Pharma expected to make progress in psoriasis with gel or cream; however, the project has been in a standstill after phase II clinical trials was conducted from 2005 to 2009. Canada pharmaceutical company, Oxalys Pharmaceuticals, research it for treating Huntington’s disease, and it was included in the orphan drug list by the USA in 2014. Till now, phase I clinical trials are still continuing.

Использование

The product may be used as a starting material to prepare 18β-glycyrrhetinic acid derivatives, which show anti-inflammatory and antioxidant properties.

Показания

Treatment of Addison’s disease, deoxycorticosterone

Определение

ChEBI: A pentacyclic triterpenoid that is olean-12-ene substituted by a hydroxy group at position 3, an oxo group at position 11 and a carboxy group at position 30.

Общее описание

18β-Glycyrrhetinic acid is a pentacyclic triterpenoid found in the Glycyrrhiza glabra L.(liquorice) roots. It is the key metabolite of glycyrrhizin and glycyrrhizic acid.

Фармаколо?гия

Thirty percent of glycyrrhetinic acid can be effectively used by the body; both 18α-glycyrrhetic acid and 18β-glycyrrhetic acid reduce by half in 2.24 h and 11.5 h separately. CYP3A promotes metabolism with hydroxyl added to 22α and 24α .There are lots of pharmacological activities : it plays an anti-inflammatory role by inhibiting the activity of phospholipase A2 and lipoxygenase to reduce mediators of inflammation; the compound promotes antiulcer activity through the production of more PGE2 and secretion of gastric mucus; it also provokes proliferation of gastric cell to protect the mucosa from ulceration. The complex which consists of glycyrrhetinic acid and carotenoid plays antioxidation by scavenging free radical. Glycyrrhetinic acid inhibits the replication of viral DNA to achieve an antiviral effect at the concentration of 4×10?5 mol/L; it also inhibits proliferation of tumor cell and promotes apoptosis and differentiation. The decreasing ability of invasion exerts an antitumor effect. Glycyrrhetinic acid is considered to have extensive antiarrhythmic effects through inhibition of L-type calcium channel. In addition, glycyrrhetinic acid functions as an anticholinesterase (1.7×10?5 mol/L), anticoagulant, and antitetanus toxin; it also improves inner ear hearing (100 mg/kg, intramuscular injection) and improves absorption of insulin.

Клиническое использование

Glycyrrhetic acid has not been applied in clinical treatment till now. Meanwhile, the ramification has come into the market for the property of antiulcer. However, with large doses and long-term usage, the drug gives rise to hypertension, sodium retention, and hypokalemia. When renin-angiotensin-aldosterone system fails to function properly, liquorice-induced pseudoaldosteronism threatens human health .

разработк И противоопухолевых препаратов

Glycyrrhetinic acid in combinationwith etoposide inhibits thetopoisomerase 2α and inducesapoptosis
Cai et al.(2017)

Эноксолон поставщик

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