SMB01016

Pomolic acid

≥90% (LC/MS-ELSD)

• Sinónimos: 19α-Hydroxyursolic acid, Benthamic acid, Randialic acid A
• Fórmula empírica (notación de Hill): C₃₀H₄₈O₄
• Número de CAS: 13849-91-7
• Peso molecular: 472.70
• Número MDL: MFCD21333659
• Código UNSPSC: 12352205
• NACRES: NA.25

Propiedades

• origen biológico: plant
• Ensayo: ≥90% (LC/MS-ELSD)
• Formulario: solid
• mol peso: 472.7
• solubilidad: water: slightly soluble
• aplicaciones: metabolomics; vitamins, nutraceuticals, and natural products
• temp. de almacenamiento: −20°C
• InChI: 1S/C30H48O4/c1-18-10-15-30(24(32)33)17-16-27(5)19(23(30)29(18,7)34)8-9-21-26(4)13-12-22(31)25(2,3)20(26)11-14-28(21,27)6/h8,18,20-23,31,34H,9-17H2,1-7H3,(H,32,33)/t18-,20+,21-,22+,23-,26+,27-,28-,29-,30+/m1/s1
• Clave InChI: ZZTYPLSBNNGEIS-OPAXANQDSA-N

Descripción

Descripción general

Pomolic acid, a pentacyclic triterpene, is a bioactive natural compound commonly derived from plants such as Euscaphis japonica, Centella asiatica, Picramnia sellowii, and Cecropia pachystachya. Current research suggests that this metabolite acts as an inhibitor and may exhibit diverse biological activities, including anticancer, anti-inflammatory, antiviral, apoptotic, and antihypertensive properties.

Natural product derived from plant source.

Aplicación

Pomolic acid is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Acciones bioquímicas o fisiológicas

Pomolic acid is highly effective in inhibiting cell growth and inducing apoptosis.

Características y beneficios

• Suitable for Biochemical and Biomedical research
• Versatile and adaptable for wide variety of laboratory and research applications

Otras notas

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Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable