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Inhibitors of HCV NS5B polymerase : Synthesis and structure-activity relationships of N-1-benzyl and N-1-[3-methylbutyl]-4-hydroxy-1,8-naphthyridon-3-yl benzothiadiazine analogs containing substituents on the aromatic ringROCKWAY, Todd W; RONG ZHANG; KATI, Warren M et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 14, pp 3833-3838, issn 0960-894X, 6 p.Article

Des-A-ring benzothiadiazines : Inhibitors of HCV genotype 1 NS5B RNA-dependent RNA polymeraseDONNER, Pamela L; QINGHUA XIE; MOLLA, Akhter et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 8, pp 2735-2738, issn 0960-894X, 4 p.Article

A new class of potent non-imidazole H3 antagonists: 2-aminoethylbenzofuransCOWART, Marion; PRATT, John K; STEWART, Andrew O et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 3, pp 689-693, issn 0960-894X, 5 p.Article

In vitro optimization of structure activity relationships of analogues of A-331440 combining radioligand receptor binding assays and micronucleus assays of potential antiobesity histamine H3 receptor antagonistsHANCOCK, Arthur A; DIEHL, Marilyn S; COWART, Marion D et al.Basic & clinical pharmacology & toxicology (Print). 2004, Vol 95, Num 3, pp 144-152, issn 1742-7835, 9 p.Article

Nonsteroidal selective glucocorticoid modulators: the effect of C-5 alkyl substitution on the transcriptional activation/repression profile of 2,5-dihydro-10-methoxy-2,2,4-trimethyl-1H-[1]benzopyrano[3,4-f]quinolinesELMORE, Steven W; COGHLAN, Michael J; JACOBSON, Peer B et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 25, pp 4481-4491, issn 0022-2623Article

Inhibitors of HCV NS5B polymerase : Synthesis and structure- activity relationships of N-alkyl-4-hydroxyquinolon-3-yl-benzothiadiazine sulfamidesKRUEGER, A. Chris; MADIGAN, Darold L; HONGMEI MO et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 13, pp 3367-3370, issn 0960-894X, 4 p.Article

Nonsteroidal selective glucocorticoid modulators: The effect of C-10 substitution on receptor selectivity and functional potency of 5-allyl-2,5-dihydro-2,2,4-trimethyl-1H-[1]benzopyrano[3,4-f]quinolinesKYM, Philip R; KORT, Michael E; FALLS, H. Douglass et al.Journal of medicinal chemistry (Print). 2003, Vol 46, Num 6, pp 1016-1030, issn 0022-2623, 15 p.Article

Pyridopyrimidine analogues as novel adenosine kinase inhibitorsGUO ZHU ZHENG; LEE, Chih-Hung; MUCHMORE, Steve et al.Bioorganic & medicinal chemistry letters (Print). 2001, Vol 11, Num 16, pp 2071-2074, issn 0960-894XArticle

Structure-activity studies for a novel series of bicyclic substituted hexahydrobenz[e]isoindole α1A adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasiaMEYER, Michael D; ALTENBACH, Robert J; TIETJE, Karin et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 12, pp 1971-1985, issn 0022-2623Article

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