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THE ALKYLATION AND HALOGENATION OF SULFONES CATALYZED BY HYDROXIDE ION IN APROTIC SOLVENTSREGIS RR; DOWEYKO AM.1982; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1982; VOL. 23; NO 25; PP. 2539-2542; BIBL. 12 REF.Article

A NOVEL CLASS OF FUNGICIDES: (2-PYRIDYLTHIO) METHYL BENZOATE N-OXIDESSTANTON DT; DAVIS RA; DOWEYKO AM et al.1983; JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY; ISSN 0021-8561; USA; DA. 1983; VOL. 31; NO 2; PP. 451-453; BIBL. 9 REF.Article

An application of 3D-QSAR to the analysis of the sequence specificity of DNA alkylation by uracil mustardDOWEYKO, A. M; MATTES, W. B.Biochemistry (Easton). 1992, Vol 31, Num 39, pp 9388-9392, issn 0006-2960Article

Antiulcer agents. 6. Analysis of the in vitro biochemical and in vivo gastric antisecretory activity of substituted imidazo[1,2-a]pyridines and related analogues using comparative molecular field analysis and hypothetical active site lattice methodologiesKAMINSKI, J. J; DOWEYKO, A. M.Journal of medicinal chemistry (Print). 1997, Vol 40, Num 4, pp 427-436, issn 0022-2623Article

Synthesis of H-3 labeled 5-fluoro-3-[3-[4-(5-methoxy-4-pyrimidinyl)-1-piperazinyl]propyl]-1H-indole, a serotonergic agent with potential antidepressant activityDISCHINO, D. D; COMBRINK, K. D; DOWEYKO, L et al.Journal of labelled compounds & radiopharmaceuticals. 1995, Vol 36, Num 8, pp 789-794, issn 0362-4803Article

Estimation of hERG inhibition of drug candidates using multivariate property and pharmacophore SARJOHNSON, Stephen R; HONGWEN YUE; LEE CONDER, Mary et al.Bioorganic & medicinal chemistry. 2007, Vol 15, Num 18, pp 6182-6192, issn 0968-0896, 11 p.Article

Benzothiazole based inhibitors of p38α MAP kinaseCHUNJIAN LIU; LIN, James; TRZASKOS, James et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 6, pp 1874-1879, issn 0960-894X, 6 p.Article

Molecular design, synthesis, and structure-activity relationships leading to the potent and selective p56lck inhibitor BMS-243117DAS, Jagabandhu; LIN, James; PITT, Sidney et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 13, pp 2145-2149, issn 0960-894X, 5 p.Article

Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56LckWITYAK, John; DAS, Jagabandhu; QIONG FANG et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 22, pp 4007-4010, issn 0960-894X, 4 p.Article

Utilization of a nitrogen-sulfur nonbonding interaction in the design of new 2-aminothiazol-5-yl-pyrimidines as p38α MAP kinase inhibitorsSHUQUN LIN; WROBLESKI, Stephen T; KIEFER, Susan E et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 19, pp 5864-5868, issn 0960-894X, 5 p.Article

Synthesis and SAR of p38α MAP kinase inhibitors based on heterobicyclic scaffoldsMURALI DHAR, T. G; WROBLESKI, Stephen T; MATHUR, Arvind et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 18, pp 5019-5024, issn 0960-894X, 6 p.Article

5-Amino-pyrazoles as potent and selective p38α inhibitorsDAS, Jagabandhu; MOQUIN, Robert V; NEWITT, John A et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 23, pp 6886-6889, issn 0960-894X, 4 p.Article

Discovery of azetidinone acids as conformationally-constrained dual PPARα/γ agonistsWEI WANG; DEVASTHALE, Pratik; ZEBO, Rachel et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 6, pp 1939-1944, issn 0960-894X, 6 p.Article

Discovery and initial SAR of imidazoquinoxalines as inhibitors of the Src-family kinase p56LckPING CHEN; NORRIS, Derek; DE FEX, Henry F et al.Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 10, pp 1361-1364, issn 0960-894XArticle

Design and synthesis of 4-substituted benzamides as potent, selective, and orally bioavailable IKs blockersLLOYD, John; SCHMIDT, Joan B; CONDER, Mary Lee et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 23, pp 3764-3767, issn 0022-2623Article

Discovery of tertiary aminoacids as dual PPARα/γ agonists-IDEVASTHALE, Pratik V; CHEN, Sean; GROVER, Gary et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 8, pp 2312-2316, issn 0960-894X, 5 p.Article

5-cyanopyrimidine derivative's as a novel class of potent, selective, and orally active inhibitors of p38α MAP kinaseCHUNJIAN LIU; WROBLESKI, Stephen T; DING REN SHEN et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 20, pp 6261-6270, issn 0022-2623, 10 p.Article

Tetrahydronaphthalene-derived amino alcohols and amino ketones as potent and selective inhibitors of the delayed rectifier potassium current IKsAHMAD, Saleem; DOWEYKO, Lidia; RUSSELL, Anita D et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 1, pp 99-102, issn 0960-894X, 4 p.Article

Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56Lck inhibitorsPING CHEN; NORRIS, Derek; DING REN SHEN et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 24, pp 6061-6066, issn 0960-894X, 6 p.Article

Pyrazolo-pyrimidines : A novel heterocyclic scaffold for potent and selective p38α inhibitorsDAS, Jagabandhu; MOQUIN, Robert V; KIEFER, Susan E et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 8, pp 2652-2657, issn 0960-894X, 6 p.Article

Synthesis and SAR of new pyrrolo[2,1-f][1,2,4]triazines as potent p38α MAP kinase inhibitorsWROBLESKI, Stephen T; SHUQUN LIN; DOWEYKO, Arthur M et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 8, pp 2739-2744, issn 0960-894X, 6 p.Article

2-Aminothiazole as a novel kinase inhibitor template. structure-activity relationship studies toward the discovery of N-(2 -chloro -6 -methylphenyl ) -2 -[ [6 -[4 -(2 -hydroxyethyl ) -1-piperazinyl ] -2 -methyl -4 -pyrimidinyl ]amino ]-1,3 -thiazole -5 -carboxamide (dasatinib, BMS-354825) as a potent pan-Src kinase inhibitorDAS, Jagabandhu; PING CHEN; SUHONG PANG et al.Journal of medicinal chemistry (Print). 2006, Vol 49, Num 23, pp 6819-6832, issn 0022-2623, 14 p.Article

N-[1-aryl-2-(1-imidazolo)ethyl]-guanidine derivatives as potent inhibitors of the bovine mitochondrial F1F0 ATP hydrolaseATWAL, Karnail S; AHMAD, Saleem; DOWEYKO, Lidia M et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 4, pp 1027-1030, issn 0960-894X, 4 p.Article

Arylcyclopropanecarboxyl guanidines as novel, potent, and selective inhibitors of the sodium hydrogen exchanger isoform-1AHMAD, Saleem; DOWEYKO, Lidia M; LAN, Shih-Jung et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 20, pp 3302-3310, issn 0022-2623Article

Discovery of N-(2-chloro-6-methylphenyl)-2-6-(4-(2-hydroxyethyl)-piperazin-1-yl)-2-methylpyr imidin-4-ylaminothiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assaysLOMBARDO, Louis J; LEE, Francis Y; FAIRCHILD, Craig et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 27, pp 6658-6661, issn 0022-2623, 4 p.Article

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