Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines von Parhi, Ajit K., Zhang, Yongzheng, Saionz, Kurt W., Pradhan, Padmanava, Kaul, Malvika, Trivedi, Kalkal, Pilch, Daniel S., LaVoie, Edmond J.

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Synthesis, biological evaluation, and pharmacokinetic study of prolyl-1-piperazinylacetic acid and prolyl-4-piperidinylacetic acid derivatives as VLA-4 antagonists von Chiba, Jun, Takayama, Gensuke, Takashi, Tohru, Yokoyama, Mika, Nakayama, Atsushi, Baldwin, John J., McDonald, Edward, Moriarty, Kevin J., Sarko, Christopher R., Saionz, Kurt W., Swanson, Robert, Hussain, Zahid, Wong, Angela, Machinaga, Nobuo

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JPC-2997, a new aminomethylphenol with high in vitro and in vivo antimalarial activities against blood stages of Plasmodium von Birrell, Geoffrey W, Chavchich, Marina, Ager, Arba L, Shieh, Hong-Ming, Heffernan, Gavin D, Zhao, Wenyi, Krasucki, Peter E, Saionz, Kurt W, Terpinski, Jacek, Schiehser, Guy A, Jacobus, Laura R, Shanks, G Dennis, Jacobus, David P, Edstein, Michael D

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(−)-Sandramycin:  Total Synthesis and Characterization of DNA Binding Properties von Boger, Dale L, Chen, Jyun-Hung, Saionz, Kurt W

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Identified a morpholinyl-4-piperidinylacetic acid derivative as a potent oral active VLA-4 antagonist von Chiba, Jun, Machinaga, Nobuo, Takashi, Tohru, Ejima, Akio, Takayama, Gensuke, Yokoyama, Mika, Nakayama, Atsushi, Baldwin, John J., McDonald, Edward, Saionz, Kurt W., Swanson, Robert, Hussain, Zahid, Wong, Angela

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Synthesis of novel substituted 3,8,11-triazaspiro[5,6]dodecan-7-ones von Qin, Lan-Ying, Cole, Andrew G., Metzger, Axel, Saionz, Kurt W., Henderson, Ian

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Folate Pathway Disruption Leads to Critical Disruption of Methionine Derivatives in Mycobacterium tuberculosis von Nixon, Molly R., Saionz, Kurt W., Koo, Mi-Sun, Szymonifka, Michael J., Jung, Hunmin, Roberts, Justin P., Nandakumar, Madhumita, Kumar, Anuradha, Liao, Reiling, Rustad, Tige, Sacchettini, James C., Rhee, Kyu Y., Freundlich, Joel S., Sherman, David R.

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Quantitative Host-Guest Complexation Studies Using Chemically Bonded Stationary Phases. A Comparison of HPLC and Solution Enthalpies von Zimmerman, Steven C, Saionz, Kurt W

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Small molecule biaryl FSH receptor agonists. Part 2: Lead optimization via parallel synthesis von Guo, Tao, Adang, Anton E.P., Dong, Guizhen, Fitzpatrick, Dan, Geng, Peng, Ho, Koc-Kan, Jibilian, Charles H., Kultgen, Steven G., Liu, Ruiyan, McDonald, Edward, Saionz, Kurt W., Valenzano, Kenneth J., van Straten, Nicole C.R., Xie, Dan, Webb, Maria L.

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Small molecule biaryl FSH receptor agonists. Part 1: Lead discovery via encoded combinatorial synthesis von Guo, Tao, Adang, Anton E.P., Dolle, Roland E., Dong, Guizhen, Fitzpatrick, Dan, Geng, Peng, Ho, Koc-Kan, Kultgen, Steven G., Liu, Ruiyan, McDonald, Edward, McGuinness, Brian F., Saionz, Kurt W., Valenzano, Kenneth J., van Straten, Nicole C.R., Xie, Dan, Webb, Maria L.

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Synthesis of key sandramycin analogs: systematic examination of the intercalation chromophore von Boger, Dale L., Chen, Jyun-Hung, Saionz, Kurt W., Jin, Qing

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Chemically Bonded Stationary Phases that Use Synthetic Hosts Containing Aromatic Binding Clefts: HPLC Analysis of Nitro-Substituted Polycyclic Aromatic Hydrocarbons von Zimmerman, Steven C., Saionz, Kurt W., Zeng, Zijian

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A facile synthesis of novel 2-amino-6-arylmethyl-7-carboxamido-7,8-dihydropyrimido[5,4- f][1,4]thiazepin-5-ones von Qin, Lan-Ying, Cole, Andrew G., Metzger, Axel, Brescia, Marc-Raleigh, Saionz, Kurt W., Zhang, Joan J., Rigollier, Pascal, Wareing, James R., Gstach, Hubert, Zimmermann, Juerg, Dolle, Roland E., Baldwin, John J., Henderson, Ian

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Combined solution-phase and solid-phase synthesis of 2-amino-7,8-dihydropteridin-6(5 H)-ones von Metzger, Axel, Qin, Lan-Ying, Cole, Andrew G., Saionz, Kurt W., Brescia, Marc-Raleigh, Gstach, Hubert, Wareing, James R., Zimmermann, Juerg, Brill, Wolfgang K-D., Baldwin, John J., Dolle, Roland E., Henderson, Ian

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DNA binding properties of key sandramycin analogues: systematic examination of the intercalation chromophore von Boger, D L, Saionz, K W

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Corrigendum to “Identified a morpholinyl-4-piperidinylacetic acid derivatives as a potent oral active VLA-4 antagonist”: [Bioorg. Med. Chem. Lett. 15 (1) (2005) 41] von Chiba, Jun, Machinaga, Nobuo, Takashi, Tohru, Ejima, Akio, Takayama, Gensuke, Yokoyama, Mika, Nakayama, Atsushi, Baldwin, John J., McDonald, Edward, Moriarty, Kevin J., Sarko, Christopher R., Saionz, Kurt W., Swanson, Robert, Hussain, Zahid, Wong, Angela

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Small molecule biaryl FSH receptor agonists. Part 1 von Guo, Tao, Adang, Anton E.P., Dolle, Roland E., Dong, Guizhen, Fitzpatrick, Dan, Geng, Peng, Ho, Koc-Kan, Kultgen, Steven G., Liu, Ruiyan, McDonald, Edward, McGuinness, Brian F., Saionz, Kurt W., Valenzano, Kenneth J., van Straten, Nicole C.R., Xie, Dan, Webb, Maria L.

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Heterocyclic aspartyl protease inhibitors von SAIONZ KURT W, GUO TAO, STAMFORD ANDREW W, ZHU ZHAONING

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LIPOPROTEIN LIPASE-ACTIVATING COMPOSITIONS COMPRISING BENZENE DERIVATES von SAIONZ, KURT W, SHIBUTANI, TADAO, IWATA, KOUSHI, OHLMEYER, MICHAEL, OKAMURA, TAKASHI, NEAGU, IRINA, PARADKAR, VIDYADHAR M

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Lipoprotein lipase-activating compositions comprising benzene derivates von NEAGU IRINA, PARADKAR VIDYADHAR M, OKAMURA TAKASHI, SAIONZ KURT W, OHLMEYER MICHAEL, SHIBUTANI TADAO, IWATA KOUSHI

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