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Drug Metabolic Roadmap (2024 update)
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Drug Information
Drug General Information
Drug ID
D08CNS
Former ID
DNC008616
Drug Name
IPRONIAZIDE
Drug Type
Small molecular drug
Indication
Discovery agent
Investigative
[
530675
]
Formula
C9H13N3O
Canonical SMILES
CC(C)NNC(=O)C1=CC=NC=C1
InChI
1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13)
InChIKey
NYMGNSNKLVNMIA-UHFFFAOYSA-N
PubChem Compound ID
3748
Target and Pathway
Target(s)
Amine oxidase [flavin-containing] A
Target Info
Inhibitor
[
530675
]
Amine oxidase [flavin-containing] B
Target Info
Inhibitor
[
530675
]
BioCyc Pathway
Superpathway of tryptophan utilization
Dopamine degradation
Putrescine degradation III
Noradrenaline and adrenaline degradation
Serotonin degradation
Superpathway of melatonin degradation
Melatonin degradation IIPWY66-401:Superpathway of tryptophan utilization
Tryptophan degradation via tryptamine
KEGG Pathway
Glycine, serine and threonine metabolism
Arginine and proline metabolism
Histidine metabolism
Tyrosine metabolism
Phenylalanine metabolism
Tryptophan metabolism
Drug metabolism - cytochrome P450
Metabolic pathways
Serotonergic synapse
Dopaminergic synapse
Cocaine addiction
Amphetamine addiction
Alcoholismhsa00260:Glycine, serine and threonine metabolism
Alcoholism
NetPath Pathway
IL4 Signaling Pathway
PANTHER Pathway
Adrenaline and noradrenaline biosynthesis
5-Hydroxytryptamine degredation
Dopamine receptor mediated signaling pathwayP00001:Adrenaline and noradrenaline biosynthesis
Dopamine receptor mediated signaling pathway
Pathway Interaction Database
Alpha-synuclein signaling
PathWhiz Pathway
Histidine Metabolism
Tyrosine Metabolism
Glycine and Serine Metabolism
Reactome
Norepinephrine Neurotransmitter Release Cycle
WikiPathways
SIDS Susceptibility Pathways
Biogenic Amine Synthesis
Oxidative Stress
Dopamine metabolism
Phase 1 - Functionalization of compounds
Neurotransmitter Release Cycle
Neurotransmitter Clearance In The Synaptic Cleft
Serotonin Transporter ActivityWP465:Tryptophan metabolism
References
Ref 530675
Bioorg Med Chem. 2010 Feb 15;18(4):1659-64. Epub 2010 Jan 4.Design of novel nicotinamides as potent and selective monoamine oxidase a inhibitors.
Ref 530675
Bioorg Med Chem. 2010 Feb 15;18(4):1659-64. Epub 2010 Jan 4.Design of novel nicotinamides as potent and selective monoamine oxidase a inhibitors.
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