MiMeDB: Showing metabocard for UDP-N-acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alanine (MMDBc0056361)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 20:23:43 UTC

Update Date

2022-08-12 20:09:42 UTC

Metabolite ID

MMDBc0056361

Metabolite Identification

Common Name

UDP-N-acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alanine

Description

UDP-N-acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alaninate(3-) 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 UDP-N-acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alaninate(3-).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172222232D          

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M  CHG  3  51  -1  52  -1  53  -1
M  END


  Mrv1652306172222232D          

 92 94  0  0  1  0            999 V2000
    8.5737    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2881    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1703    8.5519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    1.7605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964    6.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6939    5.4005    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781    6.8433    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3910    7.7796    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6563    6.9155    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
 10  9  1  0  0  0  0
 12  7  1  0  0  0  0
 13 11  2  0  0  0  0
 16  1  1  1  0  0  0
 17  2  1  6  0  0  0
 18  3  1  6  0  0  0
 19  4  1  1  0  0  0
 20  5  1  4  0  0  0
 21  8  1  0  0  0  0
 22  9  1  0  0  0  0
 23 14  1  1  0  0  0
 24 15  1  1  0  0  0
 25 10  1  0  0  0  0
 26 11  1  0  0  0  0
 28 24  1  0  0  0  0
 29 23  1  0  0  0  0
 30 28  1  0  0  0  0
 31 27  1  0  0  0  0
 31 29  1  0  0  0  0
 32 16  1  0  0  0  0
 33 17  1  0  0  0  0
 34 19  1  0  0  0  0
 35 21  1  0  0  0  0
 36 30  1  0  0  0  0
 37 18  1  0  0  0  0
 38 22  1  0  0  0  0
 39 27  1  0  0  0  0
 41 12  1  0  0  0  0
 42 17  1  0  0  0  0
 42 34  2  0  0  0  0
 43 16  1  0  0  0  0
 43 35  2  0  0  0  0
 44 18  1  0  0  0  0
 44 32  2  0  0  0  0
 45 20  2  0  0  0  0
 27 45  1  6  0  0  0
 21 46  1  6  0  0  0
 46 25  2  0  0  0  0
 22 47  1  1  0  0  0
 47 33  2  0  0  0  0
 48 26  2  0  0  0  0
 48 40  1  0  0  0  0
 49 13  1  0  0  0  0
 36 49  1  1  0  0  0
 49 40  1  0  0  0  0
 50 14  1  0  0  0  0
 51 20  1  0  0  0  0
 25 52  1  4  0  0  0
 53 26  1  0  0  0  0
 28 54  1  6  0  0  0
 29 55  1  6  0  0  0
 30 56  1  6  0  0  0
 32 57  1  4  0  0  0
 33 58  1  4  0  0  0
 34 59  1  4  0  0  0
 35 60  1  4  0  0  0
 61 37  2  0  0  0  0
 62 37  1  0  0  0  0
 63 38  2  0  0  0  0
 64 38  1  0  0  0  0
 65 40  2  0  0  0  0
 70 15  1  0  0  0  0
 71 19  1  0  0  0  0
 31 71  1  6  0  0  0
 72 24  1  0  0  0  0
 72 36  1  0  0  0  0
 73 23  1  0  0  0  0
 73 39  1  0  0  0  0
 39 74  1  6  0  0  0
 76 66  1  0  0  0  0
 76 67  2  0  0  0  0
 76 70  1  0  0  0  0
 76 75  1  0  0  0  0
 77 68  1  0  0  0  0
 77 69  2  0  0  0  0
 77 74  1  0  0  0  0
 77 75  1  0  0  0  0
 16 78  1  6  0  0  0
 17 79  1  1  0  0  0
 18 80  1  1  0  0  0
 19 81  1  6  0  0  0
 21 82  1  6  0  0  0
 22 83  1  1  0  0  0
 23 84  1  6  0  0  0
 24 85  1  6  0  0  0
 27 86  1  1  0  0  0
 28 87  1  1  0  0  0
 29 88  1  1  0  0  0
 30 89  1  1  0  0  0
 31 90  1  6  0  0  0
 36 91  1  6  0  0  0
 39 92  1  1  0  0  0
M  CHG  3  51  -1  52  -1  53  -1
M  END
> <DATABASE_ID>
MMDBc0056361

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(O[C@@]1([H])[C@]([H])(O)[C@@]([H])(CO)O[C@]([H])(OP(O)(=O)OP(O)(=O)OC[C@@]2([H])O[C@@]([H])(N3C=CC([O-])=NC3=O)[C@]([H])(O)[C@]2([H])O)[C@]1([H])N=C(C)[O-])C(O)=N[C@@]([H])(C)C(O)=N[C@]([H])(CCC([O-])=N[C@@]([H])(CCCCN)C(O)=N[C@]([H])(C)C(O)=N[C@]([H])(C)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C40H65N9O26P2/c1-16(32(57)44-18(3)37(61)62)43-35(60)21(8-6-7-12-41)46-25(52)10-9-22(38(63)64)47-33(58)17(2)42-34(59)19(4)71-31-27(45-20(5)51)39(73-23(14-50)29(31)55)74-77(68,69)75-76(66,67)70-15-24-28(54)30(56)36(72-24)49-13-11-26(53)48-40(49)65/h11,13,16-19,21-24,27-31,36,39,50,54-56H,6-10,12,14-15,41H2,1-5H3,(H,42,59)(H,43,60)(H,44,57)(H,45,51)(H,46,52)(H,47,58)(H,61,62)(H,63,64)(H,66,67)(H,68,69)(H,48,53,65)/p-3/t16-,17+,18-,19-,21+,22-,23-,24-,27-,28-,29-,30-,31-,36-,39-/m1/s1

> <INCHI_KEY>
PFMVORMCVGOQKR-XNCOKRRHSA-K

> <FORMULA>
C40H62N9O26P2

> <MOLECULAR_WEIGHT>
1146.922

> <EXACT_MASS>
1146.329767888

> <JCHEM_ACCEPTOR_COUNT>
31

> <JCHEM_ATOM_COUNT>
139

> <JCHEM_AVERAGE_POLARIZABILITY>
105.06782558267744

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
-3

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4R)-N-[(1S)-5-amino-1-{[(1R)-1-{[(1R)-1-carboxyethyl]-C-hydroxycarbonimidoyl}ethyl]-C-hydroxycarbonimidoyl}pentyl]-4-carboxy-4-{[(2S)-2-{[(2R)-2-{[(2R,3R,4R,5S,6R)-2-({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-5-hydroxy-6-(hydroxymethyl)-3-[(1-oxidoethylidene)amino]oxan-4-yl]oxy}-1-hydroxypropylidene]amino}-1-hydroxypropylidene]amino}butanecarboximidate

> <JCHEM_LOGP>
-2.4772900316666657

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
2.6293939141278457

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.6927540209592973

> <JCHEM_POLAR_SURFACE_AREA>
568.4500000000003

> <JCHEM_REFRACTIVITY>
282.57920000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
30

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-N-[(1S)-5-amino-1-{[(1R)-1-{[(1R)-1-carboxyethyl]-C-hydroxycarbonimidoyl}ethyl]-C-hydroxycarbonimidoyl}pentyl]-4-carboxy-4-{[(2S)-2-{[(2R)-2-{[(2R,3R,4R,5S,6R)-2-[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-5-hydroxy-6-(hydroxymethyl)-3-[(1-oxidoethylidene)amino]oxan-4-yl]oxy}-1-hydroxypropylidene]amino}-1-hydroxypropylidene]amino}butanecarboximidate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0      16.004   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.670   6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.779  15.481   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.874  14.235   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.004   6.160   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.153  16.887   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.421  11.685   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.897  13.150   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      14.670   3.850   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.437  13.150   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      17.338   6.930   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -3.716  15.803   0.000  0.00  0.00           C+0
HETATM   41  N   UNK     0       5.335   0.000   0.000  0.00  0.00           N+0
HETATM   42  N   UNK     0       5.335  -4.620   0.000  0.00  0.00           N+0
HETATM   43  N   UNK     0      13.337   1.540   0.000  0.00  0.00           N+0
HETATM   44  N   UNK     0      16.004   4.620   0.000  0.00  0.00           N+0
HETATM   45  N   UNK     0       4.001   2.310   0.000  0.00  0.00           N+0
HETATM   46  N   UNK     0      10.669   0.000   0.000  0.00  0.00           N+0
HETATM   47  N   UNK     0       9.336  -5.390   0.000  0.00  0.00           N+0
HETATM   48  N   UNK     0      -4.621  17.048   0.000  0.00  0.00           N+0
HETATM   49  N   UNK     0      -4.343  14.396   0.000  0.00  0.00           N+0
HETATM   50  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O-1
HETATM   52  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O-1
HETATM   53  O   UNK     0      -7.058  18.133   0.000  0.00  0.00           O-1
HETATM   54  O   UNK     0       0.043  11.209   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0      -0.992  14.396   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      13.337   4.620   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      12.003   3.850   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      18.672   6.160   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0      17.338   8.470   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      13.337  -4.620   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0      12.003  -6.930   0.000  0.00  0.00           O+0
HETATM   65  O   UNK     0      -2.185  15.964   0.000  0.00  0.00           O+0
HETATM   66  O   UNK     0      -2.874   6.930   0.000  0.00  0.00           O+0
HETATM   67  O   UNK     0       0.206   6.930   0.000  0.00  0.00           O+0
HETATM   68  O   UNK     0      -0.770   3.286   0.000  0.00  0.00           O+0
HETATM   69  O   UNK     0       0.770   5.954   0.000  0.00  0.00           O+0
HETATM   70  O   UNK     0      -1.334   8.470   0.000  0.00  0.00           O+0
HETATM   71  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   72  O   UNK     0      -3.913  11.685   0.000  0.00  0.00           O+0
HETATM   73  O   UNK     0      -0.000   1.540   0.000  0.00  0.00           O+0
HETATM   74  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   75  O   UNK     0      -1.334   5.390   0.000  0.00  0.00           O+0
HETATM   76  P   UNK     0      -1.334   6.930   0.000  0.00  0.00           P+0
HETATM   77  P   UNK     0      -0.000   4.620   0.000  0.00  0.00           P+0
HETATM   78  H   UNK     0      16.004   3.080   0.000  0.00  0.00           H+0
HETATM   79  H   UNK     0       8.002  -6.160   0.000  0.00  0.00           H+0
HETATM   80  H   UNK     0      16.004   7.700   0.000  0.00  0.00           H+0
HETATM   81  H   UNK     0       4.001  -3.850   0.000  0.00  0.00           H+0
HETATM   82  H   UNK     0      10.669   3.080   0.000  0.00  0.00           H+0
HETATM   83  H   UNK     0      12.003  -3.850   0.000  0.00  0.00           H+0
HETATM   84  H   UNK     0      -0.000  -1.540   0.000  0.00  0.00           H+0
HETATM   85  H   UNK     0      -1.295  10.081   0.000  0.00  0.00           H+0
HETATM   86  H   UNK     0       4.001   0.770   0.000  0.00  0.00           H+0
HETATM   87  H   UNK     0      -0.333  12.774   0.000  0.00  0.00           H+0
HETATM   88  H   UNK     0       2.667  -1.540   0.000  0.00  0.00           H+0
HETATM   89  H   UNK     0      -2.597  14.522   0.000  0.00  0.00           H+0
HETATM   90  H   UNK     0       1.334   0.770   0.000  0.00  0.00           H+0
HETATM   91  H   UNK     0      -4.958  12.909   0.000  0.00  0.00           H+0
HETATM   92  H   UNK     0       2.667   3.080   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6    7    8                                                       
CONECT    7    6   12                                                       
CONECT    8    6   21                                                       
CONECT    9   10   22                                                       
CONECT   10    9   25                                                       
CONECT   11   13   26                                                       
CONECT   12    7   41                                                       
CONECT   13   11   49                                                       
CONECT   14   23   50                                                       
CONECT   15   24   70                                                       
CONECT   16    1   32   43   78                                             
CONECT   17    2   33   42   79                                             
CONECT   18    3   37   44   80                                             
CONECT   19    4   34   71   81                                             
CONECT   20    5   45   51                                                  
CONECT   21    8   35   46   82                                             
CONECT   22    9   38   47   83                                             
CONECT   23   14   29   73   84                                             
CONECT   24   15   28   72   85                                             
CONECT   25   10   46   52                                                  
CONECT   26   11   48   53                                                  
CONECT   27   31   39   45   86                                             
CONECT   28   24   30   54   87                                             
CONECT   29   23   31   55   88                                             
CONECT   30   28   36   56   89                                             
CONECT   31   27   29   71   90                                             
CONECT   32   16   44   57                                                  
CONECT   33   17   47   58                                                  
CONECT   34   19   42   59                                                  
CONECT   35   21   43   60                                                  
CONECT   36   30   49   72   91                                             
CONECT   37   18   61   62                                                  
CONECT   38   22   63   64                                                  
CONECT   39   27   73   74   92                                             
CONECT   40   48   49   65                                                  
CONECT   41   12                                                            
CONECT   42   17   34                                                       
CONECT   43   16   35                                                       
CONECT   44   18   32                                                       
CONECT   45   20   27                                                       
CONECT   46   21   25                                                       
CONECT   47   22   33                                                       
CONECT   48   26   40                                                       
CONECT   49   13   36   40                                                  
CONECT   50   14                                                            
CONECT   51   20                                                            
CONECT   52   25                                                            
CONECT   53   26                                                            
CONECT   54   28                                                            
CONECT   55   29                                                            
CONECT   56   30                                                            
CONECT   57   32                                                            
CONECT   58   33                                                            
CONECT   59   34                                                            
CONECT   60   35                                                            
CONECT   61   37                                                            
CONECT   62   37                                                            
CONECT   63   38                                                            
CONECT   64   38                                                            
CONECT   65   40                                                            
CONECT   66   76                                                            
CONECT   67   76                                                            
CONECT   68   77                                                            
CONECT   69   77                                                            
CONECT   70   15   76                                                       
CONECT   71   19   31                                                       
CONECT   72   24   36                                                       
CONECT   73   23   39                                                       
CONECT   74   39   77                                                       
CONECT   75   76   77                                                       
CONECT   76   66   67   70   75                                             
CONECT   77   68   69   74   75                                             
CONECT   78   16                                                            
CONECT   79   17                                                            
CONECT   80   18                                                            
CONECT   81   19                                                            
CONECT   82   21                                                            
CONECT   83   22                                                            
CONECT   84   23                                                            
CONECT   85   24                                                            
CONECT   86   27                                                            
CONECT   87   28                                                            
CONECT   88   29                                                            
CONECT   89   30                                                            
CONECT   90   31                                                            
CONECT   91   36                                                            
CONECT   92   39                                                            
MASTER        0    0    0    0    0    0    0    0   92    0  188    0
END

Synonyms

Value	Source
UDP-N-Acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alanine	ChEBI
UDP-N-Acetyl-a-D-muramoyl-L-alanyl-g-D-glutamyl-L-lysyl-D-alanyl-D-alanine	Generator
UDP-N-Acetyl-α-D-muramoyl-L-alanyl-γ-D-glutamyl-L-lysyl-D-alanyl-D-alanine	Generator
UDP-N-Acetyl-a-D-muramoyl-L-alanyl-g-D-glutamyl-L-lysyl-D-alanyl-D-alaninate(3-)	Generator
UDP-N-Acetyl-a-D-muramoyl-L-alanyl-g-D-glutamyl-L-lysyl-D-alanyl-D-alaninic acid(3-)	Generator
UDP-N-Acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alaninic acid(3-)	Generator
UDP-N-Acetyl-α-D-muramoyl-L-alanyl-γ-D-glutamyl-L-lysyl-D-alanyl-D-alaninate(3-)	Generator
UDP-N-Acetyl-α-D-muramoyl-L-alanyl-γ-D-glutamyl-L-lysyl-D-alanyl-D-alaninic acid(3-)	Generator

Molecular Formula

C₄₀H₆₂N₉O₂₆P₂

Average Mass

1146.922

Monoisotopic Mass

1146.329767888

IUPAC Name

(4R)-N-[(1S)-5-amino-1-{[(1R)-1-{[(1R)-1-carboxyethyl]-C-hydroxycarbonimidoyl}ethyl]-C-hydroxycarbonimidoyl}pentyl]-4-carboxy-4-{[(2S)-2-{[(2R)-2-{[(2R,3R,4R,5S,6R)-2-({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxo-1,2-dihydropyrimidin-1-yl)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-5-hydroxy-6-(hydroxymethyl)-3-[(1-oxidoethylidene)amino]oxan-4-yl]oxy}-1-hydroxypropylidene]amino}-1-hydroxypropylidene]amino}butanecarboximidate

Traditional Name

(4R)-N-[(1S)-5-amino-1-{[(1R)-1-{[(1R)-1-carboxyethyl]-C-hydroxycarbonimidoyl}ethyl]-C-hydroxycarbonimidoyl}pentyl]-4-carboxy-4-{[(2S)-2-{[(2R)-2-{[(2R,3R,4R,5S,6R)-2-[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxido-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-5-hydroxy-6-(hydroxymethyl)-3-[(1-oxidoethylidene)amino]oxan-4-yl]oxy}-1-hydroxypropylidene]amino}-1-hydroxypropylidene]amino}butanecarboximidate

CAS Registry Number

Not Available

SMILES

[H][C@](C)(O[C@@]1([H])[C@]([H])(O)[C@@]([H])(CO)O[C@]([H])(OP(O)(=O)OP(O)(=O)OC[C@@]2([H])O[C@@]([H])(N3C=CC([O-])=NC3=O)[C@]([H])(O)[C@]2([H])O)[C@]1([H])N=C(C)[O-])C(O)=N[C@@]([H])(C)C(O)=N[C@]([H])(CCC([O-])=N[C@@]([H])(CCCCN)C(O)=N[C@]([H])(C)C(O)=N[C@]([H])(C)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C40H65N9O26P2/c1-16(32(57)44-18(3)37(61)62)43-35(60)21(8-6-7-12-41)46-25(52)10-9-22(38(63)64)47-33(58)17(2)42-34(59)19(4)71-31-27(45-20(5)51)39(73-23(14-50)29(31)55)74-77(68,69)75-76(66,67)70-15-24-28(54)30(56)36(72-24)49-13-11-26(53)48-40(49)65/h11,13,16-19,21-24,27-31,36,39,50,54-56H,6-10,12,14-15,41H2,1-5H3,(H,42,59)(H,43,60)(H,44,57)(H,45,51)(H,46,52)(H,47,58)(H,61,62)(H,63,64)(H,66,67)(H,68,69)(H,48,53,65)/p-3/t16-,17+,18-,19-,21+,22-,23-,24-,27-,28-,29-,30-,31-,36-,39-/m1/s1

InChI Key

PFMVORMCVGOQKR-XNCOKRRHSA-K

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
Pyrimidine nucleotide sugar
Pyrimidine ribonucleoside diphosphate
Pentose phosphate
Pentose-5-phosphate
N-acyl-alpha-hexosamine
Glutamine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Glycosyl compound
N-glycosyl compound
Alanine or derivatives
Alpha-amino acid or derivatives
Monosaccharide phosphate
Organic pyrophosphate
N-substituted-alpha-amino acid
Pyrimidone
Fatty acyl
Dicarboxylic acid or derivatives
Fatty amide
Hydropyrimidine
Alkyl phosphate
Monosaccharide
N-acyl-amine
Organic phosphoric acid derivative
Pyrimidine
Oxane
Phosphoric acid ester
Acetamide
Vinylogous amide
Tetrahydrofuran
Heteroaromatic compound
Amino acid
Amino acid or derivatives
Secondary alcohol
Carboxamide group
Carboxylic acid salt
Secondary carboxylic acid amide
Urea
Lactam
Organoheterocyclic compound
Carboxylic acid
Oxacycle
Dialkyl ether
Azacycle
Ether
Primary alcohol
Organooxygen compound
Alcohol
Organic salt
Organic nitrogen compound
Primary aliphatic amine
Organic oxygen compound
Organopnictogen compound
Organic oxide
Carbonyl group
Organonitrogen compound
Amine
Hydrocarbon derivative
Primary amine
Organic anion
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

UDP-N-acetylmuramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alanine(3-) (CHEBI:70758 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	-2.5	ChemAxon
pKa (Strongest Acidic)	1.69	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	31	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	568.45 Å²	ChemAxon
Rotatable Bond Count	30	ChemAxon
Refractivity	282.58 m³·mol⁻¹	ChemAxon
Polarizability	105.07 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

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

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
Bacteria	Firmicutes	80	Human ; Human feces; Cattle

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

34448470

KEGG Compound ID

Not Available

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

86289103

PDB ID

Not Available

ChEBI ID

70758

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for UDP-N-acetyl-alpha-D-muramoyl-L-alanyl-gamma-D-glutamyl-L-lysyl-D-alanyl-D-alanine (MMDBc0056361)

MOL for #<Metabolite:0x00007f1240f05a88>

3D MOL for #<Metabolite:0x00007f1240f05a88>

3D SDF for #<Metabolite:0x00007f1240f05a88>

3D-SDF for #<Metabolite:0x00007f1240f05a88>

PDB for #<Metabolite:0x00007f1240f05a88>

3D PDB for #<Metabolite:0x00007f1240f05a88>

SMILES for #<Metabolite:0x00007f1240f05a88>

INCHI for #<Metabolite:0x00007f1240f05a88>

Structure for #<Metabolite:0x00007f1240f05a88>

3D Structure for #<Metabolite:0x00007f1240f05a88>