Weight | 288.299 g/mol |
---|---|
Formula | C16H16O5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
Alkannin (23444-65-7, 517-88-4)
Score:
#5 in Medicinal chemistry
,
#511 in Biochemistry
,
#1877 in Chemistry
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- The Chemistry and Biology of Alkannin, Shikonin, and Related Naphthazarin Natural Products (Angewandte Chemie, 1999)
- A comparative study on anti-inflammatory activities of the enantiomers, shikonin and alkannin. (Journal of Natural Products, 1986)
- Antioxidant activities of alkannin, shikonin and Alkanna tinctoria root extracts in oil substrates (Food Chemistry, 2004)
- Alkannin and shikonin: effect on free radical processes and on inflammation - a preliminary pharmacochemical investigation. (Archiv Der Pharmazie, 2002)
- Reaction of -Alkannin (Shikonin) with Reactive Oxygen Species: Detection of -Alkannin Free Radicals (Bioorganic & Medicinal Chemistry, 2000)
- Antitumor Activity of Shikonin, Alkannin and Their Derivatives. II. X-Ray Analysis of Cyclo-alkannin Leucoacetate, Tautomerism of Alkannin and Cyclo-alkannin and Antitumor Activity of Alkannin Derivatives (Chemical & Pharmaceutical Bulletin, 1981)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C
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InChIKeyNEZONWMXZKDMKF-UHFFFAOYSA-N
- Pubchem - Alkannin
- Wikipedia - shikonin
Alkannin is a natural dye that is obtained from the extracts of plants from the borage family Alkanna tinctoria that are found in the south of France. The dye is used as a food coloring and in cosmetics. It is used as a red-brown food additive in regions such as Australia, and is designated in Europe as the E number E103, but is no longer approved for use.
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