Drug Information
Drug General Information | |||||
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Drug ID |
D0L8DL
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Former ID |
DNC004073
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Drug Name |
WIN-63395
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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 |
C19H19N5O4S2
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Canonical SMILES |
CC(C)C1=CC(=CC2=C1C(=O)N(S2(=O)=O)CSC3=NN=NN3C4=CC=CC=C<br />4)OC
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InChI |
1S/C19H19N5O4S2/c1-12(2)15-9-14(28-3)10-16-17(15)18(25)23(30(16,26)27)11-29-19-20-21-22-24(19)13-7-5-4-6-8-13/h4-10,12H,11H2,1-3H3
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InChIKey |
LZCQHGLOTYILCS-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Leukocyte elastase | Target Info | Inhibitor | [1] | |
KEGG Pathway | Transcriptional misregulation in cancer | ||||
Systemic lupus erythematosus | |||||
Pathway Interaction Database | Urokinase-type plasminogen activator (uPA) and uPAR-mediated signaling | ||||
C-MYB transcription factor network | |||||
Reactome | Collagen degradation | ||||
Degradation of the extracellular matrix | |||||
Activation of Matrix Metalloproteinases | |||||
WikiPathways | Hair Follicle Development: Cytodifferentiation (Part 3 of 3) | ||||
Human Complement System | |||||
Degradation of collagen | |||||
References | |||||
REF 1 | A comparative SAR and computer modeling study of benzisothiazolone, mechanism-based inhibitors with porcine pancreatic and human leukocyte elastase, Bioorg. Med. Chem. Lett. 6(24):2941-2946 (1996). | ||||
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