N'-[[2,4,6-trioxo-1-(2,4,6-trimethylphenyl)-1,3-diazinan-5-ylidene]methyl]-4-pyridinecarbohydrazide (CHEBI:108474)

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ChEBI Name	N'-[[2,4,6-trioxo-1-(2,4,6-trimethylphenyl)-1,3-diazinan-5-ylidene]methyl]-4-pyridinecarbohydrazide

ChEBI ID	CHEBI:108474

Stars	This entity has been manually annotated by a third party.

Supplier Information

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Formula

C20H19N5O4

Net Charge

Average Mass

393.397

Monoisotopic Mass

393.14370

InChI

InChI=1S/C20H19N5O4/c1-11-8-12(2)16(13(3)9-11)25-19(28)15(18(27)23-20(25)29)10-22-24-17(26)14-4-6-21-7-5-14/h4-10,22H,1-3H3,(H,24,26)(H,23,27,29)

InChIKey

VRMVSHOHANAVAR-UHFFFAOYSA-N

SMILES

CC1=CC(=C(C(=C1)C)N2C(=O)C(=CNNC(=O)C3=CC=NC=C3)C(=O)NC2=O)C

Roles Classification
Biological Role(s):	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. (via barbiturates )

Application(s):	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. (via barbiturates )

ChEBI Ontology
Outgoing	N'-[[2,4,6-trioxo-1-(2,4,6-trimethylphenyl)-1,3-diazinan-5-ylidene]methyl]-4-pyridinecarbohydrazide (CHEBI:108474) is a barbiturates (CHEBI:22693)