H. Maag

发表

Synthesis and anti-HIV activity of 4'-azido- and 4'-methoxynucleosides.

R. Rydzewski, M. J. Mcroberts, J. Verheyden, 1992, Journal of medicinal chemistry.

The design, synthesis, and antiviral activity of monofluoro and difluoro analogues of 4'-azidocytidine against hepatitis C virus replication: the discovery of 4'-azido-2'-deoxy-2'-fluorocytidine and 4'-azido-2'-dideoxy-2',2'-difluorocytidine.

K. Benkestock, N. Cammack, S. Le Pogam, 2009, Journal of medicinal chemistry.

An allylic azide route to 4'-azido carbocyclic nucleosides. Synthesis of (.+-.)-(1'.alpha.,2'.alpha.,3'.beta.)- and (.+-.)-(1'.alpha.,2'.beta.,3'.beta.)-1-[1-azido-2-hydroxy-1-(hydroxymethyl)-3-cyclopentyl]thymine

R. Rydzewski, H. Maag, 1992 .

Application of the “trimethyl lock”1 to Ganciclovir, a pro-prodrug with increased oral bioavailability☆

M. P. Dillon, H. Maag, H. Cai, 1996 .

Overcoming poor permeability - the role of prodrugs for oral drug delivery.

H. Maag, 2012, Drug discovery today. Technologies.

Prodrugs of Carboxylic Acids

H. Maag, 2007 .

Solid-state and solution conformations of the potent HIV inhibitor, 4'-azidothymidine.

J. L. Steiner, H. Maag, E. Prisbe, 1994, Journal of medicinal chemistry.

Structure, absolute configuration, and total synthesis of an acid-catalyzed rearrangement product of bicyclomycin

J. Blount, H. Maag, D. L. Coffen, 1978 .

The design, synthesis, and antiviral activity of 4'-azidocytidine analogues against hepatitis C virus replication: the discovery of 4'-azidoarabinocytidine.

K. Benkestock, N. Cammack, S. Le Pogam, 2009, Journal of medicinal chemistry.

Preparation and Structure Proof of the Four Isomeric Dicyanocobyrinic Acid Hexamethyl Ester Monoamides Carrying the Amide Group on a Propionic Acid Side Chain

L. Ernst, H. Maag, 2006 .

Fatty acid derivatives: Important surfactants for household, cosmetic and industrial purposes

H. Maag, 1984 .

THE REGIOSELECTIVE OPENING OF 5-O-BENZYL-1,2:3,4-O-ISOPROPYLIDENE-D-PSICOFURANOSE WITH ORGANOSTANNANES

M. P. Dillon, H. Maag, Dawn M. Myszynski, 1995 .

Prodrugs of nucleoside analogues for improved oral absorption and tissue targeting.

Fujun Li, T. Alfredson, H. Maag, 2008, Journal of pharmaceutical sciences.

Oligodeoxynucleotide probes with multiple labels linked to the 4'-position of thymidine monomers : excellent duplex stability and detection sensitivity

H. Maag, B. Schmidt, S. Rose, 1994 .

Structure-Activity Relationships Among HIV Inhibitory 4′-Substituted Nucleosides

R. Rydzewski, J. Verheyden, H. Maag, 1993 .

GMP Synthetase: Synthesis and Biological Evaluation of a Stable Analog of the Proposed AMP-XMP Reaction Intermediate

E. J. Salaski, H. Maag, 1999 .

D. Bertrand, M. Milla, F. Knoflach, 2018, Public Health Genomics.

Characterization of RO5126946, a Novel α7 Nicotinic Acetylcholine Receptor–Positive Allosteric Modulator

D. Bertrand, M. Milla, F. Knoflach, 2014, The Journal of Pharmacology and Experimental Therapeutics.

Characterization of RO 5126946 , a Novel a 7 Nicotinic Acetylcholine Receptor – Positive Allosteric Modulator s

D. Bertrand, M. Milla, F. Knoflach, 2014 .

5‐(N‐Arylnortropan‐3‐yl)‐ and 5‐(N‐Arylpiperidin‐4‐yl)‐2,4‐diaminopyrimidines. Novel Inhibitors of Dihydrofolate Reductase

J. Daly, H. Maag, I. Kompiš, 1986 .

Antibiotics and antiviral compounds : chemical synthesis and modification

K. Krohn, H. Maag, A. KirstHerbert, 1993 .