NP-MRD: Showing NP-Card for Pyridinopyrone C (NP0010188)

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Record Information

Version

1.0

Created at

2021-01-05 19:47:44 UTC

Updated at

2021-07-15 17:05:23 UTC

NP-MRD ID

NP0010188

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Pyridinopyrone C

Provided By

NPAtlas

Description

4-Methoxy-3-methyl-6-[(1E,3E,5E,7E)-3-methyl-8-(pyridin-3-yl)octa-1,3,5,7-tetraen-1-yl]-2H-pyran-2-one belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone. Pyridinopyrone C is found in Streptomyces. It was first documented in 2011 (PMID: 21751787). Based on a literature review very few articles have been published on 4-methoxy-3-methyl-6-[(1E,3E,5E,7E)-3-methyl-8-(pyridin-3-yl)octa-1,3,5,7-tetraen-1-yl]-2H-pyran-2-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106563D          

 46 47  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242106563D          

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 16 40  1  0  0  0  0
 17 41  1  0  0  0  0
 18 42  1  0  0  0  0
 20 43  1  0  0  0  0
 25 44  1  0  0  0  0
 25 45  1  0  0  0  0
 25 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010188

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]/C(=C(/[H])\C(\[H])=C(\C(\[H])=C(/[H])C1=C([H])C(OC([H])([H])[H])=C(C(=O)O1)C([H])([H])[H])/C([H])([H])[H])/C(/[H])=C(\[H])C1=C([H])C([H])=C([H])N=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H21NO3/c1-16(8-5-4-6-9-18-10-7-13-22-15-18)11-12-19-14-20(24-3)17(2)21(23)25-19/h4-15H,1-3H3/b5-4+,9-6+,12-11+,16-8+

> <INCHI_KEY>
IJOSQPCSTPSGHH-LVZZCUJTSA-N

> <FORMULA>
C21H21NO3

> <MOLECULAR_WEIGHT>
335.403

> <EXACT_MASS>
335.15214354

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
39.36387967495759

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-methoxy-3-methyl-6-[(1E,3E,5E,7E)-3-methyl-8-(pyridin-3-yl)octa-1,3,5,7-tetraen-1-yl]-2H-pyran-2-one

> <ALOGPS_LOGP>
4.50

> <JCHEM_LOGP>
3.6423762289999995

> <ALOGPS_LOGS>
-5.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
4.882567998278186

> <JCHEM_POLAR_SURFACE_AREA>
48.42

> <JCHEM_REFRACTIVITY>
106.17869999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.29e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-methoxy-3-methyl-6-[(1E,3E,5E,7E)-3-methyl-8-(pyridin-3-yl)octa-1,3,5,7-tetraen-1-yl]pyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -5.5021   -0.5729   -2.5199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3856   -0.6640   -1.4165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8467   -0.5954   -0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4684   -0.4404    0.0671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9952   -0.3791    1.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5632   -0.2174    1.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6781   -0.1252    0.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2708    0.0331    0.9938 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2800    0.0952    2.3442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    0.1221   -0.0254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9835    0.2822    0.2487 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8603    0.3746   -0.7451 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2774    0.5353   -0.3703 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2201    0.6355   -1.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6256    0.7941   -1.0498 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5169    0.8878   -2.1162 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8745    1.0408   -1.9304 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3808    1.1048   -0.6488 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5183    1.0141    0.3764 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1709    0.8624    0.2066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8464   -0.4672    2.3522 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1376   -0.6120    2.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9233   -0.6930    3.2002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6722   -0.6800    0.9577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1375   -0.8448    0.7369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7184   -1.3485   -2.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0254   -0.7961   -3.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0576    0.4353   -2.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8454   -0.3768   -0.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2628   -0.1748    2.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9984   -0.1679   -0.3475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4342   -0.0936    3.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1046   -0.6472    2.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7908    1.0923    2.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2208    0.0783   -1.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3509    0.3313    1.2638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5451    0.3333   -1.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5768    0.5748    0.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8424    0.5872   -2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0771    0.8329   -3.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5545    1.1120   -2.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4524    1.2258   -0.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5184    0.7943    1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5254   -0.1239   -0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6854   -0.7118    1.6894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3290   -1.8602    0.3735 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  5 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 24  3  2  0
 20 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  7 31  1  0
  9 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 20 43  1  0
 25 44  1  0
 25 45  1  0
 25 46  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -5.502  -0.573  -2.520  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.386  -0.664  -1.417  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.847  -0.595  -0.142  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.468  -0.440   0.067  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.995  -0.379   1.346  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.563  -0.217   1.668  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.678  -0.125   0.717  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.271   0.033   0.994  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.280   0.095   2.344  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.567   0.122  -0.025  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.984   0.282   0.249  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.860   0.375  -0.745  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.277   0.535  -0.370  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.220   0.636  -1.288  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.626   0.794  -1.050  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.517   0.888  -2.116  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.874   1.041  -1.930  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.381   1.105  -0.649  0.00  0.00           C+0
HETATM   19  N   UNK     0       8.518   1.014   0.376  0.00  0.00           N+0
HETATM   20  C   UNK     0       7.171   0.862   0.207  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.846  -0.467   2.352  0.00  0.00           O+0
HETATM   22  C   UNK     0      -6.138  -0.612   2.222  0.00  0.00           C+0
HETATM   23  O   UNK     0      -6.923  -0.693   3.200  0.00  0.00           O+0
HETATM   24  C   UNK     0      -6.672  -0.680   0.958  0.00  0.00           C+0
HETATM   25  C   UNK     0      -8.137  -0.845   0.737  0.00  0.00           C+0
HETATM   26  H   UNK     0      -4.718  -1.349  -2.394  0.00  0.00           H+0
HETATM   27  H   UNK     0      -6.025  -0.796  -3.478  0.00  0.00           H+0
HETATM   28  H   UNK     0      -5.058   0.435  -2.607  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.845  -0.377  -0.806  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.263  -0.175   2.713  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.998  -0.168  -0.348  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.434  -0.094   3.158  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.105  -0.647   2.509  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.791   1.092   2.506  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.221   0.078  -1.047  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.351   0.331   1.264  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.545   0.333  -1.770  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.577   0.575   0.666  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.842   0.587  -2.325  0.00  0.00           H+0
HETATM   40  H   UNK     0       7.077   0.833  -3.113  0.00  0.00           H+0
HETATM   41  H   UNK     0       9.555   1.112  -2.779  0.00  0.00           H+0
HETATM   42  H   UNK     0      10.452   1.226  -0.459  0.00  0.00           H+0
HETATM   43  H   UNK     0       6.518   0.794   1.076  0.00  0.00           H+0
HETATM   44  H   UNK     0      -8.525  -0.124  -0.013  0.00  0.00           H+0
HETATM   45  H   UNK     0      -8.685  -0.712   1.689  0.00  0.00           H+0
HETATM   46  H   UNK     0      -8.329  -1.860   0.374  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5   29                                                  
CONECT    5    4    6   21                                                  
CONECT    6    5    7   30                                                  
CONECT    7    6    8   31                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8   32   33   34                                             
CONECT   10    8   11   35                                                  
CONECT   11   10   12   36                                                  
CONECT   12   11   13   37                                                  
CONECT   13   12   14   38                                                  
CONECT   14   13   15   39                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   40                                                  
CONECT   17   16   18   41                                                  
CONECT   18   17   19   42                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15   43                                                  
CONECT   21    5   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25    3                                                  
CONECT   25   24   44   45   46                                             
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    4                                                            
CONECT   30    6                                                            
CONECT   31    7                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   11                                                            
CONECT   37   12                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   16                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   20                                                            
CONECT   44   25                                                            
CONECT   45   25                                                            
CONECT   46   25                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   94    0
END

RDKit          3D

46 47  0  0  0  0  0  0  0  0999 V2000
   -5.5021   -0.5729   -2.5199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3856   -0.6640   -1.4165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8467   -0.5954   -0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4684   -0.4404    0.0671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9952   -0.3791    1.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5632   -0.2174    1.6675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6781   -0.1252    0.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2708    0.0331    0.9938 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2800    0.0952    2.3442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5670    0.1221   -0.0254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9835    0.2822    0.2487 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8603    0.3746   -0.7451 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2774    0.5353   -0.3703 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2201    0.6355   -1.2882 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6256    0.7941   -1.0498 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5169    0.8878   -2.1162 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8745    1.0408   -1.9304 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3808    1.1048   -0.6488 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5183    1.0141    0.3764 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1709    0.8624    0.2066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8464   -0.4672    2.3522 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1376   -0.6120    2.2219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9233   -0.6930    3.2002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6722   -0.6800    0.9577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1375   -0.8448    0.7369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7184   -1.3485   -2.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0254   -0.7961   -3.4775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0576    0.4353   -2.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8454   -0.3768   -0.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2628   -0.1748    2.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9984   -0.1679   -0.3475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4342   -0.0936    3.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1046   -0.6472    2.5089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7908    1.0923    2.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2208    0.0783   -1.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3509    0.3313    1.2638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5451    0.3333   -1.7699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5768    0.5748    0.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8424    0.5872   -2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0771    0.8329   -3.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5545    1.1120   -2.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4524    1.2258   -0.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5184    0.7943    1.0761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5254   -0.1239   -0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6854   -0.7118    1.6894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3290   -1.8602    0.3735 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  5 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 24  3  2  0
 20 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  7 31  1  0
  9 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 20 43  1  0
 25 44  1  0
 25 45  1  0
 25 46  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Pyridinopyrone b	MeSH

Chemical Formula

C₂₁H₂₁NO₃

Average Mass

335.4030 Da

Monoisotopic Mass

335.15214 Da

IUPAC Name

4-methoxy-3-methyl-6-[(1E,3E,5E,7E)-3-methyl-8-(pyridin-3-yl)octa-1,3,5,7-tetraen-1-yl]-2H-pyran-2-one

Traditional Name

4-methoxy-3-methyl-6-[(1E,3E,5E,7E)-3-methyl-8-(pyridin-3-yl)octa-1,3,5,7-tetraen-1-yl]pyran-2-one

CAS Registry Number

Not Available

SMILES

COC1=C(C)C(=O)OC(\C=C\C(\C)=C\C=C\C=C\C2=CN=CC=C2)=C1

InChI Identifier

InChI=1S/C21H21NO3/c1-16(8-5-4-6-9-18-10-7-13-22-15-18)11-12-19-14-20(24-3)17(2)21(23)25-19/h4-15H,1-3H3/b5-4+,9-6+,12-11+,16-8+

InChI Key

IJOSQPCSTPSGHH-LVZZCUJTSA-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
Streptomyces	NPAtlas	21751787

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Pyranones and derivatives

Alternative Parents

Substituents

Alkyl aryl ether
Pyranone
Pyridine
Heteroaromatic compound
Vinylogous ester
Lactone
Ether
Oxacycle
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

pyranone (CHEBI:69244 )

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	4.5	ALOGPS
logP	3.64	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	4.88	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48.42 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	106.18 m³·mol⁻¹	ChemAxon
Polarizability	39.36 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA001677

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

27025581

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fukuda T, Miller ED, Clark BR, Alnauman A, Murphy CD, Jensen PR, Fenical W: Structures and biosynthesis of the pyridinopyrones, polyenepyrones from a marine-derived Streptomyces species. J Nat Prod. 2011 Aug 26;74(8):1773-8. doi: 10.1021/np200323e. Epub 2011 Jul 13. [PubMed:21751787 ]

Showing NP-Card for Pyridinopyrone C (NP0010188)

MOL for NP0010188 (Pyridinopyrone C)

3D MOL for NP0010188 (Pyridinopyrone C)

3D SDF for NP0010188 (Pyridinopyrone C)

3D-SDF for NP0010188 (Pyridinopyrone C)

PDB for NP0010188 (Pyridinopyrone C)

3D PDB for NP0010188 (Pyridinopyrone C)

SMILES for NP0010188 (Pyridinopyrone C)

INCHI for NP0010188 (Pyridinopyrone C)

Structure for NP0010188 (Pyridinopyrone C)

3D Structure for NP0010188 (Pyridinopyrone C)