MiMeDB: Showing metabocard for Aflatrem (MMDBc0013595)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:52:15 UTC

Update Date

2025-10-07 16:06:10 UTC

Metabolite ID

MMDBc0013595

Metabolite Identification

Common Name

Aflatrem

Description

Aflatrem is a secondary metabolite belonging to the chemical class of indole diterpenes, primarily produced by certain species of the fungus Aspergillus. It has garnered attention due to its presence alongside other mycotoxins, such as aflatoxins and cyclopiazonic acid, in various substrates, including agricultural products. Studies have shown that pulses can accumulate significant levels of aflatrem, which raises concerns regarding its potential toxicological effects (PMID:40510667 ). Moreover, genetic analyses have revealed that aflatrem biosynthesis is regulated by specific gene clusters, indicating its complex biosynthetic pathways in fungi (PMID:39227280 ). Aflatrem's role in food safety is underscored by its association with other mycotoxins that can adversely affect human health (PMID:34408970 ). Additionally, research suggests that aflatrem may influence behavior in ants, potentially disrupting feeding patterns through its effects on neurobiology (PMID:32354705 ). The regulation of aflatrem production by various genetic factors highlights its significance in the broader context of fungal secondary metabolism (PMID:30635379 ). Overall, aflatrem's biochemical properties and biological implications warrant further investigation to understand its impact on health and safety.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152106522D          

 39 45  0  0  1  0            999 V2000
    8.7171    3.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9423    2.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5516    2.4178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7284   -0.1502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5592    1.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8994    1.0416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9291    3.4046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9883    0.4307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1705    1.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2004    0.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3150    3.2155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271    2.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7756    0.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9804    0.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7423    2.7308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9770    2.5765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9208    2.6554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0679    1.9727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5648    1.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5947    0.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507    2.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5465    1.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7768    1.5508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9168    1.5206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7470    2.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9078    0.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9507    1.6062    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7386    1.8508    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3449    2.1663    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3093    1.0704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7731    0.6708    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5709    2.9429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7396    2.7269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331    1.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7365    0.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1329    2.4109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1001    1.6371    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  2  0  0  0  0
 10  9  2  0  0  0  0
 11  9  1  0  0  0  0
 13 12  1  0  0  0  0
 15 14  1  0  0  0  0
 18 12  1  0  0  0  0
 18 16  1  0  0  0  0
 19 16  1  0  0  0  0
 20 10  1  0  0  0  0
 21 11  2  0  0  0  0
 22 17  1  0  0  0  0
 23 17  2  0  0  0  0
 24 19  1  0  0  0  0
 24 20  2  0  0  0  0
 24 21  1  0  0  0  0
 25 19  2  0  0  0  0
 26 22  1  0  0  0  0
 27  2  1  0  0  0  0
 27  3  1  0  0  0  0
 27  8  1  0  0  0  0
 27 20  1  0  0  0  0
 28  4  1  0  0  0  0
 28  5  1  0  0  0  0
 28 26  1  0  0  0  0
 29  6  1  6  0  0  0
 29 14  1  0  0  0  0
 30  7  1  1  0  0  0
 30 18  1  0  0  0  0
 30 25  1  0  0  0  0
 30 29  1  0  0  0  0
 31 13  1  0  0  0  0
 31 23  1  0  0  0  0
 31 29  1  0  0  0  0
 32 15  1  0  0  0  0
 32 23  1  0  0  0  0
 33 21  1  0  0  0  0
 33 25  1  0  0  0  0
 34 22  2  0  0  0  0
 31 35  1  1  0  0  0
 36 26  1  0  0  0  0
 32 36  1  1  0  0  0
 37 28  1  0  0  0  0
 37 32  1  0  0  0  0
 18 38  1  6  0  0  0
 26 39  1  1  0  0  0
M  END


  Mrv1652305152106522D          

 39 45  0  0  1  0            999 V2000
    8.7171    3.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9423    2.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5516    2.4178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882    0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7284   -0.1502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5592    1.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8994    1.0416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9291    3.4046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9883    0.4307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1705    1.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2004    0.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3150    3.2155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271    2.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7756    0.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9804    0.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7423    2.7308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9770    2.5765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9208    2.6554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0679    1.9727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5648    1.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5947    0.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507    2.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5465    1.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7768    1.5508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4475    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9168    1.5206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7470    2.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9078    0.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9507    1.6062    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7386    1.8508    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3449    2.1663    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3093    1.0704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7731    0.6708    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5709    2.9429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7396    2.7269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6331    1.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7365    0.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1329    2.4109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1001    1.6371    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  2  0  0  0  0
 10  9  2  0  0  0  0
 11  9  1  0  0  0  0
 13 12  1  0  0  0  0
 15 14  1  0  0  0  0
 18 12  1  0  0  0  0
 18 16  1  0  0  0  0
 19 16  1  0  0  0  0
 20 10  1  0  0  0  0
 21 11  2  0  0  0  0
 22 17  1  0  0  0  0
 23 17  2  0  0  0  0
 24 19  1  0  0  0  0
 24 20  2  0  0  0  0
 24 21  1  0  0  0  0
 25 19  2  0  0  0  0
 26 22  1  0  0  0  0
 27  2  1  0  0  0  0
 27  3  1  0  0  0  0
 27  8  1  0  0  0  0
 27 20  1  0  0  0  0
 28  4  1  0  0  0  0
 28  5  1  0  0  0  0
 28 26  1  0  0  0  0
 29  6  1  6  0  0  0
 29 14  1  0  0  0  0
 30  7  1  1  0  0  0
 30 18  1  0  0  0  0
 30 25  1  0  0  0  0
 30 29  1  0  0  0  0
 31 13  1  0  0  0  0
 31 23  1  0  0  0  0
 31 29  1  0  0  0  0
 32 15  1  0  0  0  0
 32 23  1  0  0  0  0
 33 21  1  0  0  0  0
 33 25  1  0  0  0  0
 34 22  2  0  0  0  0
 31 35  1  1  0  0  0
 36 26  1  0  0  0  0
 32 36  1  1  0  0  0
 37 28  1  0  0  0  0
 37 32  1  0  0  0  0
 18 38  1  6  0  0  0
 26 39  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0013595

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12CC3=C(NC4=CC=CC(=C34)C(C)(C)C=C)[C@]1(C)[C@@]1(C)CC[C@@]34O[C@@]([H])(C(=O)C=C3[C@]1(O)CC2)C(C)(C)O4

> <INCHI_IDENTIFIER>
InChI=1S/C32H39NO4/c1-8-27(2,3)20-10-9-11-21-24(20)19-16-18-12-13-31(35)23-17-22(34)26-28(4,5)37-32(23,36-26)15-14-29(31,6)30(18,7)25(19)33-21/h8-11,17-18,26,33,35H,1,12-16H2,2-7H3/t18-,26-,29+,30+,31+,32-/m0/s1

> <INCHI_KEY>
YVDJBQQJIDPRKP-SLUQHKSNSA-N

> <FORMULA>
C32H39NO4

> <MOLECULAR_WEIGHT>
501.667

> <EXACT_MASS>
501.28790874

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
57.573640360085314

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,5S,16S,19S,23R)-19-hydroxy-4,5,24,24-tetramethyl-12-(2-methylbut-3-en-2-yl)-25,26-dioxa-7-azaheptacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{6,14}.0^{8,13}]hexacosa-6(14),8,10,12,20-pentaen-22-one

> <ALOGPS_LOGP>
6.06

> <JCHEM_LOGP>
6.052038274666668

> <ALOGPS_LOGS>
-6.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.788116584958473

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.617501355950719

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4033673277239957

> <JCHEM_POLAR_SURFACE_AREA>
71.55000000000001

> <JCHEM_REFRACTIVITY>
144.59509999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.94e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,5S,16S,19S,23R)-19-hydroxy-4,5,24,24-tetramethyl-12-(2-methylbut-3-en-2-yl)-25,26-dioxa-7-azaheptacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{6,14}.0^{8,13}]hexacosa-6(14),8,10,12,20-pentaen-22-one

> <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      16.272   6.812   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.959   5.193   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.963   4.513   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.165   1.399   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.360  -0.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.511   1.958   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.146   1.944   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.801   6.355   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.912   0.804   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.252   2.306   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.441   0.347   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.055   6.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.584   5.546   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.048   1.485   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.563   1.015   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.719   5.097   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.690   4.809   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.185   4.957   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.327   3.682   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.121   3.351   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.310   1.393   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.148   4.398   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.753   3.584   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.650   2.895   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.169   2.667   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.711   2.838   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.461   4.853   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.694   1.223   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.375   2.998   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.845   3.455   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.244   4.044   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.311   1.998   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      10.776   1.252   0.000  0.00  0.00           N+0
HETATM   34  O   UNK     0       1.066   5.493   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       5.114   5.090   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       3.049   2.483   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       3.241   0.704   0.000  0.00  0.00           O+0
HETATM   38  H   UNK     0       7.715   4.500   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.187   3.056   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2   27                                                            
CONECT    3   27                                                            
CONECT    4   28                                                            
CONECT    5   28                                                            
CONECT    6   29                                                            
CONECT    7   30                                                            
CONECT    8    1   27                                                       
CONECT    9   10   11                                                       
CONECT   10    9   20                                                       
CONECT   11    9   21                                                       
CONECT   12   13   18                                                       
CONECT   13   12   31                                                       
CONECT   14   15   29                                                       
CONECT   15   14   32                                                       
CONECT   16   18   19                                                       
CONECT   17   22   23                                                       
CONECT   18   12   16   30   38                                             
CONECT   19   16   24   25                                                  
CONECT   20   10   24   27                                                  
CONECT   21   11   24   33                                                  
CONECT   22   17   26   34                                                  
CONECT   23   17   31   32                                                  
CONECT   24   19   20   21                                                  
CONECT   25   19   30   33                                                  
CONECT   26   22   28   36   39                                             
CONECT   27    2    3    8   20                                             
CONECT   28    4    5   26   37                                             
CONECT   29    6   14   30   31                                             
CONECT   30    7   18   25   29                                             
CONECT   31   13   23   29   35                                             
CONECT   32   15   23   36   37                                             
CONECT   33   21   25                                                       
CONECT   34   22                                                            
CONECT   35   31                                                            
CONECT   36   26   32                                                       
CONECT   37   28   32                                                       
CONECT   38   18                                                            
CONECT   39   26                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   90    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₃₉NO₄

Average Mass

501.667

Monoisotopic Mass

501.28790874

IUPAC Name

(1S,4R,5S,16S,19S,23R)-19-hydroxy-4,5,24,24-tetramethyl-12-(2-methylbut-3-en-2-yl)-25,26-dioxa-7-azaheptacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{6,14}.0^{8,13}]hexacosa-6(14),8,10,12,20-pentaen-22-one

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@]12CC3=C(NC4=CC=CC(=C34)C(C)(C)C=C)[C@]1(C)[C@@]1(C)CC[C@@]34O[C@@]([H])(C(=O)C=C3[C@]1(O)CC2)C(C)(C)O4

InChI Identifier

InChI=1S/C32H39NO4/c1-8-27(2,3)20-10-9-11-21-24(20)19-16-18-12-13-31(35)23-17-22(34)26-28(4,5)37-32(23,36-26)15-14-29(31,6)30(18,7)25(19)33-21/h8-11,17-18,26,33,35H,1,12-16H2,2-7H3/t18-,26-,29+,30+,31+,32-/m0/s1

InChI Key

YVDJBQQJIDPRKP-SLUQHKSNSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
3-alkylindole
Indole
Indole or derivatives
Dihydropyranone
Ketal
Pyran
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Meta-dioxolane
Cyclic alcohol
Ketone
Acetal
Oxacycle
Azacycle
Organooxygen compound
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organonitrogen compound
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	5.9e-05 g/L	ALOGPS
logP	6.06	ALOGPS
logP	6.05	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	71.55 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	144.6 m³·mol⁻¹	ChemAxon
Polarizability	57.57 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	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_2) - 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	2	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

19976660

KEGG Compound ID

C20555

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21118293

PDB ID

Not Available

ChEBI ID

181944

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 Aflatrem (MMDBc0013595)

MOL for #<Metabolite:0x00007f6d7171cc68>

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3D SDF for #<Metabolite:0x00007f6d7171cc68>

3D-SDF for #<Metabolite:0x00007f6d7171cc68>

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Structure for #<Metabolite:0x00007f6d7171cc68>

3D Structure for #<Metabolite:0x00007f6d7171cc68>