Drug Information
Drug General Information | Top | |||
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Drug ID |
D0IX0N
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Former ID |
DNC011569
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Drug Name |
N*1*-(5-Methyl-2-nitro-phenyl)-butane-1,4-diamine
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Synonyms |
CHEMBL89454; 1,4-Butanediamine, N1-(5-methyl-2-nitrophenyl)-; N*1*-(5-Methyl-2-nitro-phenyl)-butane-1,4-diamine; BDBM50065369; AKOS018628293
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C11H17N3O2
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Canonical SMILES |
CC1=CC(=C(C=C1)[N+](=O)[O-])NCCCCN
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InChI |
1S/C11H17N3O2/c1-9-4-5-11(14(15)16)10(8-9)13-7-3-2-6-12/h4-5,8,13H,2-3,6-7,12H2,1H3
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InChIKey |
ANIBJVLRYPKMKX-UHFFFAOYSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Nitric-oxide synthase brain (NOS1) | Target Info | Inhibitor | [1] |
BioCyc | Citrulline-nitric oxide cycle | |||
KEGG Pathway | Arginine and proline metabolism | |||
Metabolic pathways | ||||
Calcium signaling pathway | ||||
Phagosome | ||||
Circadian entrainment | ||||
Long-term depression | ||||
Salivary secretion | ||||
Alzheimer's disease | ||||
Amyotrophic lateral sclerosis (ALS) | ||||
NetPath Pathway | EGFR1 Signaling Pathway | |||
Panther Pathway | CCKR signaling map ST | |||
Pathwhiz Pathway | Arginine and Proline Metabolism | |||
Reactome | ROS production in response to bacteria | |||
Nitric oxide stimulates guanylate cyclase | ||||
WikiPathways | Monoamine Transport | |||
Myometrial Relaxation and Contraction Pathways | ||||
Amyotrophic lateral sclerosis (ALS) | ||||
Quercetin and Nf-kB/ AP-1 Induced Cell Apoptosis | ||||
Spinal Cord Injury | ||||
Alzheimers Disease | ||||
Effects of Nitric Oxide | ||||
Serotonin Transporter Activity |
References | Top | |||
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REF 1 | Nitroaromatic amino acids as inhibitors of neuronal nitric oxide synthase. J Med Chem. 1998 Jul 2;41(14):2636-42. |
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