Therapeutic Targets Database
BIDD Pharmainformatics Databases


TTD Drug ID: DAP001342

Drug Information
SynonymsMolPort-004-845-383; AC1L27WP; LS-93909; NSC 208734; KBio2_003515; CID152688; Aclarubicin (USAN/INN); KBio2_006083; AC1L48VL; Aclacin; CID154943; SMP1_000003; Antibiotic MA 144A1; Aclarubicino [INN-Spanish]; BCBcMAP01_000191; CID6712061; MolPort-003-665-565; MolPort-003-983-841; 64520-15-6; NSC240619; 10-epi-Aclacinomycin A; NINDS_000678; acene-1-carboxylate; QTL1_000003; CID451415; 72711-48-9; 79617-46-2; KBio1_000678; NCIMech_000395; Spectrum_000467; HMS502B20; C42H53NO15; AC1L4DB3; CHEMBL45414; CHEBI:170281; DivK1c_000678; .alpha.-L-lyxo-hexopyranosyl]-oxy]-1-naphthacenecarboxalic acid methyl ester; Aclarubicino; Neuro_000108; AC1O8MK9; NSC-208734; Antibiotic MA144-A1; KBioGR_001156; Spectrum2_001934; AC1L9PMJ; Spectrum4_000768; Aclarubicin [USAN:BAN:INN]; STK177207; MA 144G1; IDI1_000678; LS-93950; MA 144-A1; D02756; LS-93943; A8959_SIGMA; NSC208734; Aclarubicine [INN-French]; Aclarubicine; AC1L1CQ0; Antibiotic MA 144G1; Spectrum5_001041; KBioSS_000947; NCI60_001746; CCRIS 2262; 57576-44-0; NCI60_018879; AC1O8OA8; aclarubicin; CID6713097; Aclacur; Jaclacin; UNII-74KXF8I502; SPBio_001967; AC1L7CAE; EINECS 260-824-3; CID42474; KBio2_000947; Aclacinomycin A; CID2008; HMS2089B13; 77448-81-8; CID308141; Aclucinomycin A; MA-144A1; NSC-208,734; Antibiotic MA 144A; CHEMBL502620; Aclarubicinum; Aclarubicinum [INN-Latin]
[ICD9: 140-229   ICD10: C00-C96]
Approved    [1]

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Canonical SMILESCCC1(CC(C2=C(C1C(=O)OC)C=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4O)OC5CC(C(C(O5)
Isomeric SMILESCC[C@]1(C[C@@H](C2=C([C@H]1C(=O)OC)C=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4O)O
Therapeutic ClassAntineoplastic Agents
CAS NumberCAS 57576-44-0
PubChem Compound IDCID 152688.
PubChem Substance IDSID 730204.
SuperDrug ATC IDL01DB04
SuperDrug CAS ID057576440;
TargetDNA topoisomerase IIInhibitor[2][3]
Ref 1Natural products as sources of new drugs over the last 25 years. J Nat Prod. 2007 Mar;70(3):461-77. Epub 2007 Feb 20. To Reference
Ref 2Linker length in podophyllotoxin-acridine conjugates determines potency in vivo and in vitro as well as specificity against MDR cell lines. Anticancer Drug Des. 2001 Dec;16(6):305-15. To Reference
Ref 31,3-Dihydroxyacridone derivatives as inhibitors of herpes virus replication. Antiviral Res. 2000 Feb;45(2):123-34. To Reference


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