U6628

Uvaol

≥95%

• Sinônimo(s): Urs-12-ene-3,28-diol
• Fórmula empírica (Notação de Hill): C₃₀H₅₀O₂
• Número CAS: 545-46-0
• Peso molecular: 442.72
• Número CE: 208-888-3
• Número MDL: MFCD00009620
• Código UNSPSC: 12352103
• ID de substância PubChem: 24900437
• NACRES: NA.25

Propriedades

• Nível de qualidade: 100
• Ensaio: ≥95%
• pf: 223-225 °C (lit.)
• aplicação(ões): metabolomics; vitamins, nutraceuticals, and natural products
• cadeia de caracteres SMILES: 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
• 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
• chave InChI: XUARCIYIVXVTAE-ZAPOICBTSA-N
• Informações sobre genes: mouse ... Nos2(18126)

Descrição

Descrição geral

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.).

Aplicação

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.

Ações bioquímicas/fisiológicas

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.

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable