Weight | 146.145 g/mol |
---|---|
Formula | C9H6O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
CHROMONE (491-38-3)
4-chromone
Score:
#6471 in Chemistry
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- Chromone: a valid scaffold in Medicinal Chemistry (Chemical Reviews, 2014)
- The chromone inhibitor stigmatellin - binding to the ubiquinol oxidation center at the C-side of the mitochondrial membrane (FEBS Letters, 1985)
- pH Controlled Release of Chromone from Chromone-Fe3O4 Nanoparticles (Journal of the American Chemical Society, 2008)
- The in Vitro and in Vivo Effects of 2-(4-Morpholinyl)-8-phenyl-chromone (LY294002), a Specific Inhibitor of Phosphatidylinositol 3-Kinase, in Human Colon Cancer Cells (Clinical Cancer Research, 2002)
- In vivo Antitumor, in vitro Antibacterial Activity and Alkylating Properties of Phosphorohydrazine Derivatives of Coumarin and Chromone. (European Journal of Medicinal Chemistry, 2006)
- Synthesis, characterization, and DNA-binding properties of the Ln(III) complexes with 6-hydroxy chromone-3-carbaldehyde-(2'-hydroxy) benzoyl hydrazone (Bioorganic & Medicinal Chemistry, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-chromone
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SMILESC1=CC=C2C(=C1)C(=O)C=CO2
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InChIKeyOTAFHZMPRISVEM-UHFFFAOYSA-N
- Pubchem - CHROMONE
- Wikipedia - chromone
Chromone (or 1,4-benzopyrone) is a derivative of benzopyran with a substituted keto group on the pyran ring. It is an isomer of coumarin. Derivatives of chromone are collectively known as chromones.
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