Drug Information
Drug General Information | Top | |||
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Drug ID |
D0O9QG
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Former ID |
DNC011133
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Drug Name |
S-(4-Chlorobenzyl)isothiourea hydrochloride
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Synonyms |
544-47-8; UNII-UG8Z59JOWY; 2-(4-Chlorobenzyl)-2-thiopseudourea hydrochloride; S-(4-Chlorobenzyl)Isothiouronium chloride; 4-CHLOROBENZYL CARBAMIMIDOTHIOATE HYDROCHLORIDE; 2-(p-Chlorobenzyl)isothiouronium chloride; p-Chlorobenzylpseudothiuronium chloride; EINECS 208-871-0; UG8Z59JOWY; Carbamimidothioic acid, (4-chlorophenyl)methyl ester, monohydrochloride; 4-chlorobenzyl imidothiocarbamate hydrochloride; s-(p-Chlorobenzyl)-thiuronium chloride; 4-CHLOROBENZYL CARBAMIMIDOTHIOATE HCL; Pseudourea, 2-(p-chlorobenzyl)-2-thio-,
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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 |
C8H10Cl2N2S
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Canonical SMILES |
C1=CC(=CC=C1CSC(=N)N)Cl.Cl
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InChI |
1S/C8H9ClN2S.ClH/c9-7-3-1-6(2-4-7)5-12-8(10)11;/h1-4H,5H2,(H3,10,11);1H
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InChIKey |
QAVHMIYSTFZJAU-UHFFFAOYSA-N
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CAS Number |
CAS 544-47-8
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Indoleamine 2,3-dioxygenase 1 (IDO1) | Target Info | Inhibitor | [1] |
BioCyc | 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 | Top | |||
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REF 1 | S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase. Bioorg Med Chem Lett. 2010 Sep 1;20(17):5126-9. |
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