NP-MRD: Showing NP-Card for 13-oxo-ode (NP0152290)

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Record Information

Version

2.0

Created at

2022-09-02 08:43:54 UTC

Updated at

2022-09-02 08:43:54 UTC

NP-MRD ID

NP0152290

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-oxo-ode

Description

13-OxoODE, also known as 13-KODE or 13-oxo-ode, belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Thus, 13-oxoode is considered to be an octadecanoid lipid molecule. 13-OxoODE is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 13-oxo-ode is found in Artemisia argyi, Carthamus oxyacanthus, Glycine max and Mus musculus. 13-OxoODE exists in all living organisms, ranging from bacteria to humans.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 50  0  0  0  0  0  0  0  0999 V2000
   -7.4331    0.6766   -1.8198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6213   -0.4894   -0.9171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4834   -0.1675    0.5429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1602    0.3816    0.9287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0327   -0.5746    0.6241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7300    0.0143    1.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6277    1.1541    1.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5214   -0.7688    0.8074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3176   -0.2801    1.1535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1295   -1.0555    0.9363 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0751   -0.6503    1.2457 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3472    0.6606    1.8579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2440    1.4637    0.9452 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5511    0.7286    0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3993    1.6176   -0.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7242    0.9348   -0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5563   -0.3975   -1.0263 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8925   -1.0440   -1.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7954   -0.3039   -2.1153 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5215    0.7694   -2.7029 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0679   -0.8308   -2.3176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3803    1.0035   -1.9250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1052    1.5192   -1.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7619    0.3745   -2.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8880   -1.2850   -1.1621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6185   -0.9309   -1.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6981   -1.0549    1.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2869    0.5684    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1687    0.4883    2.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9617    1.4033    0.5514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0280   -0.9422   -0.4111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1883   -1.4695    1.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5216   -1.7535    0.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2897    0.6986    1.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2327   -2.0650    0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8873   -1.3482    1.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4649    1.2579    2.1023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9341    0.5276    2.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4075    2.4925    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7763    1.5542   -0.0652 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0281    0.5154    1.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2710   -0.2090    0.1880 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5502    2.5674    0.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8496    1.7678   -1.1078 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3548    1.6527   -0.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1457    0.7609    0.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0042   -1.0482   -0.2977 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0245   -0.3435   -1.9973 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4038   -1.2054   -0.2477 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6920   -2.0330   -1.7295 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2182   -1.7420   -2.7342 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 21 51  1  0
M  END

  Mrv0541 02231219582D          

 21 20  0  0  0  0            999 V2000
   24.1800  -19.4576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.8946  -18.2201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4642  -14.5075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.7511  -16.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0366  -15.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7511  -16.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0366  -14.9200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4656  -17.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3221  -14.5075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4656  -18.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0352  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3208  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7497  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6062  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3221  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1800  -18.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4642  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8917  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6076  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1787  -13.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8932  -13.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 16  1  0  0  0  0
  2 16  2  0  0  0  0
  3 17  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  7  1  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
  9 15  1  0  0  0  0
 10 16  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 13 17  1  0  0  0  0
 14 18  1  0  0  0  0
 15 19  2  0  0  0  0
 17 20  1  0  0  0  0
 19 21  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0152290

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H30O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h7,9,12,15H,2-6,8,10-11,13-14,16H2,1H3,(H,20,21)/b9-7-,15-12+

> <INCHI_KEY>
JHXAZBBVQSRKJR-BSZOFBHHSA-N

> <FORMULA>
C18H30O3

> <MOLECULAR_WEIGHT>
294.429

> <EXACT_MASS>
294.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
36.073522142850926

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9Z,11E)-13-oxooctadeca-9,11-dienoic acid

> <ALOGPS_LOGP>
5.66

> <JCHEM_LOGP>
5.602404215333333

> <ALOGPS_LOGS>
-5.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.988167284021987

> <JCHEM_PKA_STRONGEST_BASIC>
-4.577074788947507

> <JCHEM_POLAR_SURFACE_AREA>
54.37

> <JCHEM_REFRACTIVITY>
89.13689999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-Oxo-ODE

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      45.136 -36.321   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      46.470 -34.011   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      34.467 -27.081   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      42.469 -30.161   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      41.135 -29.391   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      42.469 -31.701   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      41.135 -27.851   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      43.802 -32.471   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      39.801 -27.081   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      43.802 -34.011   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      31.799 -25.541   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.465 -24.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      33.133 -24.771   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      29.132 -25.541   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      39.801 -25.541   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      45.136 -34.781   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.467 -25.541   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      27.798 -24.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      38.468 -24.771   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      35.800 -24.771   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      37.134 -25.541   0.000  0.00  0.00           C+0
CONECT    1   16                                                            
CONECT    2   16                                                            
CONECT    3   17                                                            
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   15                                                       
CONECT   10    8   16                                                       
CONECT   11   12   13                                                       
CONECT   12   11   14                                                       
CONECT   13   11   17                                                       
CONECT   14   12   18                                                       
CONECT   15    9   19                                                       
CONECT   16    1    2   10                                                  
CONECT   17    3   13   20                                                  
CONECT   18   14                                                            
CONECT   19   15   21                                                       
CONECT   20   17   21                                                       
CONECT   21   19   20                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
13-Keto-9Z,11E-octadecadienoic acid	ChEBI
13-KetoODE	ChEBI
13-KODE	ChEBI
13-oxo-ODE	ChEBI
(9Z,11E)-13-Oxooctadeca-9,11-dienoic acid	Kegg
13-Keto-9Z,11E-octadecadienoate	Generator
(9Z,11E)-13-Oxooctadeca-9,11-dienoate	Generator
13-KODDA	HMDB
13-Keto-9,11,-octadecadienoic acid	HMDB
13-oxo-9,11-Octadecadienoic acid	HMDB
13-Oxooctadecadienoic acid	HMDB
13-OxoODE	ChEBI

Chemical Formula

C₁₈H₃₀O₃

Average Mass

294.4290 Da

Monoisotopic Mass

294.21949 Da

IUPAC Name

(9Z,11E)-13-oxooctadeca-9,11-dienoic acid

Traditional Name

13-Oxo-ODE

CAS Registry Number

Not Available

SMILES

CCCCCC(=O)\C=C\C=C/CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H30O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h7,9,12,15H,2-6,8,10-11,13-14,16H2,1H3,(H,20,21)/b9-7-,15-12+

InChI Key

JHXAZBBVQSRKJR-BSZOFBHHSA-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
Artemisia argyi	LOTUS Database	35616633
Carthamus oxyacanthus	LOTUS Database	35616633
Glycine max	LOTUS Database	35616633
Mus musculus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Long-chain fatty acid
Unsaturated fatty acid
Fatty acid
Acryloyl-group
Enone
Alpha,beta-unsaturated ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

enone (CHEBI:68947 )
OxoODE (CHEBI:68947 )
Other Octadecanoids (C14765 )
Other Octadecanoids (LMFA02000016 )

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	5.66	ALOGPS
logP	5.6	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	4.99	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	89.14 m³·mol⁻¹	ChemAxon
Polarizability	36.07 Å³	ChemAxon
Number of Rings	0	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

HMDB0004668

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB023396

KNApSAcK ID

Not Available

Chemspider ID

4949634

KEGG Compound ID

C14765

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6446027

PDB ID

Not Available

ChEBI ID

68947

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-oxo-ode (NP0152290)

MOL for NP0152290 (13-oxo-ode)

3D MOL for NP0152290 (13-oxo-ode)

3D SDF for NP0152290 (13-oxo-ode)

3D-SDF for NP0152290 (13-oxo-ode)

PDB for NP0152290 (13-oxo-ode)

3D PDB for NP0152290 (13-oxo-ode)

SMILES for NP0152290 (13-oxo-ode)

INCHI for NP0152290 (13-oxo-ode)

Structure for NP0152290 (13-oxo-ode)

3D Structure for NP0152290 (13-oxo-ode)