MiMeDB: Showing metabocard for Terreustoxin A (MMDBc0025798)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:31:03 UTC

Update Date

2022-08-31 06:51:03 UTC

MiMeDB ID

MMDBc0025798

Metabolite Identification

Common Name

Terreustoxin A

Description

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117312D          

 39 42  0  0  1  0            999 V2000
    1.5246   -1.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4709    1.9628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4731    1.6156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -0.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8165    0.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8422   -1.7945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6160   -0.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4306   -0.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3218   -1.1543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449    0.8802    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.8157    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.2834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0  0  0  0
 12  1  2  0  0  0  0
 12 11  1  0  0  0  0
 13 11  1  0  0  0  0
 14  9  1  0  0  0  0
 16 15  1  0  0  0  0
 18 15  1  0  0  0  0
 19 17  1  0  0  0  0
 22  2  1  0  0  0  0
 22  3  1  0  0  0  0
 22 14  1  0  0  0  0
 22 16  1  0  0  0  0
 23  4  1  6  0  0  0
 23 10  1  0  0  0  0
 23 13  1  0  0  0  0
 23 16  1  0  0  0  0
 24  5  1  6  0  0  0
 24 12  1  0  0  0  0
 24 17  1  0  0  0  0
 24 20  1  0  0  0  0
 25  6  1  6  0  0  0
 25 13  1  0  0  0  0
 25 17  1  0  0  0  0
 25 18  1  0  0  0  0
 26  7  1  6  0  0  0
 26 20  1  0  0  0  0
 26 21  1  1  0  0  0
 27 14  2  0  0  0  0
 15 28  1  6  0  0  0
 18 29  1  6  0  0  0
 30 19  2  0  0  0  0
 31 20  2  0  0  0  0
 32 21  2  0  0  0  0
 33  8  1  0  0  0  0
 33 21  1  0  0  0  0
 34 19  1  0  0  0  0
 34 26  1  0  0  0  0
 13 35  1  1  0  0  0
 15 36  1  1  0  0  0
 16 37  1  1  0  0  0
 17 38  1  1  0  0  0
 18 39  1  1  0  0  0
M  END


  Mrv1652305152117312D          

 39 42  0  0  1  0            999 V2000
    1.5246   -1.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4709    1.9628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4731    1.6156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -0.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8165    0.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8422   -1.7945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6160   -0.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4306   -0.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3218   -1.1543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449    0.8802    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.8157    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.2834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0  0  0  0
 12  1  2  0  0  0  0
 12 11  1  0  0  0  0
 13 11  1  0  0  0  0
 14  9  1  0  0  0  0
 16 15  1  0  0  0  0
 18 15  1  0  0  0  0
 19 17  1  0  0  0  0
 22  2  1  0  0  0  0
 22  3  1  0  0  0  0
 22 14  1  0  0  0  0
 22 16  1  0  0  0  0
 23  4  1  6  0  0  0
 23 10  1  0  0  0  0
 23 13  1  0  0  0  0
 23 16  1  0  0  0  0
 24  5  1  6  0  0  0
 24 12  1  0  0  0  0
 24 17  1  0  0  0  0
 24 20  1  0  0  0  0
 25  6  1  6  0  0  0
 25 13  1  0  0  0  0
 25 17  1  0  0  0  0
 25 18  1  0  0  0  0
 26  7  1  6  0  0  0
 26 20  1  0  0  0  0
 26 21  1  1  0  0  0
 27 14  2  0  0  0  0
 15 28  1  6  0  0  0
 18 29  1  6  0  0  0
 30 19  2  0  0  0  0
 31 20  2  0  0  0  0
 32 21  2  0  0  0  0
 33  8  1  0  0  0  0
 33 21  1  0  0  0  0
 34 19  1  0  0  0  0
 34 26  1  0  0  0  0
 13 35  1  1  0  0  0
 15 36  1  1  0  0  0
 16 37  1  1  0  0  0
 17 38  1  1  0  0  0
 18 39  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0025798

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(O)[C@@]([H])(O)[C@@]2(C)[C@@]([H])(CC(=C)[C@@]3(C)C(=O)[C@](C)(OC(=O)[C@]23[H])C(=O)OC)[C@]2(C)CCC(=O)C(C)(C)[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O8/c1-12-11-13-23(4)10-9-14(27)22(2,3)16(23)15(28)18(29)25(13,6)17-19(30)34-26(7,21(32)33-8)20(31)24(12,17)5/h13,15-18,28-29H,1,9-11H2,2-8H3/t13-,15+,16+,17-,18+,23-,24+,25-,26-/m0/s1

> <INCHI_KEY>
GVJWSIBVKQDNPN-GQNBQQLRSA-N

> <FORMULA>
C26H36O8

> <MOLECULAR_WEIGHT>
476.566

> <EXACT_MASS>
476.241018119

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
50.25088078329489

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2R,5S,7S,10S,11S,16S,17R,18S)-17,18-dihydroxy-1,5,7,11,15,15-hexamethyl-8-methylidene-3,6,14-trioxo-4-oxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadecane-5-carboxylate

> <ALOGPS_LOGP>
1.85

> <JCHEM_LOGP>
2.6491305696666676

> <ALOGPS_LOGS>
-3.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.941448899042364

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.498866167417418

> <JCHEM_PKA_STRONGEST_BASIC>
-3.281816779576028

> <JCHEM_POLAR_SURFACE_AREA>
127.20000000000002

> <JCHEM_REFRACTIVITY>
120.59759999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.60e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,5S,7S,10S,11S,16S,17R,18S)-17,18-dihydroxy-1,5,7,11,15,15-hexamethyl-8-methylidene-3,6,14-trioxo-4-oxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadecane-5-carboxylate

> <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       2.846  -3.013   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.346   3.664   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.216   3.016   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.375  -0.976   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.838  -1.849   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.350   2.516   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.524   1.228   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.572  -3.350   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.862  -1.267   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.350  -1.558   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.375   3.098   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.150  -0.716   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.415   1.352   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       6.879   4.553   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       3.854   3.971   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.342   3.680   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.326  -2.140   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -2.671  -0.472   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -0.601  -2.155   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       0.326   1.934   0.000  0.00  0.00           O+0
HETATM   35  H   UNK     0       5.870   1.643   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       7.887   3.389   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       8.391   0.770   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.334   0.770   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.366   4.262   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2   22                                                            
CONECT    3   22                                                            
CONECT    4   23                                                            
CONECT    5   24                                                            
CONECT    6   25                                                            
CONECT    7   26                                                            
CONECT    8   33                                                            
CONECT    9   10   14                                                       
CONECT   10    9   23                                                       
CONECT   11   12   13                                                       
CONECT   12    1   11   24                                                  
CONECT   13   11   23   25   35                                             
CONECT   14    9   22   27                                                  
CONECT   15   16   18   28   36                                             
CONECT   16   15   22   23   37                                             
CONECT   17   19   24   25   38                                             
CONECT   18   15   25   29   39                                             
CONECT   19   17   30   34                                                  
CONECT   20   24   26   31                                                  
CONECT   21   26   32   33                                                  
CONECT   22    2    3   14   16                                             
CONECT   23    4   10   13   16                                             
CONECT   24    5   12   17   20                                             
CONECT   25    6   13   17   18                                             
CONECT   26    7   20   21   34                                             
CONECT   27   14                                                            
CONECT   28   15                                                            
CONECT   29   18                                                            
CONECT   30   19                                                            
CONECT   31   20                                                            
CONECT   32   21                                                            
CONECT   33    8   21                                                       
CONECT   34   19   26                                                       
CONECT   35   13                                                            
CONECT   36   15                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

Synonyms

Not Available

Chemical Formula

C₂₆H₃₆O₈

Average Molecular Weight

476.566

Monoisotopic Molecular Weight

476.241018119

IUPAC Name

methyl (1S,2R,5S,7S,10S,11S,16S,17R,18S)-17,18-dihydroxy-1,5,7,11,15,15-hexamethyl-8-methylidene-3,6,14-trioxo-4-oxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadecane-5-carboxylate

Traditional Name

methyl (1S,2R,5S,7S,10S,11S,16S,17R,18S)-17,18-dihydroxy-1,5,7,11,15,15-hexamethyl-8-methylidene-3,6,14-trioxo-4-oxatetracyclo[8.8.0.0^{2,7}.0^{11,16}]octadecane-5-carboxylate

CAS Registry Number

Not Available

SMILES

[H][C@]1(O)[C@@]([H])(O)[C@@]2(C)[C@@]([H])(CC(=C)[C@@]3(C)C(=O)[C@](C)(OC(=O)[C@]23[H])C(=O)OC)[C@]2(C)CCC(=O)C(C)(C)[C@@]12[H]

InChI Identifier

InChI=1S/C26H36O8/c1-12-11-13-23(4)10-9-14(27)22(2,3)16(23)15(28)18(29)25(13,6)17-19(30)34-26(7,21(32)33-8)20(31)24(12,17)5/h13,15-18,28-29H,1,9-11H2,2-8H3/t13-,15+,16+,17-,18+,23-,24+,25-,26-/m0/s1

InChI Key

GVJWSIBVKQDNPN-GQNBQQLRSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.096 g/L	ALOGPS
logP	1.85	ALOGPS
logP	2.65	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	13.5	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	127.2 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	120.6 m³·mol⁻¹	ChemAxon
Polarizability	50.25 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_3) - 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)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		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

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Fungi	Ascomycota	1	Human Feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

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

External Links

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 Terreustoxin A (MMDBc0025798)

MOL for #<Metabolite:0x000055b76dcd4950>

3D MOL for #<Metabolite:0x000055b76dcd4950>

3D SDF for #<Metabolite:0x000055b76dcd4950>

3D-SDF for #<Metabolite:0x000055b76dcd4950>

PDB for #<Metabolite:0x000055b76dcd4950>

3D PDB for #<Metabolite:0x000055b76dcd4950>

SMILES for #<Metabolite:0x000055b76dcd4950>

INCHI for #<Metabolite:0x000055b76dcd4950>

Structure for #<Metabolite:0x000055b76dcd4950>

3D Structure for #<Metabolite:0x000055b76dcd4950>