NP-MRD: Showing NP-Card for zeinoxanthin (NP0182005)

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Record Information

Version

2.0

Created at

2022-09-03 20:37:15 UTC

Updated at

2022-09-03 20:37:15 UTC

NP-MRD ID

NP0182005

Secondary Accession Numbers

None

Natural Product Identification

Common Name

zeinoxanthin

Description

Beta-Cryptoxanthin, also known as 3-hydroxy-a-carotene, 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. Thus, Beta-cryptoxanthin is considered to be an isoprenoid lipid molecule. zeinoxanthin is found in Tagetes erecta, Aloe arborescens, Aplysia depilans, Caltha palustris, Citrus reticulata, Cladonia gracilis, Cladonia scabriuscula, Diospyros kaki, Dryopteris dilatata, Metasequoia glyptostroboides, Momordica charantia and Physalis lagascae. zeinoxanthin was first documented in 1960 (PMID: 14432452). Beta-Cryptoxanthin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral (PMID: 16076118) (PMID: 16076119) (PMID: 16492736) (PMID: 18466360).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304232018042D          

 41 42  0  0  1  0            999 V2000
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  1 30  2  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304232018042D          

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    7.3307   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0450   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7594   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0450   -3.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4740   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1883   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9029   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6173   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9029   -3.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3318   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0462   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7607   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4752   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1896   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4752   -5.7330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9040   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6186   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3329   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.0474   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3329   -5.7330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7619   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4764   -4.4955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.1908   -3.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9053   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9053   -3.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9017   -5.7330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6161   -6.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.7619   -3.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4764   -3.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7747   -3.7811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1872   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5997   -3.7811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7783   -5.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.1908   -4.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6032   -5.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4728   -5.7330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7583   -6.1455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1 30  2  0  0  0  0
  1 35  1  0  0  0  0
  1  2  1  0  0  0  0
 30  3  1  0  0  0  0
 35  4  1  0  0  0  0
  2  5  2  0  0  0  0
  3 40  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 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
 22 24  1  0  0  0  0
 23 25  2  0  0  0  0
 26 25  1  1  0  0  0
 26 33  1  0  0  0  0
 26 38  1  0  0  0  0
 33 27  2  0  0  0  0
 38 28  1  0  0  0  0
 27 29  1  0  0  0  0
  4 40  1  0  0  0  0
 28 29  1  0  0  0  0
 30 31  1  0  0  0  0
 33 32  1  0  0  0  0
 35 34  1  0  0  0  0
 35 36  1  0  0  0  0
 38 37  1  0  0  0  0
 38 39  1  0  0  0  0
 40 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0182005

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=CCCC1(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/C40H56O/c1-30(18-13-20-32(3)23-25-37-34(5)22-15-27-39(37,7)8)16-11-12-17-31(2)19-14-21-33(4)24-26-38-35(6)28-36(41)29-40(38,9)10/h11-14,16-26,36-37,41H,15,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20+,33-21+/t36-,37+/m1/s1

> <INCHI_KEY>
NBZANZVJRKXVBH-NHWXEJKLSA-N

> <FORMULA>
C40H56O

> <MOLECULAR_WEIGHT>
552.887

> <EXACT_MASS>
552.433116423

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
72.5602591867509

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-3-en-1-ol

> <ALOGPS_LOGP>
9.19

> <JCHEM_LOGP>
9.781020397666666

> <ALOGPS_LOGS>
-6.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.907213404525137

> <JCHEM_PKA_STRONGEST_BASIC>
-1.089784856860705

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
193.54790000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.35e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
α-cryptoxanthin

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 23-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-20         0                                  
HETATM    1  C   UNK     0      11.017  -9.162   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.350  -8.392   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.683 -11.472   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.349  -9.162   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.684  -9.162   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.017  -8.392   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.351  -9.162   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.017  -6.852   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.685  -8.392   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.018  -9.162   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.352  -8.392   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      21.686  -9.162   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.352  -6.852   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      23.019  -8.392   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      24.353  -9.162   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      25.687  -8.392   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      27.020  -9.162   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.354  -8.392   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      27.020 -10.702   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.687  -9.162   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      31.021  -8.392   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      32.355  -9.162   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      33.688  -8.392   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      32.355 -10.702   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      35.022  -9.162   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      36.356  -8.392   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      37.689  -6.082   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      39.023  -8.392   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      39.023  -6.852   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.017 -10.702   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.350 -11.472   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      35.022  -6.082   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      36.356  -6.852   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.913  -7.058   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.683  -8.392   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.453  -7.058   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      36.919 -10.495   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      37.689  -9.162   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      38.459 -10.495   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.349 -10.702   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.015 -11.472   0.000  0.00  0.00           O+0
CONECT    1   30   35    2                                                  
CONECT    2    1    5                                                       
CONECT    3   30   40                                                       
CONECT    4   35   40                                                       
CONECT    5    2    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6    9                                                       
CONECT    8    6                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11   14                                                       
CONECT   13   11                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   20                                                       
CONECT   19   17                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22   25                                                       
CONECT   24   22                                                            
CONECT   25   23   26                                                       
CONECT   26   25   33   38                                                  
CONECT   27   33   29                                                       
CONECT   28   38   29                                                       
CONECT   29   27   28                                                       
CONECT   30    1    3   31                                                  
CONECT   31   30                                                            
CONECT   32   33                                                            
CONECT   33   26   27   32                                                  
CONECT   34   35                                                            
CONECT   35    1    4   34   36                                             
CONECT   36   35                                                            
CONECT   37   38                                                            
CONECT   38   26   28   37   39                                             
CONECT   39   38                                                            
CONECT   40    3    4   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

View in JSmol

Synonyms

Value	Source
(3R,6'r)-beta,epsilon-Caroten-3-ol	ChEBI
3-Hydroxy-alpha-carotene	ChEBI
(3R,6'r)-b,epsilon-Caroten-3-ol	Generator
(3R,6'r)-Β,epsilon-caroten-3-ol	Generator
3-Hydroxy-a-carotene	Generator
3-Hydroxy-α-carotene	Generator
b-Cryptoxanthin	Generator
Β-cryptoxanthin	Generator

Chemical Formula

C₄₀H₅₆O

Average Mass

552.8870 Da

Monoisotopic Mass

552.43312 Da

IUPAC Name

(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]cyclohex-3-en-1-ol

Traditional Name

α-cryptoxanthin

CAS Registry Number

Not Available

SMILES

C\C(\C=C\C=C(/C)\C=C\[C@H]1C(C)=CCCC1(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/C40H56O/c1-30(18-13-20-32(3)23-25-37-34(5)22-15-27-39(37,7)8)16-11-12-17-31(2)19-14-21-33(4)24-26-38-35(6)28-36(41)29-40(38,9)10/h11-14,16-26,36-37,41H,15,27-29H2,1-10H3/b12-11+,18-13+,19-14+,25-23+,26-24+,30-16+,31-17+,32-20+,33-21+/t36-,37+/m1/s1

InChI Key

NBZANZVJRKXVBH-NHWXEJKLSA-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
African marigold	LOTUS Database	35616633
Aloe arborescens	LOTUS Database	35616633
Aplysia depilans	LOTUS Database	35616633
Caltha palustris	LOTUS Database	35616633
Citrus reticulata	LOTUS Database	35616633
Cladonia gracilis	LOTUS Database	35616633
Cladonia scabriuscula	LOTUS Database	35616633
Diospyros kaki	LOTUS Database	35616633
Dryopteris dilatata	LOTUS Database	35616633
Metasequoia glyptostroboides	LOTUS Database	35616633
Momordica charantia	LOTUS Database	35616633
Physalis lagascae	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

carotenol (CHEBI:65244 )
C40 isoprenoids (tetraterpenes) (C08590 )
Carotenoids (C08590 )
C40 isoprenoids (tetraterpenes) (LMPR01070268 )

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	9.19	ALOGPS
logP	9.78	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	18.91	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	193.55 m³·mol⁻¹	ChemAxon
Polarizability	72.56 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00003770

Chemspider ID

Not Available

KEGG Compound ID

C08590

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281234

PDB ID

Not Available

ChEBI ID

65244

Good Scents ID

Not Available

References

General References

PETZOLD EN, QUACKENBUSH FW: Zeinoxanthin, a crystalline carotenol from corn gluten. Arch Biochem Biophys. 1960 Feb;86:163-5. doi: 10.1016/0003-9861(60)90396-9. [PubMed:14432452 ]
Schlatterer J, Breithaupt DE: Cryptoxanthin structural isomers in oranges, orange juice, and other fruits. J Agric Food Chem. 2005 Aug 10;53(16):6355-61. doi: 10.1021/jf050362w. [PubMed:16076118 ]
Melendez-Martinez AJ, Britton G, Vicario IM, Heredia FJ: Identification of zeinoxanthin in orange juices. J Agric Food Chem. 2005 Aug 10;53(16):6362-7. doi: 10.1021/jf050370c. [PubMed:16076119 ]
Kim J, DellaPenna D: Defining the primary route for lutein synthesis in plants: the role of Arabidopsis carotenoid beta-ring hydroxylase CYP97A3. Proc Natl Acad Sci U S A. 2006 Feb 28;103(9):3474-9. doi: 10.1073/pnas.0511207103. Epub 2006 Feb 21. [PubMed:16492736 ]
Perez-Bueno ML, Horton P: The role of lutein in the acclimation of higher plant chloroplast membranes to suboptimal conditions. Physiol Plant. 2008 Sep;134(1):227-36. doi: 10.1111/j.1399-3054.2008.01124.x. Epub 2008 May 5. [PubMed:18466360 ]
LOTUS database [Link]

Showing NP-Card for zeinoxanthin (NP0182005)

MOL for NP0182005 (zeinoxanthin)

3D MOL for NP0182005 (zeinoxanthin)

3D SDF for NP0182005 (zeinoxanthin)

3D-SDF for NP0182005 (zeinoxanthin)

PDB for NP0182005 (zeinoxanthin)

3D PDB for NP0182005 (zeinoxanthin)

SMILES for NP0182005 (zeinoxanthin)

INCHI for NP0182005 (zeinoxanthin)

Structure for NP0182005 (zeinoxanthin)

3D Structure for NP0182005 (zeinoxanthin)