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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-11 08:54:53 UTC
Update Date2021-09-26 23:03:36 UTC
HMDB IDHMDB0251550
Secondary Accession NumbersNone
Metabolite Identification
Common Name2-Hydroxy-4-carboxybutyrylhistidylprolinamide
Description2-Hydroxy-4-carboxybutyrylhistidylprolinamide belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Based on a literature review very few articles have been published on 2-Hydroxy-4-carboxybutyrylhistidylprolinamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2-hydroxy-4-carboxybutyrylhistidylprolinamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2-Hydroxy-4-carboxybutyrylhistidylprolinamide is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Structure
Thumb
SynonymsNot Available
Chemical FormulaC16H23N5O6
Average Molecular Weight381.389
Monoisotopic Molecular Weight381.164833481
IUPAC Name4-{[1-(2-carbamoylpyrrolidin-1-yl)-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]carbamoyl}-4-hydroxybutanoic acid
Traditional Name4-{[1-(2-carbamoylpyrrolidin-1-yl)-3-(3H-imidazol-4-yl)-1-oxopropan-2-yl]carbamoyl}-4-hydroxybutanoic acid
CAS Registry NumberNot Available
SMILES
NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1)NC(=O)C(O)CCC(O)=O
InChI Identifier
InChI=1S/C16H23N5O6/c17-14(25)11-2-1-5-21(11)16(27)10(6-9-7-18-8-19-9)20-15(26)12(22)3-4-13(23)24/h7-8,10-12,22H,1-6H2,(H2,17,25)(H,18,19)(H,20,26)(H,23,24)
InChI KeyQTSAHVCUJWDFEQ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentDipeptides
Alternative Parents
Substituents
  • Alpha-dipeptide
  • Histidine or derivatives
  • Proline or derivatives
  • N-acyl-alpha amino acid or derivatives
  • Alpha-amino acid amide
  • Alpha-amino acid or derivatives
  • N-acylpyrrolidine
  • Pyrrolidine carboxylic acid or derivatives
  • Pyrrolidine-2-carboxamide
  • Imidazolyl carboxylic acid derivative
  • Fatty amide
  • N-acyl-amine
  • Monosaccharide
  • Fatty acyl
  • Pyrrolidine
  • Azole
  • Heteroaromatic compound
  • Tertiary carboxylic acid amide
  • Imidazole
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Primary carboxylic acid amide
  • Monocarboxylic acid or derivatives
  • Organoheterocyclic compound
  • Azacycle
  • Carboxylic acid
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Alcohol
  • Carbonyl group
  • Organic oxide
  • Organic oxygen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
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
logP-2ALOGPS
logP-4ChemAxon
logS-1.9ALOGPS
pKa (Strongest Acidic)3.72ChemAxon
pKa (Strongest Basic)6.74ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area178.71 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity91.3 m³·mol⁻¹ChemAxon
Polarizability36.41 ųChemAxon
Number of Rings2ChemAxon
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]+179.89130932474
DeepCCS[M-H]-177.53330932474
DeepCCS[M-2H]-211.32930932474
DeepCCS[M+Na]+186.55630932474
AllCCS[M+H]+185.132859911
AllCCS[M+H-H2O]+182.732859911
AllCCS[M+NH4]+187.332859911
AllCCS[M+Na]+188.032859911
AllCCS[M-H]-185.632859911
AllCCS[M+Na-2H]-185.632859911
AllCCS[M+HCOO]-185.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2-Hydroxy-4-carboxybutyrylhistidylprolinamideNC(=O)C1CCCN1C(=O)C(CC1=CN=CN1)NC(=O)C(O)CCC(O)=O3940.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamideNC(=O)C1CCCN1C(=O)C(CC1=CN=CN1)NC(=O)C(O)CCC(O)=O2679.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamideNC(=O)C1CCCN1C(=O)C(CC1=CN=CN1)NC(=O)C(O)CCC(O)=O3845.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #1C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)NC(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3407.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #1C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)NC(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3282.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #1C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)NC(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4864.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #10C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C3336.1Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #10C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C3282.8Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #10C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C4879.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #11C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3452.6Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #11C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3285.9Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #11C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C5367.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #12C[Si](C)(C)N(C(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(O)CCC(=O)O)[Si](C)(C)C3665.2Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #12C[Si](C)(C)N(C(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(O)CCC(=O)O)[Si](C)(C)C3447.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #12C[Si](C)(C)N(C(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(O)CCC(=O)O)[Si](C)(C)C4902.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #13C[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3436.2Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #13C[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3365.3Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #13C[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4820.1Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #14C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(O)CCC(=O)O)[Si](C)(C)C3501.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #14C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(O)CCC(=O)O)[Si](C)(C)C3375.4Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #14C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(O)CCC(=O)O)[Si](C)(C)C4940.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3358.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3180.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #2C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C5376.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O3509.1Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O3258.4Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O5394.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #4C[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3497.5Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #4C[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3352.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #4C[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4812.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #5C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(CCC(=O)O)O[Si](C)(C)C3573.6Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #5C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(CCC(=O)O)O[Si](C)(C)C3342.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #5C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(CCC(=O)O)O[Si](C)(C)C4943.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #6C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C)[Si](C)(C)C3378.9Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #6C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C)[Si](C)(C)C3283.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #6C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C)[Si](C)(C)C4863.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #7C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3522.7Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #7C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3264.3Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #7C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C5361.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #8C[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3491.5Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #8C[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3369.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #8C[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4845.1Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #9C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(O)CCC(=O)O[Si](C)(C)C3573.7Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #9C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(O)CCC(=O)O[Si](C)(C)C3349.8Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TMS,isomer #9C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(O)CCC(=O)O[Si](C)(C)C4973.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3429.2Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3359.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4402.8Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #10C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C3455.2Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #10C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C3385.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #10C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C4599.2Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #11C[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3562.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #11C[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3489.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #11C[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4543.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #2C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3498.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #2C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3357.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #2C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)NC(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4574.7Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #3C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C3339.8Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #3C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C3291.8Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #3C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C4453.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3463.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C3294.3Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #4C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C5098.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #5C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3440.1Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #5C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3371.1Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #5C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C4438.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #6C[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3613.1Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #6C[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3447.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #6C[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4529.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #7C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C)[Si](C)(C)C3507.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #7C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C)[Si](C)(C)C3380.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #7C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C)[Si](C)(C)C4592.1Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3387.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3373.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #8C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C4448.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #9C[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3604.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #9C[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3449.4Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TMS,isomer #9C[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4546.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3405.1Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3375.1Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C4005.2Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #2C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3556.6Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #2C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C3455.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #2C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C4203.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #3C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C3451.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #3C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C3398.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #3C[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N(C(=O)C(CCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C4251.7Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #4C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3583.7Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #4C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3485.9Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #4C[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C4243.0Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3524.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3492.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,5TMS,isomer #5C[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C4247.0Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,6TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3539.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,6TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3494.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,6TMS,isomer #1C[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C3929.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)NC(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4076.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)NC(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3772.1Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)NC(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4758.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4030.5Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3781.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4780.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C4188.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C3832.9Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C5206.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(C(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(O)CCC(=O)O)[Si](C)(C)C(C)(C)C4354.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(C(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(O)CCC(=O)O)[Si](C)(C)C(C)(C)C3948.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N(C(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(O)CCC(=O)O)[Si](C)(C)C(C)(C)C4781.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4140.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3855.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4721.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(O)CCC(=O)O)[Si](C)(C)C(C)(C)C4221.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(O)CCC(=O)O)[Si](C)(C)C(C)(C)C3890.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(O)CCC(=O)O)[Si](C)(C)C(C)(C)C4843.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C4066.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C3715.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C5216.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O4232.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O3806.0Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O5231.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4169.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3829.5Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4721.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C4260.7Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C3863.3Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C4838.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4056.1Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3780.2Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4787.7Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C4231.5Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C3819.6Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C5217.4Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4185.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3839.8Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4722.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C4265.8Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C3877.8Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C4840.0Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4318.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3954.3Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4399.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4325.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4041.9Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4604.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4461.8Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4112.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N(C(=O)C(O)CCC(=O)O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4557.3Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4347.8Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4005.7Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)NC(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4568.1Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4192.8Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3921.2Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N(C(=O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4478.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C4375.9Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C3974.1Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(O[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(N)=O)[Si](C)(C)C(C)(C)C5007.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4333.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3981.9Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4444.7Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4478.7Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4069.8Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(CCC(=O)O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4536.9Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4378.3Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4032.1Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N(C(=O)C(CCC(=O)O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4610.6Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4291.0Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3989.4Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4439.5Standard polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4467.4Semi standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4093.2Standard non polar33892256
2-Hydroxy-4-carboxybutyrylhistidylprolinamide,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CCC(O)C(=O)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4535.1Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0f6x-6793000000-65df0d63d796f0fdfc4c2021-09-23Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_1_1) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_1_2) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_1_3) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_1_4) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_1_5) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_2_1) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide GC-MS (TBDMS_2_2) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide 10V, Positive-QTOFsplash10-001i-0019000000-663931f4d15e81450fbf2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide 20V, Positive-QTOFsplash10-02as-1459000000-92481f6e35db81056e112021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide 40V, Positive-QTOFsplash10-01pa-8900000000-a771d6c5e1363a61d96c2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide 10V, Negative-QTOFsplash10-03xr-0029000000-a65415b4a0f6f379bde92021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide 20V, Negative-QTOFsplash10-0006-9264000000-10aeb1886c1818bf3cb62021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-Hydroxy-4-carboxybutyrylhistidylprolinamide 40V, Negative-QTOFsplash10-0006-9710000000-dff937a961676ed9eab12021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-10-13Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
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 ID19994230
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound21126480
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]