SMB01045

Isoliquiritin

≥90% (LC/MS-ELSD)

• Synonym(e): 4-beta-D-glucopyranosyloxy-2′,4′-dihydroxy-trans-chalcone, Isoliquiritoside
• Empirische Formel (Hill-System): C₂₁H₂₂O₉
• CAS-Nummer: 5041-81-6
• Molekulargewicht: 418.39
• MDL-Nummer: MFCD00272145
• UNSPSC-Code: 12352205
• NACRES: NA.25

Eigenschaften

• Biologische Quelle: plant
• Assay: ≥90% (LC/MS-ELSD)
• Form: solid
• Mol-Gew.: 418.39
• Anwendung(en): metabolomics; vitamins, nutraceuticals, and natural products
• Lagertemp.: −20°C
• InChI: 1S/C21H22O9/c22-10-17-18(26)19(27)20(28)21(30-17)29-13-5-1-11(2-6-13)3-8-15(24)14-7-4-12(23)9-16(14)25/h1-9,17-23,25-28H,10H2/b8-3+/t17-,18-,19+,20-,21-/m1/s1
• InChIKey: YNWXJFQOCHMPCK-LXGDFETPSA-N

Beschreibung

Allgemeine Beschreibung

Isoliquiritin, also known as Isoliquiritoside, is a flavonoid belongs to the class of dihydrochalcones commonly available from Glycyrrhiza Sp. plants. This plant metabolite exhibits various biological activities, including antioxidant, antifungal, anti-HIV, anticancer properties.

Anwendung

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

Biochem./physiol. Wirkung

Isoliquiritin triggers apoptotic cell death by increasing the levels of p53 and p21 in A549 non-small cell lung cancer cells while also inhibiting the p53-dependent pathway and revealing interactions with Akt activities. Futher, Isoliquiritin has demonstrated neuroprotective activity against oxidative stress and has the capability to restrain the growth of microbial pathogens.

Leistungsmerkmale und Vorteile

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

Sonstige Hinweise

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Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable