32741-05-2Relevant articles and documents
Selective angiotensin II AT2 receptor agonists: Arylbenzylimidazole structure-activity relationships
Wu, Xiongyu,Wan, Yiqian,Mahalingam,Murugaiah,Plouffe, Bianca,Botros, Milad,Karlén, Anders,Hallberg, Mathias,Gallo-Payet, Nicole,Alterman, Mathias
, p. 7160 - 7168 (2006)
Structural alterations in the 2- and 5-positions of the first drug-like selective angiotensin II AT2 receptor agonist (1) have been performed. The imidazole ring system was proven to be a strong determinant for the AT2 selectivity, and with few exceptions all variations gave good AT2 receptor affinities and with retained high AT 2/AT1 selectivities. On the contrary to the findings with AT1 receptor agonists, the impact of structural modifications in the 5-position of the AT2 selective compounds were less pronounced regarding activation of the AT2 receptor. The butyloxyphenyl (56) and the propylthienyl (50) derivatives were found to exert a high agonistic effect as deduced from their capacity to induce neurite elongation in neuronal cells, as does angiotensin II.
N-acyl sulfamide FBPase inhibitor, preparation method thereof, drug composition and application
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Paragraph 2380; 2384; 2385, (2017/09/08)
The invention discloses an N-acryl sulfamide FBPase inhibitor of a novel structure, and a preparation method thereof, a drug composition and an application, and particularly relates to an N-acryl sulfamide FBPase inhibitor shown in the formula I, a salt thereof for medicine, a preparation method, a composition comprising one or more compounds, an application of the compound in preparing the FBPase inhibitor or a drug for treating FBPase-related diseases, and an application in preparing a drug for preventing and/or treating diabetes. The formula is shown in the description.
New FBPase inhibitors for diabetes
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Page/Page column 15, (2008/06/13)
Compounds of formula as well as pharmaceutically acceptable salts and esters thereof, wherein R1 to R3 have the significance given in the application and which can be used in the form of pharmaceutical compositions.