<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <version>1.0</version>
  <creation_date>2026-04-05 13:49:57 UTC</creation_date>
  <update_date>2026-08-20 01:52:57 UTC</update_date>
  <accession/>
  <common_name>Talazoparib</common_name>
  <class>SmallMolecule</class>
  <description>Talazoparib is an organic compound with the chemical formula C19H14F2N6O and an average molecular weight of 380.36 g/mol. Talazoparib belongs to the phenylquinolines, a subclass of quinolines and derivatives within the organic compounds. 

This compound is used as an antineoplastic agent within the sector of healthcare, pharmaceuticals, and veterinary products, with oral administration as the recorded exposure route. In terms of biological activity, talazoparib acts as an inhibitor of two protein targets: Poly [ADP-ribose] polymerase 1 (PARP1) and Poly [ADP-ribose] polymerase 2 (PARP2).</description>
  <categories/>
  <types/>
  <synonyms/>
  <chemical_formula>C19H14F2N6O</chemical_formula>
  <average_molecular_weight>380.359</average_molecular_weight>
  <monisotopic_moleculate_weight>380.1197155</monisotopic_moleculate_weight>
  <iupac_name/>
  <traditional_iupac/>
  <cas_registry_number>1207456-01-6</cas_registry_number>
  <smiles>CN1N=CN=C1[C@@H]1[C@H](NC2=C3C1=NNC(=O)C3=CC(F)=C2)C1=CC=C(F)C=C1</smiles>
  <inchi>InChI=1S/C19H14F2N6O/c1-27-18(22-8-23-27)15-16(9-2-4-10(20)5-3-9)24-13-7-11(21)6-12-14(13)17(15)25-26-19(12)28/h2-8,15-16,24H,1H3,(H,26,28)/t15-,16-/m1/s1</inchi>
  <inchikey>HWGQMRYQVZSGDQ-HZPDHXFCSA-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>Talazoparib Drug Metabolism</name>
      <smpdb_id>SMP0130871</smpdb_id>
      <kegg_map_id/>
    </pathway>
    <pathway>
      <name>Talazoparib Drug Metabolism Action Pathway</name>
      <smpdb_id>SMP0144778</smpdb_id>
      <kegg_map_id/>
    </pathway>
  </pathways>
  <state/>
  <appearance/>
  <experimental_properties>
    <property>
      <kind>logp</kind>
      <value>2.11</value>
    </property>
  </experimental_properties>
  <predicted_properties>
    <property>
      <kind>average_mass</kind>
      <value>380.359</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>mono_mass</kind>
      <value>380.1197155</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>smiles</kind>
      <value>CN1N=CN=C1[C@@H]1[C@H](NC2=C3C1=NNC(=O)C3=CC(F)=C2)C1=CC=C(F)C=C1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>formula</kind>
      <value>C19H14F2N6O</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchi</kind>
      <value>InChI=1S/C19H14F2N6O/c1-27-18(22-8-23-27)15-16(9-2-4-10(20)5-3-9)24-13-7-11(21)6-12-14(13)17(15)25-26-19(12)28/h2-8,15-16,24H,1H3,(H,26,28)/t15-,16-/m1/s1</value>
      <source>ChemAxon</source>
    </property>
    <property>
      <kind>inchikey</kind>
      <value>HWGQMRYQVZSGDQ-HZPDHXFCSA-N</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:0x00007f7277712960&gt;</health_effects>
  <symptoms/>
  <treatment/>
  <drugbank_id>DB11760</drugbank_id>
  <hmdb_id/>
  <pubchem_compound_id>135565082</pubchem_compound_id>
  <chembl_id/>
  <chemspider_id/>
  <kegg_id/>
  <uniprot_id/>
  <omim_id/>
  <chebi_id/>
  <biocyc_id/>
  <ctd_id/>
  <stitch_id/>
  <actor_id/>
  <pdb_id/>
  <wikipidia/>
  <general_references/>
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</compound>
