NP-MRD: Showing NP-Card for (1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0202700)

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Record Information

Version

2.0

Created at

2022-09-04 21:58:12 UTC

Updated at

2022-09-04 21:58:12 UTC

NP-MRD ID

NP0202700

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

Description

(1R,5R,7S)-3-(3,4-dihydroxybenzoyl)-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-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. (1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione is found in Garcinia gummi-gutta. Based on a literature review very few articles have been published on (1R,5R,7S)-3-(3,4-dihydroxybenzoyl)-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]Non-3-ene-2,9-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042223582D          

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M  END

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M  END


  Mrv1652309042223582D          

 44 46  0  0  1  0            999 V2000
   -1.3244    6.0812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6100    5.6687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1045    6.0812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6100    4.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1045    4.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1045    3.6062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8190    3.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335    3.6062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8190    2.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335    1.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335    1.1312    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7713    0.8155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4555    0.0533    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3695    0.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7820    0.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6070    0.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0195    1.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0195    0.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7713   -0.7089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6636   -1.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0467   -0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335   -1.0246    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5335   -1.8496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479   -2.2621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479   -3.0871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335   -3.4996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9624   -3.4996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2957   -0.7089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8790   -1.2923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6114    0.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4364    0.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8489   -0.6612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8489    0.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4364    1.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8489    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6739    2.1967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0864    2.9112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0864    1.4822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9114    1.4822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6739    0.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2957    0.8155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8790    1.3989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8029    0.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4704    0.5382    0.0000 O   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
  2  4  2  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  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 33 40  1  0  0  0  0
 30 41  2  0  0  0  0
 11 41  1  0  0  0  0
 41 42  1  0  0  0  0
 22 43  1  0  0  0  0
 11 43  1  0  0  0  0
 43 44  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0202700

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\C[C@@]12C[C@H](CC=C(C)C)C(C)(C)[C@@](CC=C(C)C)(C(=O)C(C(=O)C3=CC=C(O)C(O)=C3)=C1O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H50O6/c1-23(2)11-10-12-26(7)18-19-37-22-28(15-13-24(3)4)36(8,9)38(35(37)44,20-17-25(5)6)34(43)31(33(37)42)32(41)27-14-16-29(39)30(40)21-27/h11,13-14,16-18,21,28,39-40,42H,10,12,15,19-20,22H2,1-9H3/b26-18+/t28-,37+,38-/m0/s1

> <INCHI_KEY>
WBBLTYZSPRMLOP-QHHXVQFASA-N

> <FORMULA>
C38H50O6

> <MOLECULAR_WEIGHT>
602.812

> <EXACT_MASS>
602.36073933

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
68.8844693333625

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,5R,7S)-3-(3,4-dihydroxybenzoyl)-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <JCHEM_LOGP>
9.240319328666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.019840130282793

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3360589245400014

> <JCHEM_PKA_STRONGEST_BASIC>
-6.329947986637856

> <JCHEM_POLAR_SURFACE_AREA>
111.9

> <JCHEM_REFRACTIVITY>
181.7089

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5R,7S)-3-(3,4-dihydroxybenzoyl)-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-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                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.472  11.352   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.139  10.582   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.195  11.352   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.139   9.042   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.195   8.272   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.195   6.732   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.529   5.962   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.862   6.732   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.529   4.422   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.862   3.652   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.862   2.112   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.440   1.522   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.850   0.099   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.690   0.099   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.460   1.433   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.000   1.433   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.770   2.767   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.770   0.099   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.440  -1.323   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.239  -2.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.087  -1.524   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.862  -1.913   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.862  -3.453   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.196  -4.223   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.196  -5.763   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.862  -6.533   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.530  -6.533   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.285  -1.323   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.374  -2.412   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.875   0.099   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.415   0.099   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.185  -1.234   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       7.185   1.433   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.415   2.767   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.185   4.101   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.725   4.101   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       9.495   5.434   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.495   2.767   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      11.035   2.767   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       8.725   1.433   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.285   1.522   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       5.374   2.611   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       3.365   0.099   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       4.611   1.005   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    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                                                       
CONECT   11   10   12   41   43                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   13   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23   28   43                                             
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   22   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   41                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   40                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   33                                                       
CONECT   41   30   11   42                                                  
CONECT   42   41                                                            
CONECT   43   22   11   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₅₀O₆

Average Mass

602.8120 Da

Monoisotopic Mass

602.36074 Da

IUPAC Name

(1R,5R,7S)-3-(3,4-dihydroxybenzoyl)-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

Traditional Name

(1R,5R,7S)-3-(3,4-dihydroxybenzoyl)-5-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-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)=CCC\C(C)=C\C[C@@]12C[C@H](CC=C(C)C)C(C)(C)[C@@](CC=C(C)C)(C(=O)C(C(=O)C3=CC=C(O)C(O)=C3)=C1O)C2=O

InChI Identifier

InChI=1S/C38H50O6/c1-23(2)11-10-12-26(7)18-19-37-22-28(15-13-24(3)4)36(8,9)38(35(37)44,20-17-25(5)6)34(43)31(33(37)42)32(41)27-14-16-29(39)30(40)21-27/h11,13-14,16-18,21,28,39-40,42H,10,12,15,19-20,22H2,1-9H3/b26-18+/t28-,37+,38-/m0/s1

InChI Key

WBBLTYZSPRMLOP-QHHXVQFASA-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 gummi-gutta	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	9.24	ChemAxon
pKa (Strongest Acidic)	3.34	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	181.71 m³·mol⁻¹	ChemAxon
Polarizability	68.88 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

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KNApSAcK ID

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Chemspider ID

31140450

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References

General References

LOTUS database [Link]

Showing NP-Card for (1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0202700)

MOL for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D MOL for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D SDF for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D-SDF for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

PDB for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D PDB for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

SMILES for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

INCHI for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

Structure for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D Structure for NP0202700 ((1r,5r,7s)-3-(3,4-dihydroxybenzoyl)-5-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-8,8-dimethyl-1,7-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)