MiMeDB: Showing metabocard for Aspersteroid A (MMDBc0028030)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 17:39:18 UTC

Update Date

2022-08-31 06:53:26 UTC

Metabolite ID

MMDBc0028030

Metabolite Identification

Common Name

Aspersteroid A

Description

Aspersteroid A belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position. Based on a literature review very few articles have been published on Aspersteroid A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152119392D          

 39 42  0  0  1  0            999 V2000
   -2.7965    5.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1616    4.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0946    2.9759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3377    3.6816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8218    4.0837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9620    3.3912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2423    2.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    4.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9665    3.8530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1278    2.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8106    2.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5256    3.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1498    3.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7135    3.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3665    1.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    4.3915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493    3.9658    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6010    3.6273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3571    3.3145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4620    2.5654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8059    3.0509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8983    2.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7104    1.9845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5544    1.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2741    2.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4182    3.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6180    2.9057    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1817    3.3413    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9907    1.2086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0226    1.0135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7291    2.7502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9246    4.1658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620    5.2685    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2774    3.0888    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9792    5.1556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6556    4.6172    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7837    3.7401    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4531    3.1590    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0862    2.2749    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  9  8  2  0  0  0  0
 11 10  1  0  0  0  0
 13  6  1  0  0  0  0
 14 12  1  0  0  0  0
 16  1  1  0  0  0  0
 16  8  1  0  0  0  0
 17  2  1  1  0  0  0
 17  9  1  0  0  0  0
 18  3  1  0  0  0  0
 18 16  1  0  0  0  0
 19 10  1  0  0  0  0
 19 17  1  6  0  0  0
 20 11  1  0  0  0  0
 21 12  1  0  0  0  0
 22 15  2  0  0  0  0
 23  7  1  0  0  0  0
 23 22  1  0  0  0  0
 24 15  1  0  0  0  0
 25 20  2  0  0  0  0
 25 21  1  0  0  0  0
 25 24  1  0  0  0  0
 26 18  1  0  0  0  0
 27  4  1  6  0  0  0
 27 13  1  0  0  0  0
 27 21  1  0  0  0  0
 27 22  1  0  0  0  0
 28  5  1  6  0  0  0
 28 14  1  0  0  0  0
 28 19  1  0  0  0  0
 28 20  1  0  0  0  0
 29 23  2  0  0  0  0
 30 24  2  0  0  0  0
 31 26  2  0  0  0  0
 32 26  1  0  0  0  0
 33  8  1  0  0  0  0
 34  9  1  0  0  0  0
 35 16  1  0  0  0  0
 17 36  1  6  0  0  0
 37 18  1  0  0  0  0
 19 38  1  1  0  0  0
 21 39  1  1  0  0  0
M  END


  Mrv1652305152119392D          

 39 42  0  0  1  0            999 V2000
   -2.7965    5.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1616    4.7300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0946    2.9759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3377    3.6816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8218    4.0837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9620    3.3912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2423    2.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    4.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9665    3.8530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1278    2.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8106    2.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5256    3.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1498    3.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7135    3.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3665    1.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    4.3915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493    3.9658    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6010    3.6273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3571    3.3145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4620    2.5654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8059    3.0509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8983    2.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7104    1.9845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5544    1.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2741    2.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4182    3.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6180    2.9057    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1817    3.3413    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9907    1.2086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0226    1.0135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7291    2.7502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9246    4.1658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620    5.2685    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2774    3.0888    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9792    5.1556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6556    4.6172    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7837    3.7401    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4531    3.1590    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0862    2.2749    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  9  8  2  0  0  0  0
 11 10  1  0  0  0  0
 13  6  1  0  0  0  0
 14 12  1  0  0  0  0
 16  1  1  0  0  0  0
 16  8  1  0  0  0  0
 17  2  1  1  0  0  0
 17  9  1  0  0  0  0
 18  3  1  0  0  0  0
 18 16  1  0  0  0  0
 19 10  1  0  0  0  0
 19 17  1  6  0  0  0
 20 11  1  0  0  0  0
 21 12  1  0  0  0  0
 22 15  2  0  0  0  0
 23  7  1  0  0  0  0
 23 22  1  0  0  0  0
 24 15  1  0  0  0  0
 25 20  2  0  0  0  0
 25 21  1  0  0  0  0
 25 24  1  0  0  0  0
 26 18  1  0  0  0  0
 27  4  1  6  0  0  0
 27 13  1  0  0  0  0
 27 21  1  0  0  0  0
 27 22  1  0  0  0  0
 28  5  1  6  0  0  0
 28 14  1  0  0  0  0
 28 19  1  0  0  0  0
 28 20  1  0  0  0  0
 29 23  2  0  0  0  0
 30 24  2  0  0  0  0
 31 26  2  0  0  0  0
 32 26  1  0  0  0  0
 33  8  1  0  0  0  0
 34  9  1  0  0  0  0
 35 16  1  0  0  0  0
 17 36  1  6  0  0  0
 37 18  1  0  0  0  0
 19 38  1  1  0  0  0
 21 39  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0028030

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(=C(\[H])[C@@]([H])(C)[C@@]1([H])CCC2=C3C(=O)C=C4C(=O)C=CC[C@]4(C)[C@@]3([H])CC[C@]12C)C([H])(C)C([H])(C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H36O4/c1-16(18(3)26(31)32)8-9-17(2)19-10-11-20-25-21(12-14-28(19,20)5)27(4)13-6-7-23(29)22(27)15-24(25)30/h6-9,15-19,21H,10-14H2,1-5H3,(H,31,32)/b9-8+/t16?,17-,18?,19-,21+,27-,28-/m1/s1

> <INCHI_KEY>
LENSREMNGPQVHG-UZDJOFILSA-N

> <FORMULA>
C28H36O4

> <MOLECULAR_WEIGHT>
436.592

> <EXACT_MASS>
436.261359639

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
49.759678288634575

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4E,6R)-6-[(1R,2R,14R,15R)-2,15-dimethyl-6,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7,10-trien-14-yl]-2,3-dimethylhept-4-enoic acid

> <ALOGPS_LOGP>
5.45

> <JCHEM_LOGP>
5.9341950216666675

> <ALOGPS_LOGS>
-5.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.117192742945836

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.839796848976434

> <JCHEM_PKA_STRONGEST_BASIC>
-6.391198427196136

> <JCHEM_POLAR_SURFACE_AREA>
71.44

> <JCHEM_REFRACTIVITY>
129.34329999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.37e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4E,6R)-6-[(1R,2R,14R,15R)-2,15-dimethyl-6,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7,10-trien-14-yl]-2,3-dimethylhept-4-enoic acid

> <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      -5.220   9.413   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.302   8.829   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.910   5.555   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.230   6.872   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.534   7.623   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.262   6.330   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.786   4.882   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.749   8.408   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.804   7.192   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.239   4.708   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.513   3.844   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.714   7.143   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.746   6.601   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.198   7.414   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.284   2.798   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.275   8.197   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.279   7.403   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.855   6.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.667   6.187   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.729   4.789   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.238   5.695   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.277   3.976   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.793   3.704   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.768   3.069   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.245   4.518   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.381   6.560   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.754   5.424   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.206   6.237   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.316   2.256   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       3.775   1.892   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -6.961   5.134   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -7.326   7.776   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0      -2.169   9.835   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.384   5.766   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.695   9.624   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.224   8.619   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.330   6.982   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.846   5.897   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.761   4.247   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6    7   13                                                       
CONECT    7    6   23                                                       
CONECT    8    9   16   33                                                  
CONECT    9    8   17   34                                                  
CONECT   10   11   19                                                       
CONECT   11   10   20                                                       
CONECT   12   14   21                                                       
CONECT   13    6   27                                                       
CONECT   14   12   28                                                       
CONECT   15   22   24                                                       
CONECT   16    1    8   18   35                                             
CONECT   17    2    9   19   36                                             
CONECT   18    3   16   26   37                                             
CONECT   19   10   17   28   38                                             
CONECT   20   11   25   28                                                  
CONECT   21   12   25   27   39                                             
CONECT   22   15   23   27                                                  
CONECT   23    7   22   29                                                  
CONECT   24   15   25   30                                                  
CONECT   25   20   21   24                                                  
CONECT   26   18   31   32                                                  
CONECT   27    4   13   21   22                                             
CONECT   28    5   14   19   20                                             
CONECT   29   23                                                            
CONECT   30   24                                                            
CONECT   31   26                                                            
CONECT   32   26                                                            
CONECT   33    8                                                            
CONECT   34    9                                                            
CONECT   35   16                                                            
CONECT   36   17                                                            
CONECT   37   18                                                            
CONECT   38   19                                                            
CONECT   39   21                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₆O₄

Average Mass

436.592

Monoisotopic Mass

436.261359639

IUPAC Name

(4E,6R)-6-[(1R,2R,14R,15R)-2,15-dimethyl-6,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7,10-trien-14-yl]-2,3-dimethylhept-4-enoic acid

Traditional Name

(4E,6R)-6-[(1R,2R,14R,15R)-2,15-dimethyl-6,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,7,10-trien-14-yl]-2,3-dimethylhept-4-enoic acid

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@@]([H])(C)[C@@]1([H])CCC2=C3C(=O)C=C4C(=O)C=CC[C@]4(C)[C@@]3([H])CC[C@]12C)C([H])(C)C([H])(C)C(O)=O

InChI Identifier

InChI=1S/C28H36O4/c1-16(18(3)26(31)32)8-9-17(2)19-10-11-20-25-21(12-14-28(19,20)5)27(4)13-6-7-23(29)22(27)15-24(25)30/h6-9,15-19,21H,10-14H2,1-5H3,(H,31,32)/b9-8+/t16?,17-,18?,19-,21+,27-,28-/m1/s1

InChI Key

LENSREMNGPQVHG-UZDJOFILSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergostane steroids

Alternative Parents

Substituents

Ergostane-skeleton
Steroid acid
7-oxosteroid
4-oxosteroid
Oxosteroid
Medium-chain fatty acid
Cyclohexenone
Methyl-branched fatty acid
Branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0024 g/L	ALOGPS
logP	5.45	ALOGPS
logP	5.93	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4.84	ChemAxon
pKa (Strongest Basic)	-6.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71.44 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	129.34 m³·mol⁻¹	ChemAxon
Polarizability	49.76 Å³	ChemAxon
Number of Rings	4	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_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	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

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	1	Human feces	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

70990746

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146684469

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 Aspersteroid A (MMDBc0028030)

MOL for #<Metabolite:0x00007f3dce89eeb0>

3D MOL for #<Metabolite:0x00007f3dce89eeb0>

3D SDF for #<Metabolite:0x00007f3dce89eeb0>

3D-SDF for #<Metabolite:0x00007f3dce89eeb0>

PDB for #<Metabolite:0x00007f3dce89eeb0>

3D PDB for #<Metabolite:0x00007f3dce89eeb0>

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INCHI for #<Metabolite:0x00007f3dce89eeb0>

Structure for #<Metabolite:0x00007f3dce89eeb0>

3D Structure for #<Metabolite:0x00007f3dce89eeb0>