MiMeDB: Showing metabocard for Chaetoglobosin E (MMDBc0011079)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 03:02:48 UTC

Update Date

2025-10-07 16:05:49 UTC

Metabolite ID

MMDBc0011079

Metabolite Identification

Common Name

Chaetoglobosin E

Description

Chaetoglobosin E is a chaetoglobosin-type alkaloid, a class of secondary metabolites produced by fungi. This compound was isolated from an endophytic fungus, Chaetomium sp., alongside other related alkaloids, including brachaetoglobosin A and chaetochalasins BF (PMID:40058224 ). Chaetoglobosin E, like its analogs, is of interest due to its potential biological activities, which may include effects on cellular processes and interactions within ecological systems. The study of chaetoglobosins contributes to our understanding of fungal metabolites and their roles in nature, as well as their potential applications in pharmaceuticals and biotechnology. Further research into the structure-activity relationships of chaetoglobosin E and its derivatives could unveil novel therapeutic properties, highlighting the importance of natural products in drug discovery.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152105022D          

 48 52  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
   -0.7667   -1.3354    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
    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
    1.8919    0.8954    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
    1.7811    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
    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
   -0.0261   -1.6989    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
    0.3857    0.9519    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
    1.4550   -2.4261    0.0000 C   0  0  1  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
    3.4587   -0.9783    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
    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  2  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
    4.9460   -0.9664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8253   -3.7088    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
    1.5105   -3.2492    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
    4.0755   -0.4305    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
    0.0848   -3.3452    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  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
 13 12  1  0  0  0  0
 17  1  1  1  0  0  0
 17  8  1  0  0  0  0
 17 14  1  0  0  0  0
 18  2  1  0  0  0  0
 18 14  2  0  0  0  0
 19  3  1  0  0  0  0
 20  4  1  0  0  0  0
 20 19  2  0  0  0  0
 21 15  1  0  0  0  0
 21 16  2  0  0  0  0
 22  9  2  0  0  0  0
 22 21  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  2  0  0  0  0
 24 22  1  0  0  0  0
 25 15  1  6  0  0  0
 26 12  1  0  0  0  0
 27 13  1  0  0  0  0
 28 19  1  0  0  0  0
 28 25  1  0  0  0  0
 29 18  1  0  0  0  0
 29 26  1  0  0  0  0
 30 20  1  0  0  0  0
 30 23  1  0  0  0  0
 32 23  1  0  0  0  0
 32 27  1  0  0  0  0
 32 28  1  0  0  0  0
 32 31  1  1  0  0  0
 33 16  1  0  0  0  0
 33 24  1  0  0  0  0
 34 25  1  0  0  0  0
 34 31  2  0  0  0  0
 26 35  1  6  0  0  0
 36 27  2  0  0  0  0
 37 29  2  0  0  0  0
 30 38  1  6  0  0  0
 39 31  1  0  0  0  0
 40  7  1  0  0  0  0
 41 10  1  0  0  0  0
 42 14  1  0  0  0  0
 17 43  1  6  0  0  0
 23 44  1  6  0  0  0
 25 45  1  1  0  0  0
 26 46  1  6  0  0  0
 28 47  1  6  0  0  0
 30 48  1  1  0  0  0
M  END


  Mrv1652305152105022D          

 48 52  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
   -0.7667   -1.3354    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
    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
    1.8919    0.8954    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
    1.7811    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
    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
   -0.0261   -1.6989    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
    0.3857    0.9519    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
    1.4550   -2.4261    0.0000 C   0  0  1  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
    3.4587   -0.9783    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
    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  2  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
    4.9460   -0.9664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8253   -3.7088    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
    1.5105   -3.2492    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
    4.0755   -0.4305    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
    0.0848   -3.3452    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  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
 13 12  1  0  0  0  0
 17  1  1  1  0  0  0
 17  8  1  0  0  0  0
 17 14  1  0  0  0  0
 18  2  1  0  0  0  0
 18 14  2  0  0  0  0
 19  3  1  0  0  0  0
 20  4  1  0  0  0  0
 20 19  2  0  0  0  0
 21 15  1  0  0  0  0
 21 16  2  0  0  0  0
 22  9  2  0  0  0  0
 22 21  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  2  0  0  0  0
 24 22  1  0  0  0  0
 25 15  1  6  0  0  0
 26 12  1  0  0  0  0
 27 13  1  0  0  0  0
 28 19  1  0  0  0  0
 28 25  1  0  0  0  0
 29 18  1  0  0  0  0
 29 26  1  0  0  0  0
 30 20  1  0  0  0  0
 30 23  1  0  0  0  0
 32 23  1  0  0  0  0
 32 27  1  0  0  0  0
 32 28  1  0  0  0  0
 32 31  1  1  0  0  0
 33 16  1  0  0  0  0
 33 24  1  0  0  0  0
 34 25  1  0  0  0  0
 34 31  2  0  0  0  0
 26 35  1  6  0  0  0
 36 27  2  0  0  0  0
 37 29  2  0  0  0  0
 30 38  1  6  0  0  0
 39 31  1  0  0  0  0
 40  7  1  0  0  0  0
 41 10  1  0  0  0  0
 42 14  1  0  0  0  0
 17 43  1  6  0  0  0
 23 44  1  6  0  0  0
 25 45  1  1  0  0  0
 26 46  1  6  0  0  0
 28 47  1  6  0  0  0
 30 48  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0011079

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C32H38N2O5/c1-17-8-7-10-23-30(38)20(4)19(3)28-25(15-21-16-33-24-11-6-5-9-22(21)24)34-31(39)32(23,28)27(36)13-12-26(35)29(37)18(2)14-17/h5-7,9-11,14,16-17,23,25-26,28,30,33,35,38H,8,12-13,15H2,1-4H3,(H,34,39)/b10-7+,18-14+/t17-,23-,25-,26-,28-,30+,32+/m0/s1

> <INCHI_KEY>
FPNAKNFLJIQADW-CNYNBRRPSA-N

> <FORMULA>
C32H38N2O5

> <MOLECULAR_WEIGHT>
530.665

> <EXACT_MASS>
530.278072332

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
58.659490492874745

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
3.63

> <JCHEM_LOGP>
3.606016661007245

> <ALOGPS_LOGS>
-4.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.332808229711873

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7620231185743624

> <JCHEM_PKA_STRONGEST_BASIC>
5.378790699792905

> <JCHEM_POLAR_SURFACE_AREA>
122.97999999999999

> <JCHEM_REFRACTIVITY>
153.06770000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S,6aR,10S,14S,17aS,17bR)-1,6,14-trihydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3H,6H,6aH,9H,10H,14H,15H,16H,17bH-cyclotrideca[e]isoindole-13,17-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      -1.431  -2.493   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.224  -5.566   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       3.532   1.671   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.098  -5.207   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       0.343   0.284   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.267   2.959   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.863  -6.565   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.039  -4.170   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.049  -3.171   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.055  -4.708   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.720   1.777   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.149   2.350   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.716  -4.529   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.046   3.887   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.448  -0.789   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.456  -1.826   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.184  -2.036   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.230  -2.313   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.935  -2.634   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.437  -5.387   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       9.233  -1.804   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       1.541  -6.923   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       5.210  -2.105   0.000  0.00  0.00           O+0
HETATM   40  H   UNK     0       2.923  -7.602   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.377  -4.349   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       5.481  -5.886   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0       6.967  -8.101   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.820  -6.065   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.009  -1.287   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0       7.608  -0.804   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0       1.334  -3.850   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.158  -6.244   0.000  0.00  0.00           H+0
CONECT    1   17                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    6    9                                                       
CONECT    6    5   11                                                       
CONECT    7    8   10   40                                                  
CONECT    8    7   17                                                       
CONECT    9    5   22                                                       
CONECT   10    7   23   41                                                  
CONECT   11    6   24                                                       
CONECT   12   13   26                                                       
CONECT   13   12   27                                                       
CONECT   14   17   18   42                                                  
CONECT   15   21   25                                                       
CONECT   16   21   33                                                       
CONECT   17    1    8   14   43                                             
CONECT   18    2   14   29                                                  
CONECT   19    3   20   28                                                  
CONECT   20    4   19   30                                                  
CONECT   21   15   16   22                                                  
CONECT   22    9   21   24                                                  
CONECT   23   10   30   32   44                                             
CONECT   24   11   22   33                                                  
CONECT   25   15   28   34   45                                             
CONECT   26   12   29   35   46                                             
CONECT   27   13   32   36                                                  
CONECT   28   19   25   32   47                                             
CONECT   29   18   26   37                                                  
CONECT   30   20   23   38   48                                             
CONECT   31   32   34   39                                                  
CONECT   32   23   27   28   31                                             
CONECT   33   16   24                                                       
CONECT   34   25   31                                                       
CONECT   35   26                                                            
CONECT   36   27                                                            
CONECT   37   29                                                            
CONECT   38   30                                                            
CONECT   39   31                                                            
CONECT   40    7                                                            
CONECT   41   10                                                            
CONECT   42   14                                                            
CONECT   43   17                                                            
CONECT   44   23                                                            
CONECT   45   25                                                            
CONECT   46   26                                                            
CONECT   47   28                                                            
CONECT   48   30                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  104    0
END

Synonyms

Value	Source
Chaetoglobosin C	MeSH
Penochalasin K	MeSH
Chaetoglobosin a	MeSH
Chaetoglobosin b	MeSH
Chaetoglobosin Q	MeSH
Chaetoglobosin R	MeSH
Chaetoglobosin W	MeSH
Chaetoglobosin F	MeSH
Chaetoglobosin K	MeSH
Chaetoglobosin u	MeSH
Chaetoglobosin D	MeSH
Chaetoglobosin T	MeSH
Chaetoglobosin V	MeSH
Chaetoglobosin y	MeSH
Chaetoglobosins	MeSH

Molecular Formula

C₃₂H₃₈N₂O₅

Average Mass

530.665

Monoisotopic Mass

530.278072332

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C32H38N2O5/c1-17-8-7-10-23-30(38)20(4)19(3)28-25(15-21-16-33-24-11-6-5-9-22(21)24)34-31(39)32(23,28)27(36)13-12-26(35)29(37)18(2)14-17/h5-7,9-11,14,16-17,23,25-26,28,30,33,35,38H,8,12-13,15H2,1-4H3,(H,34,39)/b10-7+,18-14+/t17-,23-,25-,26-,28-,30+,32+/m0/s1

InChI Key

FPNAKNFLJIQADW-CNYNBRRPSA-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

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

indoles (CHEBI:68731 )
macrocycle (CHEBI:68731 )
cytochalasan alkaloid (CHEBI:68731 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.011 g/L	ALOGPS
logP	3.63	ALOGPS
logP	3.61	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	2.76	ChemAxon
pKa (Strongest Basic)	5.38	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	122.98 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	153.07 m³·mol⁻¹	ChemAxon
Polarizability	58.66 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_3_10) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

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	4	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

C00011311

Chemspider ID

10406725

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23259929

PDB ID

Not Available

ChEBI ID

68731

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

References

Synthesis Reference

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 Chaetoglobosin E (MMDBc0011079)

MOL for #<Metabolite:0x0000564f9fe71838>

3D MOL for #<Metabolite:0x0000564f9fe71838>

3D SDF for #<Metabolite:0x0000564f9fe71838>

3D-SDF for #<Metabolite:0x0000564f9fe71838>

PDB for #<Metabolite:0x0000564f9fe71838>

3D PDB for #<Metabolite:0x0000564f9fe71838>

SMILES for #<Metabolite:0x0000564f9fe71838>

INCHI for #<Metabolite:0x0000564f9fe71838>

Structure for #<Metabolite:0x0000564f9fe71838>

3D Structure for #<Metabolite:0x0000564f9fe71838>