Search Results - "Luu, Hiep T."

Structure-Based Design of a Parallel Synthetic Array Directed Toward the Discovery of Irreversible Inhibitors of Human Rhinovirus 3C Protease by Johnson, Theodore O, Hua, Ye, Luu, Hiep T, Brown, Edward L, Chan, Fora, Chu, Shao Song, Dragovich, Peter S, Eastman, Brian W, Ferre, Rose Ann, Fuhrman, Shella A, Hendrickson, Thomas F, Maldonado, Fausto C, Matthews, David A, Meador, James W, Patick, Amy K, Reich, Siegfried H, Skalitzky, Donald J, Worland, Stephen T, Yang, Michelle, Zalman, Leora S

“…Utilizing the tools of parallel synthesis and structure-based design, a new class of Michael acceptor-containing, irreversible inhibitors of human rhinovirus…”
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On Symbol-Triple Distance of a Class of Constacyclic Codes of Length 3 p s Over F p m + u F p m by Dinh, Hai Q., Nguyen, Bac T., Luu, Hiep T., Yamaka, Woraphon

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On Symbol-Triple Distance of a Class of Constacyclic Codes of Length 3 ps Over F pm + u F pm by Dinh, Hai Q, Nguyen, Bac T, Luu, Hiep T, Yamaka, Woraphon

“…Let [Formula Omitted] be any prime. In this paper, we completely determine symbol-triple distance of all [Formula Omitted]-constacyclic codes of length…”
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On symbol-triple distance of a class of constacyclic codes of length 3ps over Fpm + uFpm by Dinh, Hai Q., Nguyen, Bac T, Thi, Hiep L, Yamaka, Woraphon

“…Let p ≠ 3 be any prime. In this paper, we completely determine symbol-triple distance of all γ-constacyclic codes of length 3 p s over the finite commutative…”
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Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 8. Pharmacological Optimization of Orally Bioavailable 2-Pyridone-Containing Peptidomimetics by Dragovich, Peter S, Prins, Thomas J, Zhou, Ru, Johnson, Theodore O, Hua, Ye, Luu, Hiep T, Sakata, Sylvie K, Brown, Edward L, Maldonado, Fausto C, Tuntland, Tove, Lee, Caroline A, Fuhrman, Shella A, Zalman, Leora S, Patick, Amy K, Matthews, David A, Wu, Ellen Y, Guo, Ming, Borer, Bennett C, Nayyar, Naresh K, Moran, Terence, Chen, Lijian, Rejto, Paul A, Rose, Peter W, Guzman, Mark C, Dovalsantos, Elena Z, Lee, Steven, McGee, Kevin, Mohajeri, Michael, Liese, Andreas, Tao, Junhua, Kosa, Maha B, Liu, Bo, Batugo, Minerva R, Gleeson, Jean-Paul R, Wu, Zhen Ping, Liu, Jia, Meador, James W, Ferre, Rose Ann

“…The optimization of the pharmacokinetic performance of various 2-pyridone-containing human rhinovirus (HRV) 3C protease (3CP) inhibitors following oral…”
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Synthesis of azolylalkylquinolines with cytotoxic activity by Abel, Mark D., Luu, Hiep T., Micetich, Ronald G., Nguyen, Dai Q., Oreski, A. Bernadette, Tempest, Mark L., Daneshtalab, Mohsen

“…The syntheses of various azolylalkylquinoline derivatives in which the nature of the linkage between the quinoline and azolylalkyl moieties of the molecule…”
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Cytotoxic quinolines (part 2). Azolylalkylamino and-thio quinolines by Abel, M D, Ha, C M, Luu, H T, Micetich, R G, Nguyen, D Q, Nukatsuka, M, Oreski, A B, Tempest, M L, Daneshtalab, M

“…A series of azolylalkylaminoquinolines and azolylalkylthioquinolines was synthesized and evaluated for cytotoxicity against various cancer cell lines…”
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Cytotoxic quinolines (part 1). Azolylalkyloxy quinolines and 1-azolylalkyl-4(1H)-quinolones by Abel, M D, Ha, C M, Luu, H T, Micetich, R G, Nguyen, D Q, Nukatsuka, M, Oreski, A B, Tempest, M L, Daneshtalab, M

“…A series of 4-azolylalkyloxyquinolines and 1-azolylalkyl-4(1H)-quinolones has been synthesized and evaluated for cytotoxicity against various cancer cell…”
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