NP-MRD: Showing NP-Card for Boviquinone 4 (NP0045523)

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Record Information

Version

2.0

Created at

2022-03-17 19:21:24 UTC

Updated at

2022-03-17 19:21:24 UTC

NP-MRD ID

NP0045523

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Boviquinone 4

Description

Boviquinone 4, also known as bovinone, belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Boviquinone 4 is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Boviquinone 4 has been detected, but not quantified in, mushrooms. Boviquinone 4 is found in Suillus bovinus . This could make boviquinone 4 a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241217332D          

 30 30  0  0  0  0            999 V2000
    1.8557    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8557    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    2.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    3.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2884    3.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308    3.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308    2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732    2.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308   -1.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308   -2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709   -2.8868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709   -2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    3.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1132    0.0829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709   -3.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5157   -0.4121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5157    1.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2066   -0.5770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2884    1.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  1 28  1  0  0  0  0
  2  3  1  0  0  0  0
  2 27  2  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4 29  1  0  0  0  0
  5  6  1  0  0  0  0
  5 30  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 23  1  0  0  0  0
 10 11  1  0  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 24  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 25  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 26  1  0  0  0  0
M  END


  Mrv0541 02241217332D          

 30 30  0  0  0  0            999 V2000
    1.8557    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8557    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    2.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709    3.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2884    3.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308    3.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308    2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732    2.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732    1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    0.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732   -0.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7732   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308   -1.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0308   -2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709   -2.8868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3709   -2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1132    3.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157    2.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1132    0.0829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3709   -3.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5157   -0.4121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5157    1.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2066   -0.5770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2884    1.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  1 28  1  0  0  0  0
  2  3  1  0  0  0  0
  2 27  2  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4 29  1  0  0  0  0
  5  6  1  0  0  0  0
  5 30  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 23  1  0  0  0  0
 10 11  1  0  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 24  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 25  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 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0045523

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC1=C(O)C(=O)C=C(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O4/c1-18(2)9-6-10-19(3)11-7-12-20(4)13-8-14-21(5)15-16-22-25(29)23(27)17-24(28)26(22)30/h9,11,13,15,17,27,30H,6-8,10,12,14,16H2,1-5H3/b19-11+,20-13+,21-15+

> <INCHI_KEY>
FXIRKSMTDSBFCE-YKBIRWAZSA-N

> <FORMULA>
C26H36O4

> <MOLECULAR_WEIGHT>
412.5616

> <EXACT_MASS>
412.26135964

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
48.967365575283324

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,5-dihydroxy-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]cyclohexa-2,5-diene-1,4-dione

> <ALOGPS_LOGP>
6.01

> <JCHEM_LOGP>
6.5766373730000005

> <ALOGPS_LOGS>
-5.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.113490509494587

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.7851911607829445

> <JCHEM_PKA_STRONGEST_BASIC>
-4.141924259568921

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
129.9301

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.93e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,5-dihydroxy-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]cyclohexa-2,5-diene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       3.464   1.539   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.464   0.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.078  -0.769   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.692   0.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.692   1.539   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.078   2.309   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.078   3.849   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.692   4.619   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.692   6.159   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.538   6.929   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.924   6.159   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.924   4.619   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.310   3.849   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.310   2.309   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.696   1.539   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.696   0.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.310  -0.769   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.310  -2.309   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.924  -3.079   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.924  -4.619   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.692  -5.389   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.692  -4.619   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.078   6.929   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.696   4.619   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.078   0.155   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.692  -6.929   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.696  -0.769   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.696   2.309   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.386  -1.077   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -0.538   2.309   0.000  0.00  0.00           O+0
CONECT    1    2    6   28                                                  
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   29                                                  
CONECT    5    4    6   30                                                  
CONECT    6    1    5    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   23                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   24                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21                                                            
CONECT   23    9                                                            
CONECT   24   13                                                            
CONECT   25   17                                                            
CONECT   26   21                                                            
CONECT   27    2                                                            
CONECT   28    1                                                            
CONECT   29    4                                                            
CONECT   30    5                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   60    0
END

View in JSmol

Synonyms

Value	Source
3-Geranylgeranyl-2,5-dihydroxy-1,4-benzoquinone	HMDB
Bovinone	HMDB

Chemical Formula

C₂₆H₃₆O₄

Average Mass

412.5616 Da

Monoisotopic Mass

412.26136 Da

IUPAC Name

2,5-dihydroxy-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]cyclohexa-2,5-diene-1,4-dione

Traditional Name

2,5-dihydroxy-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]cyclohexa-2,5-diene-1,4-dione

CAS Registry Number

28129-52-4

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC1=C(O)C(=O)C=C(O)C1=O

InChI Identifier

InChI=1S/C26H36O4/c1-18(2)9-6-10-19(3)11-7-12-20(4)13-8-14-21(5)15-16-22-25(29)23(27)17-24(28)26(22)30/h9,11,13,15,17,27,30H,6-8,10,12,14,16H2,1-5H3/b19-11+,20-13+,21-15+

InChI Key

FXIRKSMTDSBFCE-YKBIRWAZSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Agaricus bisporus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Pleurotus ostreatus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Suillus bovinus	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Prenylbenzoquinone
Quinone
P-benzoquinone
Vinylogous acid
Cyclic ketone
Ketone
Enol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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
logP	6.01	ALOGPS
logP	6.58	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	7.79	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	129.93 m³·mol⁻¹	ChemAxon
Polarizability	48.97 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0030057

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB001364

KNApSAcK ID

Not Available

Chemspider ID

30776806

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15379535

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Boviquinone 4 (NP0045523)

MOL for NP0045523 (Boviquinone 4)

3D MOL for NP0045523 (Boviquinone 4)

3D SDF for NP0045523 (Boviquinone 4)

3D-SDF for NP0045523 (Boviquinone 4)

PDB for NP0045523 (Boviquinone 4)

3D PDB for NP0045523 (Boviquinone 4)

SMILES for NP0045523 (Boviquinone 4)

INCHI for NP0045523 (Boviquinone 4)

Structure for NP0045523 (Boviquinone 4)

3D Structure for NP0045523 (Boviquinone 4)