Development of 3D-QSAR models for 5-lipoxygenase antagonists: chalcones.
暂无分享,去创建一个
Philip Prathipati | S. G. Kaskhedikar | P. Prathipati | A. Saxena | Anil K Saxena | M Arockia Babu | Neeraj Shakya | S G Kaskhedikar | Neeraj Shakya | M. Arockia Babu
[1] Michael R. Greenberg,et al. Chapter 1 – Theory, Methods, and Applications , 1978 .
[2] J. Rokach. Leukotrienes and lipoxygenases , 1989 .
[3] Y. Martin,et al. Quantitative structure-activity relationships of 5-lipoxygenase inhibitors. Inhibitory potency of pyridazinone analogues. , 1994, Journal of pharmaceutical sciences.
[4] S. Kc,et al. Depsides as non-redox inhibitors of leukotriene B4 biosynthesis and HaCaT cell growth. 1. Novel analogues of barbatic and diffractaic acid , 1999 .
[5] M. Edwards,et al. Indazolinones, a new series of redox-active 5-lipoxygenase inhibitors with built-in selectivity and oral activity. , 1991, Journal of medicinal chemistry.
[6] R. D. Dyer,et al. Hydroxamic acid inhibitors of 5-lipoxygenase: quantitative structure-activity relationships. , 1990, Journal of medicinal chemistry.
[7] M. J. D. Powell,et al. Restart procedures for the conjugate gradient method , 1977, Math. Program..
[8] P. Young,et al. 5-Lipoxygenase inhibitors: synthesis and structure-activity relationships of a series of 1-aryl-2H,4H-tetrahydro-1,2,4-triazin-3-ones. , 1996, Journal of medicinal chemistry.
[9] P. Tuchinda,et al. Anti-inflammatory cyclohexenyl chalcone derivatives in Boesenbergia pandurata. , 2002, Phytochemistry.
[10] Gordon M. Crippen,et al. Atomic physicochemical parameters for three-dimensional-structure-directed quantitative structure-activity relationships. 2. Modeling dispersive and hydrophobic interactions , 1987, J. Chem. Inf. Comput. Sci..
[11] R. Young. Inhibitors of 5-lipoxygenase: a therapeutic potential yet to be fully realized? , 1999 .
[12] Renzi Pm. Antileukotriene agents in asthma: The dart that kills the elephant? , 1999 .
[13] H. Ueda,et al. 3,4-Dihydroxychalcones as potent 5-lipoxygenase and cyclooxygenase inhibitors. , 1993, Journal of medicinal chemistry.
[14] B. Samuelsson,et al. The inhibitory effects of BW 755C on arachidonic acid metabolism in human polymorphonuclear leukocytes , 1980, FEBS letters.
[15] Arup K. Ghose,et al. Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally occurring nucleoside antibiotics , 1989, J. Chem. Inf. Comput. Sci..
[16] H. Kubinyi,et al. 3D QSAR in drug design. , 2002 .
[17] J. Petraitis,et al. 2-substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity. , 1990, Journal of medicinal chemistry.
[18] H. Degreef,et al. A double-blind vehicle-controlled study of R 68 151 in psoriasis: a topical 5-lipoxygenase inhibitor. , 1990, Journal of the American Academy of Dermatology.