Structure–activity relationships of non-opioid [des-Arg7]-dynorphin A analogues for bradykinin receptors
[Display omitted] In our earlier studies, bradykinin receptors (BRs) were identified as a potential target for the neuroexcitatory effects of dynorphin A (Dyn A) in the central nervous system (CNS), and [des-Arg7]-Dyn A-(4–11) (6) was discovered as a lead ligand to modulate Dyn A-(2–13) induced neur...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2014-11, Vol.24 (21), p.4976-4979 |
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Format: | Artikel |
Sprache: | eng |
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In our earlier studies, bradykinin receptors (BRs) were identified as a potential target for the neuroexcitatory effects of dynorphin A (Dyn A) in the central nervous system (CNS), and [des-Arg7]-Dyn A-(4–11) (6) was discovered as a lead ligand to modulate Dyn A-(2–13) induced neuroexcitatory effects in the CNS as an antagonist. In an effort to gain insights into key structural features of the Dyn A for the BRs, we pursued further structure–activity relationships (SAR) study on the [des-Arg7]-Dyn A analogs and confirmed that all of the [des-Arg7]-Dyn A analogues showed good binding affinities at the BRs. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2014.09.033 |