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Uvaol

SIGMA/U6628 - ≥95%

Synonym: Urs-12-ene-3,28-diol

CAS Number: 545-46-0
Empirical Formula (Hill Notation): C30H50O2
Molecular Weight: 442.72
EC Number: 208-888-3
MDL Number: MFCD00009620
Linear Formula: C30H50O2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-U6628-25MG 25 mg
 $94.60
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application(s) metabolomics
vitamins, nutraceuticals, and natural products
assay ≥95%
InChI 1S/C30H50O2/c1-19-10-15-30(18-31)17-16-28(6)21(25(30)20(19)2)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3/t19-,20+,22+,23-,24+,25+,27+,28-,29-,30-/m1/s1
InChI key XUARCIYIVXVTAE-ZAPOICBTSA-N
mp 223-225 °C (lit.)
Quality Level 100 
SMILES string C[C@@H]1CC[C@]2(CO)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C
Application: Uvaol has been used as retinoic acid receptor-related orphan receptor gamma t (RORγt) inhibitor to study the role of cardiac glycoside reductase 2 (Cgr2) enzyme on its metabolism.
Biochem/physiol Actions: Uvaolexerts pharmacological properties such as antioxidant, anticancer, anti-inflammatory, and wound healing. It also displays vasodilator, hepatoprotective, and antimicrobial effects. Uvaol has inhibitory effects on nitric oxide (NO) release.
General description: Uvaolis a pentacyclic triterpene compound usually extracted from plant leaves such as Apocynum venetum L., olive leaves (Olea europaea L.), and oregano (Origanum vulgare L.).
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95%
mp 223-225 °C (lit.)
UNSPSC 12352103

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