K. Saionz

发表

Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitors.

A. Stamford, J. Cumming, L. Zhang, 2008, Bioorganic & medicinal chemistry letters.

DNA binding properties of key sandramycin analogues: systematic examination of the intercalation chromophore.

D. Boger, K. Saionz, 1999, Bioorganic & medicinal chemistry.

Small molecule biaryl FSH receptor agonists. Part 1: Lead discovery via encoded combinatorial synthesis.

M. Webb, R. Dolle, T. Guo, 2004, Bioorganic & medicinal chemistry letters.

(-)-SANDRAMYCIN : TOTAL SYNTHESIS AND CHARACTERIZATION OF DNA BINDING PROPERTIES

D. Boger, K. Saionz, J.‐H. Chen, 1996 .

Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines.

E. LaVoie, D. S. Pilch, M. Kaul, 2013, Bioorganic & medicinal chemistry letters.

Discovery of novel quinolinone adenosine A2B antagonists.

A. Klon, M. Webb, V. Srivastava, 2010, Bioorganic & medicinal chemistry letters.

Synthesis of key sandramycin analogs: systematic examination of the intercalation chromophore.

D. Boger, K. Saionz, Q. Jin, 1998, Bioorganic & medicinal chemistry.

Synthesis, biological evaluation, and pharmacokinetic study of prolyl-1-piperazinylacetic acid and prolyl-4-piperidinylacetic acid derivatives as VLA-4 antagonists.

J. Chiba, M. Yokoyama, J. Baldwin, 2006, Bioorganic & medicinal chemistry.

Chemically bonded stationary phases that use synthetic hosts containing aromatic binding clefts: HPLC analysis of nitro-substituted polycyclic aromatic hydrocarbons.

S. Zimmerman, K. Saionz, Z. Zeng, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Identified a morpholinyl-4-piperidinylacetic acid derivative as a potent oral active VLA-4 antagonist.

J. Chiba, M. Yokoyama, J. Baldwin, 2005, Bioorganic & medicinal chemistry letters.

Quantitative Host-Guest Complexation Studies Using Chemically Bonded Stationary Phases. A Comparison of HPLC and Solution Enthalpies

S. Zimmerman, K. Saionz, 1995 .

Folate pathway disruption leads to critical disruption of methionine derivatives in Mycobacterium tuberculosis.

Joel S. Freundlich, D. Sherman, M. Nixon, 2014, Chemistry & biology.

Piperazine sulfonamide BACE1 inhibitors: design, synthesis, and in vivo characterization.

Andrew Stamford, William Greenlee, Guoqing Li, 2010, Bioorganic & medicinal chemistry letters.

Combined solution-phase and solid-phase synthesis of 2-amino-7,8-dihydropteridin-6(5H)-ones

H. Gstach, J. Baldwin, A. Metzger, 2009 .

JPC-2997, a New Aminomethylphenol with High In Vitro and In Vivo Antimalarial Activities against Blood Stages of Plasmodium

G. Birrell, G. Shanks, M. Chavchich, 2014, Antimicrobial Agents and Chemotherapy.

Design, synthesis, and activity of 2-imidazol-1-ylpyrimidine derived inducible nitric oxide synthase dimerization inhibitors.

M. Adler, M. Whitlow, M. Ohlmeyer, 2007, Journal of medicinal chemistry.

Folate pathway disruption leads to critical disruption of methionine derivatives in Mycobacterium tuberculosis.

Joel S. Freundlich, D. Sherman, M. Nixon, 2014, Chemistry & biology.