NP-MRD: Showing NP-Card for 8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one (NP0171913)

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Record Information

Version

2.0

Created at

2022-09-03 08:37:35 UTC

Updated at

2022-09-03 08:37:35 UTC

NP-MRD ID

NP0171913

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032210372D          

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M  END


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   -2.0572   -0.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8091   -2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8091   -0.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6216   -0.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9037    0.5995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1519   -0.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256    0.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    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  4  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 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
 31 33  1  0  0  0  0
 27 33  2  0  0  0  0
 33 34  1  0  0  0  0
 20 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 38 45  1  0  0  0  0
 35 46  2  0  0  0  0
 11 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171913

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CCC1(CC=C(C)C)C(O)=C(C(=O)C2=CC=C(O)C(O)=C2)C2=C(C(CC(C)(C)O2)C2=C(O)C(=O)C=CO2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H44O9/c1-21(2)9-8-10-23(5)14-17-38(16-13-22(3)4)35(44)29-25(33-32(43)27(40)15-18-46-33)20-37(6,7)47-34(29)30(36(38)45)31(42)24-11-12-26(39)28(41)19-24/h9,11-15,18-19,25,39,41,43,45H,8,10,16-17,20H2,1-7H3

> <INCHI_KEY>
HGUQYROCEMPGDU-UHFFFAOYSA-N

> <FORMULA>
C38H44O9

> <MOLECULAR_WEIGHT>
644.761

> <EXACT_MASS>
644.298532997

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
69.19440356767845

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxo-4H-pyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4,5,6-tetrahydro-2H-1-benzopyran-5-one

> <ALOGPS_LOGP>
5.23

> <JCHEM_LOGP>
6.366627248

> <ALOGPS_LOGS>
-5.58

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.492234964549189

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.3153888054465783

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4597270662030346

> <JCHEM_POLAR_SURFACE_AREA>
150.59

> <JCHEM_REFRACTIVITY>
187.4484

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.71e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.896  -1.288   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.380  -1.020   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.853   0.427   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.390  -2.200   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.873  -1.933   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.883  -3.112   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.367  -2.845   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.840  -1.398   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.377  -4.025   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.860  -3.757   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.850  -2.043   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.377  -0.595   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.894  -0.328   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.420   1.119   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.883  -1.508   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.518  -1.037   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.528   0.677   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -2.667   0.000   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   17   46                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   26                                                  
CONECT   20   19   21   35                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25   19   27                                                  
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   27   34                                                  
CONECT   34   33                                                            
CONECT   35   20   36   46                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   45                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   38                                                       
CONECT   46   35   11   47                                                  
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₄O₉

Average Mass

644.7610 Da

Monoisotopic Mass

644.29853 Da

IUPAC Name

8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxo-4H-pyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4,5,6-tetrahydro-2H-1-benzopyran-5-one

Traditional Name

8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCC1(CC=C(C)C)C(O)=C(C(=O)C2=CC=C(O)C(O)=C2)C2=C(C(CC(C)(C)O2)C2=C(O)C(=O)C=CO2)C1=O

InChI Identifier

InChI=1S/C38H44O9/c1-21(2)9-8-10-23(5)14-17-38(16-13-22(3)4)35(44)29-25(33-32(43)27(40)15-18-46-33)20-37(6,7)47-34(29)30(36(38)45)31(42)24-11-12-26(39)28(41)19-24/h9,11-15,18-19,25,39,41,43,45H,8,10,16-17,20H2,1-7H3

InChI Key

HGUQYROCEMPGDU-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

Not Available

Chemical Taxonomy

Classification

Not classified

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	5.23	ALOGPS
logP	6.37	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	-0.32	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	150.59 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	187.45 m³·mol⁻¹	ChemAxon
Polarizability	69.19 Å³	ChemAxon
Number of Rings	4	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one (NP0171913)

MOL for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

3D MOL for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

3D SDF for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

3D-SDF for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

PDB for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

3D PDB for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

SMILES for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

INCHI for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

Structure for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)

3D Structure for NP0171913 (8-(3,4-dihydroxybenzoyl)-6-(3,7-dimethylocta-2,6-dien-1-yl)-7-hydroxy-4-(3-hydroxy-4-oxopyran-2-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-1-benzopyran-5-one)