NP-MRD: Showing NP-Card for 2-Geranyl-4-isobutyrylphloroglucinol (NP0138038)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-31 16:44:12 UTC

Updated at

2022-05-31 16:44:12 UTC

NP-MRD ID

NP0138038

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-Geranyl-4-isobutyrylphloroglucinol

Description

2-Geranyl-4-isobutyrylphloroglucinol 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. 2-Geranyl-4-isobutyrylphloroglucinol is found in Achyrocline alata, Helichrysum platypterum and Hypericum roeperianum. Based on a literature review very few articles have been published on 2-Geranyl-4-isobutyrylphloroglucinol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 52  0  0  0  0  0  0  0  0999 V2000
    6.6609    0.3612   -0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2108   -1.0403    0.0220 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1161   -2.1441   -0.3641 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0175   -1.3041    0.5146 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0947   -0.1914    0.9072 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8156   -0.2398    0.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8850    0.8807    0.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2613    2.2899    0.3766 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6903    0.5860    1.0410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3344    1.5622    1.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5796    1.2717    0.7033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8858    2.0728   -0.3660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1339    3.1630   -0.7889 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0196    1.7973   -1.0905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8429    0.7185   -0.7393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9858    0.4657   -1.4917 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5626   -0.0944    0.3194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3844   -1.1963    0.7165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9791   -1.8443    1.7650 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6116   -1.7109    0.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4671   -2.2488   -1.2826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7993   -0.7675    0.2655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4000    0.2085    1.0427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0646   -0.5660    2.1179 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6205    0.8827    0.8469 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9613    0.9342   -0.7988 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6709    0.3950   -0.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6716   -2.8052   -1.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0972   -1.7531   -0.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3517   -2.7603    0.5479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7086   -2.3225    0.6338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5798    0.7918    0.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9219   -0.2945    1.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3274   -1.2100    0.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9477   -0.1872   -0.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9881    2.9048    1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9136    2.7044   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3865    2.3376    0.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4505   -0.4873    1.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060    1.4004    2.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0079    2.6051    1.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2975    3.5049   -0.3809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2994    2.4047   -1.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1767    1.0774   -2.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9303   -2.6185    0.7306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6466   -3.3714   -1.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2721   -1.8525   -1.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4471   -2.1527   -1.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3152   -0.7068   -0.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5931   -1.1928    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5417    0.1983    0.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2810   -0.4561    2.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0
 10 11  1  0
 11 23  2  0
 23 24  1  0
 23 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 17 15  2  0
 15 16  1  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
  9  7  2  0
  7  8  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
 12 11  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 24 52  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 16 44  1  0
 14 43  1  0
 13 42  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  6 34  1  0
  6 35  1  0
  5 32  1  0
  5 33  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
M  END


  Mrv1652305312218442D          

 25 25  0  0  0  0            999 V2000
   -0.7145    2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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
    0.7145    1.2375    0.0000 C   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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   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
    2.8579   -0.0000    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   -1.6500    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
    0.7145   -0.4125    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
    0.0000    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
    0.0000    3.3000    0.0000 C   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
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  7 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
  2 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138038

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(CC1=C(O)C(C(=O)C(C)C)=C(O)C=C1O)=C(\C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-12(2)7-6-8-14(5)9-10-15-16(21)11-17(22)18(20(15)24)19(23)13(3)4/h7,9,11,13,21-22,24H,6,8,10H2,1-5H3/b14-9+

> <INCHI_KEY>
TXDNBNXWWCEVMG-NTEUORMPSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.36255578999685

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-{3-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,4,6-trihydroxyphenyl}-2-methylpropan-1-one

> <JCHEM_LOGP>
6.5520007693333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.553778708463318

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.784285718692649

> <JCHEM_PKA_STRONGEST_BASIC>
-4.611527526248396

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
99.6503

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1-{3-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,4,6-trihydroxyphenyl}-2-methylpropan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-MAY-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-MAY-22         0                                  
HETATM    1  H   UNK     0      -1.334   3.850   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.001  11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   13                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    7   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    4   17                                                  
CONECT   17   16                                                            
CONECT   18    2   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

72008-03-8

SMILES

[H]\C(CC1=C(O)C(C(=O)C(C)C)=C(O)C=C1O)=C(\C)CCC=C(C)C

InChI Identifier

InChI=1S/C20H28O4/c1-12(2)7-6-8-14(5)9-10-15-16(21)11-17(22)18(20(15)24)19(23)13(3)4/h7,9,11,13,21-22,24H,6,8,10H2,1-5H3/b14-9+

InChI Key

TXDNBNXWWCEVMG-NTEUORMPSA-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
Achyrocline alata	LOTUS Database	35616633
Helichrysum platypterum	LOTUS Database	35616633
Hypericum roeperanum	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
Acylphloroglucinol derivative
Aromatic monoterpenoid
Monocyclic monoterpenoid
Monoterpenoid
Benzenetriol
Phenylpropane
Phloroglucinol derivative
Benzoyl
Aryl alkyl ketone
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Polyol
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

8602316

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10426888

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2-Geranyl-4-isobutyrylphloroglucinol (NP0138038)

MOL for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

3D MOL for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

3D SDF for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

3D-SDF for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

PDB for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

3D PDB for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

SMILES for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

INCHI for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

Structure for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)

3D Structure for NP0138038 (2-Geranyl-4-isobutyrylphloroglucinol)