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Showing metabocard for Chloroacetyl chloride (HMDB0060452)

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enzymes (19) Show 19 proteins
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-17 01:21:49 UTC
Update Date2023-02-21 17:30:00 UTC
HMDB IDHMDB0060452
Secondary Accession Numbers
  • HMDB60452
Metabolite Identification
Common NameChloroacetyl chloride
DescriptionChloroacetyl chloride belongs to the class of organic compounds known as acyl chlorides. These are organic compounds containing the functional group -CO-Cl. Chloroacetyl chloride is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1677000600
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0060452 (Chloroacetyl chloride)

 
  Mrv0541 07191213112D          
 
  5  4  0  0  0  0            999 V2000
    9.9363  -11.2985    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   10.6174  -11.6991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3385  -11.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0197  -11.6991    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   11.3385  -10.4972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  2  0  0  0  0
M  END
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3D MOL for HMDB0060452 (Chloroacetyl chloride)

HMDB0060452
     RDKit          3D
Chloroacetyl chloride
  7  6  0  0  0  0  0  0  0  0999 V2000
    1.3883   -1.2612   -0.3393 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8033   -0.2180   -0.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7440    1.1883    0.3255 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.6808   -0.1196    0.0520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1265    1.4403   -0.6585 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.9212   -0.1404    1.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2071   -0.8895   -0.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  4  7  1  0
M  END
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3D SDF for HMDB0060452 (Chloroacetyl chloride)

 
  Mrv0541 07191213112D          
 
  5  4  0  0  0  0            999 V2000
    9.9363  -11.2985    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   10.6174  -11.6991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3385  -11.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0197  -11.6991    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   11.3385  -10.4972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060452

> <DATABASE_NAME>
hmdb

> <SMILES>
ClCC(Cl)=O

> <INCHI_IDENTIFIER>
InChI=1S/C2H2Cl2O/c3-1-2(4)5/h1H2

> <INCHI_KEY>
VGCXGMAHQTYDJK-UHFFFAOYSA-N

> <FORMULA>
C2H2Cl2O

> <MOLECULAR_WEIGHT>
112.943

> <EXACT_MASS>
111.9482701

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
8.408763628942323

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-chloroacetyl chloride

> <ALOGPS_LOGP>
0.46

> <JCHEM_LOGP>
0.8473277406666666

> <ALOGPS_LOGS>
-1.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.74523565689425

> <JCHEM_PKA_STRONGEST_BASIC>
-9.428350634540257

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
21.2554

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.71e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
chloroacetyl chloride

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0060452 (Chloroacetyl chloride)

HMDB0060452
     RDKit          3D
Chloroacetyl chloride
  7  6  0  0  0  0  0  0  0  0999 V2000
    1.3883   -1.2612   -0.3393 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8033   -0.2180   -0.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7440    1.1883    0.3255 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.6808   -0.1196    0.0520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1265    1.4403   -0.6585 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.9212   -0.1404    1.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2071   -0.8895   -0.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  4  7  1  0
M  END
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PDB for HMDB0060452 (Chloroacetyl chloride)

HEADER    PROTEIN                                 19-JUL-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUL-12         0                                  
HETATM    1 Cl   UNK     0      18.548 -21.091   0.000  0.00  0.00          Cl+0
HETATM    2  C   UNK     0      19.819 -21.838   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.165 -21.091   0.000  0.00  0.00           C+0
HETATM    4 Cl   UNK     0      22.437 -21.838   0.000  0.00  0.00          Cl+0
HETATM    5  O   UNK     0      21.165 -19.595   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3                                                            
MASTER        0    0    0    0    0    0    0    0    5    0    8    0
END
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3D PDB for HMDB0060452 (Chloroacetyl chloride)

COMPND    HMDB0060452
HETATM    1  O1  UNL     1       1.388  -1.261  -0.339  1.00  0.00           O  
HETATM    2  C1  UNL     1       0.803  -0.218  -0.031  1.00  0.00           C  
HETATM    3 CL1  UNL     1       1.744   1.188   0.326  1.00  0.00          CL  
HETATM    4  C2  UNL     1      -0.681  -0.120   0.052  1.00  0.00           C  
HETATM    5 CL2  UNL     1      -1.126   1.440  -0.658  1.00  0.00          CL  
HETATM    6  H1  UNL     1      -0.921  -0.140   1.152  1.00  0.00           H  
HETATM    7  H2  UNL     1      -1.207  -0.889  -0.500  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    4    5    6    7
END
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SMILES for HMDB0060452 (Chloroacetyl chloride)

ClCC(Cl)=O
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INCHI for HMDB0060452 (Chloroacetyl chloride)

InChI=1S/C2H2Cl2O/c3-1-2(4)5/h1H2
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
Monochloroacetyl chlorideHMDB
Chemical FormulaC2H2Cl2O
Average Molecular Weight112.943
Monoisotopic Molecular Weight111.9482701
IUPAC Name2-chloroacetyl chloride
Traditional Namechloroacetyl chloride
CAS Registry NumberNot Available
SMILES
ClCC(Cl)=O
InChI Identifier
InChI=1S/C2H2Cl2O/c3-1-2(4)5/h1H2
InChI KeyVGCXGMAHQTYDJK-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as acyl chlorides. These are organic compounds containing the functional group -CO-Cl.
KingdomOrganic compounds
Super ClassOrganohalogen compounds
ClassAcyl halides
Sub ClassAcyl chlorides
Direct ParentAcyl chlorides
Alternative Parents
Substituents
  • Acyl chloride
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organochloride
  • Carbonyl group
  • Alkyl halide
  • Alkyl chloride
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Source
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 Solubility7.71 g/LALOGPS
logP0.46ALOGPS
logP0.85ChemAxon
logS-1.2ALOGPS
pKa (Strongest Acidic)16.75ChemAxon
pKa (Strongest Basic)-9.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity21.26 m³·mol⁻¹ChemAxon
Polarizability8.41 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+125.60830932474
DeepCCS[M-H]-123.71230932474
DeepCCS[M-2H]-159.37830932474
DeepCCS[M+Na]+133.78430932474
AllCCS[M+H]+126.832859911
AllCCS[M+H-H2O]+122.532859911
AllCCS[M+NH4]+130.732859911
AllCCS[M+Na]+131.932859911
AllCCS[M-H]-140.432859911
AllCCS[M+Na-2H]-146.032859911
AllCCS[M+HCOO]-152.132859911

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, 2022.3.48 minutes32390414
Predicted by Siyang on May 30, 202213.2986 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20222.0 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1546.7 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid592.9 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid234.9 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid458.2 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid294.3 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid495.8 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 Acid645.1 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)618.5 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid1057.5 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid382.6 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid1071.6 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid434.8 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid418.3 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate782.2 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA531.7 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water268.3 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Chloroacetyl chlorideClCC(Cl)=O1161.4Standard polar33892256
Chloroacetyl chlorideClCC(Cl)=O630.2Standard non polar33892256
Chloroacetyl chlorideClCC(Cl)=O710.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Chloroacetyl chloride GC-MS (Non-derivatized) - 70eV, Positivesplash10-01t9-9200000000-a8124f4b787bbe8f1bce2017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Chloroacetyl chloride GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 10V, Positive-QTOFsplash10-03di-0900000000-b64bc72ba067beace9e32016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 20V, Positive-QTOFsplash10-03di-0900000000-091175abad51f63a4f3c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 40V, Positive-QTOFsplash10-0006-9100000000-bd5052211d152f46a8a82016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 10V, Negative-QTOFsplash10-03di-0900000000-1a36eddf5b39ee6eb64f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 20V, Negative-QTOFsplash10-03k9-6900000000-c653aaa6576e597b906f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 40V, Negative-QTOFsplash10-03k9-7900000000-393d57f04b27dd5e4fd52016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 10V, Positive-QTOFsplash10-03di-0900000000-a3d58fb14ea7afd59b1e2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 20V, Positive-QTOFsplash10-03di-2900000000-58ee68ef0fcfda3c601a2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 40V, Positive-QTOFsplash10-004l-9000000000-ef8cc9e7a1f93e525c682021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 10V, Negative-QTOFsplash10-03di-0900000000-46c67a826c5a9b724e0c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 20V, Negative-QTOFsplash10-001i-9000000000-c2fa753da65a4bac80a12021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Chloroacetyl chloride 40V, Negative-QTOFsplash10-001i-9000000000-c2fa753da65a4bac80a12021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 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, 1000 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, 200 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, 300 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, 400 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, 500 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, 600 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, 700 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, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX 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 IDNot Available
KEGG Compound IDC14859
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkChloroacetyl chloride
METLIN IDNot Available
PubChem Compound6577
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDM01444
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.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Glutathione S-transferase Mu 2
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
Enzyme Details
2. Glutathione S-transferase Mu 1
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
Enzyme Details
3. Glutathione S-transferase kappa 1
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
Enzyme Details
4. Microsomal glutathione S-transferase 3
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
Enzyme Details
5. Glutathione S-transferase Mu 3
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
Enzyme Details
6. Glutathione S-transferase A1
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
Enzyme Details
7. Microsomal glutathione S-transferase 1
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
Enzyme Details
8. Glutathione S-transferase Mu 4
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
Enzyme Details
9. Glutathione S-transferase Mu 5
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
Enzyme Details
10. Microsomal glutathione S-transferase 2
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.

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