MiMeDB: Showing metabocard for Malformin B4 (MMDBc0013506)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:48:29 UTC

Update Date

2022-08-31 06:36:20 UTC

MiMeDB ID

MMDBc0013506

Metabolite Identification

Common Name

Malformin B4

Description

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152106482D          

 42 43  0  0  1  0            999 V2000
    3.5483    2.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8226   -0.6708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2478   -4.0842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654   -4.4458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5791    1.5923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9157   -2.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2481    2.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9990   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3634   -0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2474   -2.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4522   -3.8659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7635    1.4681    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5455   -1.3120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1870   -0.2307    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0710   -2.2190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2434   -3.0678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4633    0.6996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7219   -1.2639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7354   -0.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6509   -2.8058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6492    0.8335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5977   -0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6873   -1.6706    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8511    0.6247    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4193   -3.1061    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5037   -2.0596    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1525    0.2462    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8983   -1.2159    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
  8  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11  4  1  0  0  0  0
 12  5  1  6  0  0  0
 12  7  1  0  0  0  0
 13  6  1  1  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  1  0  0  0
 17 12  1  1  0  0  0
 18 13  1  6  0  0  0
 19 14  1  0  0  0  0
 20 15  1  0  0  0  0
 21 16  1  0  0  0  0
 22 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 15  1  0  0  0  0
 24 19  2  0  0  0  0
 25 14  1  0  0  0  0
 25 22  2  0  0  0  0
 26 16  1  0  0  0  0
 26 20  2  0  0  0  0
 27 18  1  0  0  0  0
 27 21  2  0  0  0  0
 28 17  1  0  0  0  0
 28 23  2  0  0  0  0
 19 29  1  4  0  0  0
 20 30  1  4  0  0  0
 21 31  1  4  0  0  0
 22 32  1  4  0  0  0
 23 33  1  4  0  0  0
 34  9  1  0  0  0  0
 35 10  1  0  0  0  0
 35 34  1  0  0  0  0
 12 36  1  1  0  0  0
 13 37  1  6  0  0  0
 14 38  1  6  0  0  0
 15 39  1  6  0  0  0
 16 40  1  1  0  0  0
 17 41  1  1  0  0  0
 18 42  1  6  0  0  0
M  END


  Mrv1652305152106482D          

 42 43  0  0  1  0            999 V2000
    3.5483    2.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8226   -0.6708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2478   -4.0842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654   -4.4458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5791    1.5923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9157   -2.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2481    2.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9990   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3634   -0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2474   -2.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4522   -3.8659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7635    1.4681    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5455   -1.3120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1870   -0.2307    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0710   -2.2190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2434   -3.0678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4633    0.6996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7219   -1.2639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7354   -0.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6509   -2.8058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9807   -2.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6492    0.8335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5977   -0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6873   -1.6706    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8511    0.6247    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4193   -3.1061    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5037   -2.0596    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1525    0.2462    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5147   -0.5763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1974   -3.4951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4961   -3.3418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6109    1.6576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3697   -0.1573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2530   -0.7310    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3010   -1.5546    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.0637    2.2365    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3691   -1.3601    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8274   -0.9732    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7309   -2.9707    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0346   -2.2696    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1631   -0.0688    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8983   -1.2159    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
  8  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11  4  1  0  0  0  0
 12  5  1  6  0  0  0
 12  7  1  0  0  0  0
 13  6  1  1  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  1  0  0  0
 17 12  1  1  0  0  0
 18 13  1  6  0  0  0
 19 14  1  0  0  0  0
 20 15  1  0  0  0  0
 21 16  1  0  0  0  0
 22 17  1  0  0  0  0
 23 18  1  0  0  0  0
 24 15  1  0  0  0  0
 24 19  2  0  0  0  0
 25 14  1  0  0  0  0
 25 22  2  0  0  0  0
 26 16  1  0  0  0  0
 26 20  2  0  0  0  0
 27 18  1  0  0  0  0
 27 21  2  0  0  0  0
 28 17  1  0  0  0  0
 28 23  2  0  0  0  0
 19 29  1  4  0  0  0
 20 30  1  4  0  0  0
 21 31  1  4  0  0  0
 22 32  1  4  0  0  0
 23 33  1  4  0  0  0
 34  9  1  0  0  0  0
 35 10  1  0  0  0  0
 35 34  1  0  0  0  0
 12 36  1  1  0  0  0
 13 37  1  6  0  0  0
 14 38  1  6  0  0  0
 15 39  1  6  0  0  0
 16 40  1  1  0  0  0
 17 41  1  1  0  0  0
 18 42  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0013506

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)[C@]1([H])N=C(O)[C@]([H])(N=C(O)[C@@]([H])(N=C(O)[C@@]2([H])CSSC[C@@]([H])(N=C1O)C(O)=N2)C(C)C)[C@]([H])(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C23H39N5O5S2/c1-7-12(5)17-22(32)25-14-9-34-35-10-15(24-19(14)29)20(30)26-16(11(3)4)21(31)27-18(13(6)8-2)23(33)28-17/h11-18H,7-10H2,1-6H3,(H,24,29)(H,25,32)(H,26,30)(H,27,31)(H,28,33)/t12-,13+,14+,15+,16-,17-,18+/m0/s1

> <INCHI_KEY>
PIXYPRXKMCTYQV-RJBILPHGSA-N

> <FORMULA>
C23H39N5O5S2

> <MOLECULAR_WEIGHT>
529.72

> <EXACT_MASS>
529.239261724

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
55.0701035194063

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4S,7R,10S,13S)-7-[(2R)-butan-2-yl]-4-[(2S)-butan-2-yl]-10-(propan-2-yl)-15,16-dithia-2,5,8,11,19-pentaazabicyclo[11.4.2]nonadeca-2,5,8,11,18-pentaene-3,6,9,12,18-pentol

> <ALOGPS_LOGP>
2.60

> <JCHEM_LOGP>
0.005563501819209803

> <ALOGPS_LOGS>
-3.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
2.228091605964535

> <JCHEM_PKA_STRONGEST_ACIDIC>
-8.864184874335283

> <JCHEM_PKA_STRONGEST_BASIC>
14.617004831264536

> <JCHEM_POLAR_SURFACE_AREA>
162.95

> <JCHEM_REFRACTIVITY>
139.1615

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.96e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,7R,10S,13S)-7-[(2R)-butan-2-yl]-4-[(2S)-butan-2-yl]-10-isopropyl-15,16-dithia-2,5,8,11,19-pentaazabicyclo[11.4.2]nonadeca-2,5,8,11,18-pentaene-3,6,9,12,18-pentol

> <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       6.624   5.377   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.735  -1.252   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.929  -7.624   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.349  -8.299   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.548   2.972   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.043  -3.825   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.063   3.943   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.198  -1.163   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.678  -0.341   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.462  -4.052   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.444  -7.216   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.025   2.740   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.352  -2.449   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.216  -0.431   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.999  -4.142   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.054  -5.727   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.465   1.306   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.814  -2.359   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.239  -1.581   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.082  -5.238   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.431  -5.036   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.945   1.556   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.582  -0.837   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       3.150  -3.119   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       3.455   1.166   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0       4.516  -5.798   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0       8.407  -3.844   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       7.751   0.460   0.000  0.00  0.00           N+0
HETATM   29  O   UNK     0       4.694  -1.076   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.235  -6.524   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       8.393  -6.238   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       4.874   3.094   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      10.023  -0.294   0.000  0.00  0.00           O+0
HETATM   34  S   UNK     0      -0.472  -1.365   0.000  0.00  0.00           S+0
HETATM   35  S   UNK     0      -0.562  -2.902   0.000  0.00  0.00           S+0
HETATM   36  H   UNK     0       7.586   4.175   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      11.889  -2.539   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.545  -1.817   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.364  -5.545   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.665  -4.237   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.904  -0.128   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       7.277  -2.270   0.000  0.00  0.00           H+0
CONECT    1    7                                                            
CONECT    2    8                                                            
CONECT    3   11                                                            
CONECT    4   11                                                            
CONECT    5   12                                                            
CONECT    6   13                                                            
CONECT    7    1   12                                                       
CONECT    8    2   13                                                       
CONECT    9   14   34                                                       
CONECT   10   15   35                                                       
CONECT   11    3    4   16                                                  
CONECT   12    5    7   17   36                                             
CONECT   13    6    8   18   37                                             
CONECT   14    9   19   25   38                                             
CONECT   15   10   20   24   39                                             
CONECT   16   11   21   26   40                                             
CONECT   17   12   22   28   41                                             
CONECT   18   13   23   27   42                                             
CONECT   19   14   24   29                                                  
CONECT   20   15   26   30                                                  
CONECT   21   16   27   31                                                  
CONECT   22   17   25   32                                                  
CONECT   23   18   28   33                                                  
CONECT   24   15   19                                                       
CONECT   25   14   22                                                       
CONECT   26   16   20                                                       
CONECT   27   18   21                                                       
CONECT   28   17   23                                                       
CONECT   29   19                                                            
CONECT   30   20                                                            
CONECT   31   21                                                            
CONECT   32   22                                                            
CONECT   33   23                                                            
CONECT   34    9   35                                                       
CONECT   35   10   34                                                       
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   14                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   86    0
END

Synonyms

Not Available

Chemical Formula

C₂₃H₃₉N₅O₅S₂

Average Molecular Weight

529.72

Monoisotopic Molecular Weight

529.239261724

IUPAC Name

(1S,4S,7R,10S,13S)-7-[(2R)-butan-2-yl]-4-[(2S)-butan-2-yl]-10-(propan-2-yl)-15,16-dithia-2,5,8,11,19-pentaazabicyclo[11.4.2]nonadeca-2,5,8,11,18-pentaene-3,6,9,12,18-pentol

Traditional Name

(1S,4S,7R,10S,13S)-7-[(2R)-butan-2-yl]-4-[(2S)-butan-2-yl]-10-isopropyl-15,16-dithia-2,5,8,11,19-pentaazabicyclo[11.4.2]nonadeca-2,5,8,11,18-pentaene-3,6,9,12,18-pentol

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)[C@]1([H])N=C(O)[C@]([H])(N=C(O)[C@@]([H])(N=C(O)[C@@]2([H])CSSC[C@@]([H])(N=C1O)C(O)=N2)C(C)C)[C@]([H])(C)CC

InChI Identifier

InChI=1S/C23H39N5O5S2/c1-7-12(5)17-22(32)25-14-9-34-35-10-15(24-19(14)29)20(30)26-16(11(3)4)21(31)27-18(13(6)8-2)23(33)28-17/h11-18H,7-10H2,1-6H3,(H,24,29)(H,25,32)(H,26,30)(H,27,31)(H,28,33)/t12-,13+,14+,15+,16-,17-,18+/m0/s1

InChI Key

PIXYPRXKMCTYQV-RJBILPHGSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.08 g/L	ALOGPS
logP	2.6	ALOGPS
logP	0.0056	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	-8.9	ChemAxon
pKa (Strongest Basic)	14.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	162.95 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	139.16 m³·mol⁻¹	ChemAxon
Polarizability	55.07 Å³	ChemAxon
Number of Rings	2	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_1_5) - 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
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 Malformin B4 (MMDBc0013506)

MOL for #<Metabolite:0x00007f0920068fd0>

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