184969-61-7Relevant academic research and scientific papers
SUBSTITUTED OXIMES AS NEUROKININ ANTAGONISTS
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Page 25, (2010/02/05)
Compounds within the genus represented by structural formula (I) or a pharmaceutically acceptable salt thereof, wherein: T is substituted phenyl or substituted pyridyl; R is H, methyl, ethyl, -CH2CN, -CH2C(O)NH2, -(CH2)3SO3H, -CH2C(O)NHCH3, -CH2C(O)NHOH, -CH2C(O)NHOCH3, -CH2C(O)NHCH2CN, -CH2F, -CH2C(O)NHCH2SO3H, (a), (b), (c), (d) or (e); R is methyl or ethyl; and Z is substituted piperidinyl.
Synthesis and structure-activity relationships of oxime neurokinin antagonists: Discovery of potent arylamides
Shih, Neng-Yang,Albanese, Margaret,Anthes, John C.,Carruthers, Nicholas I.,Grice, Cheryl A.,Lin, Ling,Mangiaracina, Pietro,Reichard, Gregory A.,Schwerdt, John,Seidl, Vera,Wong, Shing-Chung,Piwinski, John J.
, p. 141 - 145 (2007/10/03)
The structural modification of the benzylic ether region of oxime 1 has resulted in the identification of several novel aryl amides as selective or dual NK1/NK2 antagonists.
Substituted oximes as neurokinin antagonists
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, (2008/06/13)
Compounds within the genus represented by the structural formula I or a pharmaceutically acceptable salt thereof, wherein: T is substituted phenyl or substituted pyridyl; R4 is methyl or ethyl; and Z is substituted piperidinyl.
SUBSTITUTED OXIMES, HYDRAZONES AND OLEFINS AS NEUROKININ ANTAGONISTS
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, (2008/06/13)
Compound represented by the structural formula STR1 or a pharmaceutically acceptable salt thereof, wherein: a is 0, 1, 2 or 3;b, d and e are independently 0, 1 or 2;R is H, C 1-6 alkyl,--OH or C 2-C 6 hydroxyalkyl; A is an optionally s
