Drug General Information
Drug ID
DX6K0N
Drug Name
2-(4-Acetylphenylureido)-1-(4-methoxyphenyl)-6,7-methylenedioxy-2H-isoquinolin-3-one
Synonyms
CHEMBL594623
Indication Discovery agent Investigative [1587926]
Formula
C26H21N3O6
Canonical SMILES
COc1ccc(cc1)C2=C3C=C4OCOC4=CC3=CC(=O)N2NC(=O)Nc5ccc(cc5)C(=O)C
InChI
InChI=1S/C26H21N3O6/c1-15(30)16-3-7-19(8-4-16)27-26(32)28-29-24(31)12-18-11-22-23(35-14-34-22)13-21(18)25(29)17-5-9-20(33-2)10-6-17/h3-13H,14H2,1-2H3,(H2,27,28,32)
InChIKey
BMSSNHJLONKLJW-UHFFFAOYSA-N
Target and Pathway
Target(s) Cathepsin L Target Info [1587926]
Cathepsin B Target Info [1587926]
KEGG Pathway Lysosome
Phagosome
Antigen processing and presentation
Proteoglycans in cancer
Rheumatoid arthritishsa04142:Lysosome
NetPath Pathway IL4 Signaling Pathway
TGF_beta_Receptor Signaling PathwayNetPath_11:TCR Signaling Pathway
IL2 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 presentationR-HSA-1442490:Collagen degradation
MHC class II antigen presentation
WikiPathways Primary Focal Segmental Glomerulosclerosis FSGS
References
Ref 1587926URL: https://www.ebi.ac.uk/chembl/ The ChEMBL database in 2017
Ref 1587926URL: https://www.ebi.ac.uk/chembl/ The ChEMBL database in 2017

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