MiMeDB: Showing metabocard for Versicotide A (MMDBc0015357)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:11:53 UTC

Update Date

2025-10-07 16:06:24 UTC

Metabolite ID

MMDBc0015357

Metabolite Identification

Common Name

Versicotide A

Description

Versicotide A is a secondary metabolite belonging to the class of polyketides. This compound has garnered attention in the field of organic chemistry due to its structural complexity and potential biological activities. Recent research has successfully achieved the first total synthesis of versicotide A, along with its analogs versicotide B and C, demonstrating the feasibility of producing these compounds in a laboratory setting (PMID:35519702 ). The synthesis of versicotide A not only provides insights into its chemical properties but also paves the way for further exploration of its biological functions. Polyketides, like versicotide A, are known for their diverse range of bioactivities, including antimicrobial and anticancer properties, making them valuable targets for drug discovery. Understanding the chemical structure and synthesis pathways of versicotide A could lead to the development of novel therapeutic agents. As research progresses, the biological implications of versicotide A and its derivatives will likely be elucidated, enhancing our understanding of their role in natural product chemistry and potential applications in medicine.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108112D          

 38 40  0  0  1  0            999 V2000
    9.1160    2.2842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8838    2.2842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -3.3958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9358    2.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3910   -3.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1097   -0.9241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1160   -1.7176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8839   -1.7176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902   -0.9241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5353   -0.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9161   -1.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0838   -1.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4645   -0.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6817    1.5828    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3181    1.5828    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4999   -2.5708    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7353   -0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4904   -1.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5095   -1.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2646   -0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7085    1.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3109   -2.4192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6591    0.2885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9124    1.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9875   -1.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2914    1.0270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0123   -1.9849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3407    0.2885    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0874    1.8808    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6890   -2.4192    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0501    1.5242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6089   -3.1885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4526    0.5142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0640    2.6918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4317   -2.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2474    0.8813    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7524    0.8813    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -1.7458    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  2  0  0  0  0
  9  7  2  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  1  0  0  0  0
 13  9  1  0  0  0  0
 14  1  1  1  0  0  0
 15  2  1  1  0  0  0
 16  3  1  1  0  0  0
 17 10  2  0  0  0  0
 18 11  2  0  0  0  0
 19 12  2  0  0  0  0
 19 17  1  0  0  0  0
 20 13  2  0  0  0  0
 20 18  1  0  0  0  0
 21 15  1  0  0  0  0
 22 16  1  0  0  0  0
 23 17  1  0  0  0  0
 24 14  1  0  0  0  0
 25 18  1  0  0  0  0
 26 14  1  0  0  0  0
 26 23  2  0  0  0  0
 27 19  1  4  0  0  0
 27 22  2  0  0  0  0
 28 20  1  4  0  0  0
 28 21  2  0  0  0  0
 29  4  1  0  0  0  0
 29 15  1  0  0  0  0
 29 24  1  0  0  0  0
 30  5  1  0  0  0  0
 30 16  1  0  0  0  0
 30 25  1  0  0  0  0
 31 21  1  0  0  0  0
 32 22  1  0  0  0  0
 23 33  1  4  0  0  0
 34 24  2  0  0  0  0
 35 25  2  0  0  0  0
 14 36  1  1  0  0  0
 15 37  1  1  0  0  0
 16 38  1  1  0  0  0
M  END


  Mrv1652305152108112D          

 38 40  0  0  1  0            999 V2000
    9.1160    2.2842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8838    2.2842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -3.3958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9358    2.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3910   -3.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1097   -0.9241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1160   -1.7176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8839   -1.7176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8902   -0.9241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5353   -0.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9161   -1.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0838   -1.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4645   -0.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6817    1.5828    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3181    1.5828    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4999   -2.5708    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7353   -0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4904   -1.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5095   -1.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2646   -0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7085    1.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3109   -2.4192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6591    0.2885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9124    1.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9875   -1.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2914    1.0270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0123   -1.9849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3407    0.2885    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0874    1.8808    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6890   -2.4192    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0501    1.5242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6089   -3.1885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4526    0.5142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0640    2.6918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4317   -2.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2474    0.8813    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7524    0.8813    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -1.7458    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  2  0  0  0  0
  9  7  2  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  1  0  0  0  0
 13  9  1  0  0  0  0
 14  1  1  1  0  0  0
 15  2  1  1  0  0  0
 16  3  1  1  0  0  0
 17 10  2  0  0  0  0
 18 11  2  0  0  0  0
 19 12  2  0  0  0  0
 19 17  1  0  0  0  0
 20 13  2  0  0  0  0
 20 18  1  0  0  0  0
 21 15  1  0  0  0  0
 22 16  1  0  0  0  0
 23 17  1  0  0  0  0
 24 14  1  0  0  0  0
 25 18  1  0  0  0  0
 26 14  1  0  0  0  0
 26 23  2  0  0  0  0
 27 19  1  4  0  0  0
 27 22  2  0  0  0  0
 28 20  1  4  0  0  0
 28 21  2  0  0  0  0
 29  4  1  0  0  0  0
 29 15  1  0  0  0  0
 29 24  1  0  0  0  0
 30  5  1  0  0  0  0
 30 16  1  0  0  0  0
 30 25  1  0  0  0  0
 31 21  1  0  0  0  0
 32 22  1  0  0  0  0
 23 33  1  4  0  0  0
 34 24  2  0  0  0  0
 35 25  2  0  0  0  0
 14 36  1  1  0  0  0
 15 37  1  1  0  0  0
 16 38  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015357

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C)N=C(O)C2=CC=CC=C2N=C(O)[C@]([H])(C)N(C)C(=O)C2=CC=CC=C2N=C(O)[C@]([H])(C)N(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H29N5O5/c1-14-24(34)29(4)15(2)21(31)28-20-13-9-7-11-18(20)25(35)30(5)16(3)22(32)27-19-12-8-6-10-17(19)23(33)26-14/h6-16H,1-5H3,(H,26,33)(H,27,32)(H,28,31)/t14-,15-,16-/m0/s1

> <INCHI_KEY>
SRHCZSHNDDEHKH-JYJNAYRXSA-N

> <FORMULA>
C25H29N5O5

> <MOLECULAR_WEIGHT>
479.537

> <EXACT_MASS>
479.216869054

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
48.7957474611653

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,15S,18S)-3,14,20-trihydroxy-4,5,15,16,18-pentamethyl-2,5,13,16,19-pentaazatricyclo[19.4.0.0^{7,12}]pentacosa-1(25),2,7,9,11,13,19,21,23-nonaene-6,17-dione

> <ALOGPS_LOGP>
2.04

> <JCHEM_LOGP>
1.9585353878241125

> <ALOGPS_LOGS>
-3.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
4.096010761723088

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.840870334003223

> <JCHEM_PKA_STRONGEST_BASIC>
5.037711437477432

> <JCHEM_POLAR_SURFACE_AREA>
138.39000000000001

> <JCHEM_REFRACTIVITY>
134.78450000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.59e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,15S,18S)-3,14,20-trihydroxy-4,5,15,16,18-pentamethyl-2,5,13,16,19-pentaazatricyclo[19.4.0.0^{7,12}]pentacosa-1(25),2,7,9,11,13,19,21,23-nonaene-6,17-dione

> <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      17.017   4.264   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.983   4.264   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.000  -6.339   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.947   5.025   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.930  -5.952   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.738  -1.725   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.683  -3.206   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.317  -3.206   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.262  -1.725   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.666  -0.619   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.177  -3.582   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.823  -3.582   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.334  -0.619   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.206   2.955   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.794   2.955   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.000  -4.799   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.172  -0.995   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.249  -2.476   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.751  -2.476   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.827  -0.995   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.656   1.917   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.514  -4.516   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.030   0.538   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.770   3.511   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.177  -3.705   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      17.344   1.917   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0      16.823  -3.705   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       9.969   0.538   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0      13.230   3.511   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0      12.486  -4.516   0.000  0.00  0.00           N+0
HETATM   31  O   UNK     0       9.427   2.845   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      16.070  -5.952   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      19.512   0.960   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      15.053   5.025   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      10.139  -4.843   0.000  0.00  0.00           O+0
HETATM   36  H   UNK     0      15.395   1.645   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      12.605   1.645   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      14.000  -3.259   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   15                                                            
CONECT    3   16                                                            
CONECT    4   29                                                            
CONECT    5   30                                                            
CONECT    6    8   10                                                       
CONECT    7    9   11                                                       
CONECT    8    6   12                                                       
CONECT    9    7   13                                                       
CONECT   10    6   17                                                       
CONECT   11    7   18                                                       
CONECT   12    8   19                                                       
CONECT   13    9   20                                                       
CONECT   14    1   24   26   36                                             
CONECT   15    2   21   29   37                                             
CONECT   16    3   22   30   38                                             
CONECT   17   10   19   23                                                  
CONECT   18   11   20   25                                                  
CONECT   19   12   17   27                                                  
CONECT   20   13   18   28                                                  
CONECT   21   15   28   31                                                  
CONECT   22   16   27   32                                                  
CONECT   23   17   26   33                                                  
CONECT   24   14   29   34                                                  
CONECT   25   18   30   35                                                  
CONECT   26   14   23                                                       
CONECT   27   19   22                                                       
CONECT   28   20   21                                                       
CONECT   29    4   15   24                                                  
CONECT   30    5   16   25                                                  
CONECT   31   21                                                            
CONECT   32   22                                                            
CONECT   33   23                                                            
CONECT   34   24                                                            
CONECT   35   25                                                            
CONECT   36   14                                                            
CONECT   37   15                                                            
CONECT   38   16                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₂₉N₅O₅

Average Mass

479.537

Monoisotopic Mass

479.216869054

IUPAC Name

(4S,15S,18S)-3,14,20-trihydroxy-4,5,15,16,18-pentamethyl-2,5,13,16,19-pentaazatricyclo[19.4.0.0^{7,12}]pentacosa-1(25),2,7,9,11,13,19,21,23-nonaene-6,17-dione

Traditional Name

(4S,15S,18S)-3,14,20-trihydroxy-4,5,15,16,18-pentamethyl-2,5,13,16,19-pentaazatricyclo[19.4.0.0^{7,12}]pentacosa-1(25),2,7,9,11,13,19,21,23-nonaene-6,17-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C)N=C(O)C2=CC=CC=C2N=C(O)[C@]([H])(C)N(C)C(=O)C2=CC=CC=C2N=C(O)[C@]([H])(C)N(C)C1=O

InChI Identifier

InChI=1S/C25H29N5O5/c1-14-24(34)29(4)15(2)21(31)28-20-13-9-7-11-18(20)25(35)30(5)16(3)22(32)27-19-12-8-6-10-17(19)23(33)26-14/h6-16H,1-5H3,(H,26,33)(H,27,32)(H,28,31)/t14-,15-,16-/m0/s1

InChI Key

SRHCZSHNDDEHKH-JYJNAYRXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
Macrolactam
Alpha-amino acid or derivatives
Benzenoid
Vinylogous amide
Tertiary carboxylic acid amide
Secondary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Carbonyl group
Organopnictogen 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	0.056 g/L	ALOGPS
logP	2.04	ALOGPS
logP	1.96	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	2.84	ChemAxon
pKa (Strongest Basic)	5.04	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	138.39 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	134.78 m³·mol⁻¹	ChemAxon
Polarizability	48.8 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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_3_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

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated 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

Other Exposures

Source Type	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

28185128

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53381962

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Versicotide A (MMDBc0015357)

MOL for #<Metabolite:0x00007f8de970b498>

3D MOL for #<Metabolite:0x00007f8de970b498>

3D SDF for #<Metabolite:0x00007f8de970b498>

3D-SDF for #<Metabolite:0x00007f8de970b498>

PDB for #<Metabolite:0x00007f8de970b498>

3D PDB for #<Metabolite:0x00007f8de970b498>

SMILES for #<Metabolite:0x00007f8de970b498>

INCHI for #<Metabolite:0x00007f8de970b498>

Structure for #<Metabolite:0x00007f8de970b498>

3D Structure for #<Metabolite:0x00007f8de970b498>