MiMeDB: Showing metabocard for S-(Formylmethyl)glutathione (MMDBc0030092)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-17 23:53:36 UTC

Update Date

2022-08-31 17:39:39 UTC

MiMeDB ID

MMDBc0030092

Metabolite Identification

Common Name

S-(Formylmethyl)glutathione

Description

S-(formylmethyl)glutathione belongs to the class of Peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. (inferred from compound structure)

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0060507
     RDKit          3D
S-(Formylmethyl)glutathione
 42 41  0  0  0  0  0  0  0  0999 V2000
    3.5795   -1.1424    0.8146 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2114   -0.6679   -0.4233 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2688    0.3939   -0.9679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8861   -0.1905   -1.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0298    0.9080   -1.7696 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4543    1.4614   -2.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    1.3637   -1.2067 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5741    0.9184    0.0220 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1274    2.0063    0.8973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4214    2.9465    0.1432 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9797    2.0921   -0.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5670    1.8113    1.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6339    1.2337    1.3784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4969   -0.2211   -0.1232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0547   -0.5052   -1.3863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8417   -0.9983    0.8439 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7456   -2.1061    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2628   -3.0974   -0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -2.9211   -0.8640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189   -4.2252   -0.6444 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5079   -0.0321   -0.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1648    0.3958   -1.1294 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9835    0.0911    1.1473 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0160   -0.3665    1.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9169   -1.9114    0.5540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2404   -1.5041   -1.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6945    0.7761   -1.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2000    1.2497   -0.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5095   -0.6835   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0428   -0.9674   -2.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2388    2.3840   -3.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2961    0.4719    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2999    2.6627    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4717    1.4762    1.8456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7032    2.7126   -0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9125    1.1172   -0.5344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0387    2.1227    2.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9833   -0.9317   -1.4583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9234   -2.6451    1.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7609   -1.7638    0.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6841   -4.2070   -1.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4305    0.4927    1.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
  8 14  1  0
 14 15  1  0
 14 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
  2 21  1  0
 21 22  2  0
 21 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  6 31  1  0
  8 32  1  1
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 17 39  1  0
 17 40  1  0
 20 41  1  0
 23 42  1  0
M  END


  Mrv0541 08131209322D          

 25 24  0  0  0  0            999 V2000
    4.4783    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638    1.1270    0.0000 C   0  0  0  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
   -0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1927    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6204    0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0493    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0493   -1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9072    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1927    1.9520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.5230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349    1.1270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0493   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7638   -1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0493   -2.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6217    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9072   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914    0.7145    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.1927    0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059    0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  4  3  1  0  0  0  0
  7  1  1  0  0  0  0
  8  6  1  0  0  0  0
  9  2  1  0  0  0  0
 10  5  1  0  0  0  0
 11  8  1  0  0  0  0
 12  7  1  0  0  0  0
  7 13  1  1  0  0  0
 14  5  1  4  0  0  0
 14 11  2  0  0  0  0
  8 15  1  1  0  0  0
 15  9  2  0  0  0  0
 16  3  2  0  0  0  0
  9 17  1  4  0  0  0
 18 10  2  0  0  0  0
 19 10  1  0  0  0  0
 20 11  1  0  0  0  0
 21 12  2  0  0  0  0
 22 12  1  0  0  0  0
 23  4  1  0  0  0  0
 23  6  1  0  0  0  0
  7 24  1  1  0  0  0
  8 25  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0030092

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](N)(CCC(O)=N[C@@]([H])(CSCC=O)C(O)=NCC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H19N3O7S/c13-7(12(21)22)1-2-9(17)15-8(6-23-4-3-16)11(20)14-5-10(18)19/h3,7-8H,1-2,4-6,13H2,(H,14,20)(H,15,17)(H,18,19)(H,21,22)/t7-,8-/m0/s1

> <INCHI_KEY>
VKLQBAQSSOPXGF-YUMQZZPRSA-N

> <FORMULA>
C12H19N3O7S

> <MOLECULAR_WEIGHT>
349.36

> <EXACT_MASS>
349.094370667

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
33.850632714377696

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-oxoethyl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <ALOGPS_LOGP>
-2.59

> <JCHEM_LOGP>
-3.864897705231508

> <ALOGPS_LOGS>
-3.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.675460862044939

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9148908954198953

> <JCHEM_PKA_STRONGEST_BASIC>
9.538644202326036

> <JCHEM_POLAR_SURFACE_AREA>
182.87

> <JCHEM_REFRACTIVITY>
80.1161

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.88e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
S-(formylmethyl)glutathione

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060507
     RDKit          3D
S-(Formylmethyl)glutathione
 42 41  0  0  0  0  0  0  0  0999 V2000
    3.5795   -1.1424    0.8146 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2114   -0.6679   -0.4233 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2688    0.3939   -0.9679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8861   -0.1905   -1.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0298    0.9080   -1.7696 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4543    1.4614   -2.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    1.3637   -1.2067 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5741    0.9184    0.0220 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1274    2.0063    0.8973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4214    2.9465    0.1432 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9797    2.0921   -0.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5670    1.8113    1.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6339    1.2337    1.3784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4969   -0.2211   -0.1232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0547   -0.5052   -1.3863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8417   -0.9983    0.8439 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7456   -2.1061    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2628   -3.0974   -0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -2.9211   -0.8640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189   -4.2252   -0.6444 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5079   -0.0321   -0.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1648    0.3958   -1.1294 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9835    0.0911    1.1473 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0160   -0.3665    1.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9169   -1.9114    0.5540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2404   -1.5041   -1.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6945    0.7761   -1.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2000    1.2497   -0.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5095   -0.6835   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0428   -0.9674   -2.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2388    2.3840   -3.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2961    0.4719    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2999    2.6627    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4717    1.4762    1.8456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7032    2.7126   -0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9125    1.1172   -0.5344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0387    2.1227    2.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9833   -0.9317   -1.4583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9234   -2.6451    1.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7609   -1.7638    0.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6841   -4.2070   -1.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4305    0.4927    1.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
  8 14  1  0
 14 15  1  0
 14 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
  2 21  1  0
 21 22  2  0
 21 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  6 31  1  0
  8 32  1  1
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 17 39  1  0
 17 40  1  0
 20 41  1  0
 23 42  1  0
M  END

HEADER    PROTEIN                                 13-AUG-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-AUG-12         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   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  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   23  S   UNK     0       0.000   0.000   0.000  0.00  0.00           S+0
HETATM   24  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
CONECT    1    2    7                                                       
CONECT    2    1    9                                                       
CONECT    3    4   16                                                       
CONECT    4    3   23                                                       
CONECT    5   10   14                                                       
CONECT    6    8   23                                                       
CONECT    7    1   12   13   24                                             
CONECT    8    6   11   15   25                                             
CONECT    9    2   15   17                                                  
CONECT   10    5   18   19                                                  
CONECT   11    8   14   20                                                  
CONECT   12    7   21   22                                                  
CONECT   13    7                                                            
CONECT   14    5   11                                                       
CONECT   15    8    9                                                       
CONECT   16    3                                                            
CONECT   17    9                                                            
CONECT   18   10                                                            
CONECT   19   10                                                            
CONECT   20   11                                                            
CONECT   21   12                                                            
CONECT   22   12                                                            
CONECT   23    4    6                                                       
CONECT   24    7                                                            
CONECT   25    8                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

COMPND    HMDB0060507
HETATM    1  N1  UNL     1       3.579  -1.142   0.815  1.00  0.00           N  
HETATM    2  C1  UNL     1       4.211  -0.668  -0.423  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.269   0.394  -0.968  1.00  0.00           C  
HETATM    4  C3  UNL     1       1.886  -0.190  -1.256  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.030   0.908  -1.770  1.00  0.00           C  
HETATM    6  O1  UNL     1       1.454   1.461  -2.990  1.00  0.00           O  
HETATM    7  N2  UNL     1      -0.015   1.364  -1.207  1.00  0.00           N  
HETATM    8  C5  UNL     1      -0.574   0.918   0.022  1.00  0.00           C  
HETATM    9  C6  UNL     1      -1.127   2.006   0.897  1.00  0.00           C  
HETATM   10  S1  UNL     1      -2.421   2.946   0.143  1.00  0.00           S  
HETATM   11  C7  UNL     1      -3.980   2.092  -0.035  1.00  0.00           C  
HETATM   12  C8  UNL     1      -4.567   1.811   1.322  1.00  0.00           C  
HETATM   13  O2  UNL     1      -5.634   1.234   1.378  1.00  0.00           O  
HETATM   14  C9  UNL     1      -1.497  -0.221  -0.123  1.00  0.00           C  
HETATM   15  O3  UNL     1      -2.055  -0.505  -1.386  1.00  0.00           O  
HETATM   16  N3  UNL     1      -1.842  -0.998   0.844  1.00  0.00           N  
HETATM   17  C10 UNL     1      -2.746  -2.106   0.679  1.00  0.00           C  
HETATM   18  C11 UNL     1      -2.263  -3.097  -0.312  1.00  0.00           C  
HETATM   19  O4  UNL     1      -1.155  -2.921  -0.864  1.00  0.00           O  
HETATM   20  O5  UNL     1      -3.019  -4.225  -0.644  1.00  0.00           O  
HETATM   21  C12 UNL     1       5.508  -0.032  -0.141  1.00  0.00           C  
HETATM   22  O6  UNL     1       6.165   0.396  -1.129  1.00  0.00           O  
HETATM   23  O7  UNL     1       5.984   0.091   1.147  1.00  0.00           O  
HETATM   24  H1  UNL     1       3.016  -0.367   1.240  1.00  0.00           H  
HETATM   25  H2  UNL     1       2.917  -1.911   0.554  1.00  0.00           H  
HETATM   26  H3  UNL     1       4.240  -1.504  -1.128  1.00  0.00           H  
HETATM   27  H4  UNL     1       3.694   0.776  -1.921  1.00  0.00           H  
HETATM   28  H5  UNL     1       3.200   1.250  -0.263  1.00  0.00           H  
HETATM   29  H6  UNL     1       1.509  -0.684  -0.365  1.00  0.00           H  
HETATM   30  H7  UNL     1       2.043  -0.967  -2.067  1.00  0.00           H  
HETATM   31  H8  UNL     1       1.239   2.384  -3.289  1.00  0.00           H  
HETATM   32  H9  UNL     1       0.296   0.472   0.641  1.00  0.00           H  
HETATM   33  H10 UNL     1      -0.300   2.663   1.273  1.00  0.00           H  
HETATM   34  H11 UNL     1      -1.472   1.476   1.846  1.00  0.00           H  
HETATM   35  H12 UNL     1      -4.703   2.713  -0.631  1.00  0.00           H  
HETATM   36  H13 UNL     1      -3.912   1.117  -0.534  1.00  0.00           H  
HETATM   37  H14 UNL     1      -4.039   2.123   2.194  1.00  0.00           H  
HETATM   38  H15 UNL     1      -2.983  -0.932  -1.458  1.00  0.00           H  
HETATM   39  H16 UNL     1      -2.923  -2.645   1.635  1.00  0.00           H  
HETATM   40  H17 UNL     1      -3.761  -1.764   0.348  1.00  0.00           H  
HETATM   41  H18 UNL     1      -3.684  -4.207  -1.426  1.00  0.00           H  
HETATM   42  H19 UNL     1       5.431   0.493   1.916  1.00  0.00           H  
CONECT    1    2   24   25
CONECT    2    3   21   26
CONECT    3    4   27   28
CONECT    4    5   29   30
CONECT    5    6    7    7
CONECT    6   31
CONECT    7    8
CONECT    8    9   14   32
CONECT    9   10   33   34
CONECT   10   11
CONECT   11   12   35   36
CONECT   12   13   13   37
CONECT   14   15   16   16
CONECT   15   38
CONECT   16   17
CONECT   17   18   39   40
CONECT   18   19   19   20
CONECT   20   41
CONECT   21   22   22   23
CONECT   23   42
END

HMDB0060507
     RDKit          3D
S-(Formylmethyl)glutathione
 42 41  0  0  0  0  0  0  0  0999 V2000
    3.5795   -1.1424    0.8146 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2114   -0.6679   -0.4233 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2688    0.3939   -0.9679 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8861   -0.1905   -1.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0298    0.9080   -1.7696 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4543    1.4614   -2.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0147    1.3637   -1.2067 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5741    0.9184    0.0220 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1274    2.0063    0.8973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4214    2.9465    0.1432 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9797    2.0921   -0.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5670    1.8113    1.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6339    1.2337    1.3784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4969   -0.2211   -0.1232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0547   -0.5052   -1.3863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8417   -0.9983    0.8439 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7456   -2.1061    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2628   -3.0974   -0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -2.9211   -0.8640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189   -4.2252   -0.6444 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5079   -0.0321   -0.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1648    0.3958   -1.1294 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9835    0.0911    1.1473 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0160   -0.3665    1.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9169   -1.9114    0.5540 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2404   -1.5041   -1.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6945    0.7761   -1.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2000    1.2497   -0.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5095   -0.6835   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0428   -0.9674   -2.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2388    2.3840   -3.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2961    0.4719    0.6409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2999    2.6627    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4717    1.4762    1.8456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7032    2.7126   -0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9125    1.1172   -0.5344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0387    2.1227    2.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9833   -0.9317   -1.4583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9234   -2.6451    1.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7609   -1.7638    0.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6841   -4.2070   -1.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4305    0.4927    1.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
  8 14  1  0
 14 15  1  0
 14 16  2  3
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
  2 21  1  0
 21 22  2  0
 21 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  6 31  1  0
  8 32  1  1
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 17 39  1  0
 17 40  1  0
 20 41  1  0
 23 42  1  0
M  END

Synonyms

Not Available

Chemical Formula

C₁₂H₁₉N₃O₇S

Average Molecular Weight

349.36

Monoisotopic Molecular Weight

349.094370667

IUPAC Name

(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-oxoethyl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid

Traditional Name

S-(formylmethyl)glutathione

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CCC(O)=N[C@@]([H])(CSCC=O)C(O)=NCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C12H19N3O7S/c13-7(12(21)22)1-2-9(17)15-8(6-23-4-3-16)11(20)14-5-10(18)19/h3,7-8H,1-2,4-6,13H2,(H,14,20)(H,15,17)(H,18,19)(H,21,22)/t7-,8-/m0/s1

InChI Key

VKLQBAQSSOPXGF-YUMQZZPRSA-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
Gamma-glutamyl alpha peptide
Glutamine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Cysteine or derivatives
Alpha-amino acid
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
L-alpha-amino acid
Dicarboxylic acid or derivatives
Fatty amide
Fatty acyl
Fatty acid
N-acyl-amine
Amino acid or derivatives
Carboxamide group
Amino acid
Secondary carboxylic acid amide
Carboxylic acid
Thioether
Sulfenyl compound
Dialkylthioether
Primary amine
Primary aliphatic amine
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Aldehyde
Amine
Organic oxide
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organosulfur compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

peptide (CHEBI:34962 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.29 g/L	ALOGPS
logP	-2.6	ALOGPS
logP	-3.9	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	1.91	ChemAxon
pKa (Strongest Basic)	9.54	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	182.87 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	80.12 m³·mol⁻¹	ChemAxon
Polarizability	33.85 Å³	ChemAxon
Number of Rings	0	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 (Non-derivatized) - 70eV, Positive	splash10-0f6x-9065000000-86d1cba61a3dca3ccc6b	2017-09-20	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (4 TMS) - 70eV, Positive	splash10-00di-5211297000-d93bf9d76a2d2fd8d369	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0v59-4189000000-5d5c6497e41130a4bc98	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-9150000000-1a124010fc5e38195c38	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-00di-9330000000-0d45185377c925296f38	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-00ea-3149000000-2ead9ab4ff107e706425	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00di-9242000000-144fc7fc48f1fe4545b2	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0006-9400000000-3beac58433b00fad5b88	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0udi-0149000000-53de86e2588eb657c655	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-015i-2952000000-86890d48f98ecf0342c9	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-000i-9210000000-bd4daba3840bdfffead2	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0592-2189000000-984b1c7e888bfb65e46f	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-05fu-1690000000-ba60c0a835976ac6512d	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-006x-8900000000-1d7b2d35cf7231763801	2021-10-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

#<MetaboliteProteinLink:0x000055b76e13fdf0>

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
	Proteobacteria	1	Human	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB		details

External Links

HMDB ID

HMDB0060507

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10128369

KEGG Compound ID

C14871

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11954074

PDB ID

Not Available

ChEBI ID

34962

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Showing metabocard for S-(Formylmethyl)glutathione (MMDBc0030092)

MOL for #<Metabolite:0x000055b76db96700>

3D MOL for #<Metabolite:0x000055b76db96700>

3D SDF for #<Metabolite:0x000055b76db96700>

3D-SDF for #<Metabolite:0x000055b76db96700>

PDB for #<Metabolite:0x000055b76db96700>

3D PDB for #<Metabolite:0x000055b76db96700>

SMILES for #<Metabolite:0x000055b76db96700>

INCHI for #<Metabolite:0x000055b76db96700>

Structure for #<Metabolite:0x000055b76db96700>

3D Structure for #<Metabolite:0x000055b76db96700>