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CHEBI:48202 - nanaomycin A

ChEBI IDCHEBI:48202
ChEBI Namenanaomycin A
Stars
DefinitionA pyranonaphthoquinone antibiotic from strain OS-3966 of Streptomyces rosa var. notoensis.
Secondary ChEBI IDCHEBI:163
Last Modified6 June 2016
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC16H14O6
Net Charge0
Average Mass302.282
Monoisotopic Mass302.07904
SMILESC[C@@H]1O[C@@H](CC(=O)O)CC2=C1C(=O)c1c(O)cccc1C2=O
InChIInChI=1S/C16H14O6/c1-7-13-10(5-8(22-7)6-12(18)19)15(20)9-3-2-4-11(17)14(9)16(13)21/h2-4,7-8,17H,5-6H2,1H3,(H,18,19)/t7-,8+/m0/s1
InChIKeyZCJHPTKRISJQTN-JGVFFNPUSA-N
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Roles:
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
ChEBI Ontology
Outgoing Relation(s)
nanaomycin A (CHEBI:48202) has role bacterial metabolite (CHEBI:76969)
nanaomycin A (CHEBI:48202) is a p-quinones (CHEBI:25830)
nanaomycin A (CHEBI:48202) is a benzoisochromanequinone (CHEBI:48129)
nanaomycin A (CHEBI:48202) is a monocarboxylic acid (CHEBI:25384)
nanaomycin A (CHEBI:48202) is a organooxygen heterocyclic antibiotic (CHEBI:25807)
IUPAC Name 
[(1S,3R)-9-hydroxy-1-methyl-5,10-dioxo-3,4,5,10-tetrahydro-1H-benzo[g]isochromen-3-yl]acetic acid
INNs  Source
NanafrocinChemIDplus
NanafrocineChemIDplus
NanafrocinumChemIDplus
Synonyms  Source
(1S,3R)-Nanaomycin AKEGG COMPOUND
[(1S,3R)-9-hydroxy-1-methyl-5,10-dioxo-3,4,5,10-tetrahydro-1H-naphtho[2,3-c]pyran-3-yl]acetic acidIUPAC
Rosanomycin AChemIDplus
Nanomycin AChemIDplus
Manual XrefsDatabases
C10377KEGG COMPOUND
C00002845KNApSAcK
Registry NumbersSources
Beilstein:7182745Beilstein
CAS:52934-83-5KEGG COMPOUND
CAS:52934-83-5ChemIDplus