Sorafenib has soluble epoxide hydrolase inhibitory activity, which contributes to its effect profile in vivo.
Ontology highlight
ABSTRACT: The advent of multikinase inhibitors targeting the vascular endothelial growth factor (VEGF) receptor has revolutionized the treatment of highly angiogenic malignancies such as renal cell carcinoma. Interestingly, several such inhibitors are commercially available, and they each possess diverse specific beneficial and adverse effect profiles. In examining the structure of sorafenib, it was hypothesized that this compound would possess inhibitory effects on the soluble epoxide hydrolase, an enzyme with pleiotropic effects on inflammation and vascular disease. We now show that sorafenib but not another VEGF receptor targeted inhibitor sunitinib is a potent inhibitor of the human soluble epoxide hydrolase in vitro (K(I) = 17 +/- 4 nmol/L). Furthermore, sorafenib causes the expected in vivo sh
SUBMITTER: Liu JY
PROVIDER: S-EPMC2728155 | biostudies-literature | 2009 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA