Kay Lin Goh

Structure-based design of Aurora A & B inhibitors

Eric Sun, Anders Poulsen, Anthony William, 2008, J. Comput. Aided Mol. Des..

Discovery of (2E)-3-{2-butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl}-N-hydroxyacrylamide (SB939), an orally active histone deacetylase inhibitor with a superior preclinical profile.

Kay Lin Goh, Z. Bonday, J. Wood, 2011, Journal of medicinal chemistry.

2-anilino-4-aryl-8H-purine derivatives as inhibitors of PDK1.

Chang Kai Soh, Kay Lin Goh, Z. Bonday, 2012, Bioorganic & medicinal chemistry letters.

Identification of a Plasmodium berghei antigen sharing common features with P. falciparum and P. chabaudi parasitophorous-vacuole membrane antigens

Kay Lin Goh, U. Kara, T. Tan, 1996, Parasitology Research.

Synthesis and evaluation of alkenyl indazoles as selective Aurora kinase inhibitors.

Kay Lin Goh, Z. Bonday, A. Poulsen, 2010, Bioorganic & medicinal chemistry letters.

Thieno[3,2-d]pyrimidin-4(3H)-one derivatives as PDK1 inhibitors discovered by fragment-based screening.

Kay Lin Goh, Z. Bonday, J. Wood, 2012, Bioorganic & medicinal chemistry letters.