MiMeDB: Showing metabocard for Aureobasidin S2a (MMDBc0020611)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 10:45:23 UTC

Update Date

2022-08-31 06:47:02 UTC

Metabolite ID

MMDBc0020611

Metabolite Identification

Common Name

Aureobasidin S2a

Description

(3S,6R,9R,12S,15S,18S,21R,24S,29aS)-21-benzyl-3,15-bis[(2S)-butan-2-yl]-1,7,19-trihydroxy-24-[(4-hydroxyphenyl)methyl]-12-(2-hydroxypropan-2-yl)-5,11,17,23-tetramethyl-9-(2-methylpropyl)-6,18-bis(propan-2-yl)-3H,4H,5H,6H,9H,10H,11H,12H,13H,15H,16H,17H,18H,21H,22H,23H,24H,25H,27H,28H,29H,29aH-pyrrolo[1,2-m]1-oxa-4,7,10,13,16,19,22,25-octaazacycloheptacosane-4,10,13,16,22,25-hexone belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. Based on a literature review very few articles have been published on (3S,6R,9R,12S,15S,18S,21R,24S,29aS)-21-benzyl-3,15-bis[(2S)-butan-2-yl]-1,7,19-trihydroxy-24-[(4-hydroxyphenyl)methyl]-12-(2-hydroxypropan-2-yl)-5,11,17,23-tetramethyl-9-(2-methylpropyl)-6,18-bis(propan-2-yl)-3H,4H,5H,6H,9H,10H,11H,12H,13H,15H,16H,17H,18H,21H,22H,23H,24H,25H,27H,28H,29H,29aH-pyrrolo[1,2-m]1-oxa-4,7,10,13,16,19,22,25-octaazacycloheptacosane-4,10,13,16,22,25-hexone.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152112452D          

 91 94  0  0  1  0            999 V2000
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M  END


  Mrv1652305152112452D          

 91 94  0  0  1  0            999 V2000
   -1.2576    0.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
MMDBc0020611

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)[C@]1([H])OC(=O)[C@@]([H])(N(C)C(=O)[C@@]([H])(CC(C)C)N=C(O)[C@@]([H])(C(C)C)N(C)C(=O)[C@@]([H])(N=C(O)[C@]2([H])CCCN2C(=O)[C@]([H])(CC2=CC=C(O)C=C2)N(C)C(=O)[C@@]([H])(CC2=CC=CC=C2)N=C(O)[C@]([H])(C(C)C)N(C)C1=O)[C@@]([H])(C)CC)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C60H92N8O12/c1-17-37(9)46-57(76)65(14)47(35(5)6)52(71)61-42(31-34(3)4)55(74)67(16)50(60(11,12)79)59(78)80-49(38(10)18-2)58(77)66(15)48(36(7)8)53(72)62-43(32-39-23-20-19-21-24-39)54(73)64(13)45(33-40-26-28-41(69)29-27-40)56(75)68-30-22-25-44(68)51(70)63-46/h19-21,23-24,26-29,34-38,42-50,69,79H,17-18,22,25,30-33H2,1-16H3,(H,61,71)(H,62,72)(H,63,70)/t37-,38-,42+,43+,44-,45-,46-,47+,48-,49-,50+/m0/s1

> <INCHI_KEY>
AZWNOPVZWSHWAA-URQULGPXSA-N

> <FORMULA>
C60H92N8O12

> <MOLECULAR_WEIGHT>
1117.44

> <EXACT_MASS>
1116.683470434

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
172

> <JCHEM_AVERAGE_POLARIZABILITY>
120.89510451895445

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6R,9R,12S,15S,18S,21R,24S,29aS)-21-benzyl-3,15-bis[(2S)-butan-2-yl]-1,7,19-trihydroxy-24-[(4-hydroxyphenyl)methyl]-12-(2-hydroxypropan-2-yl)-5,11,17,23-tetramethyl-9-(2-methylpropyl)-6,18-bis(propan-2-yl)-3H,4H,5H,6H,9H,10H,11H,12H,13H,15H,16H,17H,18H,21H,22H,23H,24H,25H,27H,28H,29H,29aH-pyrrolo[1,2-m]1-oxa-4,7,10,13,16,19,22,25-octaazacycloheptacosane-4,10,13,16,22,25-hexone

> <ALOGPS_LOGP>
4.66

> <JCHEM_LOGP>
7.879229361000002

> <ALOGPS_LOGS>
-5.28

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.495121513881555

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.003828211601321

> <JCHEM_PKA_STRONGEST_BASIC>
1.6151658153131048

> <JCHEM_POLAR_SURFACE_AREA>
266.08

> <JCHEM_REFRACTIVITY>
303.24539999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.84e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6R,9R,12S,15S,18S,21R,24S,29aS)-21-benzyl-3,15-bis[(2S)-butan-2-yl]-1,7,19-trihydroxy-24-[(4-hydroxyphenyl)methyl]-12-(2-hydroxypropan-2-yl)-6,18-diisopropyl-5,11,17,23-tetramethyl-9-(2-methylpropyl)-3H,6H,9H,12H,15H,18H,21H,24H,27H,28H,29H,29aH-pyrrolo[1,2-m]1-oxa-4,7,10,13,16,19,22,25-octaazacycloheptacosane-4,10,13,16,22,25-hexone

> <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      -2.348   0.883   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.531 -12.768   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.430   0.421   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.819  -2.217   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.740   0.652   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.792   1.493   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.941 -13.101   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.850 -14.757   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.101  -2.120   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.091  -9.004   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.182  -4.649   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.095  -4.026   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.434  -8.565   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.456  -3.794   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.296  -9.332   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.700  -5.791   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.702   0.151   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.554 -11.617   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.482 -15.603   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.170 -16.410   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.438 -14.064   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.949  -7.466   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.816 -15.678   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.083 -13.332   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.013  -5.927   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -7.167  -8.590   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -7.704 -11.203   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.675  -8.280   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -9.213 -10.893   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.226  -8.244   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.340  -1.235   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.417 -13.407   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -5.173 -10.362   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.863  -1.010   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.769   0.342   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.417 -13.326   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.746  -1.388   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.068 -10.156   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -2.772 -14.139   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -6.681 -10.052   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -9.698  -9.432   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.772  -2.666   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -1.374 -11.868   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -4.569  -5.391   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -4.150  -9.211   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.435  -2.195   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       1.255  -1.119   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       2.461 -12.118   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.560  -9.846   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       6.472  -6.113   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -4.002  -3.959   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       2.763  -1.429   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       0.937 -12.343   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -2.685 -11.060   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       5.728  -3.874   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -4.636  -7.749   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -1.080  -1.463   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       4.537 -10.997   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       6.429  -7.652   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       7.827  -5.381   0.000  0.00  0.00           C+0
HETATM   61  N   UNK     0       3.249  -2.891   0.000  0.00  0.00           N+0
HETATM   62  N   UNK     0      -0.019 -11.136   0.000  0.00  0.00           N+0
HETATM   63  N   UNK     0      -2.478  -3.735   0.000  0.00  0.00           N+0
HETATM   64  N   UNK     0      -2.642  -9.521   0.000  0.00  0.00           N+0
HETATM   65  N   UNK     0       0.232  -2.271   0.000  0.00  0.00           N+0
HETATM   66  N   UNK     0       3.028 -10.687   0.000  0.00  0.00           N+0
HETATM   67  N   UNK     0       5.161  -5.305   0.000  0.00  0.00           N+0
HETATM   68  N   UNK     0      -3.613  -6.598   0.000  0.00  0.00           N+0
HETATM   69  O   UNK     0     -11.207  -9.121   0.000  0.00  0.00           O+0
HETATM   70  O   UNK     0      -4.958  -2.752   0.000  0.00  0.00           O+0
HETATM   71  O   UNK     0       3.786  -0.278   0.000  0.00  0.00           O+0
HETATM   72  O   UNK     0       0.370 -13.774   0.000  0.00  0.00           O+0
HETATM   73  O   UNK     0      -4.040 -11.792   0.000  0.00  0.00           O+0
HETATM   74  O   UNK     0       7.108  -3.189   0.000  0.00  0.00           O+0
HETATM   75  O   UNK     0      -6.038  -8.385   0.000  0.00  0.00           O+0
HETATM   76  O   UNK     0      -1.036   0.076   0.000  0.00  0.00           O+0
HETATM   77  O   UNK     0       5.022 -12.458   0.000  0.00  0.00           O+0
HETATM   78  O   UNK     0       7.740  -8.459   0.000  0.00  0.00           O+0
HETATM   79  O   UNK     0       8.559  -6.736   0.000  0.00  0.00           O+0
HETATM   80  O   UNK     0       5.074  -8.384   0.000  0.00  0.00           O+0
HETATM   81  H   UNK     0      -5.057  -0.581   0.000  0.00  0.00           H+0
HETATM   82  H   UNK     0       8.577 -10.466   0.000  0.00  0.00           H+0
HETATM   83  H   UNK     0       6.296  -2.442   0.000  0.00  0.00           H+0
HETATM   84  H   UNK     0      -0.062 -12.675   0.000  0.00  0.00           H+0
HETATM   85  H   UNK     0      -5.646  -4.290   0.000  0.00  0.00           H+0
HETATM   86  H   UNK     0      -3.664 -10.672   0.000  0.00  0.00           H+0
HETATM   87  H   UNK     0      -3.789  -2.927   0.000  0.00  0.00           H+0
HETATM   88  H   UNK     0      -0.254  -0.809   0.000  0.00  0.00           H+0
HETATM   89  H   UNK     0       3.985 -11.894   0.000  0.00  0.00           H+0
HETATM   90  H   UNK     0       6.582  -8.694   0.000  0.00  0.00           H+0
HETATM   91  H   UNK     0       6.516  -4.573   0.000  0.00  0.00           H+0
CONECT    1   17                                                            
CONECT    2   18                                                            
CONECT    3   34                                                            
CONECT    4   34                                                            
CONECT    5   35                                                            
CONECT    6   35                                                            
CONECT    7   36                                                            
CONECT    8   36                                                            
CONECT    9   37                                                            
CONECT   10   38                                                            
CONECT   11   60                                                            
CONECT   12   60                                                            
CONECT   13   64                                                            
CONECT   14   65                                                            
CONECT   15   66                                                            
CONECT   16   67                                                            
CONECT   17    1   37                                                       
CONECT   18    2   38                                                       
CONECT   19   20   21                                                       
CONECT   20   19   23                                                       
CONECT   21   19   24                                                       
CONECT   22   25   30                                                       
CONECT   23   20   39                                                       
CONECT   24   21   39                                                       
CONECT   25   22   44                                                       
CONECT   26   28   40                                                       
CONECT   27   29   40                                                       
CONECT   28   26   41                                                       
CONECT   29   27   41                                                       
CONECT   30   22   68                                                       
CONECT   31   34   42                                                       
CONECT   32   39   43                                                       
CONECT   33   40   45                                                       
CONECT   34    3    4   31                                                  
CONECT   35    5    6   47                                                  
CONECT   36    7    8   48                                                  
CONECT   37    9   17   46   81                                             
CONECT   38   10   18   49   82                                             
CONECT   39   23   24   32                                                  
CONECT   40   26   27   33                                                  
CONECT   41   28   29   69                                                  
CONECT   42   31   55   61   83                                             
CONECT   43   32   54   62   84                                             
CONECT   44   25   51   68   85                                             
CONECT   45   33   56   64   86                                             
CONECT   46   37   57   63   87                                             
CONECT   47   35   52   65   88                                             
CONECT   48   36   53   66   89                                             
CONECT   49   38   58   80   90                                             
CONECT   50   59   60   67   91                                             
CONECT   51   44   63   70                                                  
CONECT   52   47   61   71                                                  
CONECT   53   48   62   72                                                  
CONECT   54   43   64   73                                                  
CONECT   55   42   67   74                                                  
CONECT   56   45   68   75                                                  
CONECT   57   46   65   76                                                  
CONECT   58   49   66   77                                                  
CONECT   59   50   78   80                                                  
CONECT   60   11   12   50   79                                             
CONECT   61   42   52                                                       
CONECT   62   43   53                                                       
CONECT   63   46   51                                                       
CONECT   64   13   45   54                                                  
CONECT   65   14   47   57                                                  
CONECT   66   15   48   58                                                  
CONECT   67   16   50   55                                                  
CONECT   68   30   44   56                                                  
CONECT   69   41                                                            
CONECT   70   51                                                            
CONECT   71   52                                                            
CONECT   72   53                                                            
CONECT   73   54                                                            
CONECT   74   55                                                            
CONECT   75   56                                                            
CONECT   76   57                                                            
CONECT   77   58                                                            
CONECT   78   59                                                            
CONECT   79   60                                                            
CONECT   80   49   59                                                       
CONECT   81   37                                                            
CONECT   82   38                                                            
CONECT   83   42                                                            
CONECT   84   43                                                            
CONECT   85   44                                                            
CONECT   86   45                                                            
CONECT   87   46                                                            
CONECT   88   47                                                            
CONECT   89   48                                                            
CONECT   90   49                                                            
CONECT   91   50                                                            
MASTER        0    0    0    0    0    0    0    0   91    0  188    0
END

Synonyms

Not Available

Molecular Formula

C₆₀H₉₂N₈O₁₂

Average Mass

1117.44

Monoisotopic Mass

1116.683470434

IUPAC Name

Traditional Name

(3S,6R,9R,12S,15S,18S,21R,24S,29aS)-21-benzyl-3,15-bis[(2S)-butan-2-yl]-1,7,19-trihydroxy-24-[(4-hydroxyphenyl)methyl]-12-(2-hydroxypropan-2-yl)-6,18-diisopropyl-5,11,17,23-tetramethyl-9-(2-methylpropyl)-3H,6H,9H,12H,15H,18H,21H,24H,27H,28H,29H,29aH-pyrrolo[1,2-m]1-oxa-4,7,10,13,16,19,22,25-octaazacycloheptacosane-4,10,13,16,22,25-hexone

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)[C@]1([H])OC(=O)[C@@]([H])(N(C)C(=O)[C@@]([H])(CC(C)C)N=C(O)[C@@]([H])(C(C)C)N(C)C(=O)[C@@]([H])(N=C(O)[C@]2([H])CCCN2C(=O)[C@]([H])(CC2=CC=C(O)C=C2)N(C)C(=O)[C@@]([H])(CC2=CC=CC=C2)N=C(O)[C@]([H])(C(C)C)N(C)C1=O)[C@@]([H])(C)CC)C(C)(C)O

InChI Identifier

InChI=1S/C60H92N8O12/c1-17-37(9)46-57(76)65(14)47(35(5)6)52(71)61-42(31-34(3)4)55(74)67(16)50(60(11,12)79)59(78)80-49(38(10)18-2)58(77)66(15)48(36(7)8)53(72)62-43(32-39-23-20-19-21-24-39)54(73)64(13)45(33-40-26-28-41(69)29-27-40)56(75)68-30-22-25-44(68)51(70)63-46/h19-21,23-24,26-29,34-38,42-50,69,79H,17-18,22,25,30-33H2,1-16H3,(H,61,71)(H,62,72)(H,63,70)/t37-,38-,42+,43+,44-,45-,46-,47+,48-,49-,50+/m0/s1

InChI Key

AZWNOPVZWSHWAA-URQULGPXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Macrolide
Macrolactam
Alpha-amino acid ester
Alpha-amino acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrrolidine
Lactone
Lactam
Carboxylic acid ester
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	0.0058 g/L	ALOGPS
logP	4.66	ALOGPS
logP	7.88	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4	ChemAxon
pKa (Strongest Basic)	1.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	266.08 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	303.25 m³·mol⁻¹	ChemAxon
Polarizability	120.9 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Not Available

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

Metabolic Reactions

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		Metabolic reconstruction

Exposure Sources

Source Type	Activity	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

78442893

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588891

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

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 Aureobasidin S2a (MMDBc0020611)

MOL for #<Metabolite:0x00007f5394e33e30>

3D MOL for #<Metabolite:0x00007f5394e33e30>

3D SDF for #<Metabolite:0x00007f5394e33e30>

3D-SDF for #<Metabolite:0x00007f5394e33e30>

PDB for #<Metabolite:0x00007f5394e33e30>

3D PDB for #<Metabolite:0x00007f5394e33e30>

SMILES for #<Metabolite:0x00007f5394e33e30>

INCHI for #<Metabolite:0x00007f5394e33e30>

Structure for #<Metabolite:0x00007f5394e33e30>

3D Structure for #<Metabolite:0x00007f5394e33e30>