906077-49-4Relevant academic research and scientific papers
Integrated Flow Synthesis of α-Amino Acids byIn SituGeneration of Aldimines and Subsequent Electrochemical Carboxylation
Naito, Yuki,Nakamura, Yuto,Shida, Naoki,Senboku, Hisanori,Tanaka, Kenta,Atobe, Mahito
, p. 15953 - 15960 (2021)
The synthesis of α-amino acids was carried out in a continuous flow system. In this system, aldimines were efficiently generatedin situvia the dehydration-condensation of aldehydes with anilines in a desiccant bed column filled with 4 ? molecular sieves d
Arylglycine derivatives as potent transient receptor potential melastatin 8 (TRPM8) antagonists
Zhu, Bin,Xia, Mingde,Xu, Xiaoqing,Ludovici, Donald W.,Tennakoon, Manomi,Youngman, Mark A.,Matthews, Jay M.,Dax, Scott L.,Colburn, Raymond W.,Qin, Ning,Hutchinson, Tasha L.,Lubin, Mary Lou,Brandt, Michael R.,Stone, Dennis J.,Flores, Christopher M.,MacIelag, Mark J.
, p. 2234 - 2237 (2013/04/23)
A series of arylglycine-based analogs was synthesized and tested for TRPM8 antagonism in a cell-based functional assay. Following structure-activity relationship studies in vitro, a number of compounds were identified as potent TRPM8 antagonists and were subsequently evaluated in an in vivo pharmacodynamic assay of icilin-induced 'wet-dog' shaking in which compound 12 was fully effective. TRPM8 antagonists of the type described here may be useful in treating pain conditions wherein cold hypersensitivity is a dominant feature.
Cold Menthol Receptor Antagonists
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Page/Page column 71, (2010/03/31)
Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula I as follows: wherein A, B, L, Q, R1, R2, and R3 /s
