NP-MRD: Showing NP-Card for Epipyridone (NP0007079)

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Record Information

Version

2.0

Created at

2020-12-09 03:58:05 UTC

Updated at

2021-07-15 16:56:36 UTC

NP-MRD ID

NP0007079

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epipyridone

Provided By

NPAtlas

Description

Epipyridone is found in Epicoccum sp. Epipyridone was first documented in 2007 (PMID: 17520137). Based on a literature review very few articles have been published on Epipyridone (PMID: 28704977).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


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    3.9866    3.2756   -0.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8068    3.4240    1.7096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    4.0581    2.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6933    0.0467    1.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602    0.8713   -0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6906    2.9284   -0.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6455    3.1103    0.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1288    3.3172   -0.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.8237    0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6687    0.7845    1.9171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5292   -1.3843    0.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4654   -0.9585    2.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3799   -2.1949    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   -2.4616    2.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0172   -1.4365   -1.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1570   -2.3462   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4039   -0.0280   -2.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3087    1.3165   -1.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1586   -0.1039   -2.4578 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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
  6 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26  3  1  0  0  0  0
 18  5  2  0  0  0  0
 26 19  1  0  0  0  0
 13  7  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  2 31  1  0  0  0  0
  2 32  1  0  0  0  0
  3 33  1  1  0  0  0
  8 34  1  0  0  0  0
  9 35  1  0  0  0  0
 11 36  1  0  0  0  0
 12 37  1  0  0  0  0
 13 38  1  0  0  0  0
 14 39  1  0  0  0  0
 15 40  1  0  0  0  0
 19 41  1  1  0  0  0
 20 42  1  6  0  0  0
 21 43  1  0  0  0  0
 21 44  1  0  0  0  0
 21 45  1  0  0  0  0
 22 46  1  0  0  0  0
 22 47  1  0  0  0  0
 23 48  1  6  0  0  0
 24 49  1  0  0  0  0
 24 50  1  0  0  0  0
 24 51  1  0  0  0  0
 25 52  1  0  0  0  0
 25 53  1  0  0  0  0
 27 54  1  0  0  0  0
 27 55  1  0  0  0  0
 27 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007079

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])N([H])C(=O)C2=C1O[C@]([H])(C([H])([H])C([H])([H])[H])[C@@]1(C([H])([H])[H])C([H])([H])[C@@]([H])(C([H])([H])[H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@]21[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H29NO3/c1-5-18-23(4)11-13(2)10-14(3)20(23)19-21(27-18)17(12-24-22(19)26)15-6-8-16(25)9-7-15/h6-9,12-14,18,20,25H,5,10-11H2,1-4H3,(H,24,26)/t13-,14+,18+,20+,23+/m0/s1

> <INCHI_KEY>
ZUJBUMRATOLVJT-VIBJKCLASA-N

> <FORMULA>
C23H29NO3

> <MOLECULAR_WEIGHT>
367.489

> <EXACT_MASS>
367.214743798

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.01859700971939

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6R,6aS,8S,10R,10aS)-6-ethyl-4-(4-hydroxyphenyl)-6a,8,10-trimethyl-1H,2H,6H,6aH,7H,8H,9H,10H,10aH-isochromeno[4,3-c]pyridin-1-one

> <ALOGPS_LOGP>
4.96

> <JCHEM_LOGP>
4.278135064666666

> <ALOGPS_LOGS>
-5.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.30344861308113

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.19050625670404

> <JCHEM_PKA_STRONGEST_BASIC>
-1.7125789861337037

> <JCHEM_POLAR_SURFACE_AREA>
58.56

> <JCHEM_REFRACTIVITY>
107.13129999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.86e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6R,6aS,8S,10R,10aS)-6-ethyl-4-(4-hydroxyphenyl)-6a,8,10-trimethyl-2H,6H,7H,8H,9H,10H,10aH-isochromeno[4,3-c]pyridin-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
   -0.3491   -3.3854   -1.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4368   -2.1393   -1.3002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212   -1.1404   -0.3060 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0360   -0.0858   -0.4689 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8738    1.0453    0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452    1.7244    0.6289 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3430    1.3425    0.0897 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6780    0.0054    0.1378 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8976   -0.4592   -0.3530 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7678    0.4501   -0.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9896    0.0188   -1.3876 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4541    1.7849   -0.9483 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2411    2.2224   -0.4565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9248    2.8295    1.4563 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7373    3.1996    1.9659 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998    2.5268    1.7060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4479    2.9650    2.2462 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3464    1.4239    0.8896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5187    0.6677    0.5610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7665    1.2599    0.0555 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9909    2.7028   -0.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588    0.5047    0.8597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5520   -0.9536    0.6544 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3672   -1.6711    1.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5108   -1.3095   -0.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2926   -0.4779   -0.4586 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3200    0.2339   -1.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4444   -3.9395   -0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2938   -4.0769   -2.0833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2798   -3.3059   -2.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4720   -2.4835   -0.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6733   -1.7299   -2.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002   -1.5323    0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0264   -0.7596    0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1362   -1.5198   -0.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8182   -0.0337   -0.8156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1651    2.4552   -1.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9866    3.2756   -0.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8068    3.4240    1.7096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    4.0581    2.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6933    0.0467    1.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602    0.8713   -0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6906    2.9284   -0.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6455    3.1103    0.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1288    3.3172   -0.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.8237    0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6687    0.7845    1.9171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5292   -1.3843    0.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4654   -0.9585    2.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3799   -2.1949    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   -2.4616    2.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0172   -1.4365   -1.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1570   -2.3462   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4039   -0.0280   -2.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3087    1.3165   -1.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1586   -0.1039   -2.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
  6 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  6
 26  3  1  0
 18  5  2  0
 26 19  1  0
 13  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  1
  8 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  0
 19 41  1  1
 20 42  1  6
 21 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 23 48  1  6
 24 49  1  0
 24 50  1  0
 24 51  1  0
 25 52  1  0
 25 53  1  0
 27 54  1  0
 27 55  1  0
 27 56  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      -0.349  -3.385  -1.452  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.437  -2.139  -1.300  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.021  -1.140  -0.306  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.036  -0.086  -0.469  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.874   1.045   0.372  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.045   1.724   0.629  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.343   1.343   0.090  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.678   0.005   0.138  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.898  -0.459  -0.353  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.768   0.450  -0.891  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.990   0.019  -1.388  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.454   1.785  -0.948  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.241   2.222  -0.457  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.925   2.829   1.456  0.00  0.00           C+0
HETATM   15  N   UNK     0       0.737   3.200   1.966  0.00  0.00           N+0
HETATM   16  C   UNK     0      -0.400   2.527   1.706  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.448   2.965   2.246  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.346   1.424   0.890  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.519   0.668   0.561  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.767   1.260   0.056  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.991   2.703  -0.024  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.859   0.505   0.860  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.552  -0.954   0.654  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.367  -1.671   1.997  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.511  -1.310  -0.333  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.293  -0.478  -0.459  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.320   0.234  -1.825  0.00  0.00           C+0
HETATM   28  H   UNK     0      -0.444  -3.939  -0.496  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.294  -4.077  -2.083  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.280  -3.306  -2.033  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.472  -2.483  -0.972  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.673  -1.730  -2.329  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.200  -1.532   0.707  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.026  -0.760   0.553  0.00  0.00           H+0
HETATM   35  H   UNK     0       5.136  -1.520  -0.302  0.00  0.00           H+0
HETATM   36  H   UNK     0       7.818  -0.034  -0.816  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.165   2.455  -1.377  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.987   3.276  -0.499  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.807   3.424   1.710  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.700   4.058   2.599  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.693   0.047   1.521  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.060   0.871  -0.998  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.691   2.928  -0.916  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.646   3.110   0.806  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.129   3.317  -0.270  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.850   0.824   0.547  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.669   0.785   1.917  0.00  0.00           H+0
HETATM   48  H   UNK     0      -4.529  -1.384   0.266  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.465  -0.959   2.847  0.00  0.00           H+0
HETATM   50  H   UNK     0      -2.380  -2.195   2.026  0.00  0.00           H+0
HETATM   51  H   UNK     0      -4.123  -2.462   2.174  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.017  -1.437  -1.339  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.157  -2.346  -0.036  0.00  0.00           H+0
HETATM   54  H   UNK     0      -0.404  -0.028  -2.406  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.309   1.317  -1.759  0.00  0.00           H+0
HETATM   56  H   UNK     0      -2.159  -0.104  -2.458  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3   31   32                                             
CONECT    3    2    4   26   33                                             
CONECT    4    3    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9   34                                                  
CONECT    9    8   10   35                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   36                                                       
CONECT   12   10   13   37                                                  
CONECT   13   12    7   38                                                  
CONECT   14    6   15   39                                                  
CONECT   15   14   16   40                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19    5                                                  
CONECT   19   18   20   26   41                                             
CONECT   20   19   21   22   42                                             
CONECT   21   20   43   44   45                                             
CONECT   22   20   23   46   47                                             
CONECT   23   22   24   25   48                                             
CONECT   24   23   49   50   51                                             
CONECT   25   23   26   52   53                                             
CONECT   26   25   27    3   19                                             
CONECT   27   26   54   55   56                                             
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    2                                                            
CONECT   32    2                                                            
CONECT   33    3                                                            
CONECT   34    8                                                            
CONECT   35    9                                                            
CONECT   36   11                                                            
CONECT   37   12                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   15                                                            
CONECT   41   19                                                            
CONECT   42   20                                                            
CONECT   43   21                                                            
CONECT   44   21                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
CONECT   47   22                                                            
CONECT   48   23                                                            
CONECT   49   24                                                            
CONECT   50   24                                                            
CONECT   51   24                                                            
CONECT   52   25                                                            
CONECT   53   25                                                            
CONECT   54   27                                                            
CONECT   55   27                                                            
CONECT   56   27                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  118    0
END

RDKit          3D

56 59  0  0  0  0  0  0  0  0999 V2000
   -0.3491   -3.3854   -1.4522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4368   -2.1393   -1.3002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212   -1.1404   -0.3060 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0360   -0.0858   -0.4689 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8738    1.0453    0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452    1.7244    0.6289 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3430    1.3425    0.0897 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6780    0.0054    0.1378 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8976   -0.4592   -0.3530 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7678    0.4501   -0.8908 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9896    0.0188   -1.3876 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4541    1.7849   -0.9483 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2411    2.2224   -0.4565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9248    2.8295    1.4563 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7373    3.1996    1.9659 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998    2.5268    1.7060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4479    2.9650    2.2462 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5187    0.6677    0.5610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7665    1.2599    0.0555 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9909    2.7028   -0.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588    0.5047    0.8597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5520   -0.9536    0.6544 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3672   -1.6711    1.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5108   -1.3095   -0.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2926   -0.4779   -0.4586 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3200    0.2339   -1.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4444   -3.9395   -0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2938   -4.0769   -2.0833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2798   -3.3059   -2.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4720   -2.4835   -0.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6733   -1.7299   -2.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002   -1.5323    0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0264   -0.7596    0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1362   -1.5198   -0.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8182   -0.0337   -0.8156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1651    2.4552   -1.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9866    3.2756   -0.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8068    3.4240    1.7096 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    4.0581    2.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6933    0.0467    1.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602    0.8713   -0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6906    2.9284   -0.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6455    3.1103    0.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1288    3.3172   -0.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.8237    0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6687    0.7845    1.9171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5292   -1.3843    0.2657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4654   -0.9585    2.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3799   -2.1949    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227   -2.4616    2.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0172   -1.4365   -1.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1570   -2.3462   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4039   -0.0280   -2.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3087    1.3165   -1.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1586   -0.1039   -2.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
  6 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  6
 26  3  1  0
 18  5  2  0
 26 19  1  0
 13  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  1
  8 34  1  0
  9 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  0
 19 41  1  1
 20 42  1  6
 21 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 23 48  1  6
 24 49  1  0
 24 50  1  0
 24 51  1  0
 25 52  1  0
 25 53  1  0
 27 54  1  0
 27 55  1  0
 27 56  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₃H₂₉NO₃

Average Mass

367.4890 Da

Monoisotopic Mass

367.21474 Da

IUPAC Name

(6R,6aS,8S,10R,10aS)-6-ethyl-4-(4-hydroxyphenyl)-6a,8,10-trimethyl-1H,2H,6H,6aH,7H,8H,9H,10H,10aH-isochromeno[4,3-c]pyridin-1-one

Traditional Name

(6R,6aS,8S,10R,10aS)-6-ethyl-4-(4-hydroxyphenyl)-6a,8,10-trimethyl-2H,6H,7H,8H,9H,10H,10aH-isochromeno[4,3-c]pyridin-1-one

CAS Registry Number

Not Available

SMILES

CC[C@H]1OC2=C([C@H]3[C@H](C)C[C@H](C)C[C@]13C)C(=O)NC=C2C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C23H29NO3/c1-5-18-23(4)11-13(2)10-14(3)20(23)19-21(27-18)17(12-24-22(19)26)15-6-8-16(25)9-7-15/h6-9,12-14,18,20,25H,5,10-11H2,1-4H3,(H,24,26)/t13-,14+,18+,20+,23+/m0/s1

InChI Key

ZUJBUMRATOLVJT-VIBJKCLASA-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
Epicoccum sp.	NPAtlas	17520137

Chemical Taxonomy

Classification

Not classified

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	4.96	ALOGPS
logP	4.28	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	9.19	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.56 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	107.13 m³·mol⁻¹	ChemAxon
Polarizability	42.02 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

NPA012329

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

17597258

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16664201

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kemami Wangun HV, Hertweck C: Epicoccarines A, B and epipyridone: tetramic acids and pyridone alkaloids from an Epicoccum sp. associated with the tree fungus Pholiota squarrosa. Org Biomol Chem. 2007 Jun 7;5(11):1702-5. doi: 10.1039/b702378b. Epub 2007 Apr 24. [PubMed:17520137 ]
Li C, Sarotti AM, Yang B, Turkson J, Cao S: A New N-methoxypyridone from the Co-Cultivation of Hawaiian Endophytic Fungi Camporesia sambuci FT1061 and Epicoccum sorghinum FT1062. Molecules. 2017 Jul 12;22(7). pii: molecules22071166. doi: 10.3390/molecules22071166. [PubMed:28704977 ]

Showing NP-Card for Epipyridone (NP0007079)

MOL for NP0007079 (Epipyridone)

3D MOL for NP0007079 (Epipyridone)

3D SDF for NP0007079 (Epipyridone)

3D-SDF for NP0007079 (Epipyridone)

PDB for NP0007079 (Epipyridone)

3D PDB for NP0007079 (Epipyridone)

SMILES for NP0007079 (Epipyridone)

INCHI for NP0007079 (Epipyridone)

Structure for NP0007079 (Epipyridone)

3D Structure for NP0007079 (Epipyridone)