<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2016-06-03 10:27:17 UTC</creation_date>
  <update_date>2026-08-20 00:57:23 UTC</update_date>
  <accession/>
  <common_name>isoxuprine</common_name>
  <class>SmallMolecule</class>
  <description>Isoxuprine is an organic compound with the formula C18H23NO3 and an average molecular weight of 301.38 g/mol. It is found in or released from two recorded sources: healthcare, pharmaceuticals &amp; veterinary products, where it is used as a peripheral vasodilator, and electrical &amp; electronic equipment, specifically electrically stimulated smoking devices. The recorded route of exposure for this compound is oral. Isoxuprine belongs to the phenylpropanes, a subclass of benzene and substituted derivatives within the organic compounds.</description>
  <categories/>
  <types/>
  <synonyms/>
  <chemical_formula>C18H23NO3</chemical_formula>
  <average_molecular_weight>301.3801</average_molecular_weight>
  <monisotopic_moleculate_weight>301.167793607</monisotopic_moleculate_weight>
  <iupac_name>4-{1-hydroxy-2-[(1-phenoxypropan-2-yl)amino]propyl}phenol</iupac_name>
  <traditional_iupac>isoxsuprine</traditional_iupac>
  <cas_registry_number>395-28-8</cas_registry_number>
  <smiles>CC(COC1=CC=CC=C1)NC(C)C(O)C1=CC=C(O)C=C1</smiles>
  <inchi>InChI=1S/C18H23NO3/c1-13(12-22-17-6-4-3-5-7-17)19-14(2)18(21)15-8-10-16(20)11-9-15/h3-11,13-14,18-21H,12H2,1-2H3</inchi>
  <inchikey>BMUKKTUHUDJSNZ-UHFFFAOYSA-N</inchikey>
  <taxonomy>
    <kingdom/>
    <super_class/>
    <class/>
    <sub_class/>
    <direct_parent/>
    <alternate_parents/>
    <substituents/>
    <molecular_framework/>
    <descriptors/>
  </taxonomy>
  <status>Detected and Not Quantified</status>
  <origin/>
  <cellular_locations/>
  <biofluid_locations/>
  <tissue_locations/>
  <pathways>
    <pathway>
      <name>Isoxsuprine Drug Metabolism Action Pathway</name>
      <smpdb_id>SMP0144231</smpdb_id>
      <kegg_map_id/>
    </pathway>
  </pathways>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>2.56</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>logp</kind>
      <value>2.06</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logs</kind>
      <value>-3.77</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>solubility</kind>
      <value>5.07e-02 g/l</value>
      <source>ALOGPS</source>
    </property>
    <property>
      <kind>logp</kind>
      <value>2.56</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_acidic</kind>
      <value>9.65</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>pka_strongest_basic</kind>
      <value>9</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>iupac</kind>
      <value>4-{1-hydroxy-2-[(1-phenoxypropan-2-yl)amino]propyl}phenol</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>average_mass</kind>
      <value>301.3801</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>301.167793607</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CC(COC1=CC=CC=C1)NC(C)C(O)C1=CC=C(O)C=C1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C18H23NO3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C18H23NO3/c1-13(12-22-17-6-4-3-5-7-17)19-14(2)18(21)15-8-10-16(20)11-9-15/h3-11,13-14,18-21H,12H2,1-2H3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>BMUKKTUHUDJSNZ-UHFFFAOYSA-N</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polar_surface_area</kind>
      <value>61.72</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>refractivity</kind>
      <value>86.64</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>polarizability</kind>
      <value>33.32</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>rotatable_bond_count</kind>
      <value>7</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>acceptor_count</kind>
      <value>4</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>donor_count</kind>
      <value>3</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>physiological_charge</kind>
      <value>1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formal_charge</kind>
      <value>0</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
  <mechanism_of_toxicity/>
  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3bf02424e8&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id>DB08941</drugbank_id>
  <hmdb_id/>
  <pubchem_compound_id>3783</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id>3651</chemspider_id>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
  <targets>
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</compound>
