5-(Butan-2-yl)-1,3-dimethyl-5-(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione (CHEBI:184312)

Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search

CHEBI:184312 - 5-(Butan-2-yl)-1,3-dimethyl-5-(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione

ChEBI ID	CHEBI:184312
ChEBI Name	5-(Butan-2-yl)-1,3-dimethyl-5-(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione
Stars
Submitter	MetaboLights
Downloads	Molfile

Formula	C13H20N2O3
Net Charge	0
Average Mass	252.314
Monoisotopic Mass	252.14739
SMILES	C=CCC1(C(C)CC)C(=O)N(C)C(=O)N(C)C1=O
InChI	InChI=1S/C13H20N2O3/c1-6-8-13(9(3)7-2)10(16)14(4)12(18)15(5)11(13)17/h6,9H,1,7-8H2,2-5H3
InChIKey	CDKJETHMMUVSNV-UHFFFAOYSA-N

Species of Metabolite	Component	Source	Comments
Bos taurus (ncbitaxon:9913)
	spermatozoon (BTO:0001277)	MetaboLights (MTBLS1071)	Strain: Holstein-Friesian cattle [26105007]
	spermatozoon (FMA:67338)	MetaboLights (MTBLS1071)	Strain: Holstein-Friesian cattle [26105007]

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:

ChEBI Ontology

Outgoing Relation(s)
	5-(Butan-2-yl)-1,3-dimethyl-5-(prop-2-en-1-yl)-1,3-diazinane-2,4,6-trione (CHEBI:184312) is a barbiturates (CHEBI:22693)

IUPAC Name
5-butan-2-yl-1,3-dimethyl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione

Manual Xrefs	Databases
527603	ChemSpider
HMDB0014451	HMDB