CHEBI:177359 - mansouramycin A

ChEBI IDCHEBI:177359
ChEBI Namemansouramycin A
Stars
DefinitionA member of the class of isoquinolines that is 5,8-dihydroisoquinoline substituted by methyl, methyl, oxo, methylamino and oxo groups at positions 3, 4, 5, 7 and 8, respectively. It was isolated from Streptomyces Sp. strain Mei37 from North Sea coast, Germany.
Last Modified10 August 2021
SubmitterAdnan
DownloadsMolfile
FormulaC12H12N2O2
Net Charge0
Average Mass216.240
Monoisotopic Mass216.08988
SMILESCNC1=CC(=O)c2c(cnc(C)c2C)C1=O
InChIInChI=1S/C12H12N2O2/c1-6-7(2)14-5-8-11(6)10(15)4-9(13-3)12(8)16/h4-5,13H,1-3H3
InChIKeySDLNCVBYFYLESJ-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Streptomyces albus J1074 (ncbitaxon:457425) - PubMed (30816348) produced via heterologously introduced biosynthetic gene cluster in a bacterial host.
Streptomyces sp. (ncbitaxon:1931) - PubMed (19921834) Strain: Mei37
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
marine metabolite  Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
antibacterial agent  A substance (or active part thereof) that kills or slows the growth of bacteria.
ChEBI Ontology
Outgoing Relation(s)
mansouramycin A (CHEBI:177359) has role antibacterial agent (CHEBI:33282)
mansouramycin A (CHEBI:177359) has role bacterial metabolite (CHEBI:76969)
mansouramycin A (CHEBI:177359) has role marine metabolite (CHEBI:76507)
mansouramycin A (CHEBI:177359) is a p-quinones (CHEBI:25830)
mansouramycin A (CHEBI:177359) is a isoquinolines (CHEBI:24922)
mansouramycin A (CHEBI:177359) is a secondary amino compound (CHEBI:50995)
IUPAC Name 
3,4-dimethyl-7-(methylamino)isoquinoline-5,8-dione
Synonym  Source
7-methylamino-3,4-dimethylisoquinoline-5,8-dioneChEBI
Manual XrefsDatabases
24659745ChemSpider
C00047986KNApSAcK
Registry NumbersSources
CAS:1199808-44-0KNApSAcK
Citations