ChemSpider 2D Image | Zeaxanthin | C40H56O2

Zeaxanthin

  • Molecular FormulaC40H56O2
  • Average mass568.871 Da
  • Monoisotopic mass568.428040 Da
  • ChemSpider ID4444421
  • Double-bond stereo - Double-bond stereo

    defined stereocentres - 2 of 2 defined stereocentres


More details:



Featured data source



Validated by Experts, Validated by Users, Non-Validated, Removed by Users

Zeaxanthin [Wiki]
(1R,1'R)-4,4'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaen-1,18-diyl]bis(3,5,5-trimethyl-3-cyclohexen-1-ol)
(1R,1'R)-4,4'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tetramethyl-1,3,5,7,9,11,13,15,17-octadecanonaene-1,18-diyl]bis(3,5,5-trimethyl-3-cyclohexen-1-ol)
(1R,1'R)-4,4'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-Tétraméthyl-1,3,5,7,9,11,13,15,17-octadécanonaène-1,18-diyl]bis(3,5,5-triméthyl-3-cyclohexén-1-ol) [French]
(3R,3'R)-Dihydroxy-b-carotene
(3R,3'R)-β,β-Carotene-3,3'-diol [ACD/IUPAC Name]
(3R,3'R)-β,β-Carotene-3,3'-diol
(3R,3'R)-β,β-Carotène-3,3'-diol [French] [ACD/IUPAC Name]
(3R,3'R)-β,β-Carotin-3,3'-diol [German] [ACD/IUPAC Name]
144-68-3 [RN]
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

14681_FLUKA [DBID]
C06098 [DBID]
CHEBI:27547 [DBID]
NSC713073 [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Compound Source:

      Aegilops tauschii PlantCyc CPD1F-130
      Amaranthus hypochondriacus PlantCyc CPD1F-130
      Amborella trichopoda PlantCyc CPD1F-130
      Anacardium occidentale PlantCyc CPD1F-130
      Ananas comosus PlantCyc CPD1F-130
      Aquilegia coerulea PlantCyc CPD1F-130
      Arabidopsis halleri PlantCyc CPD1F-130
      Arabidopsis lyrata PlantCyc CPD1F-130
      Arabidopsis thaliana col PlantCyc CPD1F-130
      Asparagus officinalis PlantCyc CPD1F-130
      astaxanthin biosynthesis (bacteria, fungi, algae) PlantCyc CPD1F-130
      Beta vulgaris subsp. vulgaris PlantCyc CPD1F-130
      beta-carotene + 4 a reduced ferredoxin [iron-sulfur] cluster + 4 H+ + 2 oxygen -> zeaxanthin + 4 an oxidized ferredoxin [iron-sulfur] cluster + 2 H2O PlantCyc CPD1F-130
      Boechera stricta PlantCyc CPD1F-130
      Brachypodium distachyon PlantCyc CPD1F-130
      Brassica napus PlantCyc CPD1F-130
      Brassica oleracea var. capitata PlantCyc CPD1F-130
      Brassica oleracea var. oleracea PlantCyc CPD1F-130
      Brassica rapa FPsc PlantCyc CPD1F-130
      Brassica rapa subsp. pekinensis PlantCyc CPD1F-130
      Calotropis gigantea PlantCyc CPD1F-130
      Camptotheca acuminata PlantCyc CPD1F-130
      Cannabis sativa PlantCyc CPD1F-130
      Capsella grandiflora PlantCyc CPD1F-130
      Capsella rubella PlantCyc CPD1F-130
      Capsicum annuum PlantCyc CPD1F-130
      Carica papaya PlantCyc CPD1F-130
      carotenoid cleavage PlantCyc CPD1F-130
      Catharanthus roseus PlantCyc CPD1F-130
      Chenopodium quinoa PlantCyc CPD1F-130
      Chlamydomonas reinhardtii PlantCyc CPD1F-130
      Chromochloris zofingiensis PlantCyc CPD1F-130
      Cicer arietinum PlantCyc CPD1F-130
      Citrus clementina PlantCyc CPD1F-130
      Citrus sinensis PlantCyc CPD1F-130
      Coccomyxa subellipsoidea C-169 PlantCyc CPD1F-130
      Corchorus capsularis PlantCyc CPD1F-130
      crocetin biosynthesis PlantCyc CPD1F-130
      Cucumis sativus PlantCyc CPD1F-130
      Daucus carota subsp. sativus PlantCyc CPD1F-130
      Dianthus caryophyllus PlantCyc CPD1F-130
      Dioscorea rotundata PlantCyc CPD1F-130
      Eucalyptus grandis PlantCyc CPD1F-130
      Eutrema salsugineum PlantCyc CPD1F-130
      Fragaria vesca subsp. vesca PlantCyc CPD1F-130
      Glycine max PlantCyc CPD1F-130
      Gossypium raimondii PlantCyc CPD1F-130
      Helianthus annuus PlantCyc CPD1F-130
      Hordeum vulgare subsp. vulgare PlantCyc CPD1F-130
      Humulus lupulus var. lupulus PlantCyc CPD1F-130
      Kalanchoe fedtschenkoi PlantCyc CPD1F-130
      Kalanchoe laxiflora PlantCyc CPD1F-130
      Leersia perrieri PlantCyc CPD1F-130
      Linum usitatissimum PlantCyc CPD1F-130
      Lotus japonicus PlantCyc CPD1F-130
      Malus domestica PlantCyc CPD1F-130
      Manihot esculenta PlantCyc CPD1F-130
      Marchantia polymorpha PlantCyc CPD1F-130
      Medicago truncatula PlantCyc CPD1F-130
      Micromonas commoda RCC299 PlantCyc CPD1F-130
      Micromonas pusilla CCMP1545 PlantCyc CPD1F-130
      Mimulus guttatus PlantCyc CPD1F-130
      Miscanthus sinensis PlantCyc CPD1F-130
      Musa acuminata PlantCyc CPD1F-130
      Nicotiana tabacum PlantCyc CPD1F-130
      nostoxanthin biosynthesis PlantCyc CPD1F-130
      Olea europaea var. sylvestris PlantCyc CPD1F-130
      Oropetium thomaeum PlantCyc CPD1F-130
      Oryza brachyantha PlantCyc CPD1F-130
      Oryza glaberrima PlantCyc CPD1F-130
      Oryza punctata PlantCyc CPD1F-130
      Oryza rufipogon PlantCyc CPD1F-130
      Oryza sativa Japonica Group PlantCyc CPD1F-130
      Ostreococcus lucimarinus PlantCyc CPD1F-130
      Panicum hallii PlantCyc CPD1F-130
      Panicum virgatum PlantCyc CPD1F-130
      Petunia axillaris PlantCyc CPD1F-130
      Phaseolus vulgaris PlantCyc CPD1F-130
      Physcomitrella patens PlantCyc CPD1F-130
      Populus trichocarpa PlantCyc CPD1F-130
      Prunus persica PlantCyc CPD1F-130
      Ricinus communis PlantCyc CPD1F-130
      Rosa chinensis PlantCyc CPD1F-130
      Rosa multiflora PlantCyc CPD1F-130
      Salvia miltiorrhiza PlantCyc CPD1F-130
      Selaginella moellendorffii PlantCyc CPD1F-130
      Setaria italica PlantCyc CPD1F-130
      Setaria viridis PlantCyc CPD1F-130
      Solanum lycopersicum PlantCyc CPD1F-130
      Solanum melongena PlantCyc CPD1F-130
      Solanum pennellii PlantCyc CPD1F-130
      Solanum tuberosum PlantCyc CPD1F-130
      Sorghum bicolor PlantCyc CPD1F-130
      Sphagnum fallax PlantCyc CPD1F-130
      Spinacia oleracea PlantCyc CPD1F-130
      Spirodela polyrhiza PlantCyc CPD1F-130
      Thellungiella parvula PlantCyc CPD1F-130
      Theobroma cacao PlantCyc CPD1F-130
      Trifolium pratense PlantCyc CPD1F-130
      Triticum aestivum PlantCyc CPD1F-130
      Triticum urartu PlantCyc CPD1F-130
      violaxanthin + 2 L-ascorbate + 2 H+ = zeaxanthin + 2 L-dehydro-ascorbate + 2 H2O PlantCyc CPD1F-130
      violaxanthin, antheraxanthin and zeaxanthin interconversion PlantCyc CPD1F-130
      Vitis vinifera PlantCyc CPD1F-130
      Volvox carteri PlantCyc CPD1F-130
      Zea mays subsp. mays PlantCyc CPD1F-130
      zeaxanthin + 2 a reduced electron acceptor + 2 oxygen -> adonixanthin + 2 an oxidized electron acceptor + 3 H2O PlantCyc CPD1F-130
      zeaxanthin + 2 NADH + 2 H+ + 2 oxygen -> nostoxanthin + 2 NAD+ + 2 H2O PlantCyc CPD1F-130
      zeaxanthin + 2 oxygen -> crocetin dialdehyde + 2 3beta-hydroxy-beta-cyclocitral PlantCyc CPD1F-130
      zeaxanthin + 4 a reduced ferredoxin [iron-sulfur] cluster + 4 H+ + 2 oxygen -> violaxanthin + 4 an oxidized ferredoxin [iron-sulfur] cluster + 2 H2O PlantCyc CPD1F-130
      zeaxanthin biosynthesis PlantCyc CPD1F-130
      Zostera marina PlantCyc CPD1F-130
    • Bio Activity:

      antheraxanthin + L-ascorbate + H+ -> zeaxanthin + L-dehydro-ascorbate + H2O PlantCyc CPD1F-130
      beta-cryptoxanthin + 2 a reduced ferredoxin [iron-sulfur] cluster + oxygen + 2 H+ -> zeaxanthin + 2 an oxidized ferredoxin [iron-sulfur] cluster + H2O PlantCyc CPD1F-130
      zeaxanthin + 2 a reduced electron acceptor + 2 oxygen -> adonixanthin + 2 an oxidized electron acceptor + 3 H2O PlantCyc CPD1F-130
      zeaxanthin + 2 a reduced ferredoxin [iron-sulfur] cluster + 2 H+ + oxygen -> antheraxanthin + 2 an oxidized ferredoxin [iron-sulfur] cluster + H2O PlantCyc CPD1F-130
      zeaxanthin + 2 oxygen -> 2 3-hydroxy-beta-ionone + 4,9-dimethyldodeca-2,4,6,8,10-pentaene-1,12-dial PlantCyc CPD1F-130
      zeaxanthin + 2 oxygen -> crocetin dialdehyde + 2 3beta-hydroxy-beta-cyclocitral PlantCyc CPD1F-130
      zeaxanthin + a reduced electron acceptor + oxygen -> 4-hydroxyzeaxanthin + an oxidized electron acceptor + H2O PlantCyc CPD1F-130
      zeaxanthin + NADH + oxygen + H+ -> caloxanthin + NAD+ + H2O PlantCyc CPD1F-130
      zeaxanthin + oxygen -> beta-citraurin + 3beta-hydroxy-beta-cyclocitral PlantCyc CPD1F-130

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

Density: 1.0±0.1 g/cm3
Boiling Point: 711.4±55.0 °C at 760 mmHg
Vapour Pressure: 0.0±5.2 mmHg at 25°C
Enthalpy of Vaporization: 118.9±6.0 kJ/mol
Flash Point: 273.4±26.1 °C
Index of Refraction: 1.585
Molar Refractivity: 189.1±0.3 cm3
#H bond acceptors: 2
#H bond donors: 2
#Freely Rotating Bonds: 10
#Rule of 5 Violations: 2
ACD/LogP: 11.84
ACD/LogD (pH 5.5): 10.76
ACD/BCF (pH 5.5): 1000000.00
ACD/KOC (pH 5.5): 10000000.00
ACD/LogD (pH 7.4): 10.76
ACD/BCF (pH 7.4): 1000000.00
ACD/KOC (pH 7.4): 10000000.00
Polar Surface Area: 40 Å2
Polarizability: 75.0±0.5 10-24cm3
Surface Tension: 41.3±3.0 dyne/cm
Molar Volume: 564.1±3.0 cm3

Click to predict properties on the Chemicalize site






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