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European Journal of Medicinal Chemistry|July 16, 2014
Inhibition of the HIF1α-p300 interaction by quinone- and indandione-mediated ejection of structural Zn(II)Madura K P Jayatunga, Sam Thompson, Tawnya C McKee, et al.Journal of Medicinal Chemistry|September 15, 2006
Structurally simple, potent, Plasmodium selective farnesyltransferase inhibitors that arrest the growth of malaria parasitesMatthew P Glenn, Sung-Youn Chang, Carrie Hornéy, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 23, 2019
Dual Farnesyl and Geranylgeranyl Transferase Inhibitor Thwarts Mutant KRAS-Driven Patient-Derived Pancreatic TumorsAslamuzzaman Kazi, Shengyan Xiang, Hua Yang, et al.Nature Communications|June 26, 2021
Protein mimetic amyloid inhibitor potently abrogates cancer-associated mutant p53 aggregation and restores tumor suppressor functionL Palanikumar, Laura Karpauskaite, Mohamed Al-Sayegh, et al.Journal of Medicinal Chemistry|September 9, 2010
Structure-based design and synthesis of potent, ethylenediamine-based, mammalian farnesyltransferase inhibitors as anticancer agentsSteven Fletcher, Erin Pusateri Keaney, Christopher G Cummings, et al.Antimicrobial Agents and Chemotherapy|July 4, 2007
Efficacy, pharmacokinetics, and metabolism of tetrahydroquinoline inhibitors of Plasmodium falciparum protein farnesyltransferaseWesley C Van Voorhis, Kasey L Rivas, Pravin Bendale, et al.Pageof 22