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Drug Development and Industrial Pharmacy|December 1, 2005
Reversible Z-E isomerism and pharmaceutical implications for SU5416Anand Sistla, Narmada ShenoyPDA Journal of Pharmaceutical Science and Technology|July 30, 2008
Development of an intravenous formulation of SU010382 (prodrug of SU5416, an anti-angiogenesis agent)Anand Sistla, Adriana Kertelj, Narmada ShenoyJournal of Chromatography. A|February 14, 2006
High-performance liquid chromatographic method for determination of reversible isomers of SU5416Anand Sistla, Wei-Lien Yang, Narmada ShenoyPharmaceutical Development and Technology|January 22, 2010
Medium-throughput hydrate screening using the Crystal 16™Anand Sistla, Yi Wu, Penney Khamphavong, et al.Drug Delivery|October 21, 2009
Pharmacokinetics and tissue distribution of liposomal etoposide in ratsAnand Sistla, David J Smith, Nathan L Kobrinsky, et al.Drug Development and Industrial Pharmacy|March 6, 2004
Powder-in-bottle formulation of SU011248. Enabling rapid progression into human clinical trialsAnand Sistla, Alan Sunga, Kenneth Phung, et al.Journal of Medicinal Chemistry|March 21, 2003
Discovery of 5-[5-fluoro-2-oxo-1,2- dihydroindol-(3Z)-ylidenemethyl]-2,4- dimethyl-1H-pyrrole-3-carboxylic acid (2-diethylaminoethyl)amide, a novel tyrosine kinase inhibitor targeting vascular endothelial and platelet-derived growth factor receptor tyrosine kinaseLi Sun, Chris Liang, Sheri Shirazian, et al.Molecular Cancer Therapeutics|June 15, 2014
Chemogenetic evaluation of the mitotic kinesin CENP-E reveals a critical role in triple-negative breast cancerPei-Pei Kung, Ricardo Martinez, Zhou Zhu, et al.Journal of Medicinal Chemistry|March 29, 2011
Optimization of potent, selective, and orally bioavailable pyrrolodinopyrimidine-containing inhibitors of heat shock protein 90. Identification of development candidate 2-amino-4-{4-chloro-2-[2-(4-fluoro-1H-pyrazol-1-yl)ethoxy]-6-methylphenyl}-N-(2,2-difluoropropyl)-5,7-dihydro-6H-pyrrolo[3,4-d]pyrimidine-6-carboxamideLuke Zehnder, Michael Bennett, Jerry Meng, et al.Pageof 1