Table 2.
Receptor Tyrosine Kinases | ||
Pan-ErbB receptors | ||
CI-1033 | Pfizer | phase II[57,58] |
BIBW-2992 | Boehringer Ingelheim | phase II[57,59] |
Neratinib | Wyeth-Ayerst | phase III[60,61] |
MET | ||
MK-2461 | Merck | phase I/II[62] |
XL184 | Exelixis | phase II/III[62] |
MetMAb | Genentech | phase I[63] |
FGFR | ||
MK-2461 | Merck | phase I/II[62] |
Brivanib | BMS | phase II[64] |
K-RAS-RAF | ||
PLX4032 | Plexxikon Inc/Roche | phase I[65] |
PI3K-AKT Inhibitors-mTOR | ||
Dual PI3K-mTOR | ||
BEZ235 | Novartis | phase I/II[30,66,67] |
XL765 | Exelixis | phase I[68] |
SF1126 | Semafore | phase I/II[68,69] |
BGT226 | Novartis | phase II[68] |
PI3K Inhibitors | ||
XL147 | Exelixis | phase I[68] |
BKM120 | Novartis | phase I[68] |
GDC0941 | Genentech | phase I[70,71] |
AKT inhibitors | ||
Perifosine | Keryx | phsae I/II[72-74] |
GSK690693 | GSK | phase I[75-77] |
MK2206 | Merck | phase I[68] |
mTOR | ||
OSI027 | OSI Pharmaceuticals | phase I[68] |
AZD8055 | AstraZeneca | phase I/II[68] |
MAPK inhibitors | ||
MEK Inhibitors | ||
CI-1040 | Pfizer | phase I/II[78,79] |
AZD6244 | AstraZeneca | phase I/II[80,81] |
XL518 | Genentech | phase I[71] |
Cell Cycle | ||
Flavopiridol | Sanofi-aventis | phase II/III[82] |
SNS-032 | BMS | phase I/II[31] |
R-547 | Roche | Phase I/II[83,84] |
Seleciclib | Cyclacel Pharmaceuticals | Phase I/II[85] |
Histone Deacetylase inhibitors | ||
Vorinostat (SAHA) | Merck | Phase I/II[86] |
Romidepsin | Gloucester Pharmaceuticals | Phase I/II[87,88] |
MGCD0103 | MethylGene, Inc | phase I/II[89] |
LBH589 | Novartis | phase I/II[90,91] |
Demethylating agents | ||
Azacitidine | Celgene | approved[92,93] |
Decitabine | Eisai Pharmaceuticals | approved[94] |
DNA repair | ||
PARP | ||
Olaparib | KuDOS Pharmaceuticals/AstraZeneca | phase II[95] |
AG-014699 | Pfizer | phase II[96] |
ATM | ||
KU-55933 | KuDOS Pharmaceuticals | preclinical[97] |
Matrix Metalloproteinases | ||
Neovastat | Æterna Laboratories | phase III[98,99] |
Prinomastat | Pfizer | phase III[98,100,101] |