| Literature DB >> 26568411 |
Erik L Meredith1, Nello Mainolfi1, Stephen Poor2, Yubin Qiu2, Karl Miranda1, James Powers1, Donglei Liu1, Fupeng Ma1, Catherine Solovay1, Chang Rao1, Leland Johnson1, Nan Ji1, Gerald Artman1, Leo Hardegger1, Shawn Hanks2, Siyuan Shen2, Amber Woolfenden2, Elizabeth Fassbender2, Jeremy M Sivak2, Yiqin Zhang2, Debby Long2, Rosemarie Cepeda2, Fang Liu2, Vinayak P Hosagrahara3, Wendy Lee3, Peter Tarsa4, Karen Anderson2, Jason Elliott1, Bruce Jaffee2.
Abstract
The benefit of intravitreal anti-VEGF therapy in treating wet age-related macular degeneration (AMD) is well established. Identification of VEGFR-2 inhibitors with optimal ADME properties for an ocular indication provides opportunities for dosing routes beyond intravitreal injection. We employed a high-throughput in vivo screening strategy with rodent models of choroidal neovascularization and iterative compound design to identify VEGFR-2 inhibitors with potential to benefit wet AMD patients. These compounds demonstrate preferential ocular tissue distribution and efficacy after oral administration while minimizing systemic exposure.Entities:
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Year: 2015 PMID: 26568411 DOI: 10.1021/acs.jmedchem.5b01227
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446