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Discovery of 3-(3-(4-(1-Aminocyclobutyl)phenyl)-5-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amine (ARQ 092): An Orally Bioavailable, Selective, and Potent Allosteric AKT Inhibitor.
J Med Chem. 2016 Jul 14;59(13):6455-69. doi: 10.1021/acs.jmedchem.6b00619. Epub 2016 Jun 29.
J Med Chem. 2016.
PMID: 27305487
Discovery and optimization of a series of 3-(3-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amines: orally bioavailable, selective, and potent ATP-independent Akt inhibitors.
Ashwell MA, Lapierre JM, Brassard C, Bresciano K, Bull C, Cornell-Kennon S, Eathiraj S, France DS, Hall T, Hill J, Kelleher E, Khanapurkar S, Kizer D, Koerner S, Link J, Liu Y, Makhija S, Moussa M, Namdev N, Nguyen K, Nicewonger R, Palma R, Szwaya J, Tandon M, Uppalapati U, Vensel D, Volak LP, Volckova E, Westlund N, Wu H, Yang RY, Chan TC.
Ashwell MA, et al. Among authors: vensel d.
J Med Chem. 2012 Jun 14;55(11):5291-310. doi: 10.1021/jm300276x. Epub 2012 May 31.
J Med Chem. 2012.
PMID: 22533986
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The design and preparation of metabolically protected new arylpiperazine 5-HT1A ligands.
Tandon M, O'Donnell MM, Porte A, Vensel D, Yang D, Palma R, Beresford A, Ashwell MA.
Tandon M, et al. Among authors: vensel d.
Bioorg Med Chem Lett. 2004 Apr 5;14(7):1709-12. doi: 10.1016/j.bmcl.2004.01.045.
Bioorg Med Chem Lett. 2004.
PMID: 15026055
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Calix[4]arene, calix[4]resorcarene, and cyclodextrin derivatives and their lanthanide complexes as chiral NMR shift reagents.
Smith KJ, Wilcox JD, Mirick GE, Wacker LS, Ryan NS, Vensel DA, Readling R, Domush HL, Amonoo EP, Shariff SS, Wenzel TJ.
Smith KJ, et al. Among authors: vensel da.
Chirality. 2003;15 Suppl:S150-8. doi: 10.1002/chir.10254.
Chirality. 2003.
PMID: 12884386
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