Search Results - "DOOSEOP KIM"

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    Potent, orally absorbed glucagon receptor antagonists by de Laszlo, Stephen E., Hacker, Candice, Li, Bing, Kim, Dooseop, MacCoss, Malcolm, Mantlo, Nathan, Pivnichny, James V., Colwell, Larry, Koch, Gregory E., Cascieri, Margaret A., Hagmann, William K.

    Published in Bioorganic & medicinal chemistry letters (08-03-1999)
    “…The SAR of 2-pyridyl-3,5-diaryl pyrroles, ligands of the human glucagon receptor and inhibitors of p38 kinase, were investigated. This effort resulted in the…”
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    Journal Article
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    Characterization of Two Cyclic Metabolites of Sitagliptin by LIU, David Q, ARISON, Byron H, STEARNS, Ralph A, KIM, Dooseop, VINCENT, Stella H

    Published in Drug metabolism and disposition (01-04-2007)
    “…Two novel metabolites of the dipeptidyl peptidase inhibitor sitagliptin (MK-0431, (2 R )-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3- a…”
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    Journal Article
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    NMR uncovers direct interaction between human NEDD4-1 and p34SEI−1 by Shrestha, Pravesh, Yun, Ji-Hye, Ko, Yoon-Joo, Yeon, Kyu Jeong, Kim, Dooseop, Lee, Heejong, Jin, Dong-Hoon, Nam, Ki-Yup, Yoo, Hye Dong, Lee, Weontae

    “…PTEN, an important tumor suppressor and a key regulator of the PI3K/AKT signaling pathway, is often deleted/mutated in different types of cancer. The E3…”
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    Journal Article
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    NMR uncovers direct interaction between human NEDD4-1 and p34 SEI-1 by Shrestha, Pravesh, Yun, Ji-Hye, Ko, Yoon-Joo, Yeon, Kyu Jeong, Kim, Dooseop, Lee, Heejong, Jin, Dong-Hoon, Nam, Ki-Yup, Yoo, Hye Dong, Lee, Weontae

    “…PTEN, an important tumor suppressor and a key regulator of the PI3K/AKT signaling pathway, is often deleted/mutated in different types of cancer. The E3…”
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    Journal Article
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    AT1/AT2-BALANCED ANGIOTENSIN II ANTAGONISTS by Ashton, Wallace T., Chang, Linda L., Flanagan, Kelly L., Mantlo, Nathan B., Ondeyka, Debra L., Kim, Dooseop, de Laszlo, Stephen E., Glinka, Tomasz W., Rivero, Ralph A., Kevin, Nancy J., Chang, Raymond S.L., Siegl, Peter K.S., Kivlighn, Salah D., Greenlee, William J.

    “…Three heterocyclic series of nonpeptide angiotensin II receptor antagonists (quinazolinones, imidazo[4,5-b]pyridines, and triazolinones) have been transformed…”
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    Journal Article Conference Proceeding