| Identification | Back Directory |  [Name]
  UVAOL |  [CAS]
  545-46-0 |  [Synonyms]
  UVAOL UVAOL(SH) UVAOL hplc UVAOL WITH HPLC 12-URSEN-3B,28-DIOL URS-12-ENE-3,28-DIOL 12-URSEN-3BETA, 28 DIOL urs-12-ene-3beta,28-diol 3B,28-DIHYDROXY-URSA-12-EN Uvaol,Urs-12-ene-3,28-diol 3BETA,28-DIHYDROXY-URSA-12-EN (3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol |  [EINECS(EC#)]
  208-888-3 |  [Molecular Formula]
  C30H50O2 |  [MDL Number]
  MFCD00009620 |  [MOL File]
  545-46-0.mol |  [Molecular Weight]
  442.72 |  
 | Chemical Properties | Back Directory |  [Melting point ]
  223-225 °C(lit.) 
 |  [Boiling point ]
  523.7±50.0 °C(Predicted) |  [density ]
  1.05±0.1 g/cm3(Predicted) |  [storage temp. ]
  -20°C Freezer |  [solubility ]
  Chloroform (Slightly), Ethyl Acetate (Slightly) |  [form ]
  Solid |  [pka]
  15.09±0.10(Predicted) |  [color ]
  White to Off-White |  [LogP]
  9.130 (est) |  [CAS DataBase Reference]
  545-46-0 |  
 | Hazard Information | Back Directory |  [Definition]
  ChEBI: A natural product found in Rhododendron ferrugineum. |  [Uses]
  Uvaol can attenuate pleuritis and eosinophillic inflammation in mice that is induced by ovalbumin. It is an essential reagent in the synthesis of aminopropoxytriterpenoids that have anticancer activity. |  [Biological Activity]
  Uvaolexerts pharmacological properties such as antioxidantanticanceranti-inflammatoryand wound healing. It also displays vasodilatorhepatoprotectiveand antimicrobial effects. Uvaol has inhibitory effects on nitric oxide (NO) release. |  [in vivo]
 
 Uvaol (100-500 μmol/kg; orally administered; 60 min before antigen challenge) can reduce pleural eosinophilic inflammation and IL-5 concentration in a murine pleurisy model induced by ovalbumin[1]. | Animal Model: | Male Swiss mice (weighing 25-30 g) with subcutaneous (s.c.) injection on days 0 and 7 with 0.2 mL of a solution containing 50 μg of Ovalbumins (OVA) (HY-W250978) adsorbed to 5 mg of aluminum hydroxide[1]. |  | Dosage: | 100 μmol/kg, 200 μmol/kg, 500 μmol/kg (2% DMSO in sterile saline) |  | Administration: | Oral administration; 60 min before antigen challenge |  | Result: | Caused a significant decrease in total leukocyte accumulation. 
Induced a significant reduction in the levels of this cytokine.  |  
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                            | Company Name: | 
                            
                                BioBioPha Co., Ltd.  
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                            0871-65217109 13211707573; | 
                         
                        
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                            http://www.biobiopha.com | 
                         
                    
                 
                
                
                
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