<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-03 19:53:43 UTC</creation_date>
  <update_date>2026-04-03 19:53:43 UTC</update_date>
  <accession/>
  <common_name>Tyropanic acid</common_name>
  <class>SmallMolecule</class>
  <description>Tyropanic acid belongs to the phenylpropanoic acids, a class of phenylpropanoids and polyketides within the organic compounds. It has the chemical formula C15H18I3N1O3. With an average molecular weight of 641.03 g/mol, Tyropanic acid is a heavy molecule.</description>
  <categories/>
  <types/>
  <synonyms>
    <synonym>2-(3-(Butyrylamino)-2,4,6-triiodobenzyl)butanoic acid</synonym>
    <synonym>2-(3-(Butyrylamino)-2,4,6-triiodobenzyl)butyric acid</synonym>
    <synonym>2-[3-(Butyrylamino)-2,4,6-triiodobenzyl]butanoic acid</synonym>
    <synonym>2-[3-(butyrylamino)-2,4,6-triiodobenzyl]butyric acid</synonym>
    <synonym>248-389-8</synonym>
    <synonym>4F05V145YR</synonym>
    <synonym>Acidum tyropanoicum</synonym>
    <synonym>Benzenepropanoic acid, alpha-ethyl-2,4,6-triiodo-3-((1-oxobutyl)amino)-</synonym>
    <synonym>Benzenepropanoic acid, alpha-ethyl-2,4,6-triiodo-3-[(1-oxobutyl)amino]-</synonym>
    <synonym>Hydrocinnamic acid, 3-butyramido-.alpha.-ethyl-2,4,6-triiodo-</synonym>
    <synonym>TYROPANIC ACID</synonym>
    <synonym>tyropanoate</synonym>
    <synonym>Tyropanoic acid</synonym>
    <synonym>UNII:4F05V145YR</synonym>
  </synonyms>
  <chemical_formula>C15H18I3N1O3</chemical_formula>
  <average_molecular_weight>641.026</average_molecular_weight>
  <monisotopic_moleculate_weight>640.842087</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number/>
  <smiles>CCCC(=O)NC1=C(I)C(CC(CC)C(O)=O)=C(I)C=C1I</smiles>
  <inchi>InChI=1S/C15H18I3NO3/c1-3-5-12(20)19-14-11(17)7-10(16)9(13(14)18)6-8(4-2)15(21)22/h7-8H,3-6H2,1-2H3,(H,19,20)(H,21,22)/t8-/m1/s1</inchi>
  <inchikey>YMOXVLQZFAUUKI-UHFFFAOY-N</inchikey>
  <taxonomy>
    <kingdom>Organic compounds</kingdom>
    <super_class>Phenylpropanoids and polyketides</super_class>
    <class>Phenylpropanoic acids</class>
    <sub_class/>
    <direct_parent>Phenylpropanoic acids</direct_parent>
    <alternate_parents>
      <alternative_parent>Anilides</alternative_parent>
      <alternative_parent>Aryl iodides</alternative_parent>
      <alternative_parent>Carbonyl compounds</alternative_parent>
      <alternative_parent>Carboxylic acids</alternative_parent>
      <alternative_parent>Fatty amides</alternative_parent>
      <alternative_parent>Hydrocarbon derivatives</alternative_parent>
      <alternative_parent>Iodobenzenes</alternative_parent>
      <alternative_parent>Monocarboxylic acids and derivatives</alternative_parent>
      <alternative_parent>N-arylamides</alternative_parent>
      <alternative_parent>Organic oxides</alternative_parent>
      <alternative_parent>Organoiodides</alternative_parent>
      <alternative_parent>Organopnictogen compounds</alternative_parent>
      <alternative_parent>Secondary carboxylic acid amides</alternative_parent>
    </alternate_parents>
    <substituents>
      <substituent>3-phenylpropanoic-acid</substituent>
      <substituent>Anilide</substituent>
      <substituent>Aromatic homomonocyclic compound</substituent>
      <substituent>Aryl halide</substituent>
      <substituent>Aryl iodide</substituent>
      <substituent>Benzenoid</substituent>
      <substituent>Carbonyl group</substituent>
      <substituent>Carboxamide group</substituent>
      <substituent>Carboxylic acid</substituent>
      <substituent>Carboxylic acid derivative</substituent>
      <substituent>Fatty acyl</substituent>
      <substituent>Fatty amide</substituent>
      <substituent>Halobenzene</substituent>
      <substituent>Hydrocarbon derivative</substituent>
      <substituent>Iodobenzene</substituent>
      <substituent>Monocarboxylic acid or derivatives</substituent>
      <substituent>Monocyclic benzene moiety</substituent>
      <substituent>N-arylamide</substituent>
      <substituent>Organic nitrogen compound</substituent>
      <substituent>Organic oxide</substituent>
      <substituent>Organic oxygen compound</substituent>
      <substituent>Organohalogen compound</substituent>
      <substituent>Organoiodide</substituent>
      <substituent>Organonitrogen compound</substituent>
      <substituent>Organooxygen compound</substituent>
      <substituent>Organopnictogen compound</substituent>
      <substituent>Secondary carboxylic acid amide</substituent>
    </substituents>
    <molecular_framework>Aromatic homomonocyclic compounds</molecular_framework>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways/>
  <state/>
  <appearance/>
  <experimental_properties/>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>641.026</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>640.842087</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CCCC(=O)NC1=C(I)C(CC(CC)C(O)=O)=C(I)C=C1I</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C15H18I3N1O3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C15H18I3NO3/c1-3-5-12(20)19-14-11(17)7-10(16)9(13(14)18)6-8(4-2)15(21)22/h7-8H,3-6H2,1-2H3,(H,19,20)(H,21,22)/t8-/m1/s1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>YMOXVLQZFAUUKI-UHFFFAOY-N</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
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  <chemspider_id>5409</chemspider_id>
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</compound>
