Weight | 596.852 g/mol |
---|---|
Formula | C40H52O4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 10 |
Astaxanthin (472-61-7)
astaxanthine · E-astaxanthin
Score:
#2269 in Biology
,
#2795 in Chemistry
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- Sigma-Aldrich - Astaxanthin248.80 USD
- Fisher Scientific - Search for Astaxanthin
- TCI - Search for Astaxanthin
- Haematococcus astaxanthin: applications for human health and nutrition (Trends in Biotechnology, 2003)
- Commercial potential for Haematococcus microalgae as a natural source of astaxanthin (Trends in Biotechnology, 2000)
- Antioxidant Activities of Astaxanthin and Related Carotenoids (Journal of Agricultural and Food Chemistry, 2000)
- Astaxanthin: A Review of its Chemistry and Applications (Critical Reviews in Food Science and Nutrition, 2006)
- Astaxanthin from Microbial Sources (Critical Reviews in Biotechnology, 1991)
- Structure and functional analysis of a marine bacterial carotenoid biosynthesis gene cluster and astaxanthin biosynthetic pathway proposed at the gene level. (Journal of Bacteriology, 1995)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - astaxanthine
- E-astaxanthin
-
SMILESCC1=C(C(CC(C1=O)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(=O)C(CC2(C)C)O)C)C)C
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InChIKeyMQZIGYBFDRPAKN-UHFFFAOYSA-N
- Pubchem - Astaxanthin
- Wikipedia - astaxanthin
Astaxanthin is a keto-carotenoid. It belongs to a larger class of chemical compounds known as terpenes (in Asthaxanthin's case, a tetraterpenoid); terpenes are built from five carbon precursors; isopentenyl diphosphate (or IPP) and dimethylallyl diphosphate (or DMAPP). Astaxanthin is classified as a xanthophyll (originally derived from a word meaning "yellow leaves" since yellow plant leaf pigments were the first recognized of the xanthophyll family of carotenoids), but currently employed to describe carotenoid compounds that have oxygen-containing moities, hydroxyl (-OH) or ketone (C=O), such as zeaxanthin and canthaxanthin.
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