Drug Information
Drug General Information | |||||
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Drug ID |
D00QIA
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Former ID |
DNC006244
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Drug Name |
(S)-tert-butyl 4-methyl-1-oxopentan-2-ylcarbamate
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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 |
C11H21NO3
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Canonical SMILES |
CC(C)CC(C=O)NC(=O)OC(C)(C)C
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InChI |
1S/C11H21NO3/c1-8(2)6-9(7-13)12-10(14)15-11(3,4)5/h7-9H,6H2,1-5H3,(H,12,14)/t9-/m0/s1/i7+1
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InChIKey |
RQSBRFZHUKLKNO-WQVCYBKOSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Cathepsin K | Target Info | Inhibitor | [1] | |
KEGG Pathway | Lysosome | ||||
Osteoclast differentiation | |||||
Toll-like receptor signaling pathway | |||||
Rheumatoid arthritis | |||||
NetPath Pathway | TGF_beta_Receptor Signaling Pathway | ||||
RANKL Signaling Pathway | |||||
IL2 Signaling Pathway | |||||
Reactome | Collagen degradation | ||||
Degradation of the extracellular matrix | |||||
Activation of Matrix Metalloproteinases | |||||
Trafficking and processing of endosomal TLR | |||||
MHC class II antigen presentation | |||||
WikiPathways | RANKL/RANK Signaling Pathway | ||||
Osteoclast Signaling | |||||
References | |||||
REF 1 | Bioorg Med Chem Lett. 2006 Feb 15;16(4):978-83. Epub 2005 Nov 15.Semicarbazone-based inhibitors of cathepsin K, are they prodrugs for aldehyde inhibitors?. | ||||
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