NP-MRD: Showing NP-Card for 2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one (NP0269455)

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Record Information

Version

2.0

Created at

2022-09-08 14:56:42 UTC

Updated at

2022-09-08 14:56:42 UTC

NP-MRD ID

NP0269455

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one

Description

2-[2,3-Dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one is found in Verticillium dahliae. 2-[2,3-Dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171522032D          

 41 42  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171522032D          

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   -2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7309   -9.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059   -9.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4934   -8.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316   -8.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7441   -9.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691   -9.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7441  -11.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316  -11.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7441  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9816  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2191  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4566  -14.5993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4566  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2816  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6941  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9316  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7566  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1691  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9941  -12.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4066  -11.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2316  -11.7414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4066  -13.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9941  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4066  -14.5993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1691  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7566  -14.5993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9316  -14.5993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6941  -13.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9316  -11.7414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5691  -11.0270    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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  4  0  0  0
 12 13  1  0  0  0  0
 14 12  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 17 15  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 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  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 27 35  1  0  0  0  0
 35 36  1  0  0  0  0
 26 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 23 39  1  0  0  0  0
 25 40  1  0  0  0  0
 10 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0269455

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC(C)CC(C)=CC(C)C=C(C)C=CC(O)C(C)C1=CC(O)=C(C2CC(CO)CC(O)C2O)C(=O)C1

> <INCHI_IDENTIFIER>
InChI=1S/C35H56O6/c1-7-8-9-10-11-22(2)14-24(4)16-25(5)15-23(3)12-13-30(37)26(6)28-19-31(38)34(32(39)20-28)29-17-27(21-36)18-33(40)35(29)41/h12-13,15-16,19,22,25-27,29-30,33,35-38,40-41H,7-11,14,17-18,20-21H2,1-6H3

> <INCHI_KEY>
AROKSOHGURMMLT-UHFFFAOYSA-N

> <FORMULA>
C35H56O6

> <MOLECULAR_WEIGHT>
572.827

> <EXACT_MASS>
572.407689523

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
68.64834145492439

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one

> <ALOGPS_LOGP>
4.88

> <JCHEM_LOGP>
5.460610784333332

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.65466228312389

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.6771746767793365

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1737261234971776

> <JCHEM_POLAR_SURFACE_AREA>
118.22000000000001

> <JCHEM_REFRACTIVITY>
172.10750000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.42e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -5.541 -19.250   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001 -19.250   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.231 -17.916   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.691 -17.916   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.921 -16.583   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.619 -16.583   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.389 -17.916   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.929 -17.916   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.619 -19.250   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.389 -20.584   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.619 -21.917   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.389 -23.251   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.619 -24.585   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.929 -23.251   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.699 -24.585   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.929 -25.918   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.239 -24.585   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.009 -25.918   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.549 -25.918   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.319 -27.252   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.319 -24.585   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.549 -23.251   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.859 -24.585   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.629 -23.251   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.169 -23.251   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.939 -24.585   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.479 -24.585   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.249 -23.251   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.789 -23.251   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.559 -21.917   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      19.099 -21.917   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      17.559 -24.585   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.789 -25.918   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      17.559 -27.252   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      15.249 -25.918   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      14.479 -27.252   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      12.169 -25.918   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.939 -27.252   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      10.629 -25.918   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      12.939 -21.917   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.929 -20.584   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   41                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   39                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   40                                                  
CONECT   26   25   27   37                                                  
CONECT   27   26   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   27   36                                                  
CONECT   36   35                                                            
CONECT   37   26   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   23                                                       
CONECT   40   25                                                            
CONECT   41   10                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₆O₆

Average Mass

572.8270 Da

Monoisotopic Mass

572.40769 Da

IUPAC Name

2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one

Traditional Name

2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one

CAS Registry Number

Not Available

SMILES

CCCCCCC(C)CC(C)=CC(C)C=C(C)C=CC(O)C(C)C1=CC(O)=C(C2CC(CO)CC(O)C2O)C(=O)C1

InChI Identifier

InChI=1S/C35H56O6/c1-7-8-9-10-11-22(2)14-24(4)16-25(5)15-23(3)12-13-30(37)26(6)28-19-31(38)34(32(39)20-28)29-17-27(21-36)18-33(40)35(29)41/h12-13,15-16,19,22,25-27,29-30,33,35-38,40-41H,7-11,14,17-18,20-21H2,1-6H3

InChI Key

AROKSOHGURMMLT-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

Species Name	Source	Reference
Verticillium dahliae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Long chain fatty alcohol
Fatty alcohol
Cyclohexanol
Fatty acyl
Vinylogous acid
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Enol
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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	4.88	ALOGPS
logP	5.46	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	5.68	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	118.22 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	172.11 m³·mol⁻¹	ChemAxon
Polarizability	68.65 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one (NP0269455)

MOL for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

3D MOL for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

3D SDF for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

3D-SDF for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

PDB for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

3D PDB for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

SMILES for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

INCHI for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

Structure for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)

3D Structure for NP0269455 (2-[2,3-dihydroxy-5-(hydroxymethyl)cyclohexyl]-3-hydroxy-5-(3-hydroxy-6,8,10,12-tetramethyloctadeca-4,6,9-trien-2-yl)cyclohexa-2,4-dien-1-one)