NP-MRD: Showing NP-Card for Citridone B' (NP0005953)

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Record Information

Version

2.0

Created at

2020-12-09 03:03:31 UTC

Updated at

2021-07-15 16:53:26 UTC

NP-MRD ID

NP0005953

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Citridone B'

Provided By

NPAtlas

Description

Citridone B' belongs to the class of organic compounds known as phenylpyridines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond. Citridone B' is found in Penicillium. Based on a literature review very few articles have been published on Citridone B'.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118243D          

 46 49  0  0  0  0            999 V2000
    4.5354    0.5504   -1.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5548    0.1845   -0.2131 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.2539   -0.3966    0.2684 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4789   -0.8059    1.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8612   -1.5216   -0.4051 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863   -1.5213   -0.5219 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8490   -2.1882    0.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0718   -0.0667   -0.6002 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -6.2299   -0.3705    0.8211 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242118243D          

 46 49  0  0  0  0            999 V2000
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    4.5548    0.1845   -0.2131 C   0  0  2  0  0  0  0  0  0  0  0  0
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 25 46  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0005953

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]([H])(C([H])([H])[H])[C@@]1(O[C@@]([H])(O[H])[C@]2(C3=C(O[C@@]12[H])N([H])C([H])=C(C3=O)C1=C([H])C([H])=C([H])C([H])=C1[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H21NO5/c1-10(21)19(3)16-18(2,17(23)25-19)13-14(22)12(9-20-15(13)24-16)11-7-5-4-6-8-11/h4-10,16-17,21,23H,1-3H3,(H,20,22)/t10-,16+,17+,18-,19-/m0/s1

> <INCHI_KEY>
HKJGXZQUAMKOKS-HMCFAXLDSA-N

> <FORMULA>
C19H21NO5

> <MOLECULAR_WEIGHT>
343.379

> <EXACT_MASS>
343.14197278

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
35.9722943058741

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,5S,6R)-3-hydroxy-5-[(1S)-1-hydroxyethyl]-2,5-dimethyl-11-phenyl-4,7-dioxa-9-azatricyclo[6.4.0.0^{2,6}]dodeca-1(8),10-dien-12-one

> <ALOGPS_LOGP>
1.83

> <JCHEM_LOGP>
1.808829968333334

> <ALOGPS_LOGS>
-2.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.115151298636874

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.399712657167898

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1631958998520933

> <JCHEM_POLAR_SURFACE_AREA>
88.02

> <JCHEM_REFRACTIVITY>
99.8699

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.15e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,5S,6R)-3-hydroxy-5-[(1S)-1-hydroxyethyl]-2,5-dimethyl-11-phenyl-4,7-dioxa-9-azatricyclo[6.4.0.0^{2,6}]dodeca-1(8),10-dien-12-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
    4.5354    0.5504   -1.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5548    0.1845   -0.2131 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5361   -0.7984   -0.0405 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2539   -0.3966    0.2684 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4789   -0.8059    1.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8612   -1.5216   -0.4051 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863   -1.5213   -0.5219 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8490   -2.1882    0.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0718   -0.0667   -0.6002 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0845    0.4745   -1.9935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2127    0.1941    0.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1040    0.6264    1.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8856    0.9487    2.2422 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1736    0.8442    1.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5587    0.4144    0.6177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9691    0.3144    0.2611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8944   -0.2625    1.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2299   -0.3705    0.8211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6776    0.1047   -0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8040    0.6814   -1.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4684    0.7769   -0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    0.0963   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8506   -0.2980   -1.4073 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4719    0.6578    1.5146 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    0.5938    0.2590 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9052    1.4178   -1.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5807    0.8428   -1.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2992   -0.3398   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8323    1.0349    0.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4072   -1.5761   -0.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5443   -0.7358    2.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2424   -0.1561    2.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9038   -1.8343    1.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -1.9810   -1.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0316   -2.6297    0.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5076    1.5006   -1.9555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7260   -0.1388   -2.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0628    0.5623   -2.4380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6235    1.2788    3.2087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9669    1.0996    2.5783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5385   -0.6353    2.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9468   -0.8292    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7387    0.0247   -0.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2125    1.0397   -2.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7850    1.2296   -1.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4082    1.5923   -0.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 15 22  1  0
 22 23  2  0
 12 24  1  0
 24 25  1  0
 25  4  1  0
 25  9  1  0
 22 11  1  0
 21 16  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  5 31  1  0
  5 32  1  0
  5 33  1  0
  7 34  1  6
  8 35  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
 13 39  1  0
 14 40  1  0
 17 41  1  0
 18 42  1  0
 19 43  1  0
 20 44  1  0
 21 45  1  0
 25 46  1  6
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       4.535   0.550  -1.669  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.555   0.185  -0.213  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.536  -0.798  -0.041  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.254  -0.397   0.268  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.479  -0.806   1.730  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.861  -1.522  -0.405  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.486  -1.521  -0.522  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.849  -2.188   0.503  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.072  -0.067  -0.600  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.085   0.475  -1.994  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.213   0.194   0.093  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.104   0.626   1.358  0.00  0.00           C+0
HETATM   13  N   UNK     0      -0.886   0.949   2.242  0.00  0.00           N+0
HETATM   14  C   UNK     0      -2.174   0.844   1.878  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.559   0.414   0.618  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.969   0.314   0.261  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.894  -0.263   1.130  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.230  -0.371   0.821  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.678   0.105  -0.386  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.804   0.681  -1.275  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.468   0.777  -0.939  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.535   0.096  -0.253  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.851  -0.298  -1.407  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.472   0.658   1.515  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.121   0.594   0.259  0.00  0.00           C+0
HETATM   26  H   UNK     0       3.905   1.418  -1.902  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.581   0.843  -1.941  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.299  -0.340  -2.289  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.832   1.035   0.410  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.407  -1.576  -0.633  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.544  -0.736   2.311  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.242  -0.156   2.210  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.904  -1.834   1.717  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.212  -1.981  -1.506  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.032  -2.630   0.153  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.508   1.501  -1.956  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.726  -0.139  -2.657  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.063   0.562  -2.438  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.624   1.279   3.209  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.967   1.100   2.578  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.539  -0.635   2.078  0.00  0.00           H+0
HETATM   42  H   UNK     0      -6.947  -0.829   1.520  0.00  0.00           H+0
HETATM   43  H   UNK     0      -7.739   0.025  -0.644  0.00  0.00           H+0
HETATM   44  H   UNK     0      -6.213   1.040  -2.214  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.785   1.230  -1.638  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.408   1.592  -0.095  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3    4   29                                             
CONECT    3    2   30                                                       
CONECT    4    2    5    6   25                                             
CONECT    5    4   31   32   33                                             
CONECT    6    4    7                                                       
CONECT    7    6    8    9   34                                             
CONECT    8    7   35                                                       
CONECT    9    7   10   11   25                                             
CONECT   10    9   36   37   38                                             
CONECT   11    9   12   22                                                  
CONECT   12   11   13   24                                                  
CONECT   13   12   14   39                                                  
CONECT   14   13   15   40                                                  
CONECT   15   14   16   22                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18   41                                                  
CONECT   18   17   19   42                                                  
CONECT   19   18   20   43                                                  
CONECT   20   19   21   44                                                  
CONECT   21   20   16   45                                                  
CONECT   22   15   23   11                                                  
CONECT   23   22                                                            
CONECT   24   12   25                                                       
CONECT   25   24    4    9   46                                             
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    3                                                            
CONECT   31    5                                                            
CONECT   32    5                                                            
CONECT   33    5                                                            
CONECT   34    7                                                            
CONECT   35    8                                                            
CONECT   36   10                                                            
CONECT   37   10                                                            
CONECT   38   10                                                            
CONECT   39   13                                                            
CONECT   40   14                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   19                                                            
CONECT   44   20                                                            
CONECT   45   21                                                            
CONECT   46   25                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   98    0
END

RDKit          3D

46 49  0  0  0  0  0  0  0  0999 V2000
    4.5354    0.5504   -1.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5548    0.1845   -0.2131 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5361   -0.7984   -0.0405 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2539   -0.3966    0.2684 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4789   -0.8059    1.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8612   -1.5216   -0.4051 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863   -1.5213   -0.5219 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8490   -2.1882    0.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0718   -0.0667   -0.6002 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0845    0.4745   -1.9935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2127    0.1941    0.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1040    0.6264    1.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8856    0.9487    2.2422 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1736    0.8442    1.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5587    0.4144    0.6177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9691    0.3144    0.2611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8944   -0.2625    1.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2299   -0.3705    0.8211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6776    0.1047   -0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8040    0.6814   -1.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4684    0.7769   -0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    0.0963   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8506   -0.2980   -1.4073 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4719    0.6578    1.5146 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    0.5938    0.2590 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9052    1.4178   -1.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5807    0.8428   -1.9408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2992   -0.3398   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8323    1.0349    0.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4072   -1.5761   -0.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5443   -0.7358    2.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2424   -0.1561    2.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9038   -1.8343    1.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -1.9810   -1.5064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0316   -2.6297    0.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5076    1.5006   -1.9555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7260   -0.1388   -2.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0628    0.5623   -2.4380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6235    1.2788    3.2087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9669    1.0996    2.5783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5385   -0.6353    2.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9468   -0.8292    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7387    0.0247   -0.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2125    1.0397   -2.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7850    1.2296   -1.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4082    1.5923   -0.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 15 22  1  0
 22 23  2  0
 12 24  1  0
 24 25  1  0
 25  4  1  0
 25  9  1  0
 22 11  1  0
 21 16  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  5 31  1  0
  5 32  1  0
  5 33  1  0
  7 34  1  6
  8 35  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
 13 39  1  0
 14 40  1  0
 17 41  1  0
 18 42  1  0
 19 43  1  0
 20 44  1  0
 21 45  1  0
 25 46  1  6
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₉H₂₁NO₅

Average Mass

343.3790 Da

Monoisotopic Mass

343.14197 Da

IUPAC Name

(2S,3R,5S,6R)-3-hydroxy-5-[(1S)-1-hydroxyethyl]-2,5-dimethyl-11-phenyl-4,7-dioxa-9-azatricyclo[6.4.0.0^{2,6}]dodeca-1(8),10-dien-12-one

Traditional Name

(2S,3R,5S,6R)-3-hydroxy-5-[(1S)-1-hydroxyethyl]-2,5-dimethyl-11-phenyl-4,7-dioxa-9-azatricyclo[6.4.0.0^{2,6}]dodeca-1(8),10-dien-12-one

CAS Registry Number

Not Available

SMILES

CC(O)[C@]1(C)O[C@@H](O)[C@]2(C)[C@H]1OC1=C2C(=O)C(=CN1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C19H21NO5/c1-10(21)19(3)16-18(2,17(23)25-19)13-14(22)12(9-20-15(13)24-16)11-7-5-4-6-8-11/h4-10,16-17,21,23H,1-3H3,(H,20,22)/t10?,16-,17-,18+,19+/m1/s1

InChI Key

HKJGXZQUAMKOKS-HMCFAXLDSA-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
Penicillium	NPAtlas	16060383

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpyridines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

Phenylpyridines

Direct Parent

Phenylpyridines

Alternative Parents

Substituents

3-phenylpyridine
Furofuran
Alkyl aryl ether
Monocyclic benzene moiety
Monosaccharide
Benzenoid
Heteroaromatic compound
Oxolane
Vinylogous amide
Vinylogous ester
Secondary alcohol
Hemiacetal
Ether
Oxacycle
Azacycle
Organic nitrogen compound
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.83	ALOGPS
logP	1.81	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	11.4	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	88.02 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.87 m³·mol⁻¹	ChemAxon
Polarizability	35.97 Å³	ChemAxon
Number of Rings	4	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

NPA012901

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442683

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101723009

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Citridone B' (NP0005953)

MOL for NP0005953 (Citridone B')

3D MOL for NP0005953 (Citridone B')

3D SDF for NP0005953 (Citridone B')

3D-SDF for NP0005953 (Citridone B')

PDB for NP0005953 (Citridone B')

3D PDB for NP0005953 (Citridone B')

SMILES for NP0005953 (Citridone B')

INCHI for NP0005953 (Citridone B')

Structure for NP0005953 (Citridone B')

3D Structure for NP0005953 (Citridone B')