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CHEBI:207922 - Usabamycin C

Default Structure
ChEBI IDCHEBI:207922
ChEBI NameUsabamycin C
Stars
SubmitterMetaboLights
DownloadsMolfile
FormulaC15H18N2O
Net Charge0
Average Mass242.322
Monoisotopic Mass242.14191
SMILESCC/C=C1\C[C@H]2CNc3ccccc3C(=O)N2C1
InChIInChI=1S/C15H18N2O/c1-2-5-11-8-12-9-16-14-7-4-3-6-13(14)15(18)17(12)10-11/h3-7,12,16H,2,8-10H2,1H3/b11-5+/t12-/m0/s1
InChIKeyMGYWULAVXWGTIC-JVOXIWMLSA-N
Species of MetaboliteComponentSourceComments
Streptomyces (ncbitaxon:1883) - PubMed (22001031)
Roles Classification
Biological Role:
GABA modulator  A substance that does not act as agonist or antagonist but does affect the gamma-aminobutyric acid receptor-ionophore complex. GABA-A receptors appear to have at least three allosteric sites at which modulators act: a site at which benzodiazepines act by increasing the opening frequency of gamma-aminobutyric acid-activated chloride channels; a site at which barbiturates act to prolong the duration of channel opening; and a site at which some steroids may act.
Application:
GABA modulator  A substance that does not act as agonist or antagonist but does affect the gamma-aminobutyric acid receptor-ionophore complex. GABA-A receptors appear to have at least three allosteric sites at which modulators act: a site at which benzodiazepines act by increasing the opening frequency of gamma-aminobutyric acid-activated chloride channels; a site at which barbiturates act to prolong the duration of channel opening; and a site at which some steroids may act.
ChEBI Ontology
Outgoing Relation(s)
Usabamycin C (CHEBI:207922) is a benzodiazepine (CHEBI:22720)
IUPAC Name 
(6aS,8E)-8-propylidene-6,6a,7,9-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-11-one
Manual XrefsDatabases
27025750ChemSpider