MiMeDB: Showing metabocard for Penochalasin J (MMDBc0023047)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 13:05:46 UTC

Update Date

2025-10-07 16:07:16 UTC

Metabolite ID

MMDBc0023047

Metabolite Identification

Common Name

Penochalasin J

Description

Penochalasin J is a member of the chaetoglobosin chemical class, characterized by its complex cyclic structure. It features a unique six-cyclic fused ring system, which contributes to its distinct chemical properties and potential biological activities. Isolated from the culture of Penicillium chrysogenum V11, penochalasin J, along with other chaetoglobosins, exemplifies the diverse secondary metabolites produced by fungi. These compounds are often involved in various biochemical pathways, including those related to fungal development and interaction with other organisms. The intricate structure of penochalasin J suggests potential roles in cellular signaling or as bioactive agents, although specific pathways remain to be fully elucidated. The isolation of penochalasin J alongside other chaetoglobosins highlights the rich chemical diversity present in fungal metabolites and their potential applications in pharmaceuticals and biotechnology (PMID:27690061 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152115052D          

 45 49  0  0  1  0            999 V2000
    4.4173   -3.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0470   -2.5976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6558   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7667   -1.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5771    1.3550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5217    2.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2510   -3.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916   -3.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1956   -2.7896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8919    0.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7811    2.5417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1516   -0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3285   -0.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6213   -2.6936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2510   -1.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7699   -2.8856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    0.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1430    1.5853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6767   -3.5168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3065   -2.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0293   -2.5221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0261   -1.6989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3857    0.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4550   -2.4261    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4587   -0.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1514    1.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0959    2.0821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7760   -0.4227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2413   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6590   -1.2394    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9742   -1.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3996   -1.6029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2960    2.2838    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5888   -0.2815    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1852   -1.5938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8116   -1.5281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7909   -1.1279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5659   -4.0723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8808   -2.3301    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9362   -3.1532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7322   -4.3399    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7112   -2.1585    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1402   -1.9665    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0048   -0.6893    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  8  7  1  0  0  0  0
  9  7  2  0  0  0  0
 10  5  1  0  0  0  0
 11  6  1  0  0  0  0
 13 12  1  0  0  0  0
 19  1  1  1  0  0  0
 19  8  1  0  0  0  0
 19 14  1  0  0  0  0
 20  2  1  0  0  0  0
 20 14  2  0  0  0  0
 20 15  1  0  0  0  0
 21  3  1  0  0  0  0
 21 16  2  0  0  0  0
 22  4  1  1  0  0  0
 22 21  1  0  0  0  0
 23 17  1  0  0  0  0
 23 18  2  0  0  0  0
 24  9  1  0  0  0  0
 24 16  1  0  0  0  0
 25 12  1  0  0  0  0
 25 15  1  0  0  0  0
 26 10  2  0  0  0  0
 26 23  1  0  0  0  0
 27 11  2  0  0  0  0
 27 26  1  0  0  0  0
 28 17  1  6  0  0  0
 29 13  1  0  0  0  0
 30 22  1  0  0  0  0
 30 28  1  0  0  0  0
 32 24  1  0  0  0  0
 32 29  1  0  0  0  0
 32 30  1  0  0  0  0
 32 31  1  1  0  0  0
 33 18  1  0  0  0  0
 33 27  1  0  0  0  0
 34 28  1  0  0  0  0
 34 31  2  0  0  0  0
 35 25  2  0  0  0  0
 36 29  2  0  0  0  0
 37 31  1  0  0  0  0
 38  7  1  0  0  0  0
 39  9  1  0  0  0  0
 40 14  1  0  0  0  0
 19 41  1  6  0  0  0
 22 42  1  6  0  0  0
 24 43  1  6  0  0  0
 28 44  1  1  0  0  0
 30 45  1  6  0  0  0
M  END


  Mrv1652305152115052D          

 45 49  0  0  1  0            999 V2000
    4.4173   -3.8803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0470   -2.5976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6558   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7667   -1.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5771    1.3550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5217    2.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2510   -3.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9916   -3.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1956   -2.7896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8919    0.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7811    2.5417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1516   -0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3285   -0.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6213   -2.6936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2510   -1.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7699   -2.8856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    0.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1430    1.5853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6767   -3.5168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3065   -2.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0293   -2.5221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0261   -1.6989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3857    0.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4550   -2.4261    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4587   -0.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1514    1.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0959    2.0821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7760   -0.4227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2413   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6590   -1.2394    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9742   -1.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3996   -1.6029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2960    2.2838    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5888   -0.2815    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1852   -1.5938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8116   -1.5281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7909   -1.1279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5659   -4.0723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8808   -2.3301    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9362   -3.1532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7322   -4.3399    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7112   -2.1585    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1402   -1.9665    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0048   -0.6893    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  8  7  1  0  0  0  0
  9  7  2  0  0  0  0
 10  5  1  0  0  0  0
 11  6  1  0  0  0  0
 13 12  1  0  0  0  0
 19  1  1  1  0  0  0
 19  8  1  0  0  0  0
 19 14  1  0  0  0  0
 20  2  1  0  0  0  0
 20 14  2  0  0  0  0
 20 15  1  0  0  0  0
 21  3  1  0  0  0  0
 21 16  2  0  0  0  0
 22  4  1  1  0  0  0
 22 21  1  0  0  0  0
 23 17  1  0  0  0  0
 23 18  2  0  0  0  0
 24  9  1  0  0  0  0
 24 16  1  0  0  0  0
 25 12  1  0  0  0  0
 25 15  1  0  0  0  0
 26 10  2  0  0  0  0
 26 23  1  0  0  0  0
 27 11  2  0  0  0  0
 27 26  1  0  0  0  0
 28 17  1  6  0  0  0
 29 13  1  0  0  0  0
 30 22  1  0  0  0  0
 30 28  1  0  0  0  0
 32 24  1  0  0  0  0
 32 29  1  0  0  0  0
 32 30  1  0  0  0  0
 32 31  1  1  0  0  0
 33 18  1  0  0  0  0
 33 27  1  0  0  0  0
 34 28  1  0  0  0  0
 34 31  2  0  0  0  0
 35 25  2  0  0  0  0
 36 29  2  0  0  0  0
 37 31  1  0  0  0  0
 38  7  1  0  0  0  0
 39  9  1  0  0  0  0
 40 14  1  0  0  0  0
 19 41  1  6  0  0  0
 22 42  1  6  0  0  0
 24 43  1  6  0  0  0
 28 44  1  1  0  0  0
 30 45  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0023047

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C1=C([H])/[C@@]2([H])C=C(C)[C@@]([H])(C)[C@@]3([H])[C@]([H])(CC4=CNC5=CC=CC=C45)N=C(O)[C@@]23C(=O)CCC(=O)CC(C)=C([H])[C@@]([H])(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H38N2O3/c1-19-8-7-9-24-16-21(3)22(4)30-28(17-23-18-33-27-11-6-5-10-26(23)27)34-31(37)32(24,30)29(36)13-12-25(35)15-20(2)14-19/h5-7,9-11,14,16,18-19,22,24,28,30,33H,8,12-13,15,17H2,1-4H3,(H,34,37)/b9-7+,20-14+/t19-,22+,24-,28-,30-,32+/m0/s1

> <INCHI_KEY>
MYTCOOYZKCVFJE-ZOHYDBOYSA-N

> <FORMULA>
C32H38N2O3

> <MOLECULAR_WEIGHT>
498.667

> <EXACT_MASS>
498.288243092

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
56.2636178415001

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4S,6aS,10S,17aR,17bR)-1-hydroxy-3-[(1H-indol-3-yl)methyl]-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,13H,14H,15H,16H,17H,17bH-cyclotrideca[e]isoindole-14,17-dione

> <ALOGPS_LOGP>
5.17

> <JCHEM_LOGP>
5.080358457872781

> <ALOGPS_LOGS>
-5.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.953555440839327

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9372287411521665

> <JCHEM_PKA_STRONGEST_BASIC>
5.622844657930697

> <JCHEM_POLAR_SURFACE_AREA>
82.52

> <JCHEM_REFRACTIVITY>
150.3518

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.35e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S,6aS,10S,17aR,17bR)-1-hydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,13H,15H,16H,17bH-cyclotrideca[e]isoindole-14,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       8.246  -7.243   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.421  -4.849   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.224  -5.566   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.431  -2.493   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.811   2.529   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.707   4.066   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.202  -6.744   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.584  -7.423   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.098  -5.207   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.532   1.671   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.325   4.744   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.883  -0.397   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.346  -0.500   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.760  -5.028   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.935  -2.634   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.437  -5.387   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.343   0.284   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.267   2.959   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.863  -6.565   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.039  -4.170   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.055  -4.708   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.049  -3.171   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.720   1.777   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.716  -4.529   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.456  -1.826   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.149   2.350   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.046   3.887   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.448  -0.789   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.184  -2.036   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.230  -2.313   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.685  -1.887   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.613  -2.992   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       0.552   4.263   0.000  0.00  0.00           N+0
HETATM   34  N   UNK     0       2.966  -0.526   0.000  0.00  0.00           N+0
HETATM   35  O   UNK     0       5.946  -2.975   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       5.248  -2.853   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       5.210  -2.105   0.000  0.00  0.00           O+0
HETATM   38  H   UNK     0       2.923  -7.602   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.377  -4.349   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.481  -5.886   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       6.967  -8.101   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.328  -4.029   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.995  -3.671   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.009  -1.287   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.334  -3.850   0.000  0.00  0.00           H+0
CONECT    1   19                                                            
CONECT    2   20                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5    6   10                                                       
CONECT    6    5   11                                                       
CONECT    7    8    9   38                                                  
CONECT    8    7   19                                                       
CONECT    9    7   24   39                                                  
CONECT   10    5   26                                                       
CONECT   11    6   27                                                       
CONECT   12   13   25                                                       
CONECT   13   12   29                                                       
CONECT   14   19   20   40                                                  
CONECT   15   20   25                                                       
CONECT   16   21   24                                                       
CONECT   17   23   28                                                       
CONECT   18   23   33                                                       
CONECT   19    1    8   14   41                                             
CONECT   20    2   14   15                                                  
CONECT   21    3   16   22                                                  
CONECT   22    4   21   30   42                                             
CONECT   23   17   18   26                                                  
CONECT   24    9   16   32   43                                             
CONECT   25   12   15   35                                                  
CONECT   26   10   23   27                                                  
CONECT   27   11   26   33                                                  
CONECT   28   17   30   34   44                                             
CONECT   29   13   32   36                                                  
CONECT   30   22   28   32   45                                             
CONECT   31   32   34   37                                                  
CONECT   32   24   29   30   31                                             
CONECT   33   18   27                                                       
CONECT   34   28   31                                                       
CONECT   35   25                                                            
CONECT   36   29                                                            
CONECT   37   31                                                            
CONECT   38    7                                                            
CONECT   39    9                                                            
CONECT   40   14                                                            
CONECT   41   19                                                            
CONECT   42   22                                                            
CONECT   43   24                                                            
CONECT   44   28                                                            
CONECT   45   30                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₃₈N₂O₃

Average Mass

498.667

Monoisotopic Mass

498.288243092

IUPAC Name

(3S,4S,6aS,10S,17aR,17bR)-1-hydroxy-3-[(1H-indol-3-yl)methyl]-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,13H,14H,15H,16H,17H,17bH-cyclotrideca[e]isoindole-14,17-dione

Traditional Name

(3S,4S,6aS,10S,17aR,17bR)-1-hydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3H,4H,6aH,9H,10H,13H,15H,16H,17bH-cyclotrideca[e]isoindole-14,17-dione

CAS Registry Number

Not Available

SMILES

[H]\C1=C([H])/[C@@]2([H])C=C(C)[C@@]([H])(C)[C@@]3([H])[C@]([H])(CC4=CNC5=CC=CC=C45)N=C(O)[C@@]23C(=O)CCC(=O)CC(C)=C([H])[C@@]([H])(C)C1

InChI Identifier

InChI=1S/C32H38N2O3/c1-19-8-7-9-24-16-21(3)22(4)30-28(17-23-18-33-27-11-6-5-10-26(23)27)34-31(37)32(24,30)29(36)13-12-25(35)15-20(2)14-19/h5-7,9-11,14,16,18-19,22,24,28,30,33H,8,12-13,15,17H2,1-4H3,(H,34,37)/b9-7+,20-14+/t19-,22+,24-,28-,30-,32+/m0/s1

InChI Key

MYTCOOYZKCVFJE-ZOHYDBOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Isoindolones

Alternative Parents

Substituents

3-alkylindole
Isoindolone
Isoindole
Indole or derivatives
Indole
Benzenoid
Substituted pyrrole
2-pyrrolidone
Pyrrolidone
Heteroaromatic compound
Pyrrolidine
Pyrrole
Cyclic ketone
Secondary carboxylic acid amide
Lactam
Ketone
Carboxamide group
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0014 g/L	ALOGPS
logP	5.17	ALOGPS
logP	5.08	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	2.94	ChemAxon
pKa (Strongest Basic)	5.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	82.52 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	150.35 m³·mol⁻¹	ChemAxon
Polarizability	56.26 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

58197351

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590395

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Penochalasin J (MMDBc0023047)

MOL for #<Metabolite:0x00007f8dc57f5af8>

3D MOL for #<Metabolite:0x00007f8dc57f5af8>

3D SDF for #<Metabolite:0x00007f8dc57f5af8>

3D-SDF for #<Metabolite:0x00007f8dc57f5af8>

PDB for #<Metabolite:0x00007f8dc57f5af8>

3D PDB for #<Metabolite:0x00007f8dc57f5af8>

SMILES for #<Metabolite:0x00007f8dc57f5af8>

INCHI for #<Metabolite:0x00007f8dc57f5af8>

Structure for #<Metabolite:0x00007f8dc57f5af8>

3D Structure for #<Metabolite:0x00007f8dc57f5af8>