699-49-0Relevant articles and documents
Cyclopropane-1,2-dicarboxylic acids as new tools for the biophysical investigation of O-acetylserine sulfhydrylases by fluorimetric methods and saturation transfer difference (STD) NMR
Annunziato, Giannamaria,Pieroni, Marco,Benoni, Roberto,Campanini, Barbara,Pertinhez, Thelma A.,Pecchini, Chiara,Bruno, Agostino,Magalh?es, Joana,Bettati, Stefano,Franko, Nina,Mozzarelli, Andrea,Costantino, Gabriele
, p. 78 - 87 (2016/12/23)
Cysteine is a building block for many biomolecules that are crucial for living organisms. O-Acetylserine sulfhydrylase (OASS), present in bacteria and plants but absent in mammals, catalyzes the last step of cysteine biosynthesis. This enzyme has been dee
Design, synthesis and activity of novel derivatives of Oxybutynin and Tolterodine
Kaur, Kirandeep,Aeron, Shelly,Bruhaspathy, Miriyala,Shetty, Shankar J.,Gupta, Suman,Hegde, Laxminarayan H.,Silamkoti, Arun D. V.,Mehta, Anita,Chugh, Anita,Gupta, Jang B.,Sarma,Kumar, Naresh
, p. 2093 - 2096 (2007/10/03)
Novel derivatives of Tolterodine (1) and Oxybutynin (2) have been designed using conformationally restricted azabicyclics as replacement for open-chain amines. The synthesis and structure-activity relationships are presented.
Alkylation, Acylation, and Cyclopropanation Reactions of α-Halo Carboxylic Acid Dianions
Johnson, Carl R.,Bade, Thomas R.
, p. 284 - 286 (2007/10/02)
-