167255-49-4Relevant articles and documents
Cyclopropane-based conformational restriction of GABA by a stereochemical diversity-oriented strategy: Identification of an efficient lead for potent inhibitors of GABA transports
Nakada, Kazuaki,Yoshikawa, Mamie,Ide, Soichiro,Suemasa, Akihiro,Kawamura, Shuhei,Kobayashi, Takaaki,Masuda, Eiji,Ito, Yoshihiko,Hayakawa, Wataru,Katayama, Takahiro,Yamada, Shizuo,Arisawa, Mitsuhiro,Minami, Masabumi,Shuto, Satoshi
, p. 4938 - 4950 (2013/09/02)
A series of cyclopropane-based conformationally restricted γ-aminobutyric acid (GABA) analogs with stereochemical diversity, that is, the trans- and cis-2,3-methano analogs Ia and Ib and their enantiomers ent-Ia and ent-Ib, and also the trans- and cis-3,4
Ornithine decarboxylase inhibiting cyclic aminooxy compounds
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, (2008/06/13)
Compounds of formula (I): H2 N--(CH2)n --A--(CH2)m --O--NH2 and salts thereof are described in which the radical A is C3 -C6 cycloalkylene; n is 0 or 1 and, independen