Zeaxanthin (Compound)

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ID	85
Name	Zeaxanthin
Synonyms	all-trans-Zeaxanthin
Structure	MOL SDF PDB SMILES InChI Structure for EE000085 (Zeaxanthin) 3D Structure for EE000085 (Zeaxanthin) Mrv0541 02231219402D 42 43 0 0 1 0 999 V2000 5.2212 -4.8736 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.3962 -4.8736 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.9837 -4.1591 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 4.3962 -3.4446 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2212 -3.4446 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.6337 -4.1591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2212 -5.6986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9357 -5.2861 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.6337 -2.7302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1587 -4.1591 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.4588 -4.1591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.8713 -3.4446 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.6963 -3.4446 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1088 -4.1591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1088 -2.7302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.9338 -4.1591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.3463 -4.8736 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.1713 -4.8736 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.5838 -5.5881 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.5838 -4.1591 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.4088 -5.5881 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.8213 -6.3025 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.4088 -7.0170 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.8213 -7.7315 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.6463 -7.7315 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.4088 -8.4459 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.0588 -8.4459 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.8838 -8.4459 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.2963 -9.1604 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.1213 -9.1604 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.5338 -9.8749 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.3588 -9.8749 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.8838 -9.8749 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.7713 -9.1604 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.7713 -10.5894 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.5963 -10.5894 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.0569 -8.7479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.0088 -9.8749 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 17.5963 -9.1604 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.7713 -8.3354 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.8339 -9.8749 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 16.3588 -11.3038 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 0 0 0 0 3 2 1 0 0 0 0 4 3 1 0 0 0 0 5 4 1 0 0 0 0 6 5 2 0 0 0 0 6 1 1 0 0 0 0 7 1 1 0 0 0 0 8 1 1 0 0 0 0 9 5 1 0 0 0 0 3 10 1 6 0 0 0 6 11 1 0 0 0 0 12 11 2 0 0 0 0 13 12 1 0 0 0 0 14 13 2 0 0 0 0 15 13 1 0 0 0 0 16 14 1 0 0 0 0 17 16 2 0 0 0 0 18 17 1 0 0 0 0 19 18 2 0 0 0 0 20 18 1 0 0 0 0 21 19 1 0 0 0 0 22 21 2 0 0 0 0 23 22 1 0 0 0 0 24 23 2 0 0 0 0 25 24 1 0 0 0 0 26 24 1 0 0 0 0 27 25 2 0 0 0 0 28 27 1 0 0 0 0 29 28 2 0 0 0 0 30 29 1 0 0 0 0 31 30 2 0 0 0 0 32 31 1 0 0 0 0 33 29 1 0 0 0 0 34 32 1 0 0 0 0 35 32 2 0 0 0 0 36 35 1 0 0 0 0 37 34 1 0 0 0 0 38 36 1 0 0 0 0 39 38 1 0 0 0 0 39 34 1 0 0 0 0 40 34 1 0 0 0 0 38 41 1 6 0 0 0 42 35 1 0 0 0 0 M END > <DATABASE_ID> EE000085 > <DATABASE_NAME> test > <SMILES> C\C(\C=C\C=C(/C)\C=C\C1=C(C)C[C@@H](O)CC1(C)C)=C\C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C > <INCHI_IDENTIFIER> InChI=1S/C40H56O2/c1-29(17-13-19-31(3)21-23-37-33(5)25-35(41)27-39(37,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-38-34(6)26-36(42)28-40(38,9)10/h11-24,35-36,41-42H,25-28H2,1-10H3/b12-11-,17-13+,18-14+,23-21+,24-22+,29-15-,30-16+,31-19+,32-20+/t35-,36-/m1/s1 > <INCHI_KEY> JKQXZKUSFCKOGQ-PWPFSTEPSA-N > <FORMULA> C40H56O2 > <MOLECULAR_WEIGHT> 568.8714 > <EXACT_MASS> 568.428031036 > <JCHEM_ACCEPTOR_COUNT> 2 > <JCHEM_AVERAGE_POLARIZABILITY> 72.82108978473056 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 2 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> (1R)-4-[(1E,3E,5E,7Z,9Z,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol > <ALOGPS_LOGP> 8.30 > <JCHEM_LOGP> 8.350644046 > <ALOGPS_LOGS> -5.94 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 2 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 18.907213404525137 > <JCHEM_PKA_STRONGEST_ACIDIC> 18.907213404525137 > <JCHEM_PKA_STRONGEST_BASIC> -0.7887548611967236 > <JCHEM_POLAR_SURFACE_AREA> 40.46 > <JCHEM_REFRACTIVITY> 194.95080000000004 > <JCHEM_ROTATABLE_BOND_COUNT> 10 > <JCHEM_RULE_OF_FIVE> 0 > <ALOGPS_SOLUBILITY> 6.49e-04 g/l > <JCHEM_TRADITIONAL_IUPAC> (1R)-4-[(1E,3E,5E,7Z,9Z,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol > <JCHEM_VEBER_RULE> 0 $$$$
Description	Can coelute with lutein.
Classification	Compounds > Chemical entities > Organic compounds > Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
CAS number	144-68-3
PubChem ID	5280899
ChEBI ID	27547
FooDB ID	FDB019865
HMDB ID	HMDB0002789

Chemical data

MolDBi data

IUPAC Name	(1R)-4-[(1E,3E,5E,7Z,9Z,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol
Traditional IUPAC Name	(1R)-4-[(1E,3E,5E,7Z,9Z,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-3-en-1-ol
Formula	C40H56O2
InChI	InChI=1S/C40H56O2/c1-29(17-13-19-31(3)21-23-37-33(5)25-35(41)27-39(37,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-38-34(6)26-36(42)28-40(38,9)10/h11-24,35-36,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t35-,36-/m1/s1
InChI Key	JKQXZKUSFCKOGQ-QAYBQHTQSA-N
Molecular weight	568.886
Exact mass	568.428031043
SMILES	C\C(\C=C\C=C(/C)\C=C\C1=C(C)C[C@@H](O)CC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C[C@@H](O)CC1(C)C

ClassyFire Taxonomy

Description	belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.
Kingdom	Organic compounds
Super Class	Lipids and lipid-like molecules
Class	Prenol lipids
Sub Class	Tetraterpenoids
Direct Parent	Xanthophylls
Alternative Parents	Secondary alcohols Hydrocarbon derivatives

Publications with Zeaxanthin

ID	Title	First author	Authors	Year	Journal	Volume	Issue	Pages	PubMed ID	DOI	Study design	No. of Biomarkers	No. of Intake values	No. of Concentration values	No. of Reproducibility values	No. of Correlation values	No. of Metabolomic associations	No. of Microbiota associations	No. of Cancer associations

Biomarker data

Measurements of Zeaxanthin in biospecimens

Concentration values

ID	Parent ID	Depth	Subject group	Population	Country	Cohort	Biomarker Time definition	Biospecimen	Analytical method	Biomarker	Biomarker detail	Measurement size	Detected (nb)	Detected (%)	Detected only?	Arithmethic mean	Arithmethic SD	Geometric mean	Geometric SD	Min	Min (detected)	Percentile_05	Percentile_10	Percentile_25	Median	Percentile_75	Percentile_90	Percentile_95	Max	Interquartile range	Mean 95% CI lower	Mean 95% CI upper	GMean 95% CI lower	GMean 95% CI upper	Unit	Converted arithmetic mean	Converted geometric mean	Converted median	Converted unit	Adjustment type	Adjusted on	Regressed on	Expressed as	Publication

Reproducibility values

ID	Excretion ID	Subject group	Population	Country	Cohort	Biomarker Time definition	Biospecimen	Analytical method	Biomarker	Biomarker detail	Arithmetic mean	Geometric mean	Median	Unit	Adjusted on	Reproducibility size	ICC	ICC 95% CI lower	ICC 95% CI upper	CV% WS	CV% BS	VAR WS	VAR BS	Publication

Associations of Zeaxanthin with exposures

Correlation values

ID	Intake ID	Excretion ID	Subject group	Population	Country	Cohort	Intake Time definition	Intake Assessment method	Intake	Intake detail	Supplement intakes included?	Intake Arithmetic mean	Intake Geometric mean	Intake Median	Intake Unit	Intake Adjusted on	Biomarker Time definition	Biospecimen	Analytical method	Biomarker	Biomarker detail	Biomarker Arithmetic mean	Biomarker Geometric mean	Biomarker Median	Biomarker Unit	Biomarker Adjusted on	Correlation size	Correlation type	Correlation value	Correlation 95% CI lower	Correlation 95% CI upper	Correlation p-value	Significant?	Measurement adjustment	Deattenuated?	Covariates	Publication

Metabolomic associations

ID	Intake ID	Excretion ID	Subject group	Population	Country	Cohort	No. of subjects	Intake Assessment method	Intake	Intervention dose	Biospecimen	Analytical method	Biomarker	Structural identification	Feature selection	Area under curve	Sensitivity	Specificity	PLS-DA VIP	Beta coefficient	Beta coefficient p-value	ANOVA p-value	Publication

Microbiota associations

ID	Biomarker	Experimental evidence	Organism	Biospecimen	Antibiotic	Bacterial source	Substrate	Publication

Associations of Zeaxanthin with cancer risk

Cancer associations

ID	Excretion ID	Subject group	Population	Country	Cohort	No. of subjects	No. of cases	No. of controls	Biospecimen	Analytical method	Biomarker	Biomarker detail	Cancer	Study design	Publication

Exposure data

Measurements of Zeaxanthin exposures in populations

Intake values

ID	Parent ID	Depth	Subject group	Population	Country	Cohort	Intake Time definition	Intake assessment tool	Intake food coverage	Intake time coverage	Intake Assessment method	Intake	Intake detail	Food description	Supplement intakes included?	Measurement size	Detected (nb)	Detected (%)	Detected only?	Arithmethic mean	Arithmethic SD	Geometric mean	Geometric SD	Min	Min (detected)	Percentile_05	Percentile_10	Percentile_25	Median	Percentile_75	Percentile_90	Percentile_95	Max	Interquartile range	Mean 95% CI lower	Mean 95% CI upper	GMean 95% CI lower	GMean 95% CI upper	Unit	Converted arithmetic mean	Converted geometric mean	Converted median	Converted unit	Adjustment type	Adjusted on	Regressed on	Expressed as	Publication

Associations of Zeaxanthin exposures with biomarkers

Correlation values

ID	Intake ID	Excretion ID	Subject group	Population	Country	Cohort	Intake Time definition	Intake Assessment method	Intake	Intake detail	Supplement intakes included?	Intake Arithmetic mean	Intake Geometric mean	Intake Median	Intake Unit	Intake Adjusted on	Biomarker Time definition	Biospecimen	Analytical method	Biomarker	Biomarker detail	Biomarker Arithmetic mean	Biomarker Geometric mean	Biomarker Median	Biomarker Unit	Biomarker Adjusted on	Correlation size	Correlation type	Correlation value	Correlation 95% CI lower	Correlation 95% CI upper	Correlation p-value	Significant?	Measurement adjustment	Deattenuated?	Covariates	Publication