NP-MRD: Showing NP-Card for Militarinone D (NP0004555)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2020-12-09 02:01:07 UTC

Updated at

2021-07-15 16:49:30 UTC

NP-MRD ID

NP0004555

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Militarinone D

Provided By

NPAtlas

Description

(2E,4E,6E,8R,10R)-1-[2,4-dihydroxy-5-(4-hydroxyphenyl)pyridin-3-yl]-6,8,10-trimethyldodeca-2,4,6-trien-1-one 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. Militarinone D is found in Cordyceps farinosa, Paecilomyces, Paecilomyces farinosus RCEF0097 and Paecilomyces militaris. It was first documented in 2003 (PMID: 12662096). Based on a literature review very few articles have been published on (2E,4E,6E,8R,10R)-1-[2,4-dihydroxy-5-(4-hydroxyphenyl)pyridin-3-yl]-6,8,10-trimethyldodeca-2,4,6-trien-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118073D          

 62 63  0  0  0  0            999 V2000
    9.2776   -0.2695   -1.4310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.4240   -1.4046 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2458    0.4538   -0.2065 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6869    1.8251   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.1183   -0.0952 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9493    0.7026    0.9744 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8577    2.1555    0.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7157   -0.0759    0.9019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845    0.3213    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0725    1.7243    0.5598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4394   -0.7492    0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1672   -0.5265    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893   -1.6455    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0999   -1.4332    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -2.5731    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697   -3.7488    0.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4162   -2.5094    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1580   -1.3526   -0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4967   -0.1486   -0.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5235   -1.3381   -0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2846   -0.1114   -0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1230    0.0486   -1.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8885    1.1783   -1.6855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8611    2.2162   -0.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6232    3.3686   -0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0392    2.0694    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2641    0.9274    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1861   -2.5602   -0.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4863   -3.6882   -0.0162 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -3.6966    0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541   -4.7874    0.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6870    0.1629   -0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7068   -1.3118   -1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323    0.3307   -2.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4955   -1.4622   -1.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3706    0.0314   -2.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8789    0.0995    0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6102    1.7210   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1113    2.4234    0.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9950    2.3968   -1.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2649    0.2570   -1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630   -1.0091    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3888    0.3939    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3453    2.6066    0.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387    2.6360    1.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125    2.6327    0.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8330   -1.2027    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9382    1.7600    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    2.1076   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4163    2.4287    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7254   -1.8041    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    0.4387    0.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4280   -2.6360    0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3803   -0.4190    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9783    0.7060   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1389   -0.7668   -2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5382    1.2882   -2.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2551    4.1766   -1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0052    2.8831    1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6311    0.8484    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -2.5682   -0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724   -4.6209    0.0055 H   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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 17  1  0  0  0  0
 27 21  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  2 35  1  0  0  0  0
  2 36  1  0  0  0  0
  3 37  1  1  0  0  0
  4 38  1  0  0  0  0
  4 39  1  0  0  0  0
  4 40  1  0  0  0  0
  5 41  1  0  0  0  0
  5 42  1  0  0  0  0
  6 43  1  1  0  0  0
  7 44  1  0  0  0  0
  7 45  1  0  0  0  0
  7 46  1  0  0  0  0
  8 47  1  0  0  0  0
 10 48  1  0  0  0  0
 10 49  1  0  0  0  0
 10 50  1  0  0  0  0
 11 51  1  0  0  0  0
 12 52  1  0  0  0  0
 13 53  1  0  0  0  0
 14 54  1  0  0  0  0
 19 55  1  0  0  0  0
 22 56  1  0  0  0  0
 23 57  1  0  0  0  0
 25 58  1  0  0  0  0
 26 59  1  0  0  0  0
 27 60  1  0  0  0  0
 28 61  1  0  0  0  0
 29 62  1  0  0  0  0
M  END

     RDKit          3D

 62 63  0  0  0  0  0  0  0  0999 V2000
    9.2776   -0.2695   -1.4310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.4240   -1.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2458    0.4538   -0.2065 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6869    1.8251   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.1183   -0.0952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9493    0.7026    0.9744 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8577    2.1555    0.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7157   -0.0759    0.9019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845    0.3213    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0725    1.7243    0.5598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4394   -0.7492    0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1672   -0.5265    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893   -1.6455    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0999   -1.4332    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -2.5731    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697   -3.7488    0.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4162   -2.5094    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1580   -1.3526   -0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4967   -0.1486   -0.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5235   -1.3381   -0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2846   -0.1114   -0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1230    0.0486   -1.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8885    1.1783   -1.6855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8611    2.2162   -0.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6232    3.3686   -0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0392    2.0694    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2641    0.9274    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1861   -2.5602   -0.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4863   -3.6882   -0.0162 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -3.6966    0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541   -4.7874    0.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6870    0.1629   -0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7068   -1.3118   -1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323    0.3307   -2.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4955   -1.4622   -1.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3706    0.0314   -2.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8789    0.0995    0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6102    1.7210   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1113    2.4234    0.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9950    2.3968   -1.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2649    0.2570   -1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630   -1.0091    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3888    0.3939    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3453    2.6066    0.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387    2.6360    1.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125    2.6327    0.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8330   -1.2027    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9382    1.7600    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    2.1076   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4163    2.4287    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7254   -1.8041    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    0.4387    0.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4280   -2.6360    0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3803   -0.4190    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9783    0.7060   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1389   -0.7668   -2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5382    1.2882   -2.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2551    4.1766   -1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0052    2.8831    1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6311    0.8484    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -2.5682   -0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724   -4.6209    0.0055 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 20 28  2  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 17  1  0
 27 21  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  1
  4 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  1
  7 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 12 52  1  0
 13 53  1  0
 14 54  1  0
 19 55  1  0
 22 56  1  0
 23 57  1  0
 25 58  1  0
 26 59  1  0
 27 60  1  0
 28 61  1  0
 29 62  1  0
M  END


  Mrv1652306242118073D          

 62 63  0  0  0  0            999 V2000
    9.2776   -0.2695   -1.4310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.4240   -1.4046 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2458    0.4538   -0.2065 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6869    1.8251   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.1183   -0.0952 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9493    0.7026    0.9744 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8577    2.1555    0.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7157   -0.0759    0.9019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845    0.3213    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0725    1.7243    0.5598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4394   -0.7492    0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1672   -0.5265    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893   -1.6455    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0999   -1.4332    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -2.5731    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697   -3.7488    0.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4162   -2.5094    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1580   -1.3526   -0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4967   -0.1486   -0.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5235   -1.3381   -0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2846   -0.1114   -0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1230    0.0486   -1.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8885    1.1783   -1.6855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8611    2.2162   -0.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6232    3.3686   -0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0392    2.0694    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2641    0.9274    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1861   -2.5602   -0.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4863   -3.6882   -0.0162 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -3.6966    0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541   -4.7874    0.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6870    0.1629   -0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7068   -1.3118   -1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323    0.3307   -2.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4955   -1.4622   -1.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3706    0.0314   -2.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8789    0.0995    0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6102    1.7210   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1113    2.4234    0.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9950    2.3968   -1.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2649    0.2570   -1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630   -1.0091    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3888    0.3939    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3453    2.6066    0.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387    2.6360    1.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125    2.6327    0.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8330   -1.2027    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9382    1.7600    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    2.1076   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4163    2.4287    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7254   -1.8041    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    0.4387    0.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4280   -2.6360    0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3803   -0.4190    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9783    0.7060   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1389   -0.7668   -2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5382    1.2882   -2.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2551    4.1766   -1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0052    2.8831    1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6311    0.8484    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -2.5682   -0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724   -4.6209    0.0055 H   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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 17  1  0  0  0  0
 27 21  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  2 35  1  0  0  0  0
  2 36  1  0  0  0  0
  3 37  1  1  0  0  0
  4 38  1  0  0  0  0
  4 39  1  0  0  0  0
  4 40  1  0  0  0  0
  5 41  1  0  0  0  0
  5 42  1  0  0  0  0
  6 43  1  1  0  0  0
  7 44  1  0  0  0  0
  7 45  1  0  0  0  0
  7 46  1  0  0  0  0
  8 47  1  0  0  0  0
 10 48  1  0  0  0  0
 10 49  1  0  0  0  0
 10 50  1  0  0  0  0
 11 51  1  0  0  0  0
 12 52  1  0  0  0  0
 13 53  1  0  0  0  0
 14 54  1  0  0  0  0
 19 55  1  0  0  0  0
 22 56  1  0  0  0  0
 23 57  1  0  0  0  0
 25 58  1  0  0  0  0
 26 59  1  0  0  0  0
 27 60  1  0  0  0  0
 28 61  1  0  0  0  0
 29 62  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0004555

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])N([H])C(=O)C(C(=O)C(\[H])=C(/[H])\C(\[H])=C(/[H])\C(=C(/[H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])\C([H])([H])[H])=C1O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H31NO4/c1-5-17(2)14-19(4)15-18(3)8-6-7-9-23(29)24-25(30)22(16-27-26(24)31)20-10-12-21(28)13-11-20/h6-13,15-17,19,28H,5,14H2,1-4H3,(H2,27,30,31)/b8-6+,9-7+,18-15+/t17-,19-/m1/s1

> <INCHI_KEY>
GBZJQQUISHXMFL-YNFQZBBQSA-N

> <FORMULA>
C26H31NO4

> <MOLECULAR_WEIGHT>
421.537

> <EXACT_MASS>
421.225308482

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
50.02010994937068

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-5-(4-hydroxyphenyl)-3-[(2E,4E,6E,8R,10R)-6,8,10-trimethyldodeca-2,4,6-trienoyl]-1,2-dihydropyridin-2-one

> <ALOGPS_LOGP>
5.16

> <JCHEM_LOGP>
5.540083675333333

> <ALOGPS_LOGS>
-5.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.579333917964298

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.871519027085117

> <JCHEM_PKA_STRONGEST_BASIC>
-4.557039601358107

> <JCHEM_POLAR_SURFACE_AREA>
86.63

> <JCHEM_REFRACTIVITY>
128.6625

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.15e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-5-(4-hydroxyphenyl)-3-[(2E,4E,6E,8R,10R)-6,8,10-trimethyldodeca-2,4,6-trienoyl]-1H-pyridin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 62 63  0  0  0  0  0  0  0  0999 V2000
    9.2776   -0.2695   -1.4310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.4240   -1.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2458    0.4538   -0.2065 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6869    1.8251   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.1183   -0.0952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9493    0.7026    0.9744 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8577    2.1555    0.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7157   -0.0759    0.9019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845    0.3213    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0725    1.7243    0.5598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4394   -0.7492    0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1672   -0.5265    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893   -1.6455    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0999   -1.4332    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -2.5731    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697   -3.7488    0.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4162   -2.5094    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1580   -1.3526   -0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4967   -0.1486   -0.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5235   -1.3381   -0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2846   -0.1114   -0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1230    0.0486   -1.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8885    1.1783   -1.6855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8611    2.2162   -0.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6232    3.3686   -0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0392    2.0694    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2641    0.9274    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1861   -2.5602   -0.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4863   -3.6882   -0.0162 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -3.6966    0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541   -4.7874    0.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6870    0.1629   -0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7068   -1.3118   -1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323    0.3307   -2.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4955   -1.4622   -1.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3706    0.0314   -2.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8789    0.0995    0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6102    1.7210   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1113    2.4234    0.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9950    2.3968   -1.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2649    0.2570   -1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630   -1.0091    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3888    0.3939    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3453    2.6066    0.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387    2.6360    1.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125    2.6327    0.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8330   -1.2027    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9382    1.7600    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    2.1076   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4163    2.4287    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7254   -1.8041    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    0.4387    0.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4280   -2.6360    0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3803   -0.4190    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9783    0.7060   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1389   -0.7668   -2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5382    1.2882   -2.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2551    4.1766   -1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0052    2.8831    1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6311    0.8484    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -2.5682   -0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724   -4.6209    0.0055 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 20 28  2  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 17  1  0
 27 21  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  1
  4 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  1
  7 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 12 52  1  0
 13 53  1  0
 14 54  1  0
 19 55  1  0
 22 56  1  0
 23 57  1  0
 25 58  1  0
 26 59  1  0
 27 60  1  0
 28 61  1  0
 29 62  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       9.278  -0.270  -1.431  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.777  -0.424  -1.405  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.246   0.454  -0.207  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.687   1.825  -0.558  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.841   0.118  -0.095  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.949   0.703   0.974  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.858   2.155   0.884  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.716  -0.076   0.902  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.485   0.321   0.728  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.072   1.724   0.560  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.439  -0.749   0.693  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.167  -0.527   0.518  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.789  -1.646   0.499  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.100  -1.433   0.321  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.982  -2.573   0.313  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.470  -3.749   0.477  0.00  0.00           O+0
HETATM   17  C   UNK     0      -4.416  -2.509   0.133  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.158  -1.353  -0.058  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.497  -0.149  -0.087  0.00  0.00           O+0
HETATM   20  C   UNK     0      -6.524  -1.338  -0.224  0.00  0.00           C+0
HETATM   21  C   UNK     0      -7.285  -0.111  -0.384  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.123   0.049  -1.494  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.889   1.178  -1.686  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.861   2.216  -0.778  0.00  0.00           C+0
HETATM   25  O   UNK     0      -9.623   3.369  -0.946  0.00  0.00           O+0
HETATM   26  C   UNK     0      -8.039   2.069   0.319  0.00  0.00           C+0
HETATM   27  C   UNK     0      -7.264   0.927   0.515  0.00  0.00           C+0
HETATM   28  C   UNK     0      -7.186  -2.560  -0.199  0.00  0.00           C+0
HETATM   29  N   UNK     0      -6.486  -3.688  -0.016  0.00  0.00           N+0
HETATM   30  C   UNK     0      -5.157  -3.697   0.146  0.00  0.00           C+0
HETATM   31  O   UNK     0      -4.554  -4.787   0.314  0.00  0.00           O+0
HETATM   32  H   UNK     0       9.687   0.163  -0.490  0.00  0.00           H+0
HETATM   33  H   UNK     0       9.707  -1.312  -1.504  0.00  0.00           H+0
HETATM   34  H   UNK     0       9.632   0.331  -2.308  0.00  0.00           H+0
HETATM   35  H   UNK     0       7.495  -1.462  -1.221  0.00  0.00           H+0
HETATM   36  H   UNK     0       7.371   0.031  -2.317  0.00  0.00           H+0
HETATM   37  H   UNK     0       7.879   0.100   0.639  0.00  0.00           H+0
HETATM   38  H   UNK     0       8.610   1.721  -1.234  0.00  0.00           H+0
HETATM   39  H   UNK     0       8.111   2.423   0.284  0.00  0.00           H+0
HETATM   40  H   UNK     0       6.995   2.397  -1.211  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.265   0.257  -1.053  0.00  0.00           H+0
HETATM   42  H   UNK     0       5.763  -1.009   0.060  0.00  0.00           H+0
HETATM   43  H   UNK     0       5.389   0.394   2.003  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.345   2.607   0.037  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.439   2.636   1.834  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.912   2.633   0.809  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.833  -1.203   1.013  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.938   1.760   0.713  0.00  0.00           H+0
HETATM   49  H   UNK     0       2.201   2.108  -0.493  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.416   2.429   1.326  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.725  -1.804   0.818  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.233   0.439   0.378  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.428  -2.636   0.629  0.00  0.00           H+0
HETATM   54  H   UNK     0      -2.380  -0.419   0.199  0.00  0.00           H+0
HETATM   55  H   UNK     0      -4.978   0.706  -0.245  0.00  0.00           H+0
HETATM   56  H   UNK     0      -8.139  -0.767  -2.199  0.00  0.00           H+0
HETATM   57  H   UNK     0      -9.538   1.288  -2.557  0.00  0.00           H+0
HETATM   58  H   UNK     0      -9.255   4.177  -1.453  0.00  0.00           H+0
HETATM   59  H   UNK     0      -8.005   2.883   1.049  0.00  0.00           H+0
HETATM   60  H   UNK     0      -6.631   0.848   1.409  0.00  0.00           H+0
HETATM   61  H   UNK     0      -8.266  -2.568  -0.329  0.00  0.00           H+0
HETATM   62  H   UNK     0      -6.972  -4.621   0.006  0.00  0.00           H+0
CONECT    1    2   32   33   34                                             
CONECT    2    1    3   35   36                                             
CONECT    3    2    4    5   37                                             
CONECT    4    3   38   39   40                                             
CONECT    5    3    6   41   42                                             
CONECT    6    5    7    8   43                                             
CONECT    7    6   44   45   46                                             
CONECT    8    6    9   47                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   48   49   50                                             
CONECT   11    9   12   51                                                  
CONECT   12   11   13   52                                                  
CONECT   13   12   14   53                                                  
CONECT   14   13   15   54                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   30                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   55                                                       
CONECT   20   18   21   28                                                  
CONECT   21   20   22   27                                                  
CONECT   22   21   23   56                                                  
CONECT   23   22   24   57                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24   58                                                       
CONECT   26   24   27   59                                                  
CONECT   27   26   21   60                                                  
CONECT   28   20   29   61                                                  
CONECT   29   28   30   62                                                  
CONECT   30   29   31   17                                                  
CONECT   31   30                                                            
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    2                                                            
CONECT   36    2                                                            
CONECT   37    3                                                            
CONECT   38    4                                                            
CONECT   39    4                                                            
CONECT   40    4                                                            
CONECT   41    5                                                            
CONECT   42    5                                                            
CONECT   43    6                                                            
CONECT   44    7                                                            
CONECT   45    7                                                            
CONECT   46    7                                                            
CONECT   47    8                                                            
CONECT   48   10                                                            
CONECT   49   10                                                            
CONECT   50   10                                                            
CONECT   51   11                                                            
CONECT   52   12                                                            
CONECT   53   13                                                            
CONECT   54   14                                                            
CONECT   55   19                                                            
CONECT   56   22                                                            
CONECT   57   23                                                            
CONECT   58   25                                                            
CONECT   59   26                                                            
CONECT   60   27                                                            
CONECT   61   28                                                            
CONECT   62   29                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  126    0
END

RDKit          3D

62 63  0  0  0  0  0  0  0  0999 V2000
    9.2776   -0.2695   -1.4310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.4240   -1.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2458    0.4538   -0.2065 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6869    1.8251   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8412    0.1183   -0.0952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9493    0.7026    0.9744 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8577    2.1555    0.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7157   -0.0759    0.9019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845    0.3213    0.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0725    1.7243    0.5598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4394   -0.7492    0.6925 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1672   -0.5265    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893   -1.6455    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0999   -1.4332    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -2.5731    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4697   -3.7488    0.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4162   -2.5094    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1580   -1.3526   -0.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4967   -0.1486   -0.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5235   -1.3381   -0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2846   -0.1114   -0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1230    0.0486   -1.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8885    1.1783   -1.6855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8611    2.2162   -0.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6232    3.3686   -0.9460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0392    2.0694    0.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2641    0.9274    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1861   -2.5602   -0.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4863   -3.6882   -0.0162 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1570   -3.6966    0.1461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541   -4.7874    0.3143 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6870    0.1629   -0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7068   -1.3118   -1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323    0.3307   -2.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4955   -1.4622   -1.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3706    0.0314   -2.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8789    0.0995    0.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6102    1.7210   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1113    2.4234    0.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9950    2.3968   -1.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2649    0.2570   -1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7630   -1.0091    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3888    0.3939    2.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3453    2.6066    0.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387    2.6360    1.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9125    2.6327    0.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8330   -1.2027    1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9382    1.7600    0.7130 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    2.1076   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4163    2.4287    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7254   -1.8041    0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    0.4387    0.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4280   -2.6360    0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3803   -0.4190    0.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9783    0.7060   -0.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1389   -0.7668   -2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5382    1.2882   -2.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2551    4.1766   -1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0052    2.8831    1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6311    0.8484    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2656   -2.5682   -0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9724   -4.6209    0.0055 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 20 28  2  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 30 17  1  0
 27 21  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  1
  4 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  1
  7 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 12 52  1  0
 13 53  1  0
 14 54  1  0
 19 55  1  0
 22 56  1  0
 23 57  1  0
 25 58  1  0
 26 59  1  0
 27 60  1  0
 28 61  1  0
 29 62  1  0
M  END

View in JSmol View NMR Assignments View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₆H₃₁NO₄

Average Mass

421.5370 Da

Monoisotopic Mass

421.22531 Da

IUPAC Name

4-hydroxy-5-(4-hydroxyphenyl)-3-[(2E,4E,6E,8R,10R)-6,8,10-trimethyldodeca-2,4,6-trienoyl]-1,2-dihydropyridin-2-one

Traditional Name

4-hydroxy-5-(4-hydroxyphenyl)-3-[(2E,4E,6E,8R,10R)-6,8,10-trimethyldodeca-2,4,6-trienoyl]-1H-pyridin-2-one

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C[C@@H](C)\C=C(/C)\C=C\C=C\C(=O)C1=C(O)C(=CNC1=O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C26H31NO4/c1-5-17(2)14-19(4)15-18(3)8-6-7-9-23(29)24-25(30)22(16-27-26(24)31)20-10-12-21(28)13-11-20/h6-13,15-17,19,28H,5,14H2,1-4H3,(H2,27,30,31)/b8-6+,9-7+,18-15+/t17-,19-/m1/s1

InChI Key

GBZJQQUISHXMFL-YNFQZBBQSA-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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Cordyceps farinosa	LOTUS Database	35616633
Paecilomyces	NPAtlas	12662096
Paecilomyces farinosus RCEF0097	Fungi	KNApSAcK
Paecilomyces militaris	Fungi	KNApSAcK

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
Aromatic monoterpenoid
Monocyclic monoterpenoid
Monoterpenoid
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Dihydropyridine
Hydroxypyridine
Phenol
Pyridinone
Monocyclic benzene moiety
Hydropyridine
Benzenoid
Acryloyl-group
Enone
Heteroaromatic compound
Vinylogous amide
Vinylogous acid
Alpha,beta-unsaturated ketone
Lactam
Ketone
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

phenylpyridine (CHEBI:31853 )

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	5.16	ALOGPS
logP	5.54	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	8.87	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.63 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	128.66 m³·mol⁻¹	ChemAxon
Polarizability	50.02 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA015800

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

552870

KEGG Compound ID

C12332

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54691338

PDB ID

Not Available

ChEBI ID

31853

Good Scents ID

Not Available

References

General References

Schmidt K, Riese U, Li Z, Hamburger M: Novel tetramic acids and pyridone alkaloids, militarinones B, C, and D, from the insect pathogenic fungus Paecilomyces militaris. J Nat Prod. 2003 Mar;66(3):378-83. doi: 10.1021/np020430y. [PubMed:12662096 ]

Showing NP-Card for Militarinone D (NP0004555)

MOL for NP0004555 (Militarinone D)

3D MOL for NP0004555 (Militarinone D)

3D SDF for NP0004555 (Militarinone D)

3D-SDF for NP0004555 (Militarinone D)

PDB for NP0004555 (Militarinone D)

3D PDB for NP0004555 (Militarinone D)

SMILES for NP0004555 (Militarinone D)

INCHI for NP0004555 (Militarinone D)

Structure for NP0004555 (Militarinone D)

3D Structure for NP0004555 (Militarinone D)