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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-17 01:25:40 UTC
Update Date2022-03-07 03:17:46 UTC
HMDB IDHMDB0060505
Secondary Accession Numbers
  • HMDB60505
Metabolite Identification
Common NameS-(2-Chloroacetyl)glutathione
DescriptionS-(2-Chloroacetyl)glutathione, also known as CLCH2COSG, 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. 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. S-(2-Chloroacetyl)glutathione is a very strong basic compound (based on its pKa). S-(2-Chloroacetyl)glutathione exists in all living organisms, ranging from bacteria to humans.
Structure
Data?1563866069
Synonyms
ValueSource
CLCH2COSGHMDB
2-ChloroacetylglutathioneHMDB
Chemical FormulaC12H18ClN3O7S
Average Molecular Weight383.805
Monoisotopic Molecular Weight383.055398342
IUPAC Name(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-chloroacetyl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid
Traditional NameClch2COSG
CAS Registry NumberNot Available
SMILES
[H][C@](N)(CCC(O)=N[C@@]([H])(CSC(=O)CCl)C(O)=NCC(O)=O)C(O)=O
InChI Identifier
InChI=1S/C12H18ClN3O7S/c13-3-10(20)24-5-7(11(21)15-4-9(18)19)16-8(17)2-1-6(14)12(22)23/h6-7H,1-5,14H2,(H,15,21)(H,16,17)(H,18,19)(H,22,23)/t6-,7-/m0/s1
InChI KeyQJDRMMRBPVHMAD-BQBZGAKWSA-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
  • S-acylglutathione
  • Glutamine or derivatives
  • N-acyl-alpha amino acid or derivatives
  • N-acyl-alpha-amino acid
  • Alpha-amino acid amide
  • Cysteine or derivatives
  • Alpha-amino acid
  • N-substituted-alpha-amino acid
  • Alpha-amino acid or derivatives
  • L-alpha-amino acid
  • Halogenated fatty acid
  • N-acyl-amine
  • Fatty acyl
  • Fatty acid
  • Fatty amide
  • Dicarboxylic acid or derivatives
  • Amino acid or derivatives
  • Secondary carboxylic acid amide
  • Amino acid
  • Thiocarboxylic acid ester
  • Carbothioic s-ester
  • Carboxamide group
  • Sulfenyl compound
  • Carboxylic acid
  • Thiocarboxylic acid or derivatives
  • Organohalogen compound
  • Primary aliphatic amine
  • Organooxygen compound
  • Organosulfur compound
  • Primary amine
  • Alkyl halide
  • Alkyl chloride
  • Carbonyl group
  • Hydrocarbon derivative
  • Amine
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organonitrogen compound
  • Organochloride
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
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 Solubility0.26 g/LALOGPS
logP-2.2ALOGPS
logP-2.9ChemAxon
logS-3.2ALOGPS
pKa (Strongest Acidic)1.78ChemAxon
pKa (Strongest Basic)9.54ChemAxon
Physiological Charge-3ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area182.87 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity84.38 m³·mol⁻¹ChemAxon
Polarizability35.59 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+178.98130932474
DeepCCS[M-H]-176.62330932474
DeepCCS[M-2H]-210.23930932474
DeepCCS[M+Na]+185.46730932474
AllCCS[M+H]+178.532859911
AllCCS[M+H-H2O]+176.332859911
AllCCS[M+NH4]+180.632859911
AllCCS[M+Na]+181.232859911
AllCCS[M-H]-177.432859911
AllCCS[M+Na-2H]-177.932859911
AllCCS[M+HCOO]-178.632859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.1.49 minutes32390414
Predicted by Siyang on May 30, 202210.3911 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20228.78 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid620.2 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid214.6 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid60.9 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid158.5 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid57.8 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid299.4 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid284.1 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)737.1 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid621.7 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid89.1 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid902.2 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid191.7 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid189.4 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate464.1 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA422.5 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water315.6 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
S-(2-Chloroacetyl)glutathione[H][C@](N)(CCC(O)=N[C@@]([H])(CSC(=O)CCl)C(O)=NCC(O)=O)C(O)=O4158.9Standard polar33892256
S-(2-Chloroacetyl)glutathione[H][C@](N)(CCC(O)=N[C@@]([H])(CSC(=O)CCl)C(O)=NCC(O)=O)C(O)=O2727.9Standard non polar33892256
S-(2-Chloroacetyl)glutathione[H][C@](N)(CCC(O)=N[C@@]([H])(CSC(=O)CCl)C(O)=NCC(O)=O)C(O)=O3355.1Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
S-(2-Chloroacetyl)glutathione,1TMS,isomer #1C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O3159.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TMS,isomer #2C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O3110.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O3154.0Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TMS,isomer #4C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O3106.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)C(=O)O3225.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C3028.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C3091.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #11C[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C3269.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #2C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C3062.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3075.0Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O3133.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O3025.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C3000.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #7C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O3115.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3032.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O3139.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C2991.9Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3037.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #11C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3180.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3063.0Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #13C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3202.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #14C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C3177.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #2C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3007.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3061.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C2997.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3100.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3101.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #7C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O3200.9Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C2955.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3053.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C2949.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3142.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #11C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3165.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3044.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3047.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3168.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3056.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #6C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C3191.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #7C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3201.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #8C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2996.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TMS,isomer #9C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3158.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3016.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2854.1Standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3873.9Standard polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3149.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2875.4Standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4068.8Standard polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)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)C3154.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)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)C2922.2Standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)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)C4226.7Standard polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3159.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2928.3Standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4029.9Standard polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3111.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2929.2Standard non polar33892256
S-(2-Chloroacetyl)glutathione,5TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4082.2Standard polar33892256
S-(2-Chloroacetyl)glutathione,6TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)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)C3140.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,6TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)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)C2936.5Standard non polar33892256
S-(2-Chloroacetyl)glutathione,6TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSC(=O)CCl)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)C3677.8Standard polar33892256
S-(2-Chloroacetyl)glutathione,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O3325.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O3275.0Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O3369.0Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O3311.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)C(=O)O3406.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C3429.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C3517.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C3630.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C3461.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C3495.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O3538.9Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O3454.9Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C3409.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O3505.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C3494.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O3574.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3624.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3671.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3823.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3736.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3888.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3846.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3650.4Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3691.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C3652.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3705.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3737.9Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #7CC(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](CSC(=O)CCl)C(O)=NCC(=O)O3848.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C3618.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3713.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC(=O)CCl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3794.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4028.1Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4072.9Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3849.8Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3884.5Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSC(=O)CCl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4052.2Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3887.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #6CC(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](CSC(=O)CCl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4053.7Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSC(=O)CCl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4076.6Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSC(=O)CCl)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3848.3Semi standard non polar33892256
S-(2-Chloroacetyl)glutathione,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSC(=O)CCl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4049.4Semi standard non polar33892256
Spectra
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 ID143757
KEGG Compound IDC14864
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound163913
PDB IDNot Available
ChEBI ID34959
Food Biomarker OntologyNot Available
VMH IDM02854
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails
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
Chloroacetyl chloride + Glutathione → S-(2-Chloroacetyl)glutathione + Hydrochloric aciddetails

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