16728-69-1Relevant academic research and scientific papers
Design, synthesis, and: In vitro and in vivo characterization of 1-{4-[4-(substituted)piperazin-1-yl]butyl}guanidines and their piperidine analogues as histamine H3 receptor antagonists
Staszewski, Marek,Stasiak, Anna,Karcz, Tadeusz,McNaught Flores, Daniel,Fogel, Wies?awa Agnieszka,Kie?-Kononowicz, Katarzyna,Leurs, Rob,Walczyński, Krzysztof
, p. 234 - 251 (2019)
Previously, we have shown that 1-substituted-[4-(7-phenoxyheptylpiperazin-1-yl)butyl]guanidine with electron withdrawing substituents at position 4 in the benzyl moiety exhibits high in vitro affinities toward the guinea pig jejunal histamine H3/sub
Derivatives of squaric acid with anti-proliferative activity
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Page/Page column 26, (2008/12/08)
The present invention provides derivatives of squaric acid, in particular derivatives of 3,4-diamino-cyclobut-3-ene-1,2-dione and tautomers and isomers thereof, as a single stereoisomer or a mixture of stereoisomers, or as a pharmaceutically acceptable sa
Derivatives of squaric acid with anti-proliferative activity
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Page/Page column 36-37, (2008/06/13)
The present invention provides derivatives of squaric acid, in particular derivatives of 3,4-diamino-cyclobut-3-ene-1,2-dione and tautomers thereof, as a single stereoisomer or a mixture of stereoisomers, or as a pharmaceutically acceptable salt thereof.
