<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-14 20:11:04 UTC</creation_date>
  <update_date>2026-08-22 06:22:51 UTC</update_date>
  <accession/>
  <common_name>Avapritinib</common_name>
  <class>SmallMolecule</class>
  <description>Avapritinib is an organic compound with the formula C26H27FN10 and an average molecular weight of 498.57 g/mol. Avapritinib belongs to the piperazines, a subclass of diazinanes within the organic compounds.

This compound is classified as an antineoplastic agent and is found in healthcare, pharmaceuticals, and veterinary products. Its recorded route of exposure is oral. Avapritinib acts as an inhibitor for two protein targets: the Platelet-derived growth factor receptor alpha (PDGFRA) and the Mast/stem cell growth factor receptor Kit (KIT).</description>
  <categories/>
  <types/>
  <synonyms/>
  <chemical_formula>C26H27FN10</chemical_formula>
  <average_molecular_weight>498.57</average_molecular_weight>
  <monisotopic_moleculate_weight>498.240419072</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>1703793-34-3</cas_registry_number>
  <smiles>CN1C=C(C=N1)C1=CN2N=CN=C(N3CCN(CC3)C3=NC=C(C=N3)[C@@](C)(N)C3=CC=C(F)C=C3)C2=C1</smiles>
  <inchi>InChI=1S/C26H27FN10/c1-26(28,20-3-5-22(27)6-4-20)21-13-29-25(30-14-21)36-9-7-35(8-10-36)24-23-11-18(16-37(23)33-17-31-24)19-12-32-34(2)15-19/h3-6,11-17H,7-10,28H2,1-2H3/t26-/m0/s1</inchi>
  <inchikey>DWYRIWUZIJHQKQ-SANMLTNESA-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>Avapritinib Drug Metabolism</name>
      <smpdb_id>SMP0130893</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Avapritinib Drug Metabolism Action Pathway</name>
      <smpdb_id>SMP0145241</smpdb_id>
      <kegg_map_id/>
    </pathway>
  </pathways>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>3.26</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>498.57</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>498.240419072</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CN1C=C(C=N1)C1=CN2N=CN=C(N3CCN(CC3)C3=NC=C(C=N3)[C@@](C)(N)C3=CC=C(F)C=C3)C2=C1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C26H27FN10</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C26H27FN10/c1-26(28,20-3-5-22(27)6-4-20)21-13-29-25(30-14-21)36-9-7-35(8-10-36)24-23-11-18(16-37(23)33-17-31-24)19-12-32-34(2)15-19/h3-6,11-17H,7-10,28H2,1-2H3/t26-/m0/s1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>DWYRIWUZIJHQKQ-SANMLTNESA-N</value>
      <source>ChemAxon</source>
    </property>
  </predicted_properties>
  <route_of_exposure/>
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  <metabolism/>
  <toxicity/>
  <lethaldose/>
  <carcinogenicity/>
  <use_source/>
  <min_risk_level/>
  <health_effects>#&lt;HealthEffect::ActiveRecord_Associations_CollectionProxy:0x00007f3bf30d44c8&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id>DB15233</drugbank_id>
  <hmdb_id/>
  <pubchem_compound_id>118023034</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id/>
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  <biocyc_id/>
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  <wikipidia/>
  <general_references/>
  <targets>
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