NP-MRD: Showing NP-Card for 3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0150103)

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Record Information

Version

2.0

Created at

2022-09-02 06:07:36 UTC

Updated at

2022-09-02 06:07:37 UTC

NP-MRD ID

NP0150103

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

Description

3-(3,4-Dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]Non-3-ene-2,9-dione belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. 3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione is found in Garcinia xanthochymus. 3-(3,4-Dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]Non-3-ene-2,9-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161513122D          

 43 45  0  0  0  0            999 V2000
    4.4390   -1.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 17 42  1  0  0  0  0
  2 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004161513122D          

 43 45  0  0  0  0            999 V2000
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    4.8515   -3.3033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4390   -4.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6210   -3.9101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9665   -4.4123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -3.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -3.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5376   -2.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8231   -3.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1086   -2.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8231   -3.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9665   -2.7623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9665   -1.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6810   -3.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8588   -5.2302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3610   -5.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9485   -6.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3610   -7.3137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1235   -6.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7110   -7.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8860   -7.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4735   -6.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3515   -6.5992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8860   -5.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4735   -5.1703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7110   -5.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1790   -5.9924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3925   -6.7893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8335   -5.4902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5480   -5.9027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5480   -6.7277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2624   -7.1402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2624   -7.9652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9769   -6.7277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0347   -4.7179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7884   -4.3823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9412   -4.6723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7503   -4.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5615   -4.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0619   -5.4437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6765   -1.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  8  9  1  0  0  0  0
  9 10  1  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
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 21 28  1  0  0  0  0
 18 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 31 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  2  0  0  0  0
 31 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 17 42  1  0  0  0  0
  2 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0150103

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1CC2(CC(CC(C)=C)C(C)=C)C(O)=C(C(=O)C3=CC=C(O)C(O)=C3)C(=O)C(CC=C(C)C)(C2=O)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H48O6/c1-21(2)11-13-27-20-36(19-26(24(7)8)17-23(5)6)32(41)30(31(40)25-12-14-28(38)29(39)18-25)33(42)37(34(36)43,35(27,9)10)16-15-22(3)4/h11-12,14-15,18,26-27,38-39,41H,5,7,13,16-17,19-20H2,1-4,6,8-10H3

> <INCHI_KEY>
LYANWIYDCXVWQE-UHFFFAOYSA-N

> <FORMULA>
C37H48O6

> <MOLECULAR_WEIGHT>
588.785

> <EXACT_MASS>
588.345089266

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
65.42673416442841

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <ALOGPS_LOGP>
5.49

> <JCHEM_LOGP>
8.754068435666667

> <ALOGPS_LOGS>
-5.80

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.019898890382631

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.492595409069363

> <JCHEM_PKA_STRONGEST_BASIC>
-6.329947932626355

> <JCHEM_POLAR_SURFACE_AREA>
111.89999999999999

> <JCHEM_REFRACTIVITY>
174.91050000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.29e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       8.286  -2.165   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.056  -3.499   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.286  -4.832   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.056  -6.166   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.286  -7.500   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.759  -7.299   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.537  -8.236   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.204  -7.466   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.204  -5.926   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.870  -5.156   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.536  -5.926   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.203  -5.156   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.536  -7.466   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.537  -5.156   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.537  -3.616   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.871  -5.926   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.336  -9.763   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.274 -10.985   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.504 -12.319   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.274 -13.652   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.964 -12.319   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.194 -13.652   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.654 -13.652   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.884 -12.319   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.656 -12.319   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.654 -10.985   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.884  -9.651   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.194 -10.985   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.801 -11.186   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.199 -12.673   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.023 -10.248   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.356 -11.018   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.356 -12.558   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.690 -13.328   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.690 -14.868   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.024 -12.558   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.532  -8.807   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       8.938  -8.180   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.224  -8.722   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.734  -9.022   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.381  -7.706   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       3.849 -10.162   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      10.596  -3.499   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   43                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   39                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   17   37                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    7   18   42                                                  
CONECT   18   17   19   29                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   28                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   21                                                       
CONECT   29   18   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   37   39                                             
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   31    7   38                                                  
CONECT   38   37                                                            
CONECT   39   31    5   40   41                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   17                                                            
CONECT   43    2                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₈O₆

Average Mass

588.7850 Da

Monoisotopic Mass

588.34509 Da

IUPAC Name

3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

Traditional Name

3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1CC2(CC(CC(C)=C)C(C)=C)C(O)=C(C(=O)C3=CC=C(O)C(O)=C3)C(=O)C(CC=C(C)C)(C2=O)C1(C)C

InChI Identifier

InChI=1S/C37H48O6/c1-21(2)11-13-27-20-36(19-26(24(7)8)17-23(5)6)32(41)30(31(40)25-12-14-28(38)29(39)18-25)33(42)37(34(36)43,35(27,9)10)16-15-22(3)4/h11-12,14-15,18,26-27,38-39,41H,5,7,13,16-17,19-20H2,1-4,6,8-10H3

InChI Key

LYANWIYDCXVWQE-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
Garcinia xanthochymus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Bicyclic monoterpenoid
Benzoyl
Catechol
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Cyclohexenone
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ketone
Enol
Organooxygen compound
Organic oxide
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	5.49	ALOGPS
logP	8.75	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	3.49	ChemAxon
pKa (Strongest Basic)	-6.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	111.9 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	174.91 m³·mol⁻¹	ChemAxon
Polarizability	65.43 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

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 3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0150103)

MOL for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D MOL for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D SDF for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D-SDF for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

PDB for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D PDB for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

SMILES for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

INCHI for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

Structure for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D Structure for NP0150103 (3-(3,4-dihydroxybenzoyl)-4-hydroxy-8,8-dimethyl-5-[4-methyl-2-(prop-1-en-2-yl)pent-4-en-1-yl]-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)