M. P. Hutt

发表

Quinolone antibacterial agents. Synthesis and structure-activity relationships of 8-substituted quinoline-3-carboxylic acids and 1,8-naphthyridine-3-carboxylic acids.

S. Hagen, J. Domagala, J. Sánchez, 1988, Journal of medicinal chemistry.

Identification of quinoline nitration products by NOE

M. P. Hutt, F. Mackellar, 1984 .

Folate antagonists. 15. 2,3-Diamino-6-(2-naphthylsulfonyl)quinazoline and related 2,4-diamino-6-[(phenyl and naphthyl)sulfinyl and sulfonyl]quinazolines, a potent new class of antimetabolites with phenomenal antimalarial activity.

J. Johnson, M. P. Hutt, P. Jacob, 1979, Journal of medicinal chemistry.

\documentclass{article}\pagestyle{empty}\begin{document}$ \left[\!\left[ {} \right.\right. $ \end{document}[(Dialkylamino)alkyl]amino\documentclass{article}\pagestyle{empty}\begin{document}$ \left.\left. {} \right]\!\right] $ \end{document}pyrimido[1,2‐a]benzimidazoles,2,3‐dihydro‐1H‐cyclopenta[4,5]

M. P. Hutt, E. Elslager, L. M. Werbel, 1969 .

2-Phenyl-5-(trichloromethyl)-1,3,4-oxadiazoles, A new class of antimalarial substances†

M. P. Hutt, E. Elslager, L. M. Werbel, 1970 .

1-Substituted 7-[3-[(ethylamino)methyl]-1-pyrrolidinyl]-6,8- difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids. New quantitative structure-activity relationships at N1 for the quinolone antibacterials.

J. Domagala, C. L. Heifetz, M. P. Hutt, 1988, Journal of medicinal chemistry.

Antimalarial and antischistosomal effects of alpha,alpha,alpha,alpha',alpha',alpha'-hexachloroxylene derivatives and related halogenated hydrocarbons.

M. P. Hutt, E. Elslager, L. M. Werbel, 1970, Journal of medicinal chemistry.

Synthesis and biological activity of a new semisynthetic cephalosporin, CN-92,982.

P. W. Woo, T. Haskell, J. Sánchez, 1980, The Journal of antibiotics.

New structure-activity relationships of the quinolone antibacterials using the target enzyme. The development and application of a DNA gyrase assay.

J. Domagala, J M Domagala, L D Hanna, 1986, Journal of medicinal chemistry.

Antimalarial agents. 6-[ [(dialkylamino)alkyl]amino]-5,8-dimethoxyquinaldines

M. P. Hutt, L. M. Werbel, Edward F. Flslager, 1969 .

Synthesis and physical properties of the antimalarial agent 4-(2-bromo-4,5-dimethoxyphenyl)-1,1,7,7-tetraethyldiethylenetriamine (RC-12) (WR-27,653).

M. P. Hutt, E. Elslager, L. M. Werbel, 1967, Journal of pharmaceutical sciences.

Antimalarial activity of 2-(substituted amino)-4,6-bis(trichloromethyl)-1,3,5-triazines and N-(chlorophenyl)-N'-[4-(substituted amino)-6-(trichloromethyl)-1,3,5-triazin-2-yl]guanidines.

M. P. Hutt, E. Elslager, L. M. Werbel, 1987, Journal of medicinal chemistry.

Quinolone antibacterials: preparation and activity of bridged bicyclic analogues of the C7-piperazine.

J. Kiely, R. Gogliotti, M. P. Hutt, 1991, Journal of Medicinal Chemistry.

Quinolone Antibacterials: Preparation and Activity of Bridged Bicyclic Analogues of the C7‐Piperazine.

J. Kiely, R. Gogliotti, M. P. Hutt, 1991 .

1-Substituted 7-(3-((Ethylamino)methyl)-1-pyrrolidinyl)-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acids. New Quantitative Structure-Activity Relationships at N1 for the Quinolone Antibacterials.

J. Domagala, C. L. Heifetz, M. P. Hutt, 1988 .

Synthesis and biological activity of peptide antagonists of luliberin (luteinizing hormone-releasing hormone).

E. Nicolaides, W. C. Dermody, J. Reel, 1979, Journal of medicinal chemistry.

7-substituted 5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3- quinolinecarboxylic acids: synthesis and biological activity of a new class of quinolone antibacterials.

S. Hagen, J. Domagala, J. Sánchez, 1988, Journal of medicinal chemistry.

Folate antagonists. 22. Antimalarial and antibacterial effects of 2,4-diamino-6-quinazolinesulfonamides.

J. Johnson, M. P. Hutt, E. Elslager, 1984, Journal of medicinal chemistry.

FOLATE ANTAGONISTS. 22. ANTIMALARIAL AND ANTIBACTERIAL EFFECTS OF 2,4-DIAMINO-6-QUINAZOLINESULFONAMIDES

Judith L. Johnson, M. P. Hutt, E. Elslager, 1985 .