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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-17 00:53:57 UTC
Update Date2022-03-07 03:17:43 UTC
HMDB IDHMDB0060327
Secondary Accession Numbers
  • HMDB60327
Metabolite Identification
Common Name1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene
Description1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 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. 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene is a very strong basic compound (based on its pKa). 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene exists in all living organisms, ranging from bacteria to humans. 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
Data?1563866045
SynonymsNot Available
Chemical FormulaC20H24N4O9S
Average Molecular Weight496.491
Monoisotopic Molecular Weight496.126399076
IUPAC Name(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(1-hydroxy-5-nitro-1,2-dihydronaphthalen-2-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid
Traditional Name(2S)-2-amino-4-{[(1R)-1-(carboxymethyl-C-hydroxycarbonimidoyl)-2-[(1-hydroxy-5-nitro-1,2-dihydronaphthalen-2-yl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid
CAS Registry NumberNot Available
SMILES
[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1([H])C=CC2=C(C=CC=C2N(=O)=O)C1([H])O)C(O)=NCC(O)=O)C(O)=O
InChI Identifier
InChI=1S/C20H24N4O9S/c21-12(20(30)31)5-7-16(25)23-13(19(29)22-8-17(26)27)9-34-15-6-4-10-11(18(15)28)2-1-3-14(10)24(32)33/h1-4,6,12-13,15,18,28H,5,7-9,21H2,(H,22,29)(H,23,25)(H,26,27)(H,30,31)/t12-,13-,15?,18?/m0/s1
InChI KeySFJZEQDXMXSLGC-RJXQQRCHSA-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.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentOligopeptides
Alternative Parents
Substituents
  • Alpha-oligopeptide
  • Gamma-glutamyl alpha peptide
  • Glutamine or derivatives
  • N-acyl-alpha-amino acid
  • N-acyl-alpha amino acid or derivatives
  • 1-nitronaphthalene
  • Alpha-amino acid amide
  • Cysteine or derivatives
  • Alpha-amino acid
  • N-substituted-alpha-amino acid
  • Alpha-amino acid or derivatives
  • L-alpha-amino acid
  • Naphthalene
  • Nitroaromatic compound
  • Dicarboxylic acid or derivatives
  • Fatty amide
  • N-acyl-amine
  • Fatty acyl
  • Benzenoid
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Amino acid or derivatives
  • C-nitro compound
  • Carboxamide group
  • Organic nitro compound
  • Amino acid
  • Sulfenyl compound
  • Thioether
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Allyl-type 1,3-dipolar organic compound
  • Organic oxoazanium
  • Dialkylthioether
  • Carboxylic acid
  • Primary amine
  • Primary aliphatic amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Alcohol
  • Hydrocarbon derivative
  • Organopnictogen compound
  • Carbonyl group
  • Organonitrogen compound
  • Amine
  • Organic zwitterion
  • Organic oxide
  • Organooxygen compound
  • Organosulfur compound
  • Aromatic homopolycyclic compound
Molecular FrameworkAromatic homopolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
DispositionNot Available
Process
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.045 g/LALOGPS
logP-1.4ALOGPS
logP-1.7ChemAxon
logS-4ALOGPS
pKa (Strongest Acidic)1.83ChemAxon
pKa (Strongest Basic)9.54ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area231.85 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity121.43 m³·mol⁻¹ChemAxon
Polarizability47.19 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+209.78131661259
DarkChem[M-H]-200.74631661259
DeepCCS[M+H]+207.1730932474
DeepCCS[M-H]-205.27530932474
DeepCCS[M-2H]-238.51630932474
DeepCCS[M+Na]+212.94830932474
AllCCS[M+H]+204.932859911
AllCCS[M+H-H2O]+203.432859911
AllCCS[M+NH4]+206.332859911
AllCCS[M+Na]+206.632859911
AllCCS[M-H]-199.332859911
AllCCS[M+Na-2H]-200.332859911
AllCCS[M+HCOO]-201.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1([H])C=CC2=C(C=CC=C2N(=O)=O)C1([H])O)C(O)=NCC(O)=O)C(O)=O5157.0Standard polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1([H])C=CC2=C(C=CC=C2N(=O)=O)C1([H])O)C(O)=NCC(O)=O)C(O)=O3589.0Standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene[H][C@](N)(CCC(O)=N[C@@]([H])(CSC1([H])C=CC2=C(C=CC=C2N(=O)=O)C1([H])O)C(O)=NCC(O)=O)C(O)=O4493.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TMS,isomer #1C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O4275.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TMS,isomer #2C[Si](C)(C)OC1C2=CC=CC([N+](=O)[O-])=C2C=CC1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O4294.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TMS,isomer #3C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O4258.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O4261.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O4212.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)C(=O)O4349.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C4099.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #10C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O4092.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #11C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C4080.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O4200.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #13C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C4074.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O4183.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #15C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C4156.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #16C[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C4351.5Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #2C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O4129.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #3C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C4147.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C4128.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O4214.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O4077.5Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #7C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O4125.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O4108.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O4221.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C3995.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4095.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #11C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O4226.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C3973.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #13C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3984.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C4068.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #15C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O3972.5Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O4103.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #17C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O4088.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #18C[Si](C)(C)OC1C2=CC=CC([N+](=O)[O-])=C2C=CC1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O4214.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #19C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3959.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C3996.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #20C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4059.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #21C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4053.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #22C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4200.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #23C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4052.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #24C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4193.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C4190.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C4002.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4071.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #5C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C4013.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #6C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C4006.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #7C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O4110.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C4008.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4103.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C3895.5Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4009.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #11C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O4149.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3980.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #13C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C4153.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #14C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4146.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #15C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3876.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3967.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #17C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3982.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #18C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C4106.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #19C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3980.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #2C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3925.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #20C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4118.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #21C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4116.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3941.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #23C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4103.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4092.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #25C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4099.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3988.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3873.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3968.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3988.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #7C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4129.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3904.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,4TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O4015.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3836.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #10C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4100.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #11C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4093.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3900.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #13C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4047.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #14C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4056.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #15C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4061.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #16C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4033.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3914.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3936.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4077.5Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3906.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4077.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #7C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4071.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #8C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3934.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,5TMS,isomer #9C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C4100.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O4462.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1C2=CC=CC([N+](=O)[O-])=C2C=CC1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O4487.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O4446.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O4501.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O4452.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)C(=O)O4532.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C4539.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O4548.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4519.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4592.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C4587.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O4625.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C4593.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C4772.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O4549.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4537.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C4586.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4618.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O4534.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O4527.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O4576.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O4626.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C4640.1Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4752.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O4888.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4600.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C4705.5Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C4715.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O4628.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4684.8Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O4748.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1C2=CC=CC([N+](=O)[O-])=C2C=CC1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O4881.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C4639.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4631.9Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4712.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4686.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4865.7Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4735.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4910.2Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4891.6Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4676.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4719.3Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4615.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C4675.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4716.0Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C4648.4Semi standard non polar33892256
1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC1C=CC2=C(C=CC=C2[N+](=O)[O-])C1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4713.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-3602900000-08a1ea646555a202d38b2017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (2 TMS) - 70eV, Positivesplash10-0096-6901144000-b14e266087a2f14e12a02017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (TBDMS_2_4) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (TBDMS_3_3) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (TBDMS_3_6) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (TBDMS_3_8) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS (TBDMS_3_10) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene GC-MS ("1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene,2TBDMS,#4" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 10V, Positive-QTOFsplash10-0002-0000900000-77a3b95f2be8c40549082015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 20V, Positive-QTOFsplash10-006t-3000900000-6ffc994cc20e79922b4a2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 40V, Positive-QTOFsplash10-00di-9120000000-da578bac9f9fcc40d0922015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 10V, Negative-QTOFsplash10-0002-0000900000-15548fccf325d21f7daf2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 20V, Negative-QTOFsplash10-0002-1110900000-0a53ffa1b9349606b2b92015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalene 40V, Negative-QTOFsplash10-001i-9840000000-f71aca527987b3e71d982015-09-15Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID10128351
KEGG Compound IDC14805
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11954056
PDB IDNot Available
ChEBI ID34101
Food Biomarker OntologyNot Available
VMH IDM00542
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. 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 ]

Only showing the first 10 proteins. There are 19 proteins in total.

Enzymes

General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM2
Uniprot ID:
P28161
Molecular weight:
25744.395
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM1
Uniprot ID:
P09488
Molecular weight:
25711.555
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in protein disulfide oxidoreductase activity
Specific function:
Significant glutathione conjugating activity is found only with the model substrate, 1-chloro-2,4-dinitrobenzene (CDNB).
Gene Name:
GSTK1
Uniprot ID:
Q9Y2Q3
Molecular weight:
31565.605
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Also functions as a glutathione peroxidase.
Gene Name:
MGST3
Uniprot ID:
O14880
Molecular weight:
16516.185
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. May govern uptake and detoxification of both endogenous compounds and xenobiotics at the testis and brain blood barriers.
Gene Name:
GSTM3
Uniprot ID:
P21266
Molecular weight:
26559.32
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTA1
Uniprot ID:
P08263
Molecular weight:
25630.785
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Has a wide substrate specificity.
Gene Name:
MGST1
Uniprot ID:
P10620
Molecular weight:
17598.45
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Active on 1-chloro-2,4-dinitrobenzene.
Gene Name:
GSTM4
Uniprot ID:
Q03013
Molecular weight:
25561.095
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM5
Uniprot ID:
P46439
Molecular weight:
25674.455
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails
General function:
Involved in enzyme activator activity
Specific function:
Can catalyze the production of LTC4 from LTA4 and reduced glutathione. Can catalyze the conjugation of 1-chloro-2,4-dinitrobenzene with reduced glutathione.
Gene Name:
MGST2
Uniprot ID:
Q99735
Molecular weight:
16620.4
Reactions
1-Nitronaphthalene-5,6-oxide + Glutathione → 1-Nitro-5-hydroxy-6-glutathionyl-5,6-dihydronaphthalenedetails

Only showing the first 10 proteins. There are 19 proteins in total.