NP-MRD: Showing NP-Card for Fucoxanthin (NP0136926)

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Record Information

Version

2.0

Created at

2022-05-30 16:28:37 UTC

Updated at

2024-11-29 00:01:16 UTC

NP-MRD ID

NP0136926

Natural Product DOI

https://doi.org/10.57994/3479

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Fucoxanthin

Description

Fucoxanthin 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. Fucoxanthin is an extremely weak basic (essentially neutral) compound (based on its pKa). Fucoxanthin is present in brown seaweeds and diatoms and was first isolated from Fucus, Dictyota, and Laminaria by Willstätter and Page in 1914. It absorbs blue and green light at bandwidth 450-540 nm, imparting a brownish-olive color to algae. Fucoxanthin also reduces weight, improves blood lipid profiles, and decreased insulin resistance in animal models of obesity. Fucoxanthin is a xanthophyll that contributes more than 10% of the estimated total production of carotenoids in nature. Fucoxanthin is found in Aequipecten opercularis, Aplidium pliciferum, Chromulina ochromonoides, Corbicula japonica, Corbicula sandai, Crassostrea gigas, Cryptochiton stelleri, Cystoclonium purpureum, Desmarestia aculeata, Dolabella auricularia, Ellisolandia elongata, Fibrocapsa japonica, Fucus serratus, Fucus vesiculosus, Fucus virsoides, Gelliodes callista, Halocynthia roretzi, Ligia exotica, Magallana gigas, Meretrix petechialis, Pelagococcus subviridis, Pseudo-nitzschia multistriata, Skeletonema costatum, Sporochnus comosus, Styela plicata and Stypopodium flabelliforme. Fucoxanthin was first documented in 2004 (PMID: 14744942). In rodents, fucoxanthin displays low toxicity when administered orally.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02231219352D          

 48 50  0  0  0  0            999 V2000
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  1 25  1  0  0  0  0
  1 30  1  0  0  0  0
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 24 26  1  0  0  0  0
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 25 29  1  0  0  0  0
 31 32  1  0  0  0  0
 32 36  2  0  0  0  0
 33 38  2  0  0  0  0
 33 40  1  0  0  0  0
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 35 46  1  0  0  0  0
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 37 43  1  0  0  0  0
 38 44  1  0  0  0  0
 39 45  1  0  0  0  0
 40 42  2  0  0  0  0
 41 43  2  0  0  0  0
 44 45  2  0  0  0  0
 46 48  2  0  0  0  0
 47 48  2  0  0  0  0
M  END

     RDKit          3D

106108  0  0  0  0  0  0  0  0999 V2000
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 44100  1  0
 46101  1  0
 46102  1  0
 46103  1  0
 47104  1  0
 48105  1  0
 48106  1  0
M  END


  Mrv0541 02231219352D          

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  1 25  1  0  0  0  0
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 44 45  2  0  0  0  0
 46 48  2  0  0  0  0
 47 48  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0136926

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC(C)(C)C(=C=C\C(C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)C(=O)CC23OC2(C)CC(O)CC3(C)C)C(C)(O)C1

> <INCHI_IDENTIFIER>
InChI=1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+

> <INCHI_KEY>
SJWWTRQNNRNTPU-BWRPRJLXSA-N

> <FORMULA>
C42H58O6

> <MOLECULAR_WEIGHT>
658.9063

> <EXACT_MASS>
658.423339588

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
78.28700382506283

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-{4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetate

> <ALOGPS_LOGP>
7.54

> <JCHEM_LOGP>
6.827701596666665

> <ALOGPS_LOGS>
-6.06

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.128038099548267

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.033714319556875

> <JCHEM_PKA_STRONGEST_BASIC>
-2.737175756069491

> <JCHEM_POLAR_SURFACE_AREA>
96.35999999999999

> <JCHEM_REFRACTIVITY>
202.75919999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.75e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-{4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      34.297 -20.259   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      30.447 -23.132   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0       3.345 -34.572   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.681 -33.032   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      34.297 -17.591   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      10.427 -32.262   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.117 -30.928   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.347 -35.342   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.243 -30.158   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.783 -30.158   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      29.113 -22.362   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.447 -17.385   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.113 -18.155   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      36.607 -18.925   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.657 -28.261   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.277 -25.593   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.977 -25.593   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      26.597 -22.926   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.347 -32.262   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.347 -33.802   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.013 -31.492   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      30.447 -21.592   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      30.447 -18.925   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.679 -33.802   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      32.757 -20.259   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.013 -34.572   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.679 -32.262   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      31.987 -21.592   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      31.987 -18.925   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      35.067 -18.925   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.657 -30.928   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.427 -29.595   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.047 -26.927   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      21.207 -24.260   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      25.827 -21.592   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.967 -29.595   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      24.287 -21.592   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.587 -26.927   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      19.667 -24.260   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      14.277 -28.261   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      21.977 -22.926   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      12.737 -28.261   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      23.517 -22.926   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.357 -25.593   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      18.897 -25.593   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      26.597 -20.259   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      29.677 -20.259   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      28.137 -20.259   0.000  0.00  0.00           C+0
CONECT    1   25   30                                                       
CONECT    2   22                                                            
CONECT    3   24                                                            
CONECT    4   19   20                                                       
CONECT    5   30                                                            
CONECT    6   31                                                            
CONECT    7   19   31                                                       
CONECT    8   20                                                            
CONECT    9   21                                                            
CONECT   10   21                                                            
CONECT   11   22                                                            
CONECT   12   23                                                            
CONECT   13   23                                                            
CONECT   14   30                                                            
CONECT   15   32                                                            
CONECT   16   33                                                            
CONECT   17   34                                                            
CONECT   18   35                                                            
CONECT   19    4    7   20   21                                             
CONECT   20    4    8   19   26                                             
CONECT   21    9   10   19   27                                             
CONECT   22    2   11   28   47                                             
CONECT   23   12   13   29   47                                             
CONECT   24    3   26   27                                                  
CONECT   25    1   28   29                                                  
CONECT   26   20   24                                                       
CONECT   27   21   24                                                       
CONECT   28   22   25                                                       
CONECT   29   23   25                                                       
CONECT   30    1    5   14                                                  
CONECT   31    6    7   32                                                  
CONECT   32   15   31   36                                                  
CONECT   33   16   38   40                                                  
CONECT   34   17   39   41                                                  
CONECT   35   18   37   46                                                  
CONECT   36   32   42                                                       
CONECT   37   35   43                                                       
CONECT   38   33   44                                                       
CONECT   39   34   45                                                       
CONECT   40   33   42                                                       
CONECT   41   34   43                                                       
CONECT   42   36   40                                                       
CONECT   43   37   41                                                       
CONECT   44   38   45                                                       
CONECT   45   39   44                                                       
CONECT   46   35   48                                                       
CONECT   47   22   23   48                                                  
CONECT   48   46   47                                                       
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

View in JSmol

Synonyms

Value	Source
3'-Acetate-(7ci)-6',7'-didehydro-5,6-epoxy-4',5,5',6,7,8-hexahydro-3,3',5'-trihydroxy-8-oxo-a-carotene	HMDB
3'-Acetate-(7ci)-6',7'-didehydro-5,6-epoxy-4',5,5',6,7,8-hexahydro-3,3',5'-trihydroxy-8-oxo-alpha-carotene	HMDB
all-trans-Fucoxanthin	HMDB
3-Hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-{4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetic acid	HMDB

Chemical Formula

C₄₂H₅₈O₆

Average Mass

658.9063 Da

Monoisotopic Mass

658.42334 Da

IUPAC Name

3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-{4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC(C)(C)C(=C=C\C(C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)C(=O)CC23OC2(C)CC(O)CC3(C)C)C(C)(O)C1

InChI Identifier

InChI=1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+

InChI Key

SJWWTRQNNRNTPU-BWRPRJLXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	eduardo.caro1@upr.edu	UPR Medical Sciences Campus	Eduardo J. Caro-Diaz	2024-11-27	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	eduardo.caro1@upr.edu	UPR Medical Sciences Campus	Eduardo J. Caro-Diaz	2024-11-27	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	eduardo.caro1@upr.edu	UPR Medical Sciences Campus	Eduardo J. Caro-Diaz	2024-11-27	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl3, experimental)	eduardo.caro1@upr.edu	UPR Medical Sciences Campus	Eduardo J. Caro-Diaz	2024-11-27	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	eduardo.caro1@upr.edu	UPR Medical Sciences Campus	Eduardo J. Caro-Diaz	2024-11-27	View Spectrum

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
Aequipecten opercularis	LOTUS Database	35616633
Aplidium pliciferum	LOTUS Database	35616633
Chromulina ochromonoides	LOTUS Database	35616633
Corbicula japonica	LOTUS Database	35616633
Corbicula sandai	LOTUS Database	35616633
Crassostrea gigas	LOTUS Database	35616633
Cryptochiton stelleri	LOTUS Database	35616633
Cystoclonium purpureum	LOTUS Database	35616633
Desmarestia aculeata	LOTUS Database	35616633
Dolabella auricularia	LOTUS Database	35616633
Ellisolandia elongata	LOTUS Database	35616633
Fibrocapsa japonica	LOTUS Database	35616633
Fucus serratus	LOTUS Database	35616633
Fucus vesiculosus	LOTUS Database	35616633
Fucus virsoides	LOTUS Database	35616633
Gelliodes callista	LOTUS Database	35616633
Halocynthia roretzi	LOTUS Database	35616633
Ligia exotica	LOTUS Database	35616633
Lobophora variegata		Not Available
Magallana gigas	LOTUS Database	35616633
Meretrix petechialis	LOTUS Database	35616633
Pelagococcus subviridis	LOTUS Database	35616633
Pseudo-nitzschia multistriata	LOTUS Database	35616633
Skeletonema costatum	LOTUS Database	35616633
Sporochnus comosus	LOTUS Database	35616633
Styela plicata	LOTUS Database	35616633
Stypopodium flabelliforme	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
Oxepane
Alpha-branched alpha,beta-unsaturated-ketone
Acryloyl-group
Cyclic alcohol
Enone
Tertiary alcohol
Alpha,beta-unsaturated ketone
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carbonyl group
Alcohol
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	7.54	ALOGPS
logP	6.83	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	14.03	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.36 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	202.76 m³·mol⁻¹	ChemAxon
Polarizability	78.29 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0002741

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB023058

KNApSAcK ID

Not Available

Chemspider ID

4516336

KEGG Compound ID

C08596

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Fucoxanthin

METLIN ID

3685

PubChem Compound

5364094

PDB ID

Not Available

ChEBI ID

5186

Good Scents ID

Not Available

References

General References

Asai A, Sugawara T, Ono H, Nagao A: Biotransformation of fucoxanthinol into amarouciaxanthin A in mice and HepG2 cells: formation and cytotoxicity of fucoxanthin metabolites. Drug Metab Dispos. 2004 Feb;32(2):205-11. doi: 10.1124/dmd.32.2.205. [PubMed:14744942 ]

Showing NP-Card for Fucoxanthin (NP0136926)

MOL for NP0136926 (Fucoxanthin)

3D MOL for NP0136926 (Fucoxanthin)

3D SDF for NP0136926 (Fucoxanthin)

3D-SDF for NP0136926 (Fucoxanthin)

PDB for NP0136926 (Fucoxanthin)

3D PDB for NP0136926 (Fucoxanthin)

SMILES for NP0136926 (Fucoxanthin)

INCHI for NP0136926 (Fucoxanthin)

Structure for NP0136926 (Fucoxanthin)

3D Structure for NP0136926 (Fucoxanthin)