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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Fluoxymesterone
rdfs:subClassOf
Concept_In_Subset
Semantic_Type
  • Pharmacologic Substance
  • Steroid
Preferred_Name
  • Fluoxymesterone
NSC_Code
  • 12165
UMLS_CUI
  • C0016366
CAS_Registry
  • 76-43-7
FDA_UNII_Code
  • 9JU12S4YFY
Contributing_Source
  • FDA
PDQ_Open_Trial_Search_ID
  • 494707
PDQ_Closed_Trial_Search_ID
  • 494707
Chemical_Formula
  • C20H29FO3
Legacy_Concept_Name
  • Fluoxymesterone
CHEBI_ID
  • CHEBI:5120
FULL_SYN
  • Ora-testrylSYDTPNSC0012165
  • 11Beta,17beta-dihydroxy-9alpha-fluoro-17alpha-methyl-4-androsten-3-oneSNNCI
  • Ora-TestrylBRNCI
  • AndrosteroloSYDTPNSC0012165
  • AndrosteroloSYNCI
  • AndrofluoreneSYNCI
  • AndrofluoreneSYDTPNSC0012165
  • FXMABNCI
  • 9Alpha-fluoro-11beta-hydroxy-17alpha-methyltestosteroneSNNCI
  • FLUOXYMESTERONEPTFDA9JU12S4YFY
  • FluoxymesteronePTNCI
  • FluoxymesteroneSYDTPNSC0012165
  • TestoralSYDTPNSC0012165
  • StenoxFBNCI
  • (11Beta,17beta)-9-fluoro-11,17-dihydroxy-17-methylandrost-4-en-3-oneSNNCI
  • UltandrenSYDTPNSC0012165
  • OratestinSYDTPNSC0012165
  • HalodrinBRNCI
  • TestoralFBNCI
  • HalotestinSYDTPNSC0012165
  • Android-FBRNCI
  • UltandrenBRNCI
  • OratestinFBNCI
  • Ora TestrylSYDTPNSC0012165
  • HalotestinBRNCI
DEFINITION
  • A halogenated derivative of 17-alpha-methyltestosterone. Similar to testosterone, fluoxymesterone binds to and activates specific nuclear receptors, resulting in an increase in protein anabolism, a decrease in amino acid catabolism, and retention of nitrogen, potassium, and phosphorus. This agent also may competitively inhibit prolactin receptors and estrogen receptors, thereby inhibiting the growth of hormone-dependent tumor lines. Fluoxymesterone is approximately five times more potent than methyltestosterone. (NCI04)NCI
code
  • C507
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