NP-MRD: Showing NP-Card for S-(Formylmethyl)glutathione (NP0084389)

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Record Information

Version

2.0

Created at

2022-04-29 05:07:54 UTC

Updated at

2022-04-29 05:07:54 UTC

NP-MRD ID

NP0084389

Secondary Accession Numbers

None

Natural Product Identification

Common Name

S-(Formylmethyl)glutathione

Description

S-(Formylmethyl)glutathione 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. S-(Formylmethyl)glutathione is a very strong basic compound (based on its pKa). S-(Formylmethyl)glutathione exists in all living organisms, ranging from bacteria to humans. S-(Formylmethyl)glutathione is found in Paraburkholderia phymatum. 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.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 41  0  0  0  0  0  0  0  0999 V2000
    4.6498   -1.9955   -0.9211 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0529   -0.7458   -0.4141 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5783   -0.7532   -0.6909 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9416    0.5017   -0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4620    0.5183   -0.4987 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1331    0.4386   -1.8465 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3614    0.6006    0.4564 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7749    0.6312    0.3952 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3338    1.3262   -0.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7984    3.0630   -0.8972 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4968    4.0162    0.4611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0074    5.4205    0.3206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6177    6.2547   -0.3228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3449   -0.7416    0.4305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0671   -1.5386    1.5584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0639   -1.2019   -0.5178 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5949   -2.5447   -0.4353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5375   -3.5668   -0.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8275   -4.7748   -0.4543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2252   -3.1804   -0.6413 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3764   -0.6122    1.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1568    0.3873    1.7320 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9895   -1.6985    1.6792 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3236   -2.8173   -0.3912 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6690   -1.9137   -1.0104 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5199    0.0754   -0.9972 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4635   -0.8866   -1.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1398   -1.6650   -0.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4526    1.3681   -0.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0863    0.5504    0.9105 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4069    1.1498   -2.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1518    1.2016    1.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4506    1.3628   -0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1737    0.7977   -1.7592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    3.6245    1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6156    4.0227    0.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0807    5.7138    0.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7619   -1.7812    2.2340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0852   -2.6431    0.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3691   -2.7191   -1.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4910   -3.6161   -0.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0089   -1.6290    1.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  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  0
 16 17  1  0
 17 18  1  0
 18 20  1  0
 18 19  2  0
  2 21  1  0
 21 23  1  0
 21 22  2  0
  2 26  1  6
  1 24  1  0
  1 25  1  0
  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>
NP0084389

> <DATABASE_NAME>
NP-MRD

> <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

$$$$

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

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₉N₃O₇S

Average Mass

349.3600 Da

Monoisotopic Mass

349.09437 Da

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

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Paraburkholderia phymatum	-	KNApSAcK

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 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
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

External Links

HMDB ID

HMDB0060507

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB 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

Good Scents ID

Not Available

References

General References

Showing NP-Card for S-(Formylmethyl)glutathione (NP0084389)

MOL for NP0084389 (S-(Formylmethyl)glutathione)

3D MOL for NP0084389 (S-(Formylmethyl)glutathione)

3D SDF for NP0084389 (S-(Formylmethyl)glutathione)

3D-SDF for NP0084389 (S-(Formylmethyl)glutathione)

PDB for NP0084389 (S-(Formylmethyl)glutathione)

3D PDB for NP0084389 (S-(Formylmethyl)glutathione)

SMILES for NP0084389 (S-(Formylmethyl)glutathione)

INCHI for NP0084389 (S-(Formylmethyl)glutathione)

Structure for NP0084389 (S-(Formylmethyl)glutathione)

3D Structure for NP0084389 (S-(Formylmethyl)glutathione)