Drug Information
Drug General Information | Top | |||
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Drug ID |
D02PLG
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Former ID |
DNC013861
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Drug Name |
4,5-Bis(4-methoxyphenyl)-3H-1,2-dithiole-3-thione
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Synonyms |
CHEMBL489899; 4,5-Bis(4-methoxyphenyl)-3H-1,2-dithiole-3-thione
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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 |
C17H14O2S3
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Canonical SMILES |
COC1=CC=C(C=C1)C2=C(SSC2=S)C3=CC=C(C=C3)OC
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InChI |
1S/C17H14O2S3/c1-18-13-7-3-11(4-8-13)15-16(21-22-17(15)20)12-5-9-14(19-2)10-6-12/h3-10H,1-2H3
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InChIKey |
CLEJIKNYKPUJCS-UHFFFAOYSA-N
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CAS Number |
CAS 35564-24-0
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Prostaglandin G/H synthase 1 (COX-1) | Target Info | Inhibitor | [1] |
BioCyc | C20 prostanoid biosynthesis | |||
KEGG Pathway | Arachidonic acid metabolism | |||
Metabolic pathways | ||||
Platelet activation | ||||
Serotonergic synapse | ||||
NetPath Pathway | TGF_beta_Receptor Signaling Pathway | |||
Panther Pathway | Inflammation mediated by chemokine and cytokine signaling pathway | |||
Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
WikiPathways | Prostaglandin Synthesis and Regulation | |||
Arachidonic acid metabolism | ||||
Phase 1 - Functionalization of compounds | ||||
Eicosanoid Synthesis | ||||
Selenium Micronutrient Network |
References | Top | |||
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REF 1 | Diaryl-dithiolanes and -isothiazoles: COX-1/COX-2 and 5-LOX-inhibitory, *OH scavenging and anti-adhesive activities. Bioorg Med Chem. 2009 Jan 15;17(2):558-68. |
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