NP-MRD: Showing NP-Card for isozeaxanthin (NP0238758)

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Record Information

Version

2.0

Created at

2022-09-06 22:12:05 UTC

Updated at

2022-09-06 22:12:06 UTC

NP-MRD ID

NP0238758

Secondary Accession Numbers

None

Natural Product Identification

Common Name

isozeaxanthin

Description

Isozeaxanthin, also known as aphanicol, 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. Isozeaxanthin is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Isozeaxanthin has been detected, but not quantified in, fishes. isozeaxanthin is found in Acanthochitona defilippii, Microcoleus paludosus, Protula tubularia and Xipholena punicea. This could make isozeaxanthin a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 01111301292D          

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M  END

     RDKit          3D

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M  END


  Mrv0541 01111301292D          

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   -6.4821    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1966    0.5304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4821   -2.3572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532   -1.5321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3387   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6243    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9098   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1953    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4809   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7664    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0519   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6626    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3770   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0915    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5204    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2349   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9494    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6639   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3783    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0928   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8073    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6243    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7664    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6639   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5217    1.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8073    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5217   -0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2362    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2362    0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0928    1.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5217    2.1804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5217   -1.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1051   -0.8780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  1  7  1  0  0  0  0
  1  8  1  0  0  0  0
  4  9  1  0  0  0  0
  5 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 13 30  1  0  0  0  0
 17 31  1  0  0  0  0
 22 32  1  0  0  0  0
 26 33  1  0  0  0  0
 35 29  2  0  0  0  0
 29 36  1  0  0  0  0
 34 35  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 34 38  1  0  0  0  0
 35 39  1  0  0  0  0
 34 40  1  0  0  0  0
 36 41  1  0  0  0  0
 36 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0238758

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\C1=C(C)C(O)CCC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C(O)CCC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O2/c1-29(17-13-19-31(3)21-23-35-33(5)37(41)25-27-39(35,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-36-34(6)38(42)26-28-40(36,9)10/h11-24,37-38,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+

> <INCHI_KEY>
GYZWNQLEQAGWGD-DKLMTRRASA-N

> <FORMULA>
C40H56O2

> <MOLECULAR_WEIGHT>
568.8714

> <EXACT_MASS>
568.428031036

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
73.19052547340993

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(3-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]-2,4,4-trimethylcyclohex-2-en-1-ol

> <ALOGPS_LOGP>
8.49

> <JCHEM_LOGP>
8.662458966

> <ALOGPS_LOGS>
-5.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.183567392005994

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.183567392005994

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1052776270725966

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
194.64280000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.83e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(3-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]-2,4,4-trimethylcyclohex-2-en-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-JAN-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-JAN-13         0                                  
HETATM    1  C   UNK     0     -12.100   0.220   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -13.434  -0.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -13.434  -2.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -12.100  -2.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.766  -2.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -10.766  -0.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -12.100   1.760   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -13.434   0.990   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0     -12.100  -4.400   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -9.433  -2.860   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.433   0.220   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.099  -0.550   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.765   0.220   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.432  -0.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.098   0.220   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.764  -0.550   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.431   0.220   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.097  -0.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.237   0.220   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.570  -0.550   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.904   0.220   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.238  -0.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.571   0.220   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.905  -0.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.239   0.220   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.573  -0.550   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.906   0.220   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.240  -0.550   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.574   0.220   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.765   1.760   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.431   1.760   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.238  -2.090   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.573  -2.090   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.907   2.530   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.574   1.760   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.907  -0.550   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      17.241   0.220   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      17.241   1.760   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.240   2.530   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      15.907   4.070   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      15.907  -2.090   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      16.996  -1.639   0.000  0.00  0.00           C+0
CONECT    1    2    6    7    8                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    1   11                                                  
CONECT    7    1                                                            
CONECT    8    1                                                            
CONECT    9    4                                                            
CONECT   10    5                                                            
CONECT   11    6   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   30                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   31                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   32                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   35   36                                                  
CONECT   30   13                                                            
CONECT   31   17                                                            
CONECT   32   22                                                            
CONECT   33   26                                                            
CONECT   34   35   38   40                                                  
CONECT   35   29   34   39                                                  
CONECT   36   29   37   41   42                                             
CONECT   37   36   38                                                       
CONECT   38   37   34                                                       
CONECT   39   35                                                            
CONECT   40   34                                                            
CONECT   41   36                                                            
CONECT   42   36                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   86    0
END

View in JSmol

Synonyms

Value	Source
4,4'-Dihydro-β,β-carotene	HMDB
Aphanicol	HMDB
b,b-Carotene-4,4'-diol	HMDB
beta,beta-Carotene-4,4'-diol	HMDB
Lactam-based compound, 12D	HMDB

Chemical Formula

C₄₀H₅₆O₂

Average Mass

568.8714 Da

Monoisotopic Mass

568.42803 Da

IUPAC Name

3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(3-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]-2,4,4-trimethylcyclohex-2-en-1-ol

Traditional Name

3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(3-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]-2,4,4-trimethylcyclohex-2-en-1-ol

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C=C(/C)\C=C\C1=C(C)C(O)CCC1(C)C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C(O)CCC1(C)C

InChI Identifier

InChI=1S/C40H56O2/c1-29(17-13-19-31(3)21-23-35-33(5)37(41)25-27-39(35,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-36-34(6)38(42)26-28-40(36,9)10/h11-24,37-38,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+

InChI Key

GYZWNQLEQAGWGD-DKLMTRRASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Acanthochitona defilippii	LOTUS Database	35616633
Microcoleus paludosus	LOTUS Database	35616633
Protula tubularia	LOTUS Database	35616633
Xipholena punicea	LOTUS Database	35616633

Chemical 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

Substituents

Xanthophyll
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	8.49	ALOGPS
logP	8.66	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	18.18	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	194.64 m³·mol⁻¹	ChemAxon
Polarizability	73.19 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0036922

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB015889

KNApSAcK ID

C00022868

Chemspider ID

9932404

KEGG Compound ID

Not Available

BioCyc ID

CPD-7853

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11757703

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for isozeaxanthin (NP0238758)

MOL for NP0238758 (isozeaxanthin)

3D MOL for NP0238758 (isozeaxanthin)

3D SDF for NP0238758 (isozeaxanthin)

3D-SDF for NP0238758 (isozeaxanthin)

PDB for NP0238758 (isozeaxanthin)

3D PDB for NP0238758 (isozeaxanthin)

SMILES for NP0238758 (isozeaxanthin)

INCHI for NP0238758 (isozeaxanthin)

Structure for NP0238758 (isozeaxanthin)

3D Structure for NP0238758 (isozeaxanthin)