Drug Information
Drug General Information | |||||
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Drug ID |
D0SH2X
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Former ID |
DIB011723
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Drug Name |
Amocarzine
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Synonyms |
Phenthiourezine; Thiocarbamazine; CGP-6140; S-80016
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Drug Type |
Small molecular drug
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Indication | Helminth infection [ICD9: 001-139; ICD10:A00-B99] | Phase 3 | [1] | ||
Company |
Novartis AG
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Structure |
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Download2D MOL |
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Formula |
C18H21N5O2S
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Canonical SMILES |
CN1CCN(CC1)C(=S)Nc2ccc(Nc3ccc(cc3)[N+](=O)[O-])cc2
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InChI |
1S/C18H21N5O2S/c1-21-10-12-22(13-11-21)18(26)20-16-4-2-14(3-5-16)19-15-6-8-17(9-7-15)23(24)25/h2-9,19H,10-13H2,1H3,(H,20,26)
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InChIKey |
UFLRJROFPAGRPN-UHFFFAOYSA-N
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CAS Number |
CAS 36590-19-9
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Acetylcholinesterase | Target Info | Inhibitor | [2] | |
KEGG Pathway | Glycerophospholipid metabolism | ||||
Cholinergic synapse | |||||
PANTHER Pathway | Muscarinic acetylcholine receptor 1 and 3 signaling pathway | ||||
Muscarinic acetylcholine receptor 2 and 4 signaling pathway | |||||
Nicotinic acetylcholine receptor signaling pathway | |||||
Pathway Interaction Database | ATF-2 transcription factor network | ||||
PathWhiz Pathway | Phospholipid Biosynthesis | ||||
WikiPathways | Monoamine Transport | ||||
Biogenic Amine Synthesis | |||||
Acetylcholine Synthesis | |||||
Integrated Pancreatic Cancer Pathway | |||||
References | |||||
REF 1 | The safety and efficacy of amocarzine in African onchocerciasis and the influence of ivermectin on the clinical and parasitological response to treatment. Ann Trop Med Parasitol. 1997 Apr;91(3):281-96. | ||||
REF 2 | Activity, mechanism of action and pharmacokinetics of 2-tert-butylbenzothiazole and CGP 6140 (amocarzine) antifilarial drugs. Acta Trop. 1992 Aug;51(3-4):195-211. | ||||
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