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Discovery of the 3-Imino-1,2,4-thiadiazinane 1,1-Dioxide Derivative Verubecestat (MK-8931)-A β-Site Amyloid Precursor Protein Cleaving Enzyme 1 Inhibitor for the Treatment of Alzheimer's Disease.

Authors :
Scott JD
Li SW
Brunskill AP
Chen X
Cox K
Cumming JN
Forman M
Gilbert EJ
Hodgson RA
Hyde LA
Jiang Q
Iserloh U
Kazakevich I
Kuvelkar R
Mei H
Meredith J
Misiaszek J
Orth P
Rossiter LM
Slater M
Stone J
Strickland CO
Voigt JH
Wang G
Wang H
Wu Y
Greenlee WJ
Parker EM
Kennedy ME
Stamford AW
Source :
Journal of medicinal chemistry [J Med Chem] 2016 Dec 08; Vol. 59 (23), pp. 10435-10450. Date of Electronic Publication: 2016 Nov 18.
Publication Year :
2016

Abstract

Verubecestat 3 (MK-8931), a diaryl amide-substituted 3-imino-1,2,4-thiadiazinane 1,1-dioxide derivative, is a high-affinity β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor currently undergoing Phase 3 clinical evaluation for the treatment of mild to moderate and prodromal Alzheimer's disease. Although not selective over the closely related aspartyl protease BACE2, verubecestat has high selectivity for BACE1 over other key aspartyl proteases, notably cathepsin D, and profoundly lowers CSF and brain Aβ levels in rats and nonhuman primates and CSF Aβ levels in humans. In this annotation, we describe the discovery of 3, including design, validation, and selected SAR around the novel iminothiadiazinane dioxide core as well as aspects of its preclinical and Phase 1 clinical characterization.

Details

Language :
English
ISSN :
1520-4804
Volume :
59
Issue :
23
Database :
MEDLINE
Journal :
Journal of medicinal chemistry
Publication Type :
Academic Journal
Accession number :
27933948
Full Text :
https://doi.org/10.1021/acs.jmedchem.6b00307