Design and synthesis of aminopyridine containing biaryls reducing c-MYC protein levels in cells by Di Marco, Christina N., Terrell, Lamont, Sanchez, Robert, Rueda, Lourdes, Shuster, Leanna, Nartey, Eldridge N., McHugh, Charles, Mack, James F., Shu, Arthur, Tian, Xinrong, Medina, Jesus R., Rivero, Ralph, Manetsch, Roman, Heerding, Dirk, Mangatt, Biju

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Cell-Based Drug Discovery: Identification and Optimization of Small Molecules that Reduce c‑MYC Protein Levels in Cells by Medina, Jesús R, Tian, Xinrong, Li, William H, Suarez, Dominic, Mack, James F, LaFrance, Louis, Martyr, Cuthbert, Brackley, James, Di Marco, Christina, Rivero, Ralph, Heerding, Dirk A, McHugh, Charles, Minthorn, Elisabeth, Bhaskar, Aishwarya, Rubin, Jacob, Butticello, Michael, Carpenter, Christopher, Nartey, Eldridge N, Berrodin, Thomas J, Kallal, Lorena A, Mangatt, Biju

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Discovery of a novel and potent series of dianilinopyrimidineurea and urea isostere inhibitors of VEGFR2 tyrosine kinase by Sammond, Douglas M., Nailor, Kristen E., Veal, James M., Nolte, Robert T., Wang, Liping, Knick, Victoria B., Rudolph, Sharon K., Truesdale, Anne T., Nartey, Eldridge N., Stafford, Jeffrey A., Kumar, Rakesh, Cheung, Mui

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Design and effective synthesis of novel templates, 3,7-diphenyl-4-amino-thieno and furo-[3,2- c]pyridines as protein kinase inhibitors and in vitro evaluation targeting angiogeneti... by Miyazaki, Yasushi, Nakano, Masato, Sato, Hideyuki, Truesdale, Anne T., Stuart, J. Darren, Nartey, Eldridge N., Hightower, Kendra E., Kane-Carson, Laurie

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Orally active 4-amino-5-diarylurea-furo[2,3- d]pyrimidine derivatives as anti-angiogenic agent inhibiting VEGFR2 and Tie-2 by Miyazaki, Yasushi, Tang, Jun, Maeda, Yutaka, Nakano, Masato, Wang, Liping, Nolte, Robert T., Sato, Hideyuki, Sugai, Masaki, Okamoto, Yuji, Truesdale, Anne T., Hassler, Daniel F., Nartey, Eldridge N., Patrick, Denis R., Ho, Maureen L., Ozawa, Kazunori

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