Betulone

Betulone Suppliers list
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: Grice Rand (Tianjin) Pharmaceutical Co., Ltd.  
Tel: 022-83705301 13752403750
Email: 2966024760@qq.com
Company Name: BOC Sciences  
Tel: 16314854226; +8616314854226
Email: inquiry@bocsci.com
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Company Name: Baoji Herbest Bio-Tech Co.,Ltd  
Tel: 0917-18628616646 18628616646
Email: info@herbest.cn
Betulone Basic information
Product Name:Betulone
Synonyms:Betulone;3-Oxobetulin;28-hydroxy-lup-20(29)-en-3-one
CAS:7020-34-0
MF:
MW:440.70092
EINECS:
Product Categories:
Mol File:7020-34-0.mol
Betulone Structure
Betulone Chemical Properties
storage temp. -20°C
solubility DMF: 30 mg/ml,DMSO: 10 mg/ml,Ethanol: 10 mg/ml
form A crystalline solid
Safety Information
MSDS Information
Betulone Usage And Synthesis
Uses3-Oxobetulin, an antifungal agent, shows antifungal activities against white rot fungus L. betulina and the brown rot fungus L. sulphureus[1].
DefinitionChEBI: Betulone is a triterpenoid. It has a role as a metabolite. It derives from a hydride of a lupane.
Biological Activity3-Oxobetulin is a pentacyclic triterpenoid and derivative of betulinic acid that has been found in I. macropoda and has diverse biological activities.1,2,3 It is active against the plant pathogenic fungi L. betulina and L. sulphureus when used at a concentration of 30 μg/ml.2 3-Oxobetulin reduces HIV-1 replication in MT-2 cells (IC50 = 4.1 μM) with a 50% cytotoxic concentration (CC50) value of greater than 100 μM.4 It inhibits cadmium-induced cytotoxicity in HepG2 cells in a concentration-dependent manner.3
References1.Kim, D.K., Nam, I.Y., Kim, J.W., et al.Pentacyclic triterpenoids from Ilex macropodaArch. Pharm. Res.25(5)617-620(2002) 2.Chien, S.-C., Xiao, J.-H., Tseng, Y.-H., et al.Composition and antifungal activity of balsam from Liquidambar formosana HanceHolzforschung67(3)345-351(2013) 3.Hiroya, K., Takahashi, T., Miura, N., et al.Synthesis of betulin derivatives and their protective effects against the cytotoxicity of cadmiumBioorg. Med. Chem.10(10)3229-3236(2002) 4.Callies, O., Bedoya, L.M., Beltrán, M., et al.Isolation, structural modification, and HIV inhibition of pentacyclic lupane-type triterpenoids from Cassine xylocarpa and Maytenus cuzcoinaJ. Nat. Prod.78(5)1045-1055(2015)
Betulone Preparation Products And Raw materials
Preparation ProductsBetulonicacid
Tag:Betulone(7020-34-0) Related Product Information
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