| Weight | 568.886 g/mol |
|---|---|
| Formula | C40H56O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
Zeaxanthin (144-68-3)
Beta Carotene 3,3' Diol · beta-carotene-3,3'-diol · 3R,3'R-Zeaxanthin
Score:
#3406 in Biology
,
#4253 in Chemistry
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- Carotenoids and photoprotection in plants: A role for the xanthophyll zeaxanthin (Biochimica et Biophysica Acta, 1990)
- Photoinhibition and Zeaxanthin Formation in Intact Leaves A Possible Role of the Xanthophyll Cycle in the Dissipation of Excess Light Energy (Plant Physiology, 1987)
- Lutein, zeaxanthin, and the macular pigment (Archives of Biochemistry and Biophysics, 2001)
- BIOLOGIC MECHANISMS OF THE PROTECTIVE ROLE OF LUTEIN AND ZEAXANTHIN IN THE EYE (Annual Review of Nutrition, 2003)
- Resolution of lutein and zeaxanthin using a non-endcapped, lightly carbon-loaded C18 high-performance liquid chromatographic column (Journal of Chromatography A, 1991)
- Lutein + zeaxanthin and omega-3 fatty acids for age-related macular degeneration: The Age-Related Eye Disease Study 2 (AREDS2) randomized clinical trial (JAMA, 2013)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Beta Carotene 3,3' Diol
- beta-carotene-3,3'-diol
- 3R,3'R-Zeaxanthin
- Zeaxanthins
- 3R,3'R Zeaxanthin
-
SMILESCC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C
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InChIKeyJKQXZKUSFCKOGQ-UHFFFAOYSA-N
- Pubchem - Zeaxanthin
- Wikipedia - zeaxanthin
Zeaxanthin is one of the most common carotenoid alcohols found in nature. It is important in the xanthophyll cycle. Synthesized in plants and some micro-organisms, it is the pigment that gives paprika (made from bell peppers), corn, saffron, wolfberries, and many other plants and microbes their characteristic color.
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