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<BioportalConcept>
  <label>Carbutamide</label>
  <id>Carbutamide</id>
  <fullId>http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Carbutamide</fullId>
  <definitions>
    <string>A first-generation sulfonylurea with hypoglycemic activity. Carbutamide was one of the first sulfonylurea compounds used but was withdrawn from the market due to toxic effects on bone marrow. This agent has a long half-life.</string>
  </definitions>
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        <string>SubClass</string>
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    </BioportalEntry>
    <BioportalEntry>
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        <string>rdfs:subClassOf</string>
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        <BioportalConcept>
          <label>Sulfonylurea Antidiabetic Agent</label>
          <id>Sulfonylurea_Antidiabetic_Agent</id>
          <fullId>http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Sulfonylurea_Antidiabetic_Agent</fullId>
          <relations/>
          <type>class</type>
        </BioportalConcept>
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    <BioportalEntry>
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        <string>rdfs:label</string>
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        <string>Carbutamide</string>
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    <BioportalEntry>
      <strings>
        <string>Concept_In_Subset</string>
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        <BioportalConcept>
          <label>FDA Established Names and Unique Ingredient Identifier Codes Terminology</label>
          <id>FDA_UNII_Code_Terminology</id>
          <fullId>http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#FDA_UNII_Code_Terminology</fullId>
          <relations/>
          <type>class</type>
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    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>FDA_UNII_Code</string>
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      <list>
        <string>E3K8P4869P</string>
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    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>code</string>
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      <list>
        <string>C83597</string>
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    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>CAS_Registry</string>
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      <list>
        <string>339-43-5</string>
      </list>
    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>SuperClass</string>
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        <BioportalConcept>
          <label>Sulfonylurea Antidiabetic Agent</label>
          <id>Sulfonylurea_Antidiabetic_Agent</id>
          <fullId>http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Sulfonylurea_Antidiabetic_Agent</fullId>
          <synonyms>
            <string>Sulphonylurea Antidiabetic Agent</string>
          </synonyms>
          <definitions>
            <string>Sulfonamide urea derivatives with antihyperglycemic activity. Sulphonylurea antidiabetic agents bind to sulfonylurea receptor type 1 (SUR1), the subunit of ATP-sensitive inwardly-rectifier potassium (IKATP) channels on the membranes of pancreatic beta cells, thereby blocking the inward current flow (influx) of positively charged K+ ions into the cell. This results in tonic membrane depolarization, and induces a calcium ion influx through voltage-sensitive calcium channels; increased intracellular calcium ion levels trigger exocytosis of insulin-containing granules. This eventually induces secretion of insulin. The IKATP channels found in pancreatic islets are complexes of four IKATP 6.2 and four SUR1 subunits. In addition, some sulfonylureas of larger molecular size may increase the sensitivity of peripheral tissues to insulin mediated through peroxisome proliferator-activated receptor gamma (PPARgamma).</string>
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            <BioportalEntry>
              <strings>
                <string>DEFINITION</string>
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              <list>
                <string>Sulfonamide urea derivatives with antihyperglycemic activity. Sulphonylurea antidiabetic agents bind to sulfonylurea receptor type 1 (SUR1), the subunit of ATP-sensitive inwardly-rectifier potassium (IKATP) channels on the membranes of pancreatic beta cells, thereby blocking the inward current flow (influx) of positively charged K+ ions into the cell. This results in tonic membrane depolarization, and induces a calcium ion influx through voltage-sensitive calcium channels; increased intracellular calcium ion levels trigger exocytosis of insulin-containing granules. This eventually induces secretion of insulin. The IKATP channels found in pancreatic islets are complexes of four IKATP 6.2 and four SUR1 subunits. In addition, some sulfonylureas of larger molecular size may increase the sensitivity of peripheral tissues to insulin mediated through peroxisome proliferator-activated receptor gamma (PPARgamma).</string>
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                <string>SubClass</string>
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            <BioportalEntry>
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                <string>RdfType</string>
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            <BioportalEntry>
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                <string>rdfs:label</string>
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                <string>Sulfonylurea Antidiabetic Agent</string>
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            <BioportalEntry>
              <strings>
                <string>rdfs:subClassOf</string>
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                <BioportalConcept>
                  <label>Anti-diabetic Agent</label>
                  <id>Anti-diabetic_Agent</id>
                  <fullId>http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Anti-diabetic_Agent</fullId>
                  <relations/>
                  <type>class</type>
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              <strings>
                <string>ChildCount</string>
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              <counter>29</counter>
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                <string>Semantic_Type</string>
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                <string>Chemical Viewed Functionally</string>
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              <strings>
                <string>code</string>
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                <string>C97936</string>
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              <strings>
                <string>FULL_SYN</string>
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                <string>Sulphonylurea Antidiabetic Agent</string>
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              <strings>
                <string>NCI_META_CUI</string>
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                <string>CL430547</string>
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                <string>Sulfonylurea Antidiabetic Agent</string>
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    <BioportalEntry>
      <strings>
        <string>Chemical_Formula</string>
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        <string>C11H17N3O3S</string>
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    <BioportalEntry>
      <strings>
        <string>DEFINITION</string>
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        <string>A first-generation sulfonylurea with hypoglycemic activity. Carbutamide was one of the first sulfonylurea compounds used but was withdrawn from the market due to toxic effects on bone marrow. This agent has a long half-life.</string>
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        <string>ChildCount</string>
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    <BioportalEntry>
      <strings>
        <string>Semantic_Type</string>
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        <string>Pharmacologic Substance</string>
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    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>UMLS_CUI</string>
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        <string>C0007080</string>
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    <BioportalEntry>
      <strings>
        <string>Contributing_Source</string>
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        <string>FDA</string>
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    <BioportalEntry>
      <strings>
        <string>Preferred_Name</string>
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      <list>
        <string>Carbutamide</string>
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    </BioportalEntry>
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</BioportalConcept>

