MiMeDB: Showing metabocard for Staphylopeptide A (MMDBc0004024)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 22:12:21 UTC

Update Date

2022-08-31 06:21:45 UTC

Metabolite ID

MMDBc0004024

Metabolite Identification

Common Name

Staphylopeptide A

Description

Staphylopeptide A belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. Based on a literature review very few articles have been published on Staphylopeptide A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152100122D          

 37 37  0  0  1  0            999 V2000
   -2.5559   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8250   -3.0789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -1.9520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -3.0789    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -4.5079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -3.7934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -2.7770    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -1.5395    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -3.0789    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -2.7770    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  3  1  0  0  0  0
  9  6  1  0  0  0  0
 10  4  1  0  0  0  0
 10  5  1  0  0  0  0
 11  6  1  1  0  0  0
 12  7  1  1  0  0  0
 13  8  1  1  0  0  0
 14  7  1  0  0  0  0
 15  8  1  0  0  0  0
 16 10  1  1  0  0  0
 17 11  1  0  0  0  0
 18 12  1  0  0  0  0
 19 13  1  0  0  0  0
 20 16  1  0  0  0  0
 21 14  2  0  0  0  0
 22 15  2  0  0  0  0
 23 11  1  0  0  0  0
 23 18  2  0  0  0  0
 24 13  1  0  0  0  0
 24 17  2  0  0  0  0
 25 12  1  0  0  0  0
 25 20  2  0  0  0  0
 26 16  1  0  0  0  0
 26 19  2  0  0  0  0
 27 14  1  0  0  0  0
 28 15  1  0  0  0  0
 17 29  1  4  0  0  0
 18 30  1  4  0  0  0
 19 31  1  4  0  0  0
 20 32  1  4  0  0  0
 33 10  1  0  0  0  0
 11 34  1  6  0  0  0
 12 35  1  6  0  0  0
 13 36  1  6  0  0  0
 16 37  1  6  0  0  0
M  END


  Mrv1652305152100122D          

 37 37  0  0  1  0            999 V2000
   -2.5559   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8250   -3.0789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -1.9520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -3.0789    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.3645    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -4.5079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -3.7934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -2.7770    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664   -1.5395    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -3.0789    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -2.7770    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  3  1  0  0  0  0
  9  6  1  0  0  0  0
 10  4  1  0  0  0  0
 10  5  1  0  0  0  0
 11  6  1  1  0  0  0
 12  7  1  1  0  0  0
 13  8  1  1  0  0  0
 14  7  1  0  0  0  0
 15  8  1  0  0  0  0
 16 10  1  1  0  0  0
 17 11  1  0  0  0  0
 18 12  1  0  0  0  0
 19 13  1  0  0  0  0
 20 16  1  0  0  0  0
 21 14  2  0  0  0  0
 22 15  2  0  0  0  0
 23 11  1  0  0  0  0
 23 18  2  0  0  0  0
 24 13  1  0  0  0  0
 24 17  2  0  0  0  0
 25 12  1  0  0  0  0
 25 20  2  0  0  0  0
 26 16  1  0  0  0  0
 26 19  2  0  0  0  0
 27 14  1  0  0  0  0
 28 15  1  0  0  0  0
 17 29  1  4  0  0  0
 18 30  1  4  0  0  0
 19 31  1  4  0  0  0
 20 32  1  4  0  0  0
 33 10  1  0  0  0  0
 11 34  1  6  0  0  0
 12 35  1  6  0  0  0
 13 36  1  6  0  0  0
 16 37  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0004024

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H34N6O6/c1-5-10(4)16-20(32)25-12(7-14(21)27)18(30)23-11(6-9(2)3)17(29)24-13(8-15(22)28)19(31)26-16/h9-13,16H,5-8H2,1-4H3,(H2,21,27)(H2,22,28)(H,23,30)(H,24,29)(H,25,32)(H,26,31)/t10?,11-,12-,13-,16-/m0/s1

> <INCHI_KEY>
JVBWTKGWUGOPJG-IFUNHYKASA-N

> <FORMULA>
C20H34N6O6

> <MOLECULAR_WEIGHT>
454.528

> <EXACT_MASS>
454.253982839

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.08640949234564

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(2S,5S,8S,11S)-11-(butan-2-yl)-3,6,9,12-tetrahydroxy-8-[(C-hydroxycarbonimidoyl)methyl]-5-(2-methylpropyl)-1,4,7,10-tetraazacyclododeca-1(12),3,6,9-tetraen-2-yl]ethanimidic acid

> <ALOGPS_LOGP>
0.69

> <JCHEM_LOGP>
-2.8417286200726415

> <ALOGPS_LOGS>
-3.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
-0.5471870109415073

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.149220613053891

> <JCHEM_PKA_STRONGEST_BASIC>
13.324630331054088

> <JCHEM_POLAR_SURFACE_AREA>
218.51999999999995

> <JCHEM_REFRACTIVITY>
136.13500000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.27e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2S,5S,8S,11S)-3,6,9,12-tetrahydroxy-8-(C-hydroxycarbonimidoylmethyl)-5-(2-methylpropyl)-11-(sec-butyl)-1,4,7,10-tetraazacyclododeca-1(12),3,6,9-tetraen-2-yl]ethanimidic 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      -4.771  -6.724   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.645  -1.334   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.311  -3.644   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.771  -3.644   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.437  -5.954   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.977  -1.334   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.310  -7.081   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.311  -2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.437  -4.414   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.644  -2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.540  -5.747   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.310   1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.850  -7.081   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.104  -3.644   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.644  -3.644   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.540  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000  -5.747   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.104  -2.104   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      -3.080   0.000   0.000  0.00  0.00           N+0
HETATM   22  N   UNK     0       4.620  -5.747   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0       2.310  -1.334   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0       2.310  -4.414   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0      -0.770  -1.334   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0      -0.770  -4.414   0.000  0.00  0.00           N+0
HETATM   27  O   UNK     0      -3.080   2.667   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.620  -8.415   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       4.977  -4.414   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.310   1.334   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -0.770  -7.081   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -3.437  -1.334   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0      -4.771  -5.184   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.977  -2.874   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.540   0.000   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.080  -5.747   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.104  -5.184   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2    9                                                            
CONECT    3    9                                                            
CONECT    4   10                                                            
CONECT    5    1   10                                                       
CONECT    6    9   11                                                       
CONECT    7   12   14                                                       
CONECT    8   13   15                                                       
CONECT    9    2    3    6                                                  
CONECT   10    4    5   16   33                                             
CONECT   11    6   17   23   34                                             
CONECT   12    7   18   25   35                                             
CONECT   13    8   19   24   36                                             
CONECT   14    7   21   27                                                  
CONECT   15    8   22   28                                                  
CONECT   16   10   20   26   37                                             
CONECT   17   11   24   29                                                  
CONECT   18   12   23   30                                                  
CONECT   19   13   26   31                                                  
CONECT   20   16   25   32                                                  
CONECT   21   14                                                            
CONECT   22   15                                                            
CONECT   23   11   18                                                       
CONECT   24   13   17                                                       
CONECT   25   12   20                                                       
CONECT   26   16   19                                                       
CONECT   27   14                                                            
CONECT   28   15                                                            
CONECT   29   17                                                            
CONECT   30   18                                                            
CONECT   31   19                                                            
CONECT   32   20                                                            
CONECT   33   10                                                            
CONECT   34   11                                                            
CONECT   35   12                                                            
CONECT   36   13                                                            
CONECT   37   16                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   74    0
END

Synonyms

Not Available

Molecular Formula

C₂₀H₃₄N₆O₆

Average Mass

454.528

Monoisotopic Mass

454.253982839

IUPAC Name

2-[(2S,5S,8S,11S)-11-(butan-2-yl)-3,6,9,12-tetrahydroxy-8-[(C-hydroxycarbonimidoyl)methyl]-5-(2-methylpropyl)-1,4,7,10-tetraazacyclododeca-1(12),3,6,9-tetraen-2-yl]ethanimidic acid

Traditional Name

2-[(2S,5S,8S,11S)-3,6,9,12-tetrahydroxy-8-(C-hydroxycarbonimidoylmethyl)-5-(2-methylpropyl)-11-(sec-butyl)-1,4,7,10-tetraazacyclododeca-1(12),3,6,9-tetraen-2-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C20H34N6O6/c1-5-10(4)16-20(32)25-12(7-14(21)27)18(30)23-11(6-9(2)3)17(29)24-13(8-15(22)28)19(31)26-16/h9-13,16H,5-8H2,1-4H3,(H2,21,27)(H2,22,28)(H,23,30)(H,24,29)(H,25,32)(H,26,31)/t10?,11-,12-,13-,16-/m0/s1

InChI Key

JVBWTKGWUGOPJG-IFUNHYKASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Cyclic alpha peptide
Macrolactam
Alpha-amino acid or derivatives
Carboxamide group
Lactam
Primary carboxylic acid amide
Secondary carboxylic acid amide
Organoheterocyclic compound
Azacycle
Carbonyl group
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.13 g/L	ALOGPS
logP	0.69	ALOGPS
logP	-2.8	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	-1.1	ChemAxon
pKa (Strongest Basic)	13.32	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	218.52 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	136.14 m³·mol⁻¹	ChemAxon
Polarizability	46.09 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

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
Bacteria	Firmicutes	1		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

40256875

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584012

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 Staphylopeptide A (MMDBc0004024)

MOL for #<Metabolite:0x00007f46ab019a20>

3D MOL for #<Metabolite:0x00007f46ab019a20>

3D SDF for #<Metabolite:0x00007f46ab019a20>

3D-SDF for #<Metabolite:0x00007f46ab019a20>

PDB for #<Metabolite:0x00007f46ab019a20>

3D PDB for #<Metabolite:0x00007f46ab019a20>

SMILES for #<Metabolite:0x00007f46ab019a20>

INCHI for #<Metabolite:0x00007f46ab019a20>

Structure for #<Metabolite:0x00007f46ab019a20>

3D Structure for #<Metabolite:0x00007f46ab019a20>