Drug Information
Drug General Information | |||||
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Drug ID |
D0M3AP
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Former ID |
DNC010339
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Drug Name |
Bis(3-Fluorophenyl)-ketone]thiosemicarbazone
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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 |
C14H11F2N3S
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Canonical SMILES |
C1=CC(=CC(=C1)F)C(=NNC(=S)N)C2=CC(=CC=C2)F
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InChI |
1S/C14H11F2N3S/c15-11-5-1-3-9(7-11)13(18-19-14(17)20)10-4-2-6-12(16)8-10/h1-8H,(H3,17,19,20)
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InChIKey |
OBIMSARJMGBMKZ-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Cathepsin L | Target Info | Inhibitor | [1] | |
KEGG Pathway | Lysosome | ||||
Phagosome | |||||
Antigen processing and presentation | |||||
Proteoglycans in cancer | |||||
Rheumatoid arthritis | |||||
NetPath Pathway | IL4 Signaling Pathway | ||||
TGF_beta_Receptor Signaling Pathway | |||||
Reactome | Endosomal/Vacuolar pathway | ||||
Collagen degradation | |||||
Degradation of the extracellular matrix | |||||
Trafficking and processing of endosomal TLR | |||||
Assembly of collagen fibrils and other multimeric structures | |||||
MHC class II antigen presentation | |||||
WikiPathways | Primary Focal Segmental Glomerulosclerosis FSGS | ||||
References | |||||
REF 1 | Bioorg Med Chem Lett. 2010 Feb 15;20(4):1415-9. Epub 2010 Jan 6.Design, synthesis, and biological evaluation of potent thiosemicarbazone based cathepsin L inhibitors. | ||||
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