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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2021-09-14 15:47:38 UTC
HMDB IDHMDB0001177
Secondary Accession Numbers
  • HMDB0001012
  • HMDB01012
  • HMDB01177
Metabolite Identification
Common Name(S)-Succinyldihydrolipoamide
Description(S)-Succinyldihydrolipoamide belongs to the class of organic compounds known as thia fatty acids. These are fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain (S)-Succinyldihydrolipoamide is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Data?1582752182
Synonyms
ValueSource
S-Succinyl-dihydrolipoamideHMDB
S-SuccinyldihydrolipoamideHMDB
Chemical FormulaC12H21NO4S2
Average Molecular Weight307.429
Monoisotopic Molecular Weight307.091199545
IUPAC Name4-{[(3R)-7-carbamoyl-1-sulfanylheptan-3-yl]sulfanyl}-4-oxobutanoic acid
Traditional Name4-{[(3R)-7-carbamoyl-1-sulfanylheptan-3-yl]sulfanyl}-4-oxobutanoic acid
CAS Registry NumberNot Available
SMILES
NC(=O)CCCC[C@H](CCS)SC(=O)CCC(O)=O
InChI Identifier
InChI=1S/C12H21NO4S2/c13-10(14)4-2-1-3-9(7-8-18)19-12(17)6-5-11(15)16/h9,18H,1-8H2,(H2,13,14)(H,15,16)/t9-/m1/s1
InChI KeyRJCJWONCSKSHES-SECBINFHSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as thia fatty acids. These are fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acids and conjugates
Direct ParentThia fatty acids
Alternative Parents
Substituents
  • Thia fatty acid
  • Fatty acyl thioester
  • Fatty amide
  • Carboxamide group
  • Primary carboxylic acid amide
  • Thiocarboxylic acid ester
  • Carbothioic s-ester
  • Sulfenyl compound
  • Thiocarboxylic acid or derivatives
  • Alkylthiol
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Carbonyl group
  • Organic oxygen compound
  • Organosulfur compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
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 Solubility0.1 g/LALOGPS
logP1.97ALOGPS
logP1.06ChemAxon
logS-3.5ALOGPS
pKa (Strongest Acidic)4.38ChemAxon
pKa (Strongest Basic)-0.58ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area97.46 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity78.12 m³·mol⁻¹ChemAxon
Polarizability32.86 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+171.13931661259
DarkChem[M-H]-168.45931661259
AllCCS[M+H]+167.23832859911
AllCCS[M-H]-170.6532859911
DeepCCS[M+H]+182.44530932474
DeepCCS[M-H]-180.08730932474
DeepCCS[M-2H]-212.97530932474
DeepCCS[M+Na]+188.53930932474
AllCCS[M+H]+167.232859911
AllCCS[M+H-H2O]+164.632859911
AllCCS[M+NH4]+169.732859911
AllCCS[M+Na]+170.432859911
AllCCS[M-H]-170.732859911
AllCCS[M+Na-2H]-171.632859911
AllCCS[M+HCOO]-172.832859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(S)-SuccinyldihydrolipoamideNC(=O)CCCC[C@H](CCS)SC(=O)CCC(O)=O4050.8Standard polar33892256
(S)-SuccinyldihydrolipoamideNC(=O)CCCC[C@H](CCS)SC(=O)CCC(O)=O2514.2Standard non polar33892256
(S)-SuccinyldihydrolipoamideNC(=O)CCCC[C@H](CCS)SC(=O)CCC(O)=O2832.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(S)-Succinyldihydrolipoamide,1TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(N)=O2659.7Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,1TMS,isomer #2C[Si](C)(C)SCC[C@@H](CCCCC(N)=O)SC(=O)CCC(=O)O2781.7Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,1TMS,isomer #3C[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O2722.6Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C2805.6Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C2773.4Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C4328.4Standard polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #2C[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C2777.4Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #2C[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C2719.2Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #2C[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C3475.7Standard polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #3C[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O2836.6Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #3C[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O2846.6Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #3C[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O3864.8Standard polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #4C[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C2779.6Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #4C[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C2702.6Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TMS,isomer #4C[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C3620.2Standard polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #1C[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)C2874.8Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #1C[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)C2905.4Standard non polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #1C[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)C3408.6Standard polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C2799.7Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C2811.1Standard non polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C3353.6Standard polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #3C[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)SC(=O)CCC(=O)O2941.3Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #3C[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)SC(=O)CCC(=O)O2934.7Standard non polar33892256
(S)-Succinyldihydrolipoamide,3TMS,isomer #3C[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)SC(=O)CCC(=O)O3513.9Standard polar33892256
(S)-Succinyldihydrolipoamide,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)CCS[Si](C)(C)C2941.8Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)CCS[Si](C)(C)C2969.2Standard non polar33892256
(S)-Succinyldihydrolipoamide,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)CCS[Si](C)(C)C3132.4Standard polar33892256
(S)-Succinyldihydrolipoamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(N)=O2950.1Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)SCC[C@@H](CCCCC(N)=O)SC(=O)CCC(=O)O3044.5Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O2979.3Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C(C)(C)C3330.3Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C(C)(C)C3192.9Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C(C)(C)C4178.4Standard polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C3285.2Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C3078.7Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C3559.3Standard polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O3393.0Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O3200.7Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O3759.2Standard polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3271.7Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3067.7Standard non polar33892256
(S)-Succinyldihydrolipoamide,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3633.2Standard polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C3627.1Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C3410.5Standard non polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C3528.9Standard polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3513.6Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3319.0Standard non polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3497.4Standard polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O3705.0Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O3437.3Standard non polar33892256
(S)-Succinyldihydrolipoamide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)O3594.3Standard polar33892256
(S)-Succinyldihydrolipoamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCS[Si](C)(C)C(C)(C)C3912.4Semi standard non polar33892256
(S)-Succinyldihydrolipoamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCS[Si](C)(C)C(C)(C)C3621.5Standard non polar33892256
(S)-Succinyldihydrolipoamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CCS[Si](C)(C)C(C)(C)C3417.5Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (S)-Succinyldihydrolipoamide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0ukc-9880000000-d66345c90ce5eb67fa602017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (S)-Succinyldihydrolipoamide GC-MS (1 TMS) - 70eV, Positivesplash10-00dl-9533000000-a1ebe0f3e168665730012017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (S)-Succinyldihydrolipoamide 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 - (S)-Succinyldihydrolipoamide 10V, Positive-QTOFsplash10-0596-0190000000-b49046dab0850898c8892015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 20V, Positive-QTOFsplash10-006y-2190000000-474bcff100b398100e492015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 40V, Positive-QTOFsplash10-0nt9-4910000000-247a7886ecdb5a884d7c2015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 10V, Positive-QTOFsplash10-0596-0190000000-b49046dab0850898c8892015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 20V, Positive-QTOFsplash10-006y-2190000000-474bcff100b398100e492015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 40V, Positive-QTOFsplash10-0nt9-4910000000-247a7886ecdb5a884d7c2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 10V, Negative-QTOFsplash10-0a4i-5294000000-672a48ef8e666cb0ee5f2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 20V, Negative-QTOFsplash10-0a4j-9360000000-f9e4f05adcb51d48447c2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 40V, Negative-QTOFsplash10-000x-9100000000-d7f410ba584f3aad89cc2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 10V, Negative-QTOFsplash10-0a4i-1229000000-d6ef878a291e343f754a2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 20V, Negative-QTOFsplash10-0a4i-7970000000-eff246297f1390d8e0372021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 40V, Negative-QTOFsplash10-000x-9500000000-66fb2d1c65f8ee705da42021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 10V, Positive-QTOFsplash10-0a4i-0369000000-035798c3620974bb7aab2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 20V, Positive-QTOFsplash10-03dl-1910000000-e3af53d75b9037036cfe2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (S)-Succinyldihydrolipoamide 40V, Positive-QTOFsplash10-0udr-5900000000-f70f4c6e3a3b250e485f2021-09-25Wishart 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 IDFDB022467
KNApSAcK IDNot Available
Chemspider ID388536
KEGG Compound IDC01169
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID6058
PubChem Compound439425
PDB IDNot Available
ChEBI ID17432
Food Biomarker OntologyNot Available
VMH IDHC00695
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Enzymes

General function:
Involved in oxoglutarate dehydrogenase (succinyl-transferring) activity
Specific function:
The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components: 2-oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3).
Gene Name:
OGDH
Uniprot ID:
Q02218
Molecular weight:
48179.59
General function:
Involved in acyltransferase activity
Specific function:
The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of 3 enzymatic components: 2-oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3).
Gene Name:
DLST
Uniprot ID:
P36957
Molecular weight:
48754.87