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n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and Muscle Relaxation

n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide has been researched along with Muscle Relaxation in 3 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.

Muscle Relaxation: That phase of a muscle twitch during which a muscle returns to a resting position.

Research

Studies (3)

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

Authors

AuthorsStudies
Lee, SY1
Lee, MY1
Park, SH1
Kim, TH1
Moon, YT1
Han, JH1
Myung, SC1
Mukai, Y1
Shimokawa, H1
Higashi, M1
Morikawa, K1
Matoba, T1
Hiroki, J1
Kunihiro, I1
Talukder, HM1
Takeshita, A1
Beverelli, F1
Béa, ML1
Puybasset, L1
Giudicelli, JF1
Berdeaux, A1

Other Studies

3 other studies available for n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and Muscle Relaxation

ArticleYear
NS-398 (a selective cyclooxygenase-2 inhibitor) decreases agonist-induced contraction of the human ureter via calcium channel inhibition.
    Journal of endourology, 2010, Volume: 24, Issue:11

    Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl e

2010
Inhibition of renin-angiotensin system ameliorates endothelial dysfunction associated with aging in rats.
    Arteriosclerosis, thrombosis, and vascular biology, 2002, Sep-01, Volume: 22, Issue:9

    Topics: Aging; Angiotensin-Converting Enzyme Inhibitors; Animals; Aorta; Blood Pressure; Bridged Bicyclo Com

2002
Chronic inhibition of NO synthase enhances the production of prostacyclin in coronary arteries through upregulation of the cyclooxygenase type 1 isoform.
    Fundamental & clinical pharmacology, 1997, Volume: 11, Issue:3

    Topics: 6-Ketoprostaglandin F1 alpha; Animals; Bradykinin; Coronary Vessels; Cyclooxygenase 1; Dogs; Enzyme

1997