Research graph
References from N -Acetyldopamine dimers from Oxya chinensis sinuosa attenuates lipopolysaccharides induced inflammation and inhibits cathepsin C activity. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1038/nature01320
10.1038/nature01320 · External reference
10.1016/j.fct.2019.01.011
10.1016/j.fct.2019.01.011 · External reference
Interleukin-6 and chronic inflammation
10.1186/ar1917 · 2006 · External reference
10.1016/j.cell.2010.01.025
10.1016/j.cell.2010.01.025 · External reference
10.1016/j.phrs.2018.11.001
10.1016/j.phrs.2018.11.001 · External reference
10.1016/j.bcp.2008.07.041
10.1016/j.bcp.2008.07.041 · External reference
10.1016/j.tips.2017.06.003
10.1016/j.tips.2017.06.003 · External reference
Up-regulated cathepsin C induces macrophage M1 polarization through FAK-triggered p38 MAPK/NF-kappa B pathway
10.1016/j.yexcr.2019.06.017 · 2019 · External reference
Up-regulation of microglial cathepsin C expression and activity in lipopolysaccharide-induced neuroinflammation
2012 · External reference
Cathepsin C promotes microglia M1 polarization and aggravates neuroinflammation via activation of Ca2+-dependent PKC/p38MAPK/NF-B pathway
2019 · External reference
10.1016/j.biotechadv.2015.08.001
10.1016/j.biotechadv.2015.08.001 · External reference
Unresolved reference
2016 · External reference
Unresolved reference
External reference
Transcriptome profiling and in silico analysis of the antimicrobial peptides of the grasshopper Oxya chinensis sinuosa
10.4014/jmb.1608.08029 · 2016 · External reference
Evaluation of novel factor Xa inhibitors from Oxya chinensis sinuosa with anti-platelet aggregation activity
2017 · External reference
Antioxidant activity and antimicrobial activity of the grasshopper, Oxya chinensis sinuosa
2015 · External reference
10.1016/j.cellsig.2018.02.017
10.1016/j.cellsig.2018.02.017 · External reference
Discovery of novel cyanamide-based inhibitors of cathepsin C
10.1021/ml100212k · 2011 · External reference
10.1016/j.lfs.2020.118080
10.1016/j.lfs.2020.118080 · External reference
10.1002/jcc.20084
10.1002/jcc.20084 · External reference
Software news and update autodock vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
10.1002/jcc.21334 · 2010 · External reference
Implementation of the CHARMM force field in GROMACS: analysis of protein stability effects from correction maps, virtual interaction sites, and water models
10.1021/ct900549r · 2010 · External reference
10.1002/jcc.21816
10.1002/jcc.21816 · External reference
Optimizing working parameters of the smooth particle mesh Ewald algorithm in terms of accuracy and efficiency
10.1063/1.3446812 · 2010 · External reference
Molecular dynamics studies of AChBP with nicotine and carbamylcholine: the role of water in the binding pocket
10.1093/protein/gzm029 · 2007 · External reference
10.1093/bioinformatics/btl461
10.1093/bioinformatics/btl461 · External reference
Unresolved reference
External reference
Open Source Drug Discovery C, Lynn A. g_mmpbsa–a GROMACS tool for high-throughput MM-PBSA calculations
10.1021/ci500020m · 2014 · External reference
10.1073/pnas.181342398
10.1073/pnas.181342398 · External reference
Anti-inflammatory effect of Oxya chinensis sinuosa ethanol extract in LPS-induced RAW 264.7 cells
10.5352/jls.2014.24.4.370 · 2014 · External reference
10.3390/nu10060735
10.3390/nu10060735 · External reference
10.1007/s10787-007-0013-x
10.1007/s10787-007-0013-x · External reference
10.1016/j.phymed.2018.06.039
10.1016/j.phymed.2018.06.039 · External reference
Synthesis, biological evaluation and docking study of a new series of di-substituted benzoxazole derivatives as selective COX-2 inhibitors and anti-inflammatory agents
10.1016/j.bmc.2018.01.007 · 2018 · External reference
Synthesis and biological evaluation of pyridazinone derivatives as selective COX-2 inhibitors and potential anti-inflammatory agents
10.1016/j.ejmech.2019.03.036 · 2019 · External reference
10.1016/j.phymed.2018.09.186
10.1016/j.phymed.2018.09.186 · External reference
10.1016/j.smim.2014.01.009
10.1016/j.smim.2014.01.009 · External reference
10.1016/j.brainresrev.2008.12.020
10.1016/j.brainresrev.2008.12.020 · External reference
10.1038/nrd3800
10.1038/nrd3800 · External reference
Insights into cyclooxygenase-2 inhibition by isolated bioactive compounds 3-caffeoyl-4-dihydrocaffeoyl quinic acid and isorhamnetin 3-O-beta-D-glucopyranoside from Salicornia herbacea
10.1016/j.phymed.2021.153638 · 2021 · External reference
Insects: an underrepresented resource for the discovery of biologically active natural products
10.1016/j.apsb.2017.05.001 · 2017 · External reference
4-methoxycinnamyl p-coumarate isolated from Etlingera pavieana rhizomes inhibits inflammatory response via suppression of NF-kappaB, Akt and AP-1 signaling in LPS-stimulated RAW 264.7 macrophages
10.1016/j.phymed.2018.09.193 · 2019 · External reference
10.1016/j.pharmthera.2018.05.011
10.1016/j.pharmthera.2018.05.011 · External reference
10.1016/j.ejmech.2021.113818
10.1016/j.ejmech.2021.113818 · 2021 · External reference
Synthesis, biological evaluation and 3D-QSAR studies of 1,2,4-triazole-5-substituted carboxylic acid bioisosteres as uric acid transporter 1 (URAT1) inhibitors for the treatment of hyperuricemia associated with gout
10.1016/j.bmcl.2018.12.036 · 2019 · External reference
