Grundinformationen
- CAS
473-98-3- Standard-SMILES
C=C(C)[C@@H]1CC[C@]2(CO)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12- InChIKey
FVWJYYTZTCVBKE-ROUWMTJPSA-N- Summenformel
- C30H50O2
- Durchschnittliche Molmasse
- 442,7 g/mol
- Monoisotopische Masse
- 442,38108083
Namen und Bezeichner
- Bevorzugter Name
- Betulin
- IUPAC
- (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol
- Lokaler Name
- Lup-20(29)-en-3,28-diol, (3β)-
- Englischer Name
- Betulin
- Summenformel
- C30H50O2
- Molmasse
- 442.72
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
473-98-3- PubChem CID
- 72326
- DTXSID
DTXSID101019934- ChEMBL
CHEMBL23236- ChEBI
CHEBI:3086- UNII
- 6W70HN7X7O
- EC Number
- 207-475-5
- Nikkaji
- J5.959E
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 8,3
- Polarare Oberfläche (TPSA)
- 40,5 Ų
- H-Brücken-Donoren
- 2
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 32
- Formalladung
- 0
- Komplexität
- 786
Experimentelle und physikochemische Eigenschaften
Collision Cross Section
193.57 Ų [M+H-H2O]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
208.3 Ų [M+Na]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
Physikochemische Eigenschaften
- Schmelzpunkt
- 256 · 256-257 °C(lit.)
- Siedepunkt
- 493.26 °C · 493.26°C (rough estimate)
- Dichte
- 0.9882 · 0.9882 (rough estimate)
- Brechungsindex
- 1.5045 · 1.5045 (estimate)
- storage temp.
- 2 · 2-8°C
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly, Heated)
- Aggregatzustand
- Off-white powder
- pka
- 15.1 · 15.10±0.10(Predicted)
- Farbe
- Pale Brown to Beige
- Merck
- 14 · 14,1189
- Stabilität
- Hygroscopic
- Major Application
- food and beverages
- Kosmetik-Inhaltsstoffe Funktionen
- SKIN CONDITIONING
- InChIKey
- FVWJYYTZTCVBKE-ROUWMTJPSA-N
- SMILES
- [H][C@]12CC[C@]3([H])[C@@]4(C)CC[C@H](O)C(C)(C)[C@]4([H])CC[C@@]3(C)[C@]1(C)CC[C@@]5(CO)CC[C@@H](C(C)=C)[C@]25[H]
- LogP
- 8.607 · 8.607 (est)
- CAS Datenbank
- 473 · 473-98-3(CAS DataBase Reference)
- NIST chemische Informationen
- Betulin(473-98-3)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Not Classified;Reported as not meeting GHS hazard criteria by 27 of 31 companies
Aggregated GHS information provided per 31 reports by companies from 4 notifications to the ECHA C&L Inventory.;Reported as not meeting GHS hazard criteria per 27 of 31 reports by companies.;There are 3 notifications provided by 4 of 31 reports by companies with hazard statement code(s).;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Gefahrenhinweise
Sicherheitsdaten
- wgk
- 3
- hs_code
- 29181985
- RTECS-Nr.
- OK5755000
- risk_code
- 36/37/38-20/21/22-68/20/21/22-68
- hazard_code
- Xn,Xi
- safety_code
- 36/37-36-26
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- STOT SE 2
Chemie und Industrie
Pharmakologische Informationen
Anwendungen
BeschreibungSterol regulatory element binding protein 2 (SREBP-2) regulates cholesterol synthesis by activating the transcription of genes for HMG-CoA reductase and other enzymes of the cholesterol synthetic pathway. When cellular sterol levels are high, SREBP is bound by SCAP and Insig to ER membranes as a glycosylated precursor protein. Upon cholesterol depletion, the protein is cleaved to its active form and translocated into the nucleus to stimulate transcription of genes involved in the uptake and synthesis of cholesterol. Betulin, the precursor of betulinic acid, is a pentacyclic triterpene found in the bark of birch trees. Betulin inhibits the SREBP-driven pathway of cholesterol and fatty acid biosynthesis by promoting SCAP–Insig binding which prevents the activation and release of SREBP-2 from the ER. At 15-30 mg/kg/day, betulin has been shown to decrease lipid levels and increase insulin sensitivity in mice fed a western-type diet. In an atherosclerosis disease model, 30 mg/kg/day betulin can reduce the size and improve the stability of atherosclerotic plaques in LDLR-knockout mice. At 2.5-5 μg/ml betulin, in combination with cholesterol, demonstrates anticancer effects by inducing apoptosis in Jurkat cells, A549 lung carcinoma cells, and HeLa cervical carcinoma cells.
VerwendenBetulin may be used in the preparation of betulinic acid, which shows anti-HIV, antimalarial and anti-inflammatory activities.
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Nachgelagerte Produkte
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Ergänzende Hinweise
DefinitionChEBI: A pentacyclic triterpenoid that is lupane having a double bond at position 20(29) as well as 3beta-hydroxy and 28-hydroxymethyl substituents.
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