Enoxolon

18β-Glycyrrhetinic Acid Struktur
471-53-4
CAS-Nr.
471-53-4
Bezeichnung:
Enoxolon
Englisch Name:
18β-Glycyrrhetinic Acid
Synonyma:
GLYCYRRHETINIC ACID;ENOXOLONE;GLYCYRRHETIC ACID;Glycyrrhetinic;Glycyrrhetinate;biosone;URALENIC ACID;18β-Glycyrrhetic acid;18B-GLYCYRRHETINIC ACID;(2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-2-carboxylic acid
CBNumber:
CB8474793
Summenformel:
C30H46O4
Molgewicht:
470.69
MOL-Datei:
471-53-4.mol

Enoxolon Eigenschaften

Schmelzpunkt:
292-295 °C(lit.)
alpha 
165 º (c=1, CHCl3,on dry ba)
Siedepunkt:
492.11°C (rough estimate)
Dichte
0.9967 (rough estimate)
Dampfdruck
10-220Pa at 20-50℃
Brechungsindex
162 ° (C=1, MeOH)
storage temp. 
2-8°C
Löslichkeit
Practically insoluble in water, soluble in ethanol, sparingly soluble in methylene chloride.
pka
pKa 5.56±0.1 (Uncertain)
Aggregatzustand
Crystalline Powder
Farbe
White to off-white
Optische Aktivität
[α]22/D +170.0°, c = 1 in chloroform
Wasserlöslichkeit
SOLUBLE IN ACETIC ACID
Merck 
14,3590
BRN 
2229654
LogP
4.5 at 20℃
CAS Datenbank
471-53-4(CAS DataBase Reference)
EPA chemische Informationen
Enoxolone (471-53-4)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 22-36
S-Sätze: 22-24/25
WGK Germany  3
RTECS-Nr. RK0180000
HS Code  29189900
Toxizität mouse,LD50,intraperitoneal,308mg/kg (308mg/kg),Drugs in Japan Vol. -, Pg. 319, 1990.
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P330 Mund ausspülen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Enoxolon Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R22:Gesundheitsschädlich beim Verschlucken.
R36:Reizt die Augen.

S-Sätze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Beschreibung

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.

Chemische Eigenschaften

white or greyish-white crystalline powder

Physikalische Eigenschaften

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.

History

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.

Verwenden

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

Definition

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.

Indications

Treatment of Addison’s disease, deoxycorticosterone

Allgemeine Beschreibung

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.

Pharmakologie

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.

Anticancer Research

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

Clinical Use

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 .

Enoxolon Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Enoxolon Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 581)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Henan Tengmao Chemical Technology Co. LTD
+8615238638457
salesvip2@hntmhg.com China 415 58
Shaanxi Haibo Biotechnology Co., Ltd
+undefined18602966907
qinhe02@xaltbio.com China 1000 58
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886
info@dakenam.com China 15928 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075
jack.li@time-chemicals.com China 1807 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714
fandachem@gmail.com China 9348 55
Shanghai Zheyan Biotech Co., Ltd.
18017610038
zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293
sales@sdzschem.com China 2931 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897
sales@biopurify.com China 3424 58

471-53-4(Enoxolon)Verwandte Suche:


  • Enoxolone, 3β-Hydroxy-11-oxo-18β,20β-olean-12-en-29-oic acid
  • Aloe Vera, Freeze Dried Powder
  • 18-β-Glycyrrhetinic acid, 98+%
  • 18-beta-glycyrrheticacid
  • Olean-12-en-29-oic acid, 3-hydroxy-11-oxo-, (3b,20b)-
  • (20S)-3β-Hydroxy-11-oxo-5α-olean-12-en-29-oic acid
  • GLYCYRRHETINIC ACID, 18B-(P)
  • Glycyrrhetinic acid ,98%
  • 18β-Glycyrrhetinic acid,3β-Hydroxy-11-oxo-18β,20β-olean-12-en-29-oic acid, Enoxolone
  • GLYCYRRHETINIC ACID, 18B-(SH)
  • 18 β-Glycyrrhetinic Acid / Enoxolone
  • Glycyrrhetinic acid (Enoxolone)
  • Rhetinic acid
  • 18 BETA
  • 18b-Glycyrrhetic acid
  • 18beta-Glycyrrhetinic acid 97%
  • Enoxolone (18-β-glycyrrhetinic acid)
  • 3β-Hydroxy-11-oxoolean-12-en-30-olic acid
  • 19β-Glycyrrhetinic acid
  • 20β-Glycyrrhetinic acid
  • 18 β-Glycyrrhetintic Acid
  • 3.beta.-Hydroxy-11-oxo-12-oleanen-30-oicacid
  • 3-beta-hydroxy-11-oxo-olean-12-en-30-oicaci
  • 3-beta-hydroxy-11-oxoolean-12-en-30-oicacid
  • 3-hydroxy-11-oxo-,(3.beta.,20.beta.)-Olean-12-en-29-oicacid
  • 3-hydroxy-11-oxo-,(3beta,20beta)-olean-12-en-29-oicaci
  • 3-Hydroxy-11-oxo-12-oleanen-30-oicacid
  • 3BETA-HYDROXY-11-OXO-18BETA, 20BETA-OLEAN-12-EN-29-OIC ACID
  • 3BETA-HYDROXY-11-OXO-18BETA-OLEAN-12-EN-30-OIC ACID
  • 3b-hydroxy-11-oxo-18b,20b-olean-12-en-29-oic acid
  • 3B-HYDROXY-11-OXO-18B-OLEAN-12-EN-30-OIC ACID
  • GLYCYRRHETINIC ACID, 18B-
  • ENOLOXONE
  • B-GLYCYRRHETINIC ACID
  • B-GLYCYRRNETINIC ACID
  • ENOXACIN GLUCONATE/18BETA-GLYCYRRHETINIC ACID
  • GLCYRRHETINIC ACID
  • CARBENOXOLONE(P)
  • Clycyrrhetinic Acid
  • 18-Beta-Glycyrrheticacid,Uralenicacid
  • Arthrodont
  • GM 1658
  • NSC 35347
  • Olean-12-en-29-oic acid, 3-hydroxy-11-oxo-, (3β,20β)-
  • Olean-12-en-30-oic acid, 3β-hydroxy-11-oxo- (8CI)
  • PO 12
  • STX 352
  • Subglycyrrhelinic acid
  • Uralenic acid (7CI)
  • GLYCERRHETINICACID
  • (3β,20b)-3-Hydroxy-11-oxo-olean-12-en-29-oic acid
  • 3β-Hydroxy-11-oxoolean-12-en-30-oic acid
  • 18-beta-Glycyrrhetinic acid, 98+%
  • 18-beta-GLYCYRRHETINIC ACID hplc
  • alpha-glycyrrhetinicacid
  • Glycyrheticacid
  • glycyrrhetin
  • Olean-12-en-29-oicacid,3-hydroxy-11-oxo-,(3.beta.,20.beta.)-
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