Lup-20(29)-en-3,28-diol, (3β)-

Betulin

HCID 72326

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

Betulin473-98-3BetulinolTrocholBetulineBetulolBetulinic alcohol(+)-betulinLup-20(30)-ene-3beta,28-diolCP BETULINNSC-46446W70HN7X7O
Weitere Namen anzeigen
Birch bark extractbetula camphorBetuLetulin
ORISTRACT BTLLup-20(29)-ene-3,28-diol, (3beta)-lup-20(29)-ene-3 beta,28-diolCHEBI:3086DTXSID101019934(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(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-olRefChem:568020

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

Experimentelle und physikochemische Eigenschaften

Boiling Point284.00 to 288.00 °C. @ 743.00 mm Hg
Melting Point251 - 252 °C
Physical DescriptionSolid
Collision Cross Section · 2 Einträge

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)

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 2 Einträge

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

Hazard Classes and CategoriesNot Classified

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

Chemie und Industrie

Pharmakologische Informationen

Cellular LocationsExtracellular;Membrane
Anwendungen · 2 Einträge

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.

Anbieter100 Anbieter

北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
成都健腾生物技术有限公司028-85159085 · [email protected]
INTATRADE GmbH+49 3493/605464 · [email protected]

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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