SMB01016

Pomolic acid

≥90% (LC/MS-ELSD)

• Sinonimo/i: 19α-Hydroxyursolic acid, Benthamic acid, Randialic acid A
• Formula empirica (notazione di Hill): C₃₀H₄₈O₄
• Numero CAS: 13849-91-7
• Peso molecolare: 472.70
• Numero MDL: MFCD21333659
• Codice UNSPSC: 12352205
• NACRES: NA.25

Proprietà

• Origine biologica: plant
• Saggio: ≥90% (LC/MS-ELSD)
• Stato: solid
• PM: 472.7
• Solubilità: water: slightly soluble
• applicazioni: metabolomics; vitamins, nutraceuticals, and natural products
• Temperatura di conservazione: −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; ZZTYPLSBNNGEIS-OPAXANQDSA-N

Descrizione

Descrizione generale

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.

Applicazioni

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

Azioni biochim/fisiol

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

Caratteristiche e vantaggi

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

Altre note

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Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable