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Frederic Cumin

Researcher at Novartis

Publications -  58
Citations -  3309

Frederic Cumin is an academic researcher from Novartis. The author has contributed to research in topics: Renin–angiotensin system & Angiotensin II. The author has an hindex of 26, co-authored 58 publications receiving 3115 citations.

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Structure-based design of aliskiren, a novel orally effective renin inhibitor.

TL;DR: Aliskiren is the first in a novel class of renin inhibitors with the potential for treatment of hypertension and related cardiovascular diseases and employs a combination of molecular modelling and crystallographic structure analysis to design renin inhibitor lacking the extended peptide-like backbone of earlier inhibitors.
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Structure-Based Drug Design: The Discovery of Novel Nonpeptide Orally Active Inhibitors of Human Renin

TL;DR: The design approach led to compounds with high in vitro affinity and specificity for renin, favourable bioavailability and excellent oral efficacy in lowering blood pressure in primates, which are potential therapeutic agents for the treatment of hypertension and related cardiovascular diseases.
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Analysis by immunocytochemistry and in situ hybridization of renin and its mRNA in kidney, testis, adrenal, and pituitary of the rat.

TL;DR: The finding of renin mRNA and renin-like immunoreactivity in these tissues supports the notion that these tissues are sites for production of renIn, and suggests that posttranslational proteolysis or glycosylation of preprorenin varies in different tissues with consequent variations in immunore activity.
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Inhibition of Food Intake by Neuropeptide Y Y5 Receptor Antisense Oligodeoxynucleotides

TL;DR: Analysis of the structure of feeding behavior revealed that prepro NPY and Y5 receptor antisense ODNs reduced food intake by inducing decreases in meal size and meal duration analogous to the orexigenic effects of NPY that are mediated by increases in these parameters.
Journal Article

Leptin is cleared from the circulation primarily by the kidney

TL;DR: The findings demonstrate that the short half life of leptin in the circulation is mainly determined by efficient renal clearance which is mediated in part by glomerular filtration.