Posted inUncategorized

Leucyl-Asparagine

July 21, 2017
Common Name

Leucyl-Asparagine Description

Leucyl-Asparagine is a dipeptide composed of leucine and asparagine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite. Structure

MOLSDF3D-SDFPDBSMILESInChI View 3D Structure

Structure for HMDB28924 (Leucyl-Asparagine)

Synonyms

Value Source L-Leucyl-L-asparagineHMDB L-N DipeptideHMDB Leu-asnHMDB Leucine asparagine dipeptideHMDB Leucine-asparagine dipeptideHMDB LeucylasparagineHMDB LN DipeptideHMDB

Chemical Formlia

C10H19N3O4 Average Molecliar Weight

245.2756 Monoisotopic Molecliar Weight

245.137556111 IUPAC Name

2-(2-amino-4-methylpentanamido)-3-carbamoylpropanoic acid Traditional Name

2-(2-amino-4-methylpentanamido)-3-carbamoylpropanoic acid CAS Registry Number

Not Available SMILES

CC(C)CC(N)C(=O)NC(CC(N)=O)C(O)=O

InChI Identifier

InChI=1S/C10H19N3O4/c1-5(2)3-6(11)9(15)13-7(10(16)17)4-8(12)14/h5-7H,3-4,11H2,1-2H3,(H2,12,14)(H,13,15)(H,16,17)

InChI Key

MLTRLIITQPXHBJ-UHFFFAOYSA-N Chemical Taxonomy Description

This compound belongs to the class of chemical entities known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Kingdom

Chemical entities Super Class

Organic compounds Class

Organic acids and derivatives Sub Class

Carboxylic acids and derivatives Direct Parent

Dipeptides Alternative Parents

  • Asparagine and derivatives
  • Leucine and derivatives
  • N-acyl-alpha amino acids
  • Alpha amino acid amides
  • Branched fatty acids
  • N-acyl amines
  • Secondary carboxylic acid amides
  • Primary carboxylic acid amides
  • Amino acids
  • Monocarboxylic acids and derivatives
  • Carboxylic acids
  • Carbonyl compounds
  • Hydrocarbon derivatives
  • Monoalkylamines
  • Organic oxides
  • Organopnictogen compounds

    • Substituents

  • Alpha-dipeptide
  • Leucine or derivatives
  • Asparagine or derivatives
  • N-acyl-alpha-amino acid
  • N-acyl-alpha amino acid or derivatives
  • Alpha-amino acid amide
  • Alpha-amino acid or derivatives
  • Branched fatty acid
  • N-acyl-amine
  • Fatty amide
  • Fatty acid
  • Fatty acyl
  • Primary carboxylic acid amide
  • Amino acid or derivatives
  • Secondary carboxylic acid amide
  • Amino acid
  • Carboxamide group
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organic nitrogen compound
  • Organonitrogen compound
  • Primary aliphatic amine
  • Organooxygen compound
  • Primary amine
  • Hydrocarbon derivative
  • Carbonyl group
  • Organic oxide
  • Organopnictogen compound
  • Amine
  • Organic oxygen compound
  • Aliphatic acyclic compound

    • Molecliar Framework

    Aliphatic acyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous

    • Biofunction

    Not Available Application

    Not Available Cellliar locations

    Not Available Physical Properties State

    Solid Experimental Properties

    Property Value Reference Melting PointNot AvailableNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogP-3.57Extrapolated

    Predicted Properties

    Property Value Source Water Solubility6.24 mg/mLALOGPS logP-2.8ALOGPS logP-3.6ChemAxon logS-1.6ALOGPS pKa (Strongest Acidic)3.71ChemAxon pKa (Strongest Basic)8.43ChemAxon Physiological Charge0ChemAxon Hydrogen Acceptor Count5ChemAxon Hydrogen Donor Count4ChemAxon Polar Surface Area135.51 Å2ChemAxon Rotatable Bond Count7ChemAxon Refractivity59.33 m3·mol-1ChemAxon Polarizability25.11 Å3ChemAxon Number of Rings0ChemAxon Bioavailability1ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Not Available Biological Properties Cellliar Locations

    Not Available Biofluid Locations

    Not Available Tissue Location

    Not Available Pathways

    Not Available Normal Concentrations Not Available Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    Not Available KNApSAcK ID

    Not Available Chemspider ID

    Not Available KEGG Compound ID

    Not Available BioCyc ID

    Not Available BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB28924 Metagene Link

    HMDB28924 METLIN ID

    Not Available PubChem Compound

    Not Available PDB ID

    Not Available ChEBI ID

    Not Available

    Product: Proguanil

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. Furuya K, Schegg KM, Wang H, King DS, Schooley DA: Isolation and identification of a diuretic hormone from the mealworm Tenebrio molitor. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12323-7. [PubMed:8618894 ]
    2. Tatemoto K, Mutt V: Chemical determination of polypeptide hormones. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4115-9. [PubMed:279902 ]

    PMID: 16687477

    Last updated on