Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Brian A. Chauder"'
Publikováno v:
Journal of Medicinal Chemistry
Cellular and genetic evidence suggest that inhibition of ATAD2 could be a useful strategy to treat several types of cancer. To discover small-molecule inhibitors of the bromodomain of ATAD2, we used a fragment-based approach. Fragment hits were ident
Autor:
Taekyu Lee, Stephen W. Fesik, Pedro M. Garcia-Barrantes, Edward T. Olejniczak, Jason P. Burke, Bin Zhao, Brian A. Chauder, Anders Friberg, R. Nathan Daniels, Dominico Vigil, DeMarco V. Camper
Publikováno v:
Journal of Medicinal Chemistry. 56:15-30
Myeloid cell leukemia 1 (Mcl-1), a member of the Bcl-2 family of proteins, is overexpressed and amplified in various cancers and promotes the aberrant survival of tumor cells that otherwise would undergo apoptosis. Here we describe the discovery of p
Autor:
Colleen M. Niswender, Kyle A. Emmitte, Karen J. Gregory, Andrew S. Felts, Danny G. Winder, Jens Meiler, Christopher M. Olsen, Alice L. Rodriguez, Jeffrey P. Lamb, Craig W. Lindsley, Usha N. Menon, Ralf Mueller, Brittney S. Bates, Eric S. Dawson, Carrie K. Jones, P. Jeffrey Conn, Alexander S. Kane, Brian A. Chauder, Sataywan B. Jadhav
Publikováno v:
ChemMedChem. 7:406-414
Glutamate, the major excitatory neurotransmitter, functions in the brain via activation of ligand gated cation channels and also the eight subtypes of Class C G protein-coupled metabotropic glutamate receptors (mGlus).[1] Selective allosteric modulat
Publikováno v:
Future Medicinal Chemistry. 2:757-774
Inward rectifier potassium (Kir) channels have been postulated as therapeutic targets for several common disorders including hypertension, cardiac arrhythmias and pain. With few exceptions, however, the small-molecule pharmacology of this family is l
Autor:
Pat Wheelan, Brian A. Chauder, Christian Watson, Terrence Peter Kenakin, Robert M. Ferris, Cecilia S. Koble, Deborah K. Jones-Hertzog, Michael Youngman, Hanbiao Yang, Christopher J Aquino, Felix Deanda, Wieslaw M. Kazmierski
Publikováno v:
Journal of Medicinal Chemistry. 51:6538-6546
We describe robust chemical approaches toward putative CCR5 scaffolds designed in our laboratories. Evaluation of analogues in the (125)I-[MIP-1beta] binding and Ba-L-HOS antiviral assays resulted in the discovery of 64 and 68 in the 4,4-disubstitite
Autor:
James B. Thompson, Brian Andrew Chauder, Elie A. Tabet, Wieslaw M. Kazmierski, Eric E. Boros, Cecilia S. Koble, Du Kien S
Publikováno v:
Synthetic Communications. 36:279-284
A four‐step, high‐yielding, kilogram‐scale protocol to prepare aldehyde 5 is reported. The key reaction is a mild, two‐step Cu2O‐mediated decarboxylation of cyanoester 3 that proceeds in excellent yield. The general applicability of this me
Publikováno v:
Synthesis. 2001:0140-0144
Publikováno v:
Pure and Applied Chemistry. 71:1521-1529
New developments from our laboratories in Directed ortho (DoM) and remote (DreM) metalation reactions are presented and connections to transition metal catalyzed cross coupling and olefin metathesis processes are described.
Publikováno v:
Angewandte Chemie International Edition. 38:1435-1438
The oxygen-rich heterocyclic compound 1-which was proposed to be the structure of plicadin, the alleged naturally occurring coumestan from the herb Psoralea plicata-was synthesized by the rational combinations of directed ortho and remote metalation
Autor:
Rosangela S. C. Lopes, Victor Snieckus, Claudio C. Lopes, Alcides J. M. da Silva, Brian A. Chauder
Publikováno v:
Synthesis. 1998:279-282