NP-MRD: Showing NP-Card for (1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0215671)

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Record Information

Version

2.0

Created at

2022-09-05 15:21:43 UTC

Updated at

2022-09-05 15:21:44 UTC

NP-MRD ID

NP0215671

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

Description

(1S,5S,7S)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-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 sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione is found in Garcinia subelliptica. Based on a literature review very few articles have been published on (1S,5S,7S)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-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


  Mrv1652309052217212D          

 44 46  0  0  1  0            999 V2000
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M  END

     RDKit          2D

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M  END


  Mrv1652309052217212D          

 44 46  0  0  1  0            999 V2000
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    0.3315   -2.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0810   -3.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1565   -2.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5690   -3.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3940   -3.6705    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8065   -4.3850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3940   -5.0995    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5760   -4.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9215   -5.4940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2070   -5.0815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2070   -4.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5074   -3.8440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5074   -3.0190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2219   -4.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8138   -6.3120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0169   -6.5255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3160   -6.9665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9035   -7.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0785   -7.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3340   -8.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0785   -9.1099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1590   -8.3954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1340   -7.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475   -7.8710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7885   -6.5719    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5030   -6.9844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2175   -6.5719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5030   -7.8094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2175   -8.2219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2175   -9.0469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5030   -9.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5030  -10.2844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7885   -9.0469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740   -9.4594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7885   -8.2219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9897   -5.7996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7434   -5.4640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8962   -5.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7053   -5.9149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5165   -5.2100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8065   -2.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3940   -2.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6315   -2.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 18 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  2  0  0  0  0
 27 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
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 26 37  1  0  0  0  0
 10 37  1  0  0  0  0
 37 38  2  0  0  0  0
 26 39  1  0  0  0  0
  8 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215671

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(O)[C@@]2(C(=O)C3=CC=C(O)C(O)=C3)C(=O)[C@@](CC=C(C)C)(C[C@H](C[C@H](CCC(C)=C)C(C)=C)C2(C)C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H50O6/c1-22(2)11-13-26(25(7)8)19-28-21-37(18-17-24(5)6)33(42)29(15-12-23(3)4)34(43)38(35(37)44,36(28,9)10)32(41)27-14-16-30(39)31(40)20-27/h12,14,16-17,20,26,28,39-40,43H,1,7,11,13,15,18-19,21H2,2-6,8-10H3/t26-,28-,37-,38-/m0/s1

> <INCHI_KEY>
DYTPLENCSKDWEM-JQUGNBNZSA-N

> <FORMULA>
C38H50O6

> <MOLECULAR_WEIGHT>
602.812

> <EXACT_MASS>
602.36073933

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
63.099223385405494

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,5S,7S)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <JCHEM_LOGP>
9.198637100666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.847063361393072

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2822178653540215

> <JCHEM_PKA_STRONGEST_BASIC>
-6.328343683475983

> <JCHEM_POLAR_SURFACE_AREA>
111.9

> <JCHEM_REFRACTIVITY>
179.5115

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5S,7S)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2S)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.151  -4.184   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.619  -5.518   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.151  -6.852   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.159  -5.518   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.929  -6.852   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.469  -6.852   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.239  -8.185   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.469  -9.519   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.942  -9.318   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.720 -10.255   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.386  -9.485   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.386  -7.945   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.947  -7.175   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.947  -5.635   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.281  -7.945   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.519 -11.782   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.032 -12.181   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.457 -13.004   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.687 -14.338   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.147 -14.338   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.623 -15.671   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.147 -17.005   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.163 -15.671   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.983 -13.205   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.382 -14.693   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.205 -12.268   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.539 -13.038   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.873 -12.268   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.539 -14.578   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.873 -15.348   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.873 -16.888   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.539 -17.658   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.539 -19.198   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.205 -16.888   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.872 -17.658   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.205 -15.348   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.714 -10.826   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       5.121 -10.200   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.406 -10.741   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.917 -11.041   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.564  -9.725   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.239  -5.518   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.469  -4.184   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.779  -5.518   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   39                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16   37                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   10   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   18   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   37   39                                             
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   29                                                       
CONECT   37   26   10   38                                                  
CONECT   38   37                                                            
CONECT   39   26    8   40   41                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42    6   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
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

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(O)[C@@]2(C(=O)C3=CC=C(O)C(O)=C3)C(=O)[C@@](CC=C(C)C)(C[C@H](C[C@H](CCC(C)=C)C(C)=C)C2(C)C)C1=O

InChI Identifier

InChI=1S/C38H50O6/c1-22(2)11-13-26(25(7)8)19-28-21-37(18-17-24(5)6)33(42)29(15-12-23(3)4)34(43)38(35(37)44,36(28,9)10)32(41)27-14-16-30(39)31(40)20-27/h12,14,16-17,20,26,28,39-40,43H,1,7,11,13,15,18-19,21H2,2-6,8-10H3/t26-,28-,37-,38-/m0/s1

InChI Key

DYTPLENCSKDWEM-JQUGNBNZSA-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 subelliptica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Alkyl-phenylketone
Phenylketone
Benzoyl
Catechol
Aryl ketone
Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
Phenol
1-hydroxy-2-unsubstituted benzenoid
Cyclohexenone
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Ketone
Enol
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organic oxide
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

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

23314693

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 (1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0215671)

MOL for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D MOL for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D SDF for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D-SDF for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

PDB for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D PDB for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

SMILES for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

INCHI for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

Structure for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D Structure for NP0215671 ((1s,5s,7s)-5-(3,4-dihydroxybenzoyl)-4-hydroxy-6,6-dimethyl-7-[(2s)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-1,3-bis(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione)