Journal of Medicinal Chemistry · 2011 · 44 citations · 23 references
MedicineOncologyPharmacologyCancer PharmacologyDrug DiscoveryMolecular OncologyCell Division InhibitionEnzyme InhibitionMicrotubule-targeting AgentsMitotic InhibitorsMitotic SpindleStructure-activity Relationship AnalysisCell Division InhibitorsClinical Development StrategyKinesin BiochemistryKinesin InhibitorsKinesin MotorsMitotic Spindle InhibitionMitotic Spindle InhibitorsMotor Protein Inhibitors
Structure-activity relationship analysis identified (+)-N-(3-aminopropyl)-N-[1-(5-benzyl-3-methyl-4-oxo-[1,2]thiazolo[5,4-d]pyrimidin-6-yl)-2-methylpropyl]-4-methylbenzamide (AZD4877), from a series of novel kinesin spindle protein (KSP) inhibitors, as exhibiting both excellent biochemical potency and pharmaceutical properties suitable for clinical development. The selected compound arrested cells in mitosis leading to the formation of the monopolar spindle phenotype characteristic of KSP inhibition and induction of cellular death. A favorable pharmacokinetic profile and notable in vivo efficacy supported the selection of this compound as a clinical candidate for the treatment of cancer.
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Mitotic spindle organization by a plus-end-directed microtubule motor
Kenneth E. Sawin, Katherine LeGuellec, Michel Philippe et al. · Nature · 1992 · 645 citations
Taxol: the first of the taxanes, an important new class of antitumor agents.
Eric K. Rowinsky, Nicole Onetto, Renzo Canetta et al. · PubMed · 1992 · 393 citations
Medicine, Oncology, Pharmacology +13