n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and n(6)-(1-iminoethyl)lysine

n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide has been researched along with n(6)-(1-iminoethyl)lysine in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's3 (50.00)24.3611
2020's2 (33.33)2.80

Authors

AuthorsStudies
Choi, JS; Kim, JC; Lee, HK; Min, BS; Nguyen, HD; Tran, MH1
Choi, HE; Choi, HY; El-Gamal, MI; Jang, HL; Lee, KT; Oh, CH1
Han, HS; Jo, AR; Kim, HJ; Lee, JY; Lee, KT; Seo, S; Shin, JS1
Hassan, AHE; Jeong, Y; Kang, SY; Kim, SY; Lee, HH; Lee, KT; Lee, KW; Lee, YS; Park, BY; Ryu, HW; Shin, JS; Yoo, SY; Yoon, YM1
Abdel-Maksoud, MS; Baek, D; Choi, J; El-Gamal, MI; Gamal El-Din, MM; Kim, HK; Kim, TW; Lee, H; Lee, HH; Lee, KT; Shin, JS1
Elkamhawy, A; Hassan, AHE; Kim, NY; Lee, BH; Lee, KT; Lee, MY; Oh, KS; Pae, AN; Paik, S; Park, JE; Roh, EJ; Shin, KJ; Yang, JE1

Other Studies

6 other study(ies) available for n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and n(6)-(1-iminoethyl)lysine

ArticleYear
Phenolic glycosides from Alangium salviifolium leaves with inhibitory activity on LPS-induced NO, PGE(2), and TNF-alpha production.
    Bioorganic & medicinal chemistry letters, 2009, Aug-01, Volume: 19, Issue:15

    Topics: Alangiaceae; Animals; Anti-Inflammatory Agents; Chemistry, Pharmaceutical; Dinoprostone; Glycosides; Lipopolysaccharides; Mice; Models, Chemical; Nitric Oxide; Phenol; Plant Extracts; Plant Leaves; Plants, Medicinal; Tumor Necrosis Factor-alpha

2009
Synthesis of tricyclic fused coumarin sulfonates and their inhibitory effects on LPS-induced nitric oxide and PGE2 productions in RAW 264.7 macrophages.
    Bioorganic & medicinal chemistry letters, 2014, Jan-15, Volume: 24, Issue:2

    Topics: Animals; Cell Line; Coumarins; Dinoprostone; Dose-Response Relationship, Drug; Lipopolysaccharides; Macrophages; Mice; Nitric Oxide; Sulfonic Acids

2014
Inhibitory effect of moschamine isolated from Carthamus tinctorius on LPS-induced inflammatory mediators via AP-1 and STAT1/3 inactivation in RAW 264.7 macrophages.
    Bioorganic & medicinal chemistry letters, 2017, 12-01, Volume: 27, Issue:23

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Carthamus tinctorius; Dose-Response Relationship, Drug; Inflammation Mediators; Lipopolysaccharides; Macrophages; Mice; Molecular Structure; RAW 264.7 Cells; Serotonin; STAT1 Transcription Factor; STAT3 Transcription Factor; Structure-Activity Relationship; Transcription Factor AP-1

2017
Repurposing mosloflavone/5,6,7-trimethoxyflavone-resveratrol hybrids: Discovery of novel p38-α MAPK inhibitors as potent interceptors of macrophage-dependent production of proinflammatory mediators.
    European journal of medicinal chemistry, 2019, Oct-15, Volume: 180

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Dose-Response Relationship, Drug; Drug Discovery; Flavones; Flavonoids; Inflammation; Inflammation Mediators; Macrophages; Mice; Molecular Structure; p38 Mitogen-Activated Protein Kinases; Protein Kinase Inhibitors; RAW 264.7 Cells; Resveratrol; Structure-Activity Relationship

2019
Inhibitory effects of triarylpyrazole derivatives on LPS-induced nitric oxide and PGE
    Bioorganic & medicinal chemistry letters, 2020, 02-15, Volume: 30, Issue:4

    Topics: Animals; Anti-Inflammatory Agents; Cell Survival; Cyclooxygenase 2; Dinoprostone; Drug Design; Lipopolysaccharides; Macrophages; Mice; Nitric Oxide; Pyrazoles; RAW 264.7 Cells; Structure-Activity Relationship

2020
Thiazolidine-2,4-dione-based irreversible allosteric IKK-β kinase inhibitors: Optimization into in vivo active anti-inflammatory agents.
    European journal of medicinal chemistry, 2020, Feb-15, Volume: 188

    Topics: Allosteric Regulation; Animals; Anti-Inflammatory Agents, Non-Steroidal; Cell Survival; Cells, Cultured; Dose-Response Relationship, Drug; I-kappa B Kinase; Male; Mice; Mice, Inbred C57BL; Molecular Structure; Protein Kinase Inhibitors; RAW 264.7 Cells; Shock, Septic; Structure-Activity Relationship; Thiazolidinediones

2020