Drug Information
Drug General Information | |||||
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Drug ID |
DXS1AO
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Drug Name |
(S)-3,3-dimethyl-1-(4-(4-(trifluoromethyl)phenyl)-1H-imidazol-1-yl)butan-2-yl (S)-2-oxo-1-(pyridine-2-sulfonamido)heptan-3-ylcarbamate
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Synonyms |
CHEMBL233706
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Indication | Discovery agent | Investigative | [1587926] | ||
Formula |
C29H36F3N5O5S
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Canonical SMILES |
CCCC[C@H](NC(=O)O[C@H](Cn1cnc(c1)c2ccc(cc2)C(F)(F)F)C(C)(C)C)C(=O)CNS(=O)(=O)c3ccccn3
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InChI |
InChI=1S/C29H36F3N5O5S/c1-5-6-9-22(24(38)16-35-43(40,41)26-10-7-8-15-33-26)36-27(39)42-25(28(2,3)4)18-37-17-23(34-19-37)20-11-13-21(14-12-20)29(30,31)32/h7-8,10-15,17,19,22,25,35H,5-6,9,16,18H2,1-4H3,(H,36,39)/t22-,25+/m0/s1
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InChIKey |
XHGOLGYGBDIOFD-WIOPSUGQSA-N
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Target and Pathway | |||||
Target(s) | Cathepsin K | Target Info | [1587926] | ||
Cathepsin B | Target Info | [1587926] | |||
Reactome | Collagen degradation | ||||
Degradation of the extracellular matrix | |||||
Activation of Matrix Metalloproteinases | |||||
Trafficking and processing of endosomal TLR | |||||
MHC class II antigen presentationR-HSA-1442490:Collagen degradation | |||||
Assembly of collagen fibrils and other multimeric structures | |||||
MHC class II antigen presentation | |||||
WikiPathways | RANKL/RANK Signaling Pathway | ||||
Osteoclast Signaling | |||||
References |
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