Grundinformationen
- Standard-SMILES
CC1(C)[C@@H](OC(=O)CCC(=O)O)CC[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@@](C)(C(=O)O)CC[C@]5(C)CC[C@@]4(C)[C@]3(C)CC[C@@H]12- InChIKey
OBZHEBDUNPOCJG-WBXJDKIVSA-N- Summenformel
- C34H50O7
- Durchschnittliche Molmasse
- 570,8 g/mol
- Monoisotopische Masse
- 570,35565394
Überblick
An agent derived from licorice root. It is used for the treatment of digestive tract ulcers, especially in the stomach. Antidiuretic side effects are frequent, but otherwise the drug is low in toxicity.
Namen und Bezeichner
- Bevorzugter Name
- Carbenoxolone
- IUPAC
- (2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-(3-carboxypropanoyloxy)-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
- Lokaler Name
- Carbenoxolon
- Englischer Name
- Carbenoxolone
- Summenformel
- C34H50O7
- Molmasse
- 570.76
Namen und Synonyme
carbenoxolone5697-56-3CarbenoxolonaCarbenoxolonumMM6384NG73DTXSID4022733(2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-(4-hydroxy-4-oxobutanoyl)oxy-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 acidOlean-12-en-29-oic acid, 3-(3-carboxy-1-oxopropoxy)-11-oxo-, (3beta,20beta)-(2S,4aS,6aR,6aS,6bR,8aR,10S,12aS,14bR)-10-(3-carboxypropanoyloxy)-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(3beta,20beta)-3-(3-Carboxy-1-oxopropoxy)-11-oxoolean-12-en-29-oic acid18alpha CarbenoxoloneCarbeneoxolone
Weitere Namen anzeigen
bioralbiogastroneCarbenoxolonCARBENOXOLONE [UCarbenoxolone-d4CARBENOXOLONE(RG)glycyrrhetnic acidCarbenoxolone (YP 003)
CarbenoxaloneGlycyrrhetinic acid hydrogen succinateRefChem:123513DTXCID702733A02BX0118alpha Glycyrrhetinic Acid 3beta O Hemisuccinate18alpha-Glycyrrhetinic Acid 3beta-O-Hemisuccinate3beta-O-Hemisuccinate, 18alpha-Glycyrrhetinic Acid
Datenbank-Bezeichner
- CAS
5697-56-3- PubChem CID
- 636403
- DTXSID
DTXSID4022733- ChEMBL
CHEMBL499915- UNII
- MM6384NG73
- EC Number
- 227-174-2
- Nikkaji
- J209.322G
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 6,4
- Polarare Oberfläche (TPSA)
- 118 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 7
- Frei drehbare Bindungen
- 6
- Schwere Atome
- 41
- Formalladung
- 0
- Komplexität
- 1.200
Experimentelle und physikochemische Eigenschaften
DrugsPharmaceuticals -> Listed in ZINC15
Collision Cross Section243.71 Ų [M+K]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
Physikochemische Eigenschaften
- Schmelzpunkt
- 291 · 291-294 °C
- Siedepunkt
- 553.75 °C · 553.75°C (rough estimate)
- Dichte
- 1.2 · 1.20
- Brechungsindex
- 1.582 · 1.5820 (estimate)
- storage temp.
- -20 °C · -20°C Freezer
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- Aggregatzustand
- Solid
- pka
- 6.7 · pKa 6.7 (Uncertain)
- Farbe
- Cream crystals
- Wasserlöslichkeit
- 6.621 mg/L · 6.621mg/L(24 ºC)
- CAS Datenbank
- 5697 · 5697-56-3(CAS DataBase Reference)
- EPA chemische Informationen
- -12 · Olean-12-en-29-oic acid, 3-(3-carboxy-1-oxopropoxy)-11-oxo-, (3.beta.,20.beta.)- (5697-56-3)
Sicherheit und Regulatorisches
Gefahrenhinweise
Regulatory InformationChemical: Olean-12-en-29-oic acid, 3-(3-carboxy-1-oxopropoxy)-11-oxo-, (3.beta.,20.beta.)-
Other Safety InformationIMAP assessments - Olean-12-en-29-oic acid, 3-(3-carboxy-1-oxopropoxy)-11-oxo-, (3.beta.,20.beta.)-: Human health tier I assessment
Sicherheitsdaten
- tsca
- TSCA listed
- Toxizität
- LD50 orl-rat: 2450 mg/kg OYYAA2 19,323,80
Chemie und Industrie
Pharmakologische Informationen
ATC Code
A - Alimentary tract and metabolism
QA - Alimentary tract and metabolism
MeSH Pharmacological Classification
Various agents with different action mechanisms used to treat or ameliorate PEPTIC ULCER or irritation of the gastrointestinal tract. This has included ANTIBIOTICS to treat HELICOBACTER INFECTIONS; HISTAMINE H2 ANTAGONISTS to reduce GASTRIC ACID secretion; and ANTACIDS for symptomatic relief.
Verwendung und Herstellung
General Manufacturing InformationOlean-12-en-29-oic acid, 3-(3-carboxy-1-oxopropoxy)-11-oxo-, (3.beta.,20.beta.)-: INACTIVE
Anwendungen
VerwendenGlucocorticoid.
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