Designing Shorter CRF Antagonists for Anxiety and Depression Treatment

Structure-activity studies on the CRF antagonist astressin identified the minimum peptide sequence needed for CRF receptor blockade, advancing toward smaller, more drug-like CRF antagonist anxiolytics.

Rijkers, Dirk T S et al.·Chembiochem : a European journal of chemical biology·2004·Preliminary Evidencein-vitro
RPEP-00966In VitroPreliminary Evidence2004RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
in-vitro
Evidence
Preliminary Evidence
Sample
Not reported

What This Study Found

SAR studies on astressin identified the minimal CRF antagonist sequence retaining biological activity at both CRF1 and CRF2 receptors, advancing design of smaller, more drug-like peptide antagonists for stress-related psychiatric disorders.

Key Numbers

How They Did This

in-vitro study on neuropeptides, anxiety-mood.

Why This Research Matters

Relevant for neuropeptides, anxiety-mood, peptide-design.

The Bigger Picture

Advances peptide research.

What This Study Doesn't Tell Us

See abstract.

Questions This Raises

  • ?Further research needed.
  • ?Clinical translation to evaluate.

Trust & Context

Key Stat:
Key finding SAR studies on astressin identified the minimal CRF antagonist sequence retaining biological activity at both CRF1 and CRF2 receptors, advancing desig
Evidence Grade:
preliminary evidence.
Study Age:
Published in 2004.
Original Title:
Structure-activity studies on the corticotropin releasing factor antagonist astressin, leading to a minimal sequence necessary for antagonistic activity.
Published In:
Chembiochem : a European journal of chemical biology, 5(3), 340-8 (2004)
Database ID:
RPEP-00966

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study
What do these levels mean? →

Frequently Asked Questions

What was studied?

Designing Shorter CRF Antagonists for Anxiety and Depression Treatment

What was found?

Structure-activity studies on the CRF antagonist astressin identified the minimum peptide sequence needed for CRF receptor blockade, advancing toward smaller, more drug-like CRF antagonist anxiolytics.

Read More on RethinkPeptides

Cite This Study

RPEP-00966·https://rethinkpeptides.com/research/RPEP-00966

APA

Rijkers, Dirk T S; Kruijtzer, John A W; van Oostenbrugge, Marja; Ronken, Eric; den Hartog, Jack A J; Liskamp, Rob M J. (2004). Structure-activity studies on the corticotropin releasing factor antagonist astressin, leading to a minimal sequence necessary for antagonistic activity.. Chembiochem : a European journal of chemical biology, 5(3), 340-8.

MLA

Rijkers, Dirk T S, et al. "Structure-activity studies on the corticotropin releasing factor antagonist astressin, leading to a minimal sequence necessary for antagonistic activity.." Chembiochem : a European journal of chemical biology, 2004.

RethinkPeptides

RethinkPeptides Research Database. "Structure-activity studies on the corticotropin releasing fa..." RPEP-00966. Retrieved from https://rethinkpeptides.com/research/rijkers-2004-structureactivity-studies-on-the

Access the Original Study

Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkPeptides research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.