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  • Title: Small-molecule negative modulators of adrenomedullin: design, synthesis, and 3D-QSAR study.
    Author: Roldós V, Martín-Santamaría S, Julián M, Martínez A, Choulier L, Altschuh D, de Pascual-Teresa B, Ramos A.
    Journal: ChemMedChem; 2008 Sep; 3(9):1345-55. PubMed ID: 18759242.
    Abstract:
    Adrenomedullin (AM) is a peptidic hormone that was isolated in 1993, the function of which is related to several diseases such as diabetes, hypertension, and cancer. Compound 1 is one of the first nonpeptidic small-molecule negative modulators of AM, identified in a high-throughput screen carried out at the National Cancer Institute. Herein we report the synthesis of a series of analogues of 1. The ability of the synthesized compounds to disrupt the binding between AM and its monoclonal antibody has been measured, together with surface plasmon resonance (SPR)-based binding assays as implemented with Biacore technology. These data were used to derive a three-dimensional quantitative structure-activity relationship (3D-QSAR) model, with a q(2) (LOO) value of 0.8240. This study has allowed us to identify relevant features for effective binding to AM: the presence of a hydrogen-bond donor group and an aromatic ring. Evaluation of the ability of selected compounds to modify cAMP production in Rat2 cells showed that the presence of a free carboxylic acid is essential for negative AM modulation.
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