69159-49-5Relevant academic research and scientific papers
Macrocyclic Spiro Pyrimidine Derivatives
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Page/Page column 78, (2009/09/28)
Macrocyclic spiro pyrimidine compounds, compositions comprising such compounds, methods for making the compounds, and methods of treating and preventing the progression of diseases, conditions, and disorders using such compounds and compositions are described herein.
MACROCYCLIC BENZOFUSED PYRIMIDINE DERIVATIVES
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Page/Page column 122-123, (2008/12/05)
Macrocyclic benzofused pyrimidine compounds, compositions comprising such compounds, methods for making the compounds, and methods of treating and preventing the progression of diseases, conditions and disorders using such compounds and compositions are described herein.
AMINO PYRIMIDINE COMPOUNDS FOR THE TREATMENT OF INFLAMMATORY DISORDERS
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Page/Page column 31, (2010/11/28)
The present invention relates to novel amino pyrimidine compounds of formula (I) for the modulation of the histamine H4 receptor and the treatment or prevention of conditions mediated by the histamine H4 receptor. The invention also relates to the preparation of such compounds.
1,8 benzonaphthyridine derivatives and antimicrobial compositions
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, (2008/06/13)
This invention relates to a novel 1,8 benzo[b]naphythyridine derivative of general formula (I), STR1 wherein R is H or a hydroxy, amino or alkylamino radical optionally substituted by amino or hydroxy, or R is dialkylamino of which the alkyl portions may
7-Azetidinylquinolones as antibacterial agents. Synthesis and structure- activity relationships
Frigola,Pares,Corbera,Vano,Merce,Torrens,Mas,Valenti
, p. 801 - 810 (2007/10/02)
A series of novel antibacterial quinolones and naphthyridones has been prepared which contain 7-azetidinyl substituents in place of the usual piperazine or aminopyrrolidine groups. These azetidinyl derivatives were evaluated for in vitro activity by deter
Quantitative structure-activity relationships of antibacterial agents, 7-heterocyclic amine substituted 1-cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic acids
Okada,Ezumi,Yamakawa,Sato,Tsuji,Tsushima,Motokawa,Komatsu
, p. 126 - 131 (2007/10/02)
Quantitative structure-activity relationships (QSAR) of various 7-(3-substituted-azetidin-1-yl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro -4-oxoquinoline-3-carboxylic acids, 14-25, were studied to clarify the structural requirements for 3-substituted azetidi
