340997-02-6

2′′,3′′-Dihydroochnaflavone Chemical Structure
340997-02-6

Chemical Structure

2′′,3′′-Dihydroochnaflavone

  • CAS No.: 340997-02-6
  • Formula:C30H20O10
  • Molecular Weight:540.47

IUPAC Name: (S)-2-(3-(4-(5,7-dihydroxy-4-oxochroman-2-yl)phenoxy)-4-hydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one

InChIKey: VNCWZYPKAQUABQ-DEOSSOPVSA-N

SMILES: O=C1C2=C(O)C=C(O)C=C2OC(C3=CC(OC4=CC=C([C@H]5OC6=CC(O)=CC(O)=C6C(C5)=O)C=C4)=C(C=C3)O)=C1

Biological Activity: 2′′,3′′-Dihydroochnaflavone is a flavonoid/flavanone-type ether-linked biflavonoid anti-leukemic compound. 2′′,3′′-Dihydroochnaflavone exhibits significant cytotoxicity against P388 murine lymphocytic leukemia cells (IC50 = 3.1 μg/mL). It can be naturally extracted from the dried leaves of Quintinia acutifolia and has also been previously isolated and identified from Ochna interrima and Luxemburgia nobilis (both Ochnaceae plants). 2′′,3′′-Dihydroochnaflavone can be used in research related to anti-tumor (especially leukemia) applications[1].

Cat. No. Product Name Purity Description Pricing
HY-N9784
2′′,3′′-Dihydroochnaflavone 2′′,3′′-Dihydroochnaflavone is a flavonoid/flavanone-type ether-linked biflavonoid anti-leukemic compound. 2′′,3′′-Dihydroochnaflavone exhibits significant cytotoxicity against P388 murine lymphocytic leukemia cells (IC50 = 3.1 μg/mL). It can be naturally extracted from the dried leaves of Quintinia acutifolia and has also been previously isolated and identified from Ochna interrima and Luxemburgia nobilis (both Ochnaceae plants). 2′′,3′′-Dihydroochnaflavone can be used in research related to anti-tumor (especially leukemia) applications.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References