Hesperaline

Common Name

Hesperaline Description

Hesperaline is found in brassicas. Hesperaline is an alkaloid from seeds of damask violet (Hesperis matronalis Cruciferae) Hesperaline belongs to the family of Benzoic Acid and Derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring. Structure

MOLSDF3D-SDFPDBSMILESInChI View 3D Structure

Structure for HMDB29560 (Hesperaline)

Synonyms

Not Available Chemical Formlia

C14H22NO4 Average Molecliar Weight

268.3288 Monoisotopic Molecliar Weight

268.154883197 IUPAC Name

[2-(3,4-dimethoxybenzoyloxy)ethyl]trimethylazanium Traditional Name

[2-(3,4-dimethoxybenzoyloxy)ethyl]trimethylazanium CAS Registry Number

15797-38-3 SMILES

COC1=C(OC)C=C(C=C1)C(=O)OCC[N+](C)(C)C

InChI Identifier

InChI=1S/C14H22NO4/c1-15(2,3)8-9-19-14(16)11-6-7-12(17-4)13(10-11)18-5/h6-7,10H,8-9H2,1-5H3/q+1

InChI Key

IXSHJXHXZYUCPK-UHFFFAOYSA-N Chemical Taxonomy Description

This compound belongs to the class of chemical entities known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group. Kingdom

Chemical entities Super Class

Organic compounds Class

Benzenoids Sub Class

Benzene and substituted derivatives Direct Parent

P-methoxybenzoic acids and derivatives Alternative Parents

  • M-methoxybenzoic acids and derivatives
  • Benzoic acid esters
  • Dimethoxybenzenes
  • Anisoles
  • Benzoyl derivatives
  • Phenoxy compounds
  • Alkyl aryl ethers
  • Tetraalkylammonium salts
  • Carboxylic acid esters
  • Monocarboxylic acids and derivatives
  • Organopnictogen compounds
  • Hydrocarbon derivatives
  • Amines
  • Organic oxides
  • Organic salts
  • Organic cations
  • Substituents

  • M-methoxybenzoic acid or derivatives
  • P-methoxybenzoic acid or derivatives
  • Benzoate ester
  • O-dimethoxybenzene
  • Dimethoxybenzene
  • Phenoxy compound
  • Anisole
  • Benzoyl
  • Methoxybenzene
  • Phenol ether
  • Alkyl aryl ether
  • Tetraalkylammonium salt
  • Quaternary ammonium salt
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Ether
  • Carboxylic acid derivative
  • Organic salt
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Amine
  • Organic cation
  • Aromatic homomonocyclic compound
  • Molecliar Framework

    Aromatic homomonocyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

    Not Available Application

  • Nutrient
  • Cellliar locations

  • Cytoplasm
  • Extracellliar
  • Physical Properties State

    Not Available Experimental Properties

    Property Value Reference Melting Point182 – 183 °CNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.008 mg/mLALOGPS logP-1.5ALOGPS logP-2.5ChemAxon logS-4.6ALOGPS pKa (Strongest Basic)-4.6ChemAxon Physiological Charge1ChemAxon Hydrogen Acceptor Count3ChemAxon Hydrogen Donor Count0ChemAxon Polar Surface Area44.76 Å2ChemAxon Rotatable Bond Count7ChemAxon Refractivity84.94 m3·mol-1ChemAxon Polarizability29.92 Å3ChemAxon Number of Rings1ChemAxon Bioavailability1ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Not Available Biological Properties Cellliar Locations

  • Cytoplasm
  • Extracellliar
  • 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

    FDB000713 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

    HMDB29560 Metagene Link

    HMDB29560 METLIN ID

    Not Available PubChem Compound

    Not Available PDB ID

    Not Available ChEBI ID

    Not Available

    Product: KNK437

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

    PMID: 18353306

    Hesperaline

    Common Name

    Hesperaline Description

    Hesperaline is found in brassicas. Hesperaline is an alkaloid from seeds of damask violet (Hesperis matronalis Cruciferae) Hesperaline belongs to the family of Benzoic Acid and Derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring. Structure

    MOLSDF3D-SDFPDBSMILESInChI View 3D Structure

    Structure for HMDB29560 (Hesperaline)

    Synonyms

    Not Available Chemical Formlia

    C14H22NO4 Average Molecliar Weight

    268.3288 Monoisotopic Molecliar Weight

    268.154883197 IUPAC Name

    [2-(3,4-dimethoxybenzoyloxy)ethyl]trimethylazanium Traditional Name

    [2-(3,4-dimethoxybenzoyloxy)ethyl]trimethylazanium CAS Registry Number

    15797-38-3 SMILES

    COC1=C(OC)C=C(C=C1)C(=O)OCC[N+](C)(C)C

    InChI Identifier

    InChI=1S/C14H22NO4/c1-15(2,3)8-9-19-14(16)11-6-7-12(17-4)13(10-11)18-5/h6-7,10H,8-9H2,1-5H3/q+1

    InChI Key

    IXSHJXHXZYUCPK-UHFFFAOYSA-N Chemical Taxonomy Description

    This compound belongs to the class of chemical entities known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group. Kingdom

    Chemical entities Super Class

    Organic compounds Class

    Benzenoids Sub Class

    Benzene and substituted derivatives Direct Parent

    P-methoxybenzoic acids and derivatives Alternative Parents

  • M-methoxybenzoic acids and derivatives
  • Benzoic acid esters
  • Dimethoxybenzenes
  • Anisoles
  • Benzoyl derivatives
  • Phenoxy compounds
  • Alkyl aryl ethers
  • Tetraalkylammonium salts
  • Carboxylic acid esters
  • Monocarboxylic acids and derivatives
  • Organopnictogen compounds
  • Hydrocarbon derivatives
  • Amines
  • Organic oxides
  • Organic salts
  • Organic cations
  • Substituents

  • M-methoxybenzoic acid or derivatives
  • P-methoxybenzoic acid or derivatives
  • Benzoate ester
  • O-dimethoxybenzene
  • Dimethoxybenzene
  • Phenoxy compound
  • Anisole
  • Benzoyl
  • Methoxybenzene
  • Phenol ether
  • Alkyl aryl ether
  • Tetraalkylammonium salt
  • Quaternary ammonium salt
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Ether
  • Carboxylic acid derivative
  • Organic salt
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Amine
  • Organic cation
  • Aromatic homomonocyclic compound
  • Molecliar Framework

    Aromatic homomonocyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

    Not Available Application

  • Nutrient
  • Cellliar locations

  • Cytoplasm
  • Extracellliar
  • Physical Properties State

    Not Available Experimental Properties

    Property Value Reference Melting Point182 – 183 °CNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility0.008 mg/mLALOGPS logP-1.5ALOGPS logP-2.5ChemAxon logS-4.6ALOGPS pKa (Strongest Basic)-4.6ChemAxon Physiological Charge1ChemAxon Hydrogen Acceptor Count3ChemAxon Hydrogen Donor Count0ChemAxon Polar Surface Area44.76 Å2ChemAxon Rotatable Bond Count7ChemAxon Refractivity84.94 m3·mol-1ChemAxon Polarizability29.92 Å3ChemAxon Number of Rings1ChemAxon Bioavailability1ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Not Available Biological Properties Cellliar Locations

  • Cytoplasm
  • Extracellliar
  • 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

    FDB000713 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

    HMDB29560 Metagene Link

    HMDB29560 METLIN ID

    Not Available PubChem Compound

    Not Available PDB ID

    Not Available ChEBI ID

    Not Available

    Product: KNK437

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

    PMID: 18353306