NP-MRD: Showing NP-Card for (1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione (NP0207042)

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Record Information

Version

2.0

Created at

2022-09-05 03:29:52 UTC

Updated at

2022-09-05 03:29:52 UTC

NP-MRD ID

NP0207042

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione

Description

Sampsonione A belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. (1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione is found in Hypericum sampsonii. Based on a literature review very few articles have been published on Sampsonione A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205292D          

 43 47  0  0  1  0            999 V2000
   -4.3130    1.1860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5069    1.0104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9518    1.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2559    0.2245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4498    0.0490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1988   -0.7369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2367   -0.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1338   -0.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511    0.2634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.2085   -0.9810    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 30 41  1  0  0  0  0
 13 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END

     RDKit          2D

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M  END


  Mrv1652309052205292D          

 43 47  0  0  1  0            999 V2000
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   -2.1988   -0.7369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2367   -0.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0919   -1.8694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7209   -0.0822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1338   -0.3050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7511    0.2634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3411   -0.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085   -0.9810    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3555   -1.2459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3502   -0.6820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1332   -0.3872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7751   -1.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9245    0.0951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0534    0.4588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1729    0.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4858    1.5289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0215    0.1625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6098   -0.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8633   -1.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5625   -2.5955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3118   -2.7600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7570   -3.4577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4970    1.0978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3248    1.9825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4962    0.6121    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0840    1.3245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3768    2.1756    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    0.9787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5170    1.4996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    1.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4193    0.3916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7796   -0.1294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0086    0.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1484    1.0861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2912    1.9641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9287   -0.2882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7859   -0.3753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4339   -1.0568    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
  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  6  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 15 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  6  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
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
 30 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  2  0  0  0  0
 30 41  1  0  0  0  0
 13 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207042

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\C[C@]12C[C@H]3C[C@H]4C(C)(C)OC1(O)[C@]4(CC=C(C)C)C(=O)[C@@](C(=O)C1=CC=CC=C1)(C2=O)C3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C38H50O5/c1-24(2)14-13-15-26(5)19-20-35-23-28-22-29-34(8,9)43-38(35,42)36(29,21-18-25(3)4)32(41)37(31(35)40,33(28,6)7)30(39)27-16-11-10-12-17-27/h10-12,14,16-19,28-29,42H,13,15,20-23H2,1-9H3/b26-19+/t28-,29+,35-,36+,37-,38?/m1/s1

> <INCHI_KEY>
PLIMGUODTPFUKP-YKIDTEAHSA-N

> <FORMULA>
C38H50O5

> <MOLECULAR_WEIGHT>
586.813

> <EXACT_MASS>
586.36582471

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
68.27079763905746

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S,7R,9R,11R)-1-benzoyl-11-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0^{3,7}.0^{4,11}]tridecane-2,12-dione

> <JCHEM_LOGP>
9.067613785999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.966057868245484

> <JCHEM_PKA_STRONGEST_BASIC>
-4.390181317103076

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
173.25209999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,7R,9R,11R)-1-benzoyl-11-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0^{3,7}.0^{4,11}]tridecane-2,12-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      -8.051   2.214   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.546   1.886   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.510   3.025   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.078   0.419   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.573   0.091   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.104  -1.376   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.309  -1.767   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.038  -3.489   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.346  -0.153   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.250  -0.569   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.402   0.492   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.503  -0.836   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.256  -1.831   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.664  -2.326   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.654  -1.273   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.115  -0.723   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.314  -2.158   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.592   0.177   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.966   0.856   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.323   1.216   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.907   2.854   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.040   0.303   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.138  -1.316   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.611  -3.227   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.050  -4.845   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.582  -5.152   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.413  -6.454   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.928   2.049   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.606   3.701   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.793   1.143   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.890   2.472   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.437   4.061   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.371   1.827   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.565   2.799   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.004   2.251   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.249   0.731   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.055  -0.241   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.616   0.306   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.144   2.027   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       2.410   3.666   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       3.600  -0.538   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.200  -0.701   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.543  -1.973   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                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   20   39                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   41                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20                                                       
CONECT   20   19   11   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   15   23   28                                             
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   39   41                                             
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   33                                                       
CONECT   39   30   11   40                                                  
CONECT   40   39                                                            
CONECT   41   30   13   42   43                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₅₀O₅

Average Mass

586.8130 Da

Monoisotopic Mass

586.36582 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\C[C@]12C[C@H]3C[C@H]4C(C)(C)OC1(O)[C@]4(CC=C(C)C)C(=O)[C@@](C(=O)C1=CC=CC=C1)(C2=O)C3(C)C

InChI Identifier

InChI=1S/C38H50O5/c1-24(2)14-13-15-26(5)19-20-35-23-28-22-29-34(8,9)43-38(35,42)36(29,21-18-25(3)4)32(41)37(31(35)40,33(28,6)7)30(39)27-16-11-10-12-17-27/h10-12,14,16-19,28-29,42H,13,15,20-23H2,1-9H3/b26-19+/t28-,29+,35-,36+,37-,38?/m1/s1

InChI Key

PLIMGUODTPFUKP-YKIDTEAHSA-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
Hypericum sampsonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Monoterpenoid
Aromatic monoterpenoid
Aryl alkyl ketone
Benzoyl
Benzenoid
Monocyclic benzene moiety
Tetrahydrofuran
Cyclic alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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

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

102600704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione (NP0207042)

MOL for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

3D MOL for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

3D SDF for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

3D-SDF for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

PDB for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

3D PDB for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

SMILES for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

INCHI for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

Structure for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)

3D Structure for NP0207042 ((1s,3s,7r,9r,11r)-1-benzoyl-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-en-1-yl)-5-oxatetracyclo[7.3.1.0³,⁷.0⁴,¹¹]tridecane-2,12-dione)