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Ashar, HR
James, L
Gray, K
Carr, D
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Maxwell, E
Black, S
Armstrong, L
Doll, RJ
Taveras, AG
Bishop, WR
Kirschmeier, P
Citation: Hr. Ashar et al., The farnesyl transferase inhibitor SCH 66336 induces a G(2) -> M or G(1) pause in sensitive human tumor cell lines, EXP CELL RE, 262(1), 2001, pp. 17-27
Authors:
Taveras, AG
Deskus, J
Chao, JP
Vaccaro, CJ
Njoroge, FG
Vibulbhan, B
Pinto, P
Remiszewski, S
del Rosario, J
Doll, RJ
Alvarez, C
Lalwani, T
Mallams, AK
Rossman, RR
Afonso, A
Girijavallabhan, VM
Ganguly, AK
Pramanik, B
Heimark, L
Bishop, WR
Wang, L
Kirschmeier, P
James, L
Carr, D
Patton, R
Bryant, MS
Nomeir, AA
Liu, M
Citation: Ag. Taveras et al., Identification of pharmacokinetically stable 3,10-dibromo-8-chlorobenzocycloheptapyridine farnesyl protein transferase inhibitors with potent enzyme and cellular activities, J MED CHEM, 42(14), 1999, pp. 2651-2661
Authors:
Strickland, CL
Weber, PC
Windsor, WT
Wu, Z
Le, HV
Albanese, MM
Alvarez, CS
Cesarz, D
del Rosario, J
Deskus, J
Mallams, AK
Njoroge, FG
Piwinski, JJ
Remiszewski, S
Rossman, RR
Taveras, AG
Vibulbhan, B
Doll, RJ
Girijavallabhan, VM
Ganguly, AK
Citation: Cl. Strickland et al., Tricyclic farnesyl protein transferase inhibitors: Crystallographic and calorimetric studies of structure-activity relationships, J MED CHEM, 42(12), 1999, pp. 2125-2135