NP-MRD: Showing NP-Card for 7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid (NP0260949)

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Record Information

Version

2.0

Created at

2022-09-08 03:15:55 UTC

Updated at

2022-09-08 03:15:55 UTC

NP-MRD ID

NP0260949

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid

Description

7,9-Dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. 7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid is found in Chitinophaga sancti. Based on a literature review very few articles have been published on 7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082205152D          

 43 45  0  0  0  0            999 V2000
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309082205152D          

 43 45  0  0  0  0            999 V2000
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   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5004   -6.0299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1648   -6.7836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2149   -6.4424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9853   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5004   -4.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1077   -4.1366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3373   -3.8863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  2  8  2  0  0  0  0
  8  9  1  4  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 14  1  4  0  0  0
 16 17  2  0  0  0  0
 18 17  1  4  0  0  0
 18 19  2  0  0  0  0
 20 19  1  4  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 30 36  1  0  0  0  0
 27 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 26 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0260949

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C(O)CC=C(C)C=CC(O)=O)C(O)C=CC=CC=CC1C(C=C2C=CC(=O)C=C2)C2C(C=C1C)C(C)(O)CC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H48O6/c1-24(14-20-34(41)42)13-19-33(40)26(3)32(39)12-10-8-7-9-11-29-25(2)21-31-35(36(4,5)23-37(31,6)43)30(29)22-27-15-17-28(38)18-16-27/h7-18,20-22,26,29-33,35,39-40,43H,19,23H2,1-6H3,(H,41,42)

> <INCHI_KEY>
VFIKYXAGOXCBHD-UHFFFAOYSA-N

> <FORMULA>
C37H48O6

> <MOLECULAR_WEIGHT>
588.785

> <EXACT_MASS>
588.345089266

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
68.05054574513704

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid

> <JCHEM_LOGP>
5.179852770666668

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.323806432473045

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.6411214755562

> <JCHEM_PKA_STRONGEST_BASIC>
-0.530015034423969

> <JCHEM_POLAR_SURFACE_AREA>
115.06000000000002

> <JCHEM_REFRACTIVITY>
182.16050000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.002 -10.780   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.669 -10.780   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -12.003 -11.550   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0     -13.337 -10.780   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0     -12.003 -13.090   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001 -13.090   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.334 -13.090   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000 -10.780   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002 -10.780   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.669 -10.780   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.336 -13.090   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.002 -15.400   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.335 -15.400   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.668 -13.090   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.134 -11.256   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.508 -12.663   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.468 -12.026   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      13.039 -10.010   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      12.134  -8.764   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      13.268  -7.722   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      11.830  -7.254   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    2    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   41                                                  
CONECT   27   26   28   37                                                  
CONECT   28   27   22   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   30                                                       
CONECT   37   27   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   37   41                                                       
CONECT   41   40   26   42   43                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Value	Source
7,9-Dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoate	Generator

Chemical Formula

C₃₇H₄₈O₆

Average Mass

588.7850 Da

Monoisotopic Mass

588.34509 Da

IUPAC Name

7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid

Traditional Name

7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2H-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid

CAS Registry Number

Not Available

SMILES

CC(C(O)CC=C(C)C=CC(O)=O)C(O)C=CC=CC=CC1C(C=C2C=CC(=O)C=C2)C2C(C=C1C)C(C)(O)CC2(C)C

InChI Identifier

InChI=1S/C37H48O6/c1-24(14-20-34(41)42)13-19-33(40)26(3)32(39)12-10-8-7-9-11-29-25(2)21-31-35(36(4,5)23-37(31,6)43)30(29)22-27-15-17-28(38)18-16-27/h7-18,20-22,26,29-33,35,39-40,43H,19,23H2,1-6H3,(H,41,42)

InChI Key

VFIKYXAGOXCBHD-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
Chitinophaga sancti	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Bicyclic monoterpenoid
Monoterpenoid
11-noriridane monoterpenoid
Quinomethane
P-quinomethane
Branched fatty acid
Methyl-branched fatty acid
Hydroxy fatty acid
Unsaturated fatty acid
Cyclic alcohol
Tertiary alcohol
Cyclic ketone
Secondary alcohol
Ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Alcohol
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.18	ChemAxon
pKa (Strongest Acidic)	4.64	ChemAxon
pKa (Strongest Basic)	-0.53	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	115.06 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	182.16 m³·mol⁻¹	ChemAxon
Polarizability	68.05 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

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

76044700

PDB ID

Not Available

ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid (NP0260949)

MOL for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

3D MOL for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

3D SDF for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

3D-SDF for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

PDB for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

3D PDB for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

SMILES for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

INCHI for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

Structure for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)

3D Structure for NP0260949 (7,9-dihydroxy-15-{1-hydroxy-1,3,3,6-tetramethyl-4-[(4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-3a,4,5,7a-tetrahydro-2h-inden-5-yl}-4,8-dimethylpentadeca-2,4,10,12,14-pentaenoic acid)