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4',5,7-Trihydroxyflavanone, 97%, Thermo Scientific Chemicals
CAS: 67604-48-2 | C15H12O5 | 272.256 g/mol
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Catalog number ALFL09834.04
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Quantity:
2 g
Specifications
Chemical Name or Material4',5,7-Trihydroxyflavanone
CAS67604-48-2
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
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(±)-Naringenin is an antioxidant flavonoid. It has anti-inflammatory and antitumor properties. (±)-Naringenin induces apoptosis. It stimulates DNA repair following oxidative damage. (±)-Naringenin inhibits the activity of PI 3-kinase (PI(3)K).
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(±)-Naringenin is an antioxidant flavonoid. It has anti-inflammatory and antitumor properties. (±)-Naringenin induces apoptosis. It stimulates DNA repair following oxidative damage. (±)-Naringenin inhibits the activity of PI 3-kinase (PI(3)K).
Solubility
Soluble in ethanol (50 mg/ml), DMSO, methanol, and ammonium hydroxide (50 mg/ml). Insoluble in water (almost)
Notes
Store at room temperature. Incompatible with strong oxidizing agents.
(±)-Naringenin is an antioxidant flavonoid. It has anti-inflammatory and antitumor properties. (±)-Naringenin induces apoptosis. It stimulates DNA repair following oxidative damage. (±)-Naringenin inhibits the activity of PI 3-kinase (PI(3)K).
Solubility
Soluble in ethanol (50 mg/ml), DMSO, methanol, and ammonium hydroxide (50 mg/ml). Insoluble in water (almost)
Notes
Store at room temperature. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- J. Foyere Ayafor.; Joseph D. Connolly. 2R,3R-(+)-3-acetoxy-4',5-dihydroxy-7-methoxyflavanone and 2R,3R-(+)-3-acetoxy-4',5,7-trihydroxyflavanone: two new 3-acetylated dihydroflavonols from Aframomum pruinosum Gagnepain (Zingiberaceae).J. Chem. Soc., Perkin Trans. 1. 1981, ,2563-2565 .