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n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and Edema

n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide has been researched along with Edema in 20 studies

N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide: structure given in first source
NS-398 : A C-nitro compound that is N-methylsulfonyl-4-nitroaniline bearing an additional cyclohexyloxy substituent at position 2.

Edema: Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE.

Research Excerpts

ExcerptRelevanceReference
" In this study, a series of novel thiazolo[3,2-b]-1,2,4-triazole-6(5H)-one derivatives bearing naproxen was synthesized and evaluated for their in vivo analgesic and anti-inflammatory properties in acute experimental pain and inflammation models."3.81Novel thiazolo[3,2-b]-1,2,4-triazoles derived from naproxen with analgesic/anti-inflammatory properties: Synthesis, biological evaluation and molecular modeling studies. ( Ertan, M; Kazkayasi, I; Okay, G; Ozadali-Sari, K; Sarigol, D; Somuncuoglu, EI; Tel, BC; Tozkoparan, B; Unsal-Tan, O; Uzgoren-Baran, A, 2015)
"60 μmol/cm²) exhibited topical antiedematous properties comparable to those of indomethacin (ID₅₀ 0."3.77Lignan derivatives from Krameria lappacea roots inhibit acute inflammation in vivo and pro-inflammatory mediators in vitro. ( Atanasov, AG; Bauer, J; Bauer, R; Baumgartner, L; Bodensieck, A; Dirsch, VM; Fakhrudin, N; Favero, GD; Heiss, EH; Ladurner, A; Loggia, RD; Ponti, C; Rollinger, JM; Schwaiger, S; Sosa, S; Stuppner, H; Tubaro, A; Werz, O; Widowitz, U, 2011)
" The anti-inflammatory potency of NS-398 in rat carrageenin-induced edema was as potent as that of indomethacin and 8 times more potent than diclofenac."3.68NS-398, a novel non-steroidal anti-inflammatory drug with potent analgesic and antipyretic effects, which causes minimal stomach lesions. ( Arai, I; Futaki, N; Hamasaka, Y; Higuchi, S; Iizuka, H; Otomo, S; Yoshikawa, K, 1993)
"Its role as a mediator of hyperalgesia (clinically defined as an augmented sensitivity to painful stimuli) is not known."1.35Cyclooxygenases 1 and 2 contribute to peroxynitrite-mediated inflammatory pain hypersensitivity. ( Cuzzocrea, S; Di Paola, R; Esposito, E; Matuschak, GM; Mazzon, E; Ndengele, MM; Salvemini, D, 2008)
"Atopic dermatitis is a chronic inflammatory disease characterized by severe pruritus, and cutaneous barrier disruption by scratching contributes to further aggravation of the condition."1.34Cyclooxygenase-1 inhibition delays recovery of the cutaneous barrier disruption caused by mechanical scratching in mice. ( Arai, I; Futaki, N; Hashimoto, Y; Honma, Y; Nakaike, S; Sakurai, T; Sugimoto, M, 2007)
"Pretreatment with indomethacin completely reversed both of the therapeutic effects of dalteparin, whereas pretreatment with NS-398, a selective inhibitor of cyclooxygenase-2, did not."1.33Dalteparin, a low molecular weight heparin, attenuates inflammatory responses and reduces ischemia-reperfusion-induced liver injury in rats. ( Harada, N; Okajima, K; Uchiba, M, 2006)
"Pretreatment with indomethacin (10 mg kg[-1], s."1.30Cyclo-oxygenase isozymes in mucosal ulcergenic and functional responses following barrier disruption in rat stomachs. ( Hirata, T; Kato, S; Takeuchi, K; Ukawa, H; Yamakuni, H, 1997)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's7 (35.00)18.2507
2000's10 (50.00)29.6817
2010's3 (15.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Li, JJ1
Anderson, GD1
Burton, EG1
Cogburn, JN1
Collins, JT1
Garland, DJ1
Gregory, SA1
Huang, HC1
Isakson, PC1
Koboldt, CM1
Song, Y2
Connor, DT2
Doubleday, R2
Sorenson, RJ2
Sercel, AD2
Unangst, PC2
Roth, BD2
Gilbertsen, RB2
Chan, K2
Schrier, DJ2
Guglietta, A2
Bornemeier, DA2
Dyer, RD2
Beylin, VG1
Inagaki, M1
Tsuri, T1
Jyoyama, H1
Ono, T1
Yamada, K1
Kobayashi, M1
Hori, Y1
Arimura, A1
Yasui, K1
Ohno, K1
Kakudo, S1
Koizumi, K1
Suzuki, R1
Kawai, S1
Kato, M1
Matsumoto, S1
Molina, P1
Aller, E1
Lorenzo, A1
López-Cremades, P1
Rioja, I1
Ubeda, A1
Terencio, MC1
Alcaraz, MJ2
Baumgartner, L1
Sosa, S1
Atanasov, AG1
Bodensieck, A1
Fakhrudin, N1
Bauer, J1
Favero, GD1
Ponti, C1
Heiss, EH1
Schwaiger, S1
Ladurner, A1
Widowitz, U1
Loggia, RD1
Rollinger, JM1
Werz, O1
Bauer, R1
Dirsch, VM1
Tubaro, A1
Stuppner, H1
Abdel-Aziz, M1
Beshr, EA1
Abdel-Rahman, IM1
Ozadali, K1
Tan, OU1
Aly, OM1
Sarigol, D1
Uzgoren-Baran, A1
Tel, BC1
Somuncuoglu, EI1
Kazkayasi, I1
Ozadali-Sari, K1
Unsal-Tan, O1
Okay, G1
Ertan, M1
Tozkoparan, B1
Devesa, I1
Riguera, R1
Ferrándiz, ML1
Harada, N1
Okajima, K1
Uchiba, M1
Pesce, C1
Grattarola, M1
Menini, S1
Fiallo, P1
Sugimoto, M2
Arai, I3
Futaki, N3
Hashimoto, Y2
Honma, Y2
Nakaike, S2
Guindon, J1
LoVerme, J1
De Léan, A1
Piomelli, D1
Beaulieu, P1
Park, H1
Kim, YH1
Chang, HW1
Kim, HP1
Sakurai, T1
Ndengele, MM1
Cuzzocrea, S1
Esposito, E1
Mazzon, E1
Di Paola, R1
Matuschak, GM1
Salvemini, D1
Yoshikawa, K1
Hamasaka, Y1
Higuchi, S1
Iizuka, H1
Otomo, S1
Huff, R1
Collins, P1
Kramer, S1
Seibert, K1
Koboldt, C1
Gregory, S1
Isakson, P1
Buritova, J1
Chapman, V1
Honoré, P1
Besson, JM1
Hirata, T1
Ukawa, H1
Yamakuni, H1
Kato, S1
Takeuchi, K1

Other Studies

20 other studies available for n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and Edema

ArticleYear
1,2-Diarylcyclopentenes as selective cyclooxygenase-2 inhibitors and orally active anti-inflammatory agents.
    Journal of medicinal chemistry, 1995, Oct-27, Volume: 38, Issue:22

    Topics: Administration, Oral; Animals; Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Experimental; Cyc

1995
Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 1. Thiazolone and oxazolone series.
    Journal of medicinal chemistry, 1999, Apr-08, Volume: 42, Issue:7

    Topics: Administration, Oral; Animals; Anti-Inflammatory Agents, Non-Steroidal; Carrageenan; Cell Line; Cycl

1999
Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2. 1,3,4- and 1,2,4-thiadiazole series.
    Journal of medicinal chemistry, 1999, Apr-08, Volume: 42, Issue:7

    Topics: Administration, Oral; Animals; Anti-Inflammatory Agents, Non-Steroidal; Blood Platelets; Carrageenan

1999
Novel antiarthritic agents with 1,2-isothiazolidine-1,1-dioxide (gamma-sultam) skeleton: cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase.
    Journal of medicinal chemistry, 2000, May-18, Volume: 43, Issue:10

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Arthritis; Arthritis, Experimental; Blood Platelet

2000
Solid-phase synthesis and inhibitory effects of some pyrido[1,2-c]pyrimidine derivatives on leukocyte formations and experimental inflammation.
    Journal of medicinal chemistry, 2001, Mar-15, Volume: 44, Issue:6

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Cells, Cultured; Cyclooxygenase 2; Dinoprostone; E

2001
Lignan derivatives from Krameria lappacea roots inhibit acute inflammation in vivo and pro-inflammatory mediators in vitro.
    Journal of natural products, 2011, Aug-26, Volume: 74, Issue:8

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Arachidonate 5-Lipoxygenase; Austria; Benzofurans;

2011
1-(4-Methoxyphenyl)-5-(3,4,5-trimethoxyphenyl)-1H-1,2,4-triazole-3-carboxamides: synthesis, molecular modeling, evaluation of their anti-inflammatory activity and ulcerogenicity.
    European journal of medicinal chemistry, 2014, Apr-22, Volume: 77

    Topics: Animals; Anisoles; Anti-Inflammatory Agents, Non-Steroidal; Carrageenan; Cyclooxygenase 1; Cyclooxyg

2014
Novel thiazolo[3,2-b]-1,2,4-triazoles derived from naproxen with analgesic/anti-inflammatory properties: Synthesis, biological evaluation and molecular modeling studies.
    Bioorganic & medicinal chemistry, 2015, May-15, Volume: 23, Issue:10

    Topics: Analgesics; Animals; Anti-Inflammatory Agents, Non-Steroidal; Carrageenan; Disease Models, Animal; D

2015
A new pyrazolo pyrimidine derivative inhibitor of cyclooxygenase-2 with anti-angiogenic activity.
    European journal of pharmacology, 2004, Mar-19, Volume: 488, Issue:1-3

    Topics: Angiogenesis Inhibitors; Animals; Carrageenan; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cycloo

2004
Dalteparin, a low molecular weight heparin, attenuates inflammatory responses and reduces ischemia-reperfusion-induced liver injury in rats.
    Critical care medicine, 2006, Volume: 34, Issue:7

    Topics: 6-Ketoprostaglandin F1 alpha; Animals; Anticoagulants; Calcium; Cyclooxygenase 2 Inhibitors; Daltepa

2006
Cyclooxygenase 2 expression in vessels and nerves in reversal reaction leprosy.
    The American journal of tropical medicine and hygiene, 2006, Volume: 74, Issue:6

    Topics: Blood Vessels; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Edema; Endothelium; Eosine Yellowish-(

2006
COX-1 inhibition enhances scratching behaviour in NC/Nga mice with atopic dermatitis.
    Experimental dermatology, 2006, Volume: 15, Issue:8

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Blotting, Western; Carrageenan; Cyclooxygenase 1;

2006
Synergistic antinociceptive effects of anandamide, an endocannabinoid, and nonsteroidal anti-inflammatory drugs in peripheral tissue: a role for endogenous fatty-acid ethanolamides?
    European journal of pharmacology, 2006, Nov-21, Volume: 550, Issue:1-3

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Arachidonic Acids; Capsaicin; Chromatography, High

2006
Anti-inflammatory activity of the synthetic C-C biflavonoids.
    The Journal of pharmacy and pharmacology, 2006, Volume: 58, Issue:12

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Biflavonoids; Blotting, Western; Carrageenan; Cell

2006
Cyclooxygenase-1 inhibition delays recovery of the cutaneous barrier disruption caused by mechanical scratching in mice.
    The British journal of dermatology, 2007, Volume: 156, Issue:6

    Topics: Animals; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors;

2007
Cyclooxygenases 1 and 2 contribute to peroxynitrite-mediated inflammatory pain hypersensitivity.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2008, Volume: 22, Issue:9

    Topics: Animals; Carrageenan; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase Inhibitors; Drug Synergism;

2008
NS-398, a novel non-steroidal anti-inflammatory drug with potent analgesic and antipyretic effects, which causes minimal stomach lesions.
    General pharmacology, 1993, Volume: 24, Issue:1

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Experimental; Carrageenan; Cyclooxygena

1993
A structural feature of N-[2-(cyclohexyloxy)-4-nitrophenyl] methanesulfonamide (NS-398) that governs its selectivity and affinity for cyclooxygenase 2 (COX2).
    Inflammation research : official journal of the European Histamine Research Society ... [et al.], 1995, Volume: 44 Suppl 2

    Topics: Animals; Cyclooxygenase Inhibitors; Edema; Humans; Isoenzymes; Male; Mice; Nitrobenzenes; Prostaglan

1995
Selective cyclooxygenase-2 inhibition reduces carrageenan oedema and associated spinal c-Fos expression in the rat.
    Brain research, 1996, Apr-09, Volume: 715, Issue:1-2

    Topics: Animals; Carrageenan; Cyclooxygenase Inhibitors; Dose-Response Relationship, Drug; Edema; Foot; Hind

1996
Cyclo-oxygenase isozymes in mucosal ulcergenic and functional responses following barrier disruption in rat stomachs.
    British journal of pharmacology, 1997, Volume: 122, Issue:3

    Topics: Animals; Carrageenan; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenas

1997