Drug Information
Drug General Information | |||||
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Drug ID |
D0S1FF
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Former ID |
DNC010098
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Drug Name |
4-(Isopropylamino)-1-naphthol
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Drug Type |
Small molecular drug
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Indication | Discovery agent | Investigative | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C13H15NO
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Canonical SMILES |
CC(C)NC1=CC=C(C2=CC=CC=C21)O
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InChI |
1S/C13H15NO/c1-9(2)14-12-7-8-13(15)11-6-4-3-5-10(11)12/h3-9,14-15H,1-2H3
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InChIKey |
TWBKFLLEYLZFHH-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Indoleamine 2,3-dioxygenase | Target Info | Inhibitor | [1] | |
BioCyc Pathway | Superpathway of tryptophan utilization | ||||
Tryptophan degradation | |||||
L-kynurenine degradation | |||||
Tryptophan degradation to 2-amino-3-carboxymuconate semialdehyde | |||||
NAD de novo biosynthesis | |||||
KEGG Pathway | Tryptophan metabolism | ||||
Metabolic pathways | |||||
African trypanosomiasis | |||||
NetPath Pathway | TSLP Signaling Pathway | ||||
IL5 Signaling Pathway | |||||
TGF_beta_Receptor Signaling Pathway | |||||
PathWhiz Pathway | Tryptophan Metabolism | ||||
Reactome | Tryptophan catabolism | ||||
WikiPathways | Tryptophan metabolism | ||||
Metabolism of amino acids and derivatives | |||||
References | |||||
REF 1 | J Med Chem. 2010 Feb 11;53(3):1172-89.Rational design of indoleamine 2,3-dioxygenase inhibitors. | ||||
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