| Identification | More | [Name]
Enoxolone | [CAS]
471-53-4 | [Synonyms]
18-BETA-GLYCYRRHETINIC ACID
18B-GLYCYRRHETINIC ACID
(2S,4AS,6AS,6BR,8AR,10S,12AS,12BR,14BR)-10-HYDROXY-2,4A,6A,6B,9,9,12A-HEPTAMETHYL-13-OXO-1,2,3,4,4A,5,6,6A,6B,7,8,8A,9,10,11,12,12A,12B,13,14B-ICOSAHYDRO-PICENE-2-CARBOXYLIC ACID
(3beta,18alpha,20beta)-3-Hydroxy-11-oxoolean-12-en-29-oic acid
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
B-GLYCYRRHETINIC ACID
B-GLYCYRRNETINIC ACID
ENOLOXONE
ENOXOLONE
GLYCYRRHETIC ACID
GLYCYRRHETINIC ACID
GLYCYRRHETINIC ACID, 18B-
URALENIC ACID
18-beta-glycyrrheticacid
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 | [EINECS(EC#)]
207-444-6 | [Molecular Formula]
C30H46O4 | [MDL Number]
MFCD00003706 | [Molecular Weight]
470.68 | [MOL File]
471-53-4.mol |
| Chemical Properties | Back Directory | [Appearance]
white or greyish-white crystalline powder | [Melting point ]
292-295 °C(lit.)
| [alpha ]
165 º (c=1, CHCl3,on dry ba) | [Boiling point ]
492.11°C (rough estimate) | [density ]
0.9967 (rough estimate) | [refractive index ]
162 ° (C=1, MeOH) | [storage temp. ]
2-8°C | [solubility ]
Practically insoluble in water, soluble in ethanol, sparingly soluble in methylene chloride. | [form ]
Crystalline Powder | [pka]
pKa 5.56±0.1 (Uncertain) | [color ]
White to off-white | [optical activity]
[α]22/D +170.0°, c = 1 in chloroform | [Water Solubility ]
SOLUBLE IN ACETIC ACID | [Merck ]
3590 | [BRN ]
2229654 | [Uses]
glycyrrhetinic acid is anti-irritant, anti-allergenic, anti-inflammatory, skin-lightening, and smoothing properties are attributed to this ingredient, which is also a carrier. It is the organic compound derived from glycyrrhizic acid or shredded licorice roots. | [CAS DataBase Reference]
471-53-4(CAS DataBase Reference) | [EPA Substance Registry System]
471-53-4(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R36:Irritating to the eyes. | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
RK0180000
| [HS Code ]
29189900 |
| Hazard Information | Back Directory | [Description]
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. | [Chemical Properties]
white or greyish-white crystalline powder | [Physical properties]
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. | [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 | [General Description]
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. | [Pharmacology]
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) | [Anticancer Research]
It was reported that GA at noncytotoxic concentrationshowed synergistic effect in combination with anticancer drug, etoposide (VP-16).Specifically, GA enhanced cytotoxicity through regulating topoisomerase II-αtargeted by etoposide. Also, GA sensitized the cells to etoposide through elevatingtopoisomerase II-α with a 2.4-fold rate at 12 h time point. From 12 to 48 h, GAhalved the expression of topoisomerase II-α and stimulated apoptosis, whichexhibited its antineoplastic effect. They reported that GA was more potentiallyeliminating the TNBC cells when compared with Glycyrrhizin Acid (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 . |
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