CHEBI:74803 - furaltadone

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ChEBI Name furaltadone ChEBI ID CHEBI:74803 Definition An oxazolidinone that is 1,3-oxazolidin-2-one substituted at position 1 by a (5-nitro-2-furyl)methylene]amino group and at position 5 by a morpholin-4-ylmethyl group. An antibacterial formerly used oraly but withdrawn due to toxicity, it is used topically (as the hydrochloride salt) for treatment of ear disorders. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C13H16N4O6 Net Charge 0 Average Mass 324.28930 Monoisotopic Mass 324.10698 InChI InChI=1S/C13H16N4O6/c18-13-16(14-7-10-1-2-12(22-10)17(19)20)9-11(23-13)8-15-3-5-21-6-4-15/h1-2,7,11H,3-6,8-9H2 InChIKey YVQVOQKFMFRVGR-UHFFFAOYSA-N SMILES [H]C(=NN1CC(CN2CCOCC2)OC1=O)c1ccc(o1)[N+]([O-])=O Roles Classification Biological Role(s): antibacterial drug A drug used to treat or prevent bacterial infections. Application(s): antibacterial drug A drug used to treat or prevent bacterial infections. View more via ChEBI Ontology ChEBI Ontology Outgoing furaltadone (CHEBI:74803) has role antibacterial drug (CHEBI:36047) furaltadone (CHEBI:74803) is a C-nitro compound (CHEBI:35716) furaltadone (CHEBI:74803) is a furans (CHEBI:24129) furaltadone (CHEBI:74803) is a morpholines (CHEBI:38785) furaltadone (CHEBI:74803) is a oxazolidinone (CHEBI:55374) IUPAC Name 5-(morpholin-4-ylmethyl)-3-{[(5-nitro-2-furyl)methylene]amino}-1,3-oxazolidin-2-one INNs Sources furaltadona ChemIDplus furaltadone WHO MedNet furaltadone ChemIDplus furaltadonum ChemIDplus Synonyms Sources 5-(morpholinomethyl)-3-((5-nitrofurfurylidene)amino)oxazolidone ChemIDplus 5-morpholinomethyl-3-(5-nitro-2-furfurylidine-amino)-2-oxazolidinone ChemIDplus Brand Name Source Altafur KEGG DRUG Manual Xrefs Databases CN101497609 Patent D02510 KEGG DRUG LSM-5034 LINCS US2802002 Patent View more database links Registry Numbers Types Sources 139-91-3 CAS Registry Number KEGG DRUG 139-91-3 CAS Registry Number ChemIDplus 363627 Reaxys Registry Number Reaxys Citations Types Sources 13689146 PubMed citation Europe PMC 21109284 PubMed citation Europe PMC 22011291 PubMed citation Europe PMC 22486660 PubMed citation Europe PMC 23200392 PubMed citation Europe PMC 23445479 PubMed citation Europe PMC 23810835 PubMed citation Europe PMC Last Modified 22 February 2017