NP-MRD: Showing NP-Card for 2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0191348)

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Record Information

Version

2.0

Created at

2022-09-04 08:16:40 UTC

Updated at

2022-09-04 08:16:40 UTC

NP-MRD ID

NP0191348

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

2-{[4-(3-{18-[5-(4-Hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 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. Based on a literature review very few articles have been published on 2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042210162D          

 63 65  0  0  0  0            999 V2000
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  1  2  1  0  0  0  0
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M  END

     RDKit          3D

145147  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309042210162D          

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M  END
> <DATABASE_ID>
NP0191348

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CO)=CCC1CCC(C)=C(C=CC(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C=CC2=C(C)CCC(CC=C(C)COC3OC(CO)C(O)C(O)C3O)C2(C)C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C56H82O7/c1-38(19-15-21-40(3)25-33-48-44(7)27-31-46(55(48,9)10)29-23-42(5)35-57)17-13-14-18-39(2)20-16-22-41(4)26-34-49-45(8)28-32-47(56(49,11)12)30-24-43(6)37-62-54-53(61)52(60)51(59)50(36-58)63-54/h13-26,33-34,46-47,50-54,57-61H,27-32,35-37H2,1-12H3

> <INCHI_KEY>
UCVXTUCEDYVMOY-UHFFFAOYSA-N

> <FORMULA>
C56H82O7

> <MOLECULAR_WEIGHT>
867.265

> <EXACT_MASS>
866.60605498

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
145

> <JCHEM_AVERAGE_POLARIZABILITY>
109.16089789639689

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
9.796032553666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.199930239721589

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210495033922667

> <JCHEM_PKA_STRONGEST_BASIC>
-2.079706692916088

> <JCHEM_POLAR_SURFACE_AREA>
119.61000000000001

> <JCHEM_REFRACTIVITY>
275.0749

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
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HETATM   18  C   UNK     0     -18.672 -32.340   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -18.672 -30.800   0.000  0.00  0.00           C+0
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HETATM   21  O   UNK     0     -21.339 -32.340   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -13.337 -32.340   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -14.060 -30.980   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -12.614 -30.980   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334 -33.110   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000 -32.340   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.334 -33.110   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667 -32.340   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.001 -33.110   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001 -34.650   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335 -32.340   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668 -33.110   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.002 -32.340   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.336 -33.110   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.336 -34.650   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.669 -32.340   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.003 -33.110   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.337 -32.340   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.337 -30.800   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.003 -30.030   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      14.670 -30.030   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      16.004 -30.800   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      16.004 -32.340   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.338 -33.110   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      18.672 -32.340   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      20.005 -33.110   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      20.005 -34.650   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      21.339 -32.340   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      21.339 -30.800   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      22.673 -30.030   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      22.673 -28.490   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      24.006 -27.720   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      24.006 -26.180   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      22.673 -25.410   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      25.340 -28.490   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      26.674 -27.720   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      25.340 -30.030   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      26.674 -30.800   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0      24.006 -30.800   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      24.006 -32.340   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      14.670 -33.110   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      15.393 -34.470   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      13.947 -34.470   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   15   10   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    2   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   61                                                  
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   61                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   59                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53   55                                                  
CONECT   53   52   54                                                       
CONECT   54   53                                                            
CONECT   55   52   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58   59                                                  
CONECT   58   57                                                            
CONECT   59   57   50   60                                                  
CONECT   60   59                                                            
CONECT   61   43   38   62   63                                             
CONECT   62   61                                                            
CONECT   63   61                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₆H₈₂O₇

Average Mass

867.2650 Da

Monoisotopic Mass

866.60605 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(CO)=CCC1CCC(C)=C(C=CC(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C=CC2=C(C)CCC(CC=C(C)COC3OC(CO)C(O)C(O)C3O)C2(C)C)C1(C)C

InChI Identifier

InChI=1S/C56H82O7/c1-38(19-15-21-40(3)25-33-48-44(7)27-31-46(55(48,9)10)29-23-42(5)35-57)17-13-14-18-39(2)20-16-22-41(4)26-34-49-45(8)28-32-47(56(49,11)12)30-24-43(6)37-62-54-53(61)52(60)51(59)50(36-58)63-54/h13-26,33-34,46-47,50-54,57-61H,27-32,35-37H2,1-12H3

InChI Key

UCVXTUCEDYVMOY-UHFFFAOYSA-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

Not Available

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
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acyl
Monosaccharide
Oxane
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Acetal
Polyol
Alcohol
Organic oxygen compound
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162937925

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0191348)

MOL for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0191348 (2-{[4-(3-{18-[5-(4-hydroxy-3-methylbut-2-en-1-yl)-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}-2,2,4-trimethylcyclohex-3-en-1-yl)-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)