ArticleACS medicinal chemistry letters2025
Development of Highly Selective Aldosterone Synthase Inhibitors.
Article in ACS medicinal chemistry letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Baxdrostat: A First-in-Class Aldosterone Synthase Inhibitor for Resistant Hypertension.ACS pharmacology & translational science · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Recent clinical studies have heralded aldosterone synthase inhibitors (ASIs) as a promising therapeutic option for managing resistant hypertension. The efficacy of these compounds is believed to stem from their ability to mitigate aldosterone production. Consequently, we delved into the potential of aldosterone synthase inhibition as a therapeutic strategy for patients with refractory hypertension. Our focus is on the synthesis and optimization of innovative heterocyclic compounds that exhibit aldosterone synthase inhibitory activity. The CYP11B2 inhibitor we have developed exhibits an encouraging pharmacokinetic (PK) profile, along with a robust pharmacokinetic-pharmacodynamic (PK-PD) relationship. This has enabled us to meticulously evaluate the trends in aldosterone inhibition and assess the compound's efficacy in vivo using nonhuman primate models.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.