MiMeDB: Showing metabocard for Fusarielin H (MMDBc0028216)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 17:51:01 UTC

Update Date

2025-10-07 16:07:50 UTC

Metabolite ID

MMDBc0028216

Metabolite Identification

Common Name

Fusarielin H

Description

Fusarielin H is a member of the chemical class of mycotoxins, specifically a metabolite produced by the fungus Fusarium sp. Its chemical structure is characterized by a complex arrangement of carbon, hydrogen, and oxygen atoms, typical of secondary metabolites from fungi. Fusarielin H is involved in various biological pathways, including the production of other mycotoxins such as deoxynivalenol (DON) and zearalenone, where its biosynthesis is regulated by the AreA transcription factor, indicating its role in nutrient response (PMID:24295920 ). Additionally, deletion mutants lacking specific transporters showed increased production of DON and zearalenone but reduced levels of fusarielin H, highlighting its interconnected biosynthetic pathway (PMID:28390508 ). Fusarielin H has been detected in infected cereals, with concentrations ranging from 392 to 1865 ng/g, suggesting its production during fungal infection (PMID:23290226 ). Furthermore, it demonstrates significant biological activity, stimulating MCF-7 cell proliferation four-fold at 25 μM, making it the most potent among tested fusarielins (PMID:22982765 ), and exhibiting higher potency against colorectal cancer cell lines compared to other fusarielins (PMID:22252016 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152119512D          

 39 41  0  0  1  0            999 V2000
    0.8083    4.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2505   -0.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1527    3.0355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7587    4.1712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2835    6.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3791    2.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3001    3.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1196    3.9819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4474    4.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    3.3194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0865    1.3321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5948    1.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392    0.4804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4309    7.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7587    0.5751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9722    3.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    4.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1031    6.2531    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7753    1.8999    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2835    2.5624    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4474    1.1429    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4640    2.4677    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5948    5.5907    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6279    1.0482    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1361    1.7107    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9392    7.6726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4144    5.6853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083    0.9536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6279    4.6443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392    4.0765    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3528    5.5585    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3684    2.9916    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    6.9155    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1031    2.6570    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7918    3.2248    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557    1.8053    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6444    2.3731    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7753    5.4960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7225    0.2287    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
  9  8  1  0  0  0  0
 10  8  2  0  0  0  0
 12 11  1  0  0  0  0
 15  2  1  0  0  0  0
 15 11  2  0  0  0  0
 15 13  1  0  0  0  0
 16  3  1  0  0  0  0
 16  7  2  0  0  0  0
 17  4  1  0  0  0  0
 17  9  2  0  0  0  0
 18  5  1  1  0  0  0
 18 14  1  0  0  0  0
 19 12  1  0  0  0  0
 20 10  1  1  0  0  0
 20 19  1  0  0  0  0
 21 13  1  0  0  0  0
 21 19  1  0  0  0  0
 22 16  1  1  0  0  0
 22 20  1  0  0  0  0
 23 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 21  1  0  0  0  0
 25  6  1  1  0  0  0
 25 22  1  0  0  0  0
 25 24  1  0  0  0  0
 26 14  1  0  0  0  0
 23 27  1  1  0  0  0
 28 24  1  0  0  0  0
 28 25  1  0  0  0  0
 29  7  1  0  0  0  0
 30  8  1  0  0  0  0
 31  9  1  0  0  0  0
 32 10  1  0  0  0  0
 18 33  1  6  0  0  0
 19 34  1  1  0  0  0
 20 35  1  6  0  0  0
 21 36  1  6  0  0  0
 22 37  1  6  0  0  0
 23 38  1  1  0  0  0
 24 39  1  1  0  0  0
M  END


  Mrv1652305152119512D          

 39 41  0  0  1  0            999 V2000
    0.8083    4.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2505   -0.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1527    3.0355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7587    4.1712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2835    6.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3791    2.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3001    3.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1196    3.9819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4474    4.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    3.3194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0865    1.3321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5948    1.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392    0.4804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4309    7.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7587    0.5751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9722    3.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670    4.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1031    6.2531    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7753    1.8999    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2835    2.5624    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4474    1.1429    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4640    2.4677    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5948    5.5907    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6279    1.0482    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1361    1.7107    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9392    7.6726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4144    5.6853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8083    0.9536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6279    4.6443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392    4.0765    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3528    5.5585    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3684    2.9916    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    6.9155    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1031    2.6570    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7918    3.2248    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557    1.8053    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6444    2.3731    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7753    5.4960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7225    0.2287    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
  9  8  1  0  0  0  0
 10  8  2  0  0  0  0
 12 11  1  0  0  0  0
 15  2  1  0  0  0  0
 15 11  2  0  0  0  0
 15 13  1  0  0  0  0
 16  3  1  0  0  0  0
 16  7  2  0  0  0  0
 17  4  1  0  0  0  0
 17  9  2  0  0  0  0
 18  5  1  1  0  0  0
 18 14  1  0  0  0  0
 19 12  1  0  0  0  0
 20 10  1  1  0  0  0
 20 19  1  0  0  0  0
 21 13  1  0  0  0  0
 21 19  1  0  0  0  0
 22 16  1  1  0  0  0
 22 20  1  0  0  0  0
 23 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 21  1  0  0  0  0
 25  6  1  1  0  0  0
 25 22  1  0  0  0  0
 25 24  1  0  0  0  0
 26 14  1  0  0  0  0
 23 27  1  1  0  0  0
 28 24  1  0  0  0  0
 28 25  1  0  0  0  0
 29  7  1  0  0  0  0
 30  8  1  0  0  0  0
 31  9  1  0  0  0  0
 32 10  1  0  0  0  0
 18 33  1  6  0  0  0
 19 34  1  1  0  0  0
 20 35  1  6  0  0  0
 21 36  1  6  0  0  0
 22 37  1  6  0  0  0
 23 38  1  1  0  0  0
 24 39  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0028216

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C(C)=C(C)[C@@]1([H])[C@@]([H])(C([H])=C([H])C(\[H])=C(/C)[C@@]([H])(O)[C@@]([H])(C)CO)[C@]2([H])CC=C(C)C[C@@]2([H])[C@]2([H])O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O3/c1-7-16(3)22-20(10-8-9-17(4)23(27)18(5)14-26)19-12-11-15(2)13-21(19)24-25(22,6)28-24/h7-11,18-24,26-27H,12-14H2,1-6H3/b10-8-,16-7+,17-9+/t18-,19-,20-,21+,22-,23+,24-,25+/m0/s1

> <INCHI_KEY>
IFASIJVLMUACLJ-MXOTVBERSA-N

> <FORMULA>
C25H38O3

> <MOLECULAR_WEIGHT>
386.576

> <EXACT_MASS>
386.282095084

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.633973443642084

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,4E,6E)-7-[(1aR,2R,3S,3aS,7aR,7bS)-2-[(2E)-but-2-en-2-yl]-1a,6-dimethyl-1aH,2H,3H,3aH,4H,7H,7aH,7bH-naphtho[1,2-b]oxiren-3-yl]-2,4-dimethylhepta-4,6-diene-1,3-diol

> <ALOGPS_LOGP>
4.92

> <JCHEM_LOGP>
3.9554517473333335

> <ALOGPS_LOGS>
-4.41

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.519295198358677

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.255467373529413

> <JCHEM_PKA_STRONGEST_BASIC>
-2.62912724451873

> <JCHEM_POLAR_SURFACE_AREA>
52.99

> <JCHEM_REFRACTIVITY>
119.14269999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4E,6E)-7-[(1aR,2R,3S,3aS,7aR,7bS)-2-[(2E)-but-2-en-2-yl]-1a,6-dimethyl-2H,3H,3aH,4H,7H,7aH,7bH-naphtho[1,2-b]oxiren-3-yl]-2,4-dimethylhepta-4,6-diene-1,3-diol

> <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       1.509   8.493   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.934  -0.163   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.285   5.666   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.016   7.786   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.263  11.496   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.708   3.805   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.427   7.256   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.957   7.433   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.569   8.846   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.875   6.196   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.628   2.487   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.710   3.723   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.486   0.897   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.404  13.086   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.016   1.073   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.815   5.843   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.098   9.023   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.792  11.672   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.180   3.547   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.263   4.783   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.569   2.133   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.733   4.606   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.710  10.436   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.039   1.957   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.121   3.193   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.486  14.322   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.240  10.613   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       1.509   1.780   0.000  0.00  0.00           O+0
HETATM   29  H   UNK     0       3.039   8.669   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.486   7.610   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.392  10.376   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       6.288   5.584   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.875  12.909   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       5.792   4.960   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.345   6.020   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.651   3.370   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.203   4.430   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       5.180  10.259   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.215   0.427   0.000  0.00  0.00           H+0
CONECT    1    7                                                            
CONECT    2   15                                                            
CONECT    3   16                                                            
CONECT    4   17                                                            
CONECT    5   18                                                            
CONECT    6   25                                                            
CONECT    7    1   16   29                                                  
CONECT    8    9   10   30                                                  
CONECT    9    8   17   31                                                  
CONECT   10    8   20   32                                                  
CONECT   11   12   15                                                       
CONECT   12   11   19                                                       
CONECT   13   15   21                                                       
CONECT   14   18   26                                                       
CONECT   15    2   11   13                                                  
CONECT   16    3    7   22                                                  
CONECT   17    4    9   23                                                  
CONECT   18    5   14   23   33                                             
CONECT   19   12   20   21   34                                             
CONECT   20   10   19   22   35                                             
CONECT   21   13   19   24   36                                             
CONECT   22   16   20   25   37                                             
CONECT   23   17   18   27   38                                             
CONECT   24   21   25   28   39                                             
CONECT   25    6   22   24   28                                             
CONECT   26   14                                                            
CONECT   27   23                                                            
CONECT   28   24   25                                                       
CONECT   29    7                                                            
CONECT   30    8                                                            
CONECT   31    9                                                            
CONECT   32   10                                                            
CONECT   33   18                                                            
CONECT   34   19                                                            
CONECT   35   20                                                            
CONECT   36   21                                                            
CONECT   37   22                                                            
CONECT   38   23                                                            
CONECT   39   24                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₈O₃

Average Mass

386.576

Monoisotopic Mass

386.282095084

IUPAC Name

(2S,3S,4E,6E)-7-[(1aR,2R,3S,3aS,7aR,7bS)-2-[(2E)-but-2-en-2-yl]-1a,6-dimethyl-1aH,2H,3H,3aH,4H,7H,7aH,7bH-naphtho[1,2-b]oxiren-3-yl]-2,4-dimethylhepta-4,6-diene-1,3-diol

Traditional Name

(2S,3S,4E,6E)-7-[(1aR,2R,3S,3aS,7aR,7bS)-2-[(2E)-but-2-en-2-yl]-1a,6-dimethyl-2H,3H,3aH,4H,7H,7aH,7bH-naphtho[1,2-b]oxiren-3-yl]-2,4-dimethylhepta-4,6-diene-1,3-diol

CAS Registry Number

Not Available

SMILES

[H]C(C)=C(C)[C@@]1([H])[C@@]([H])(C([H])=C([H])C(\[H])=C(/C)[C@@]([H])(O)[C@@]([H])(C)CO)[C@]2([H])CC=C(C)C[C@@]2([H])[C@]2([H])O[C@]12C

InChI Identifier

InChI=1S/C25H38O3/c1-7-16(3)22-20(10-8-9-17(4)23(27)18(5)14-26)19-12-11-15(2)13-21(19)24-25(22,6)28-24/h7-11,18-24,26-27H,12-14H2,1-6H3/b10-8-,16-7+,17-9+/t18-,19-,20-,21+,22-,23+,24-,25+/m0/s1

InChI Key

IFASIJVLMUACLJ-MXOTVBERSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.015 g/L	ALOGPS
logP	4.92	ALOGPS
logP	3.96	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	14.26	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	119.14 m³·mol⁻¹	ChemAxon
Polarizability	46.63 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

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 Fusarielin H (MMDBc0028216)

MOL for #<Metabolite:0x00007f8dc031fe70>

3D MOL for #<Metabolite:0x00007f8dc031fe70>

3D SDF for #<Metabolite:0x00007f8dc031fe70>

3D-SDF for #<Metabolite:0x00007f8dc031fe70>

PDB for #<Metabolite:0x00007f8dc031fe70>

3D PDB for #<Metabolite:0x00007f8dc031fe70>

SMILES for #<Metabolite:0x00007f8dc031fe70>

INCHI for #<Metabolite:0x00007f8dc031fe70>

Structure for #<Metabolite:0x00007f8dc031fe70>

3D Structure for #<Metabolite:0x00007f8dc031fe70>