Matches in DBpedia 2016-04 for { ?s ?p "JNJ-7925476 is a TRI antidepressant currently under development by Johnson & Johnson.These molecules were first prepared by Bruce E. Maryanoff, et al. during the late 1970s – 1980's. and is known as a pyrroloisoquinoline, that is benzhydryl-containing. Incorporating the pyrrolidino ring onto the THIQ scaffolding markedly improves potency, although this only works for one of the available diastereo/enantiomers. JNJ-7925476 is a racemic preparation of the more potent diastereomer. The eutomer, JNJ-39836966 has (6R,10bS)-stereochemistry whereas the distomer JNJ-39836732 will have (6S,10bR)-stereochemistry. The compounds depicted appear to be cis but Maryanoff and coworkers are of the opinion that it is trans. (see abstract)The reason for this is not known because it was referred to as \"cis\" to begin with, only reassigning it later.Cyclohexane conformation"@en }
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- JNJ-7925476 abstract "JNJ-7925476 is a TRI antidepressant currently under development by Johnson & Johnson.These molecules were first prepared by Bruce E. Maryanoff, et al. during the late 1970s – 1980's. and is known as a pyrroloisoquinoline, that is benzhydryl-containing. Incorporating the pyrrolidino ring onto the THIQ scaffolding markedly improves potency, although this only works for one of the available diastereo/enantiomers. JNJ-7925476 is a racemic preparation of the more potent diastereomer. The eutomer, JNJ-39836966 has (6R,10bS)-stereochemistry whereas the distomer JNJ-39836732 will have (6S,10bR)-stereochemistry. The compounds depicted appear to be cis but Maryanoff and coworkers are of the opinion that it is trans. (see abstract)The reason for this is not known because it was referred to as \"cis\" to begin with, only reassigning it later.Cyclohexane conformation".