| Literature DB >> 25282551 |
Yeon Sun Lee1, David Rankin2, Sara M Hall3, Cyf Ramos-Colon3, Jose Juan Ortiz3, Robert Kupp3, Frank Porreca2, Josephine Lai2, Victor J Hruby4.
Abstract
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-Arg(7)]-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-Arg(7)]-Dyn A analogs and confirmed that all of the [des-Arg(7)]-Dyn A analogues showed good binding affinities at the BRs.Entities:
Keywords: Bradykinin receptors; Chronic pain; Non-opioid dynorphin A; Structure–activity relationship; pH sensitivity
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Year: 2014 PMID: 25282551 PMCID: PMC4250343 DOI: 10.1016/j.bmcl.2014.09.033
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823