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

AttributesValues
rdf:type
rdfs:label
  • Gimatecan
rdfs:subClassOf
Has_Target
Concept_In_Subset
Semantic_Type
  • Pharmacologic Substance
Preferred_Name
  • Gimatecan
UMLS_CUI
  • C0969276
CAS_Registry
  • 292618-32-7
In_Clinical_Trial_For
  • Advanced Solid Tumor; Malignant Glioma
FDA_UNII_Code
  • 7KKS9R192F
Contributing_Source
  • FDA
ALT_DEFINITION
  • A substance that is being studied in the treatment of cancer. It belongs to the family of drugs called topoisomerase inhibitors.NCI-GLOSS
PDQ_Open_Trial_Search_ID
  • 537638
PDQ_Closed_Trial_Search_ID
  • 537638
Chemical_Formula
  • C25H25N3O5
Legacy_Concept_Name
  • Gimatecan
FULL_SYN
  • 7-t-ButoxyiminomethylcamptothecinSNNCI
  • ST1481PTNCI-GLOSSCDR0000386216
  • LBQ707CNNCI
  • STI481CNNCI
  • GIMATECANPTFDA7KKS9R192F
  • GimatecanPTNCI
  • gimatecanPTNCI-GLOSSCDR0000386214
DEFINITION
  • An orally bioavailable, semi-synthetic lipophilic analogue of camptothecin, a quinoline alkaloid extracted from the Asian tree Camptotheca acuminate, with potential antineoplastic and antiangiogenic activities. Gimatecan binds to and inhibits the activity of topoisomerase I, stabilizing the cleavable complex of topoisomerase I-DNA, which inhibits the religation of single-stranded DNA breaks generated by topoisomerase I; lethal double-stranded DNA breaks occur when the topoisomerase I-DNA complex is encountered by the DNA replication machinery, DNA replication is disrupted, and the tumor cell undergoes apoptosis. Although the mechanism of its antiangiogenic activity has yet to be full elucidated, this agent may inhibit endothelial cell migration, tumor neovascularization, and the expression of proangiogenic basic fibroblast growth factor (bFGF).NCI
code
  • C65804
http://linked.open...y/mesh/hasConcept
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