104768-34-5Relevant academic research and scientific papers
Tailoring small molecules for an allosteric site on procaspase-6
Murray, Jeremy,Giannetti, Anthony M.,Steffek, Micah,Gibbons, Paul,Hearn, Brian R.,Cohen, Frederick,Tam, Christine,Pozniak, Christine,Bravo, Brandon,Lewcock, Joe,Jaishankar, Priyadarshini,Ly, Cuong Q.,Zhao, Xianrui,Tang, Yinyan,Chugha, Preeti,Arkin, Michelle R.,Flygare, John,Renslo, Adam R.
, p. 73 - 77 (2014)
Although they represent attractive therapeutic targets, caspases have so far proven recalcitrant to the development of drugs targeting the active site. Allosteric modulation of caspase activity is an alternate strategy that potentially avoids the need for anionic and electrophilic functionality present in most active-site inhibitors. Caspase-6 has been implicated in neurodegenerative disease, including Huntington's and Alzheimer's diseases. Herein we describe a fragment-based lead discovery effort focused on caspase-6 in its active and zymogen forms. Fragments were identified for procaspase-6 using surface plasmon resonance methods and subsequently shown by X-ray crystallography to bind a putative allosteric site at the dimer interface. A fragment-merging strategy was employed to produce nanomolar-affinity ligands that contact residues in the L2 loop at the dimer interface, significantly stabilizing procaspase-6. Because rearrangement of the L2 loop is required for caspase-6 activation, our results suggest a strategy for the allosteric control of caspase activation with drug-like small molecules. Merge ahead: A fragment-based lead discovery effort revealed the presence of a putative allosteric binding site at the dimer interface of procaspase-6. A fragment merging strategy produced nanomolar-affinity lead compounds that contact residues of the L2 loop at the dimer interface, significantly stabilizing the protein. These results suggest new avenues for controlling caspase activity and/or activation for therapeutic benefit. Copyright
Phosphorus-nitrogen compounds: New spiro-cyclic phosphazene derivatives. Structure of 4′,4′,6′,6′-tetrachloro-3,4-dihydro-3-(3- methylpyridin-2-yl)spiro-[1,3,2-benzoxazaphosphinine-2,2′- (2λ5,4λ5,6λ5- cyclotriphosphazene)]
Dal, Hakan,Safran, Serap,Süzen, Yasemin,H?kelek, Tuncer,Kili?, Zeynel
, p. 84 - 91 (2007/10/03)
The condensation reactions of {N-[(2-hydroxyphenylmethyl)amino]- methylpyridines (5-8) with trimer, N3P3Cl6, have been afforded partially substituted novel spiro-cyclic phosphazene derivatives (9-12) (Scheme 1). Compounds
