Probe Reports from the NIH Molecular Libraries Program, 2011 Dec 16 (Updated 2013 Mar 7) (2013-06-14)
Allosteric modulators for G-protein-coupled receptors (GPCRs) provide numerous advantages over orthosteric ligands, including greater sub-type selectivity, reduced receptor desensitization, saturability of effect, and potential for enhanced therapeutic index. Positive allosteric modulators (PAMs) of the group I metabotropic glutamate receptor mGlu
(NHC) Copper (I)-Catalyzed [3+ 2] Cycloaddition of Azides and Mono-or Disubstituted Alkynes.
Diez-Gonzalez S, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 12(29), 7558-7564 (2006)
Ya Zhou et al.
Probe Reports from the NIH Molecular Libraries Program, 2011 Oct 31 (Updated 2013 Mar 7) (2013-06-14)
A series of acetylenic biaryl mGlu5 positive allosteric modulators (PAMs) have been optimized as pure potentiators in low receptor expressing mGlu5 cell lines. ML254 was identified and shown to competitively interact with the MPEP allosteric binding site. Preliminary data from
Beilstein journal of organic chemistry, 5, 35-35 (2009-09-25)
Methodology has been developed for laying down a thin gold-on-silver film on the inner surface of glass capillaries for the purpose of catalysing benzannulation reactions. The cycloaddition precursors are flowed through these capillaries while the metal film is being heated
Chemistry (Weinheim an der Bergstrasse, Germany), 15(43), 11668-11674 (2009-09-25)
A simple and efficient method for the synthesis of gamma,delta-alkynyl-beta-amino acid derivatives by a copper-catalyzed three-component amine-alkyne-alkyne addition reaction was developed. Various gamma,delta-alkynyl-beta-amino acid derivatives were synthesized in moderate to good yields in one step. With chiral prolinol derivatives employed
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