MiMeDB: Showing metabocard for Asporyzin C (MMDBc0009597)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:04:05 UTC

Update Date

2022-08-31 06:30:28 UTC

Metabolite ID

MMDBc0009597

Metabolite Identification

Common Name

Asporyzin C

Description

Asporyzin C belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review very few articles have been published on Asporyzin C.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104042D          

 36 40  0  0  1  0            999 V2000
   -1.6997    3.7078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9569    2.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1133    1.7236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304    0.2202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4725    0.2457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7141    0.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6030   -0.0924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2028    1.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0616    1.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8396   -0.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7000    2.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9365    2.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6034   -0.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188    2.3126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7623    0.8848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3669   -0.0924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1643    2.0022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3525    1.8552    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2981    0.9174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5549    1.2756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1871    0.0999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8255    1.2300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0490    0.0999    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9846    0.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2593    3.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0620    0.9174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4780    0.7251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2414    1.0377    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3753   -0.0471    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125   -0.2127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5617    3.4506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0271    1.5498    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1982    2.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5890    1.5426    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1730    1.7349    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7015    0.6048    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 12 11  1  0  0  0  0
 14  8  2  0  0  0  0
 15  8  1  0  0  0  0
 16 13  1  0  0  0  0
 18 11  1  0  0  0  0
 18 17  1  0  0  0  0
 19  9  2  0  0  0  0
 20 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 10  2  0  0  0  0
 21 19  1  0  0  0  0
 22 12  1  0  0  0  0
 23 13  1  0  0  0  0
 24 20  2  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 14  1  0  0  0  0
 26  3  1  6  0  0  0
 26 15  1  1  0  0  0
 26 22  1  0  0  0  0
 26 23  1  0  0  0  0
 27  4  1  6  0  0  0
 27 16  1  0  0  0  0
 27 22  1  0  0  0  0
 28  5  1  1  0  0  0
 28 18  1  0  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29 21  1  0  0  0  0
 29 24  1  0  0  0  0
 23 30  1  6  0  0  0
 31 25  1  0  0  0  0
 32  8  1  0  0  0  0
 33 14  1  0  0  0  0
 18 34  1  6  0  0  0
 22 35  1  1  0  0  0
 23 36  1  1  0  0  0
M  END


  Mrv1652305152104042D          

 36 40  0  0  1  0            999 V2000
   -1.6997    3.7078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9569    2.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1133    1.7236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304    0.2202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4725    0.2457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7141    0.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6030   -0.0924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2028    1.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0616    1.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8396   -0.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7000    2.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9365    2.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6034   -0.4050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8188    2.3126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7623    0.8848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3669   -0.0924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1643    2.0022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3525    1.8552    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2981    0.9174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5549    1.2756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1871    0.0999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8255    1.2300    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0490    0.0999    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9846    0.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2593    3.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0620    0.9174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4780    0.7251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2414    1.0377    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3753   -0.0471    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125   -0.2127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5617    3.4506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0271    1.5498    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1982    2.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5890    1.5426    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1730    1.7349    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7015    0.6048    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 12 11  1  0  0  0  0
 14  8  2  0  0  0  0
 15  8  1  0  0  0  0
 16 13  1  0  0  0  0
 18 11  1  0  0  0  0
 18 17  1  0  0  0  0
 19  9  2  0  0  0  0
 20 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 10  2  0  0  0  0
 21 19  1  0  0  0  0
 22 12  1  0  0  0  0
 23 13  1  0  0  0  0
 24 20  2  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 14  1  0  0  0  0
 26  3  1  6  0  0  0
 26 15  1  1  0  0  0
 26 22  1  0  0  0  0
 26 23  1  0  0  0  0
 27  4  1  6  0  0  0
 27 16  1  0  0  0  0
 27 22  1  0  0  0  0
 28  5  1  1  0  0  0
 28 18  1  0  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29 21  1  0  0  0  0
 29 24  1  0  0  0  0
 23 30  1  6  0  0  0
 31 25  1  0  0  0  0
 32  8  1  0  0  0  0
 33 14  1  0  0  0  0
 18 34  1  6  0  0  0
 22 35  1  1  0  0  0
 23 36  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0009597

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(C[C@]1(C)[C@@]([H])(O)CC[C@@]2(C)[C@@]1([H])CC[C@@]1([H])CC3=C(NC4=CC=CC=C34)[C@]21C)=C(\[H])C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C28H39NO2/c1-25(2,31)14-8-15-26(3)22-12-11-18-17-20-19-9-6-7-10-21(19)29-24(20)28(18,5)27(22,4)16-13-23(26)30/h6-10,14,18,22-23,29-31H,11-13,15-17H2,1-5H3/b14-8+/t18-,22-,23-,26-,27-,28+/m0/s1

> <INCHI_KEY>
UCZDOMMSHDUFIK-TWQPBVKTSA-N

> <FORMULA>
C28H39NO2

> <MOLECULAR_WEIGHT>
421.625

> <EXACT_MASS>
421.2980795

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
50.674634005336884

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,12S,15R,16S,17S,20S)-16-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,16,20-trimethyl-3-azapentacyclo[10.8.0.0^{2,10}.0^{4,9}.0^{15,20}]icosa-2(10),4,6,8-tetraen-17-ol

> <ALOGPS_LOGP>
6.38

> <JCHEM_LOGP>
5.343107977666666

> <ALOGPS_LOGS>
-6.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.781309684726832

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.859191169077373

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6028927428817404

> <JCHEM_POLAR_SURFACE_AREA>
56.25

> <JCHEM_REFRACTIVITY>
128.13790000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.60e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,12S,15R,16S,17S,20S)-16-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,16,20-trimethyl-3-azapentacyclo[10.8.0.0^{2,10}.0^{4,9}.0^{15,20}]icosa-2(10),4,6,8-tetraen-17-ol

> <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      -3.173   6.921   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.653   4.797   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.211   3.217   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.977   0.411   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.615   0.459   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.666   1.354   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.459  -0.172   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.245   2.954   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.448   2.296   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.034  -0.756   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.173   4.406   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.748   3.822   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.126  -0.756   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.529   4.317   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.423   1.652   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.552  -0.172   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.907   3.737   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.391   3.463   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.023   1.712   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.636   2.381   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.816   0.186   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.541   2.296   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.091   0.186   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.571   1.268   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.351   5.619   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.116   1.712   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.759   1.354   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.184   1.937   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       6.301  -0.088   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0      -1.517  -0.397   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -1.048   6.441   0.000  0.00  0.00           O+0
HETATM   32  H   UNK     0      -3.784   2.893   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.370   5.331   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.966   2.880   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.323   3.238   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.309   1.129   0.000  0.00  0.00           H+0
CONECT    1   25                                                            
CONECT    2   25                                                            
CONECT    3   26                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6    7    9                                                       
CONECT    7    6   10                                                       
CONECT    8   14   15   32                                                  
CONECT    9    6   19                                                       
CONECT   10    7   21                                                       
CONECT   11   12   18                                                       
CONECT   12   11   22                                                       
CONECT   13   16   23                                                       
CONECT   14    8   25   33                                                  
CONECT   15    8   26                                                       
CONECT   16   13   27                                                       
CONECT   17   18   20                                                       
CONECT   18   11   17   28   34                                             
CONECT   19    9   20   21                                                  
CONECT   20   17   19   24                                                  
CONECT   21   10   19   29                                                  
CONECT   22   12   26   27   35                                             
CONECT   23   13   26   30   36                                             
CONECT   24   20   28   29                                                  
CONECT   25    1    2   14   31                                             
CONECT   26    3   15   22   23                                             
CONECT   27    4   16   22   28                                             
CONECT   28    5   18   24   27                                             
CONECT   29   21   24                                                       
CONECT   30   23                                                            
CONECT   31   25                                                            
CONECT   32    8                                                            
CONECT   33   14                                                            
CONECT   34   18                                                            
CONECT   35   22                                                            
CONECT   36   23                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₉NO₂

Average Mass

421.625

Monoisotopic Mass

421.2980795

IUPAC Name

(1S,12S,15R,16S,17S,20S)-16-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,16,20-trimethyl-3-azapentacyclo[10.8.0.0^{2,10}.0^{4,9}.0^{15,20}]icosa-2(10),4,6,8-tetraen-17-ol

Traditional Name

(1S,12S,15R,16S,17S,20S)-16-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,16,20-trimethyl-3-azapentacyclo[10.8.0.0^{2,10}.0^{4,9}.0^{15,20}]icosa-2(10),4,6,8-tetraen-17-ol

CAS Registry Number

Not Available

SMILES

[H]\C(C[C@]1(C)[C@@]([H])(O)CC[C@@]2(C)[C@@]1([H])CC[C@@]1([H])CC3=C(NC4=CC=CC=C34)[C@]21C)=C(\[H])C(C)(C)O

InChI Identifier

InChI=1S/C28H39NO2/c1-25(2,31)14-8-15-26(3)22-12-11-18-17-20-19-9-6-7-10-21(19)29-24(20)28(18,5)27(22,4)16-13-23(26)30/h6-10,14,18,22-23,29-31H,11-13,15-17H2,1-5H3/b14-8+/t18-,22-,23-,26-,27-,28+/m0/s1

InChI Key

UCZDOMMSHDUFIK-TWQPBVKTSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
3-alkylindole
Indole
Indole or derivatives
Benzenoid
Cyclic alcohol
Pyrrole
Tertiary alcohol
Heteroaromatic compound
Secondary alcohol
Organoheterocyclic compound
Azacycle
Alcohol
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen 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	8.6e-05 g/L	ALOGPS
logP	6.38	ALOGPS
logP	5.34	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	16.86	ChemAxon
pKa (Strongest Basic)	-0.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	56.25 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	128.14 m³·mol⁻¹	ChemAxon
Polarizability	50.67 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	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

Metabolic Reactions

Not Available

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	Source Sub-type	Species	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

26367350

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46945861

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 Asporyzin C (MMDBc0009597)

MOL for #<Metabolite:0x00007fecd1e2bdd0>

3D MOL for #<Metabolite:0x00007fecd1e2bdd0>

3D SDF for #<Metabolite:0x00007fecd1e2bdd0>

3D-SDF for #<Metabolite:0x00007fecd1e2bdd0>

PDB for #<Metabolite:0x00007fecd1e2bdd0>

3D PDB for #<Metabolite:0x00007fecd1e2bdd0>

SMILES for #<Metabolite:0x00007fecd1e2bdd0>

INCHI for #<Metabolite:0x00007fecd1e2bdd0>

Structure for #<Metabolite:0x00007fecd1e2bdd0>

3D Structure for #<Metabolite:0x00007fecd1e2bdd0>