ChemicalBook--->CAS DataBase List--->545-46-0

545-46-0

545-46-0 Structure

545-46-0 Structure
IdentificationBack 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 PropertiesBack 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 InformationBack 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.
Safety DataBack Directory
[Risk Statements ]

22
[Safety Statements ]

22-45
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

UVAOL(545-46-0)1HNMR
UVAOL(545-46-0)Raman
UVAOL(545-46-0)FT-IR
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