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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
  • Amsacrine
rdfs:subClassOf
Has_Salt_Form
Concept_In_Subset
Semantic_Type
  • Organic Chemical
  • Pharmacologic Substance
Preferred_Name
  • Amsacrine
NSC_Code
  • 249992
UMLS_CUI
  • C0591085
CAS_Registry
  • 51264-14-3
In_Clinical_Trial_For
  • Myeloid leukemia
FDA_UNII_Code
  • 00DPD30SOY
Contributing_Source
  • FDA
PDQ_Open_Trial_Search_ID
  • 39142
PDQ_Closed_Trial_Search_ID
  • 39142
Chemical_Formula
  • C21H19N3O3S
Legacy_Concept_Name
  • Amsacrine
CHEBI_ID
  • CHEBI:2687
FULL_SYN
  • m-AMSASYDTPNSC0249992
  • Cain's AcridineSYNCI
  • SN 11841SYDTPNSC0156303
  • AMSAABNCI
  • 4'-(9-Acridinylamino)methane-sulfon-m-anisidideSNNCI
  • AmsidineSYDTPNSC0249992
  • CI-880CNNCI
  • m-AMSAABNCI
  • AMSACRINEPTFDA00DPD30SOY
  • N-[4-(9-Acridinylamino)-3-methoxyphenyl]methanesulfonamideSNNCI
  • AmekrinFBNCI
  • AmsidylFBNCI
  • AmsacrineSYDTPNSC0249992
  • SN-11841CNNCI
  • SN-21429CNNCI
  • Amsa P-DBRNCI
  • Acridinyl AnisidideSYNCI
  • LamasineFBNCI
  • AmsidineFBNCI
  • AmsacrinePTNCI
  • amsacrinePTNCI-GLOSSCDR0000045172
DEFINITION
  • An aminoacridine derivative with potential antineoplastic activity. Although its mechanism of action is incompletely defined, amsacrine may intercalate into DNA and inhibit topoisomerase II, resulting in DNA double-strand breaks, arrest of the S/G2 phase of the cell cycle, and cell death. This agent's cytotoxicity is maximal during the S phase of the cell cycle when topoisomerase levels are greatest. In addition, amsacrine may induce transcription of tumor promoter p53 protein and block p53 ubiquitination and proteasomal degradation, resulting in p53-dependent tumor cell apoptosis.NCI
code
  • C240
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