Weight | 288.299 g/mol |
---|---|
Formula | C16H16O5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
shikonin (54952-43-1, 517-88-4)
Score:
#466 in Biochemistry
,
#1495 in Biology
,
#1756 in Chemistry
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- The Chemistry and Biology of Alkannin, Shikonin, and Related Naphthazarin Natural Products (Angewandte Chemie, 1999)
- Cellular pharmacology studies of shikonin derivatives (Phytotherapy Research, 2002)
- Shikonin circumvents cancer drug resistance by induction of a necroptotic death (Molecular Cancer Therapeutics, 2007)
- Production of shikonin derivatives by cell suspension cultures of Lithospermum erythrorhizon (Plant Cell Reports, 1981)
- Production of shikonin derivatives by cell suspension cultures of Lithospermum erythrorhizon : II. A new Medium for the production of shikonin derivatives. (Plant Cell Reports, 1981)
- Shikonin, a Component of Chinese Herbal Medicine, Inhibits Chemokine Receptor Function and Suppresses Human Immunodeficiency Virus Type 1 (Antimicrobial Agents and Chemotherapy, 2003)
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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
-
InChIKeyNEZONWMXZKDMKF-UHFFFAOYSA-N
- Pubchem - shikonin
- 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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