ML-SYS / 2026.07NON-CLINICAL RESEARCH MATERIALSORIGIN DECLARED BY LOT

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RM-CVS / Coagulation and vascular signalling

B7-33

Also known as: Relaxin B-chain mimetic ยท Single-chain RXFP1 agonist

Preclinical evidenceEvidence grade C: Preclinical evidence

Grade describes the published research on the molecule. It is not a quality score, a safety score, or a release state.

What this is

B7-33 is a minimized relaxin-2 analog designed to favor selected RXFP1 signaling pathways. It is distinct from native two-chain relaxin and from serelaxin.

Evidence position

Cell and animal studies support Grade C. The cited work does not include human exposure.

What the record does not establish

Anti-fibrotic findings in rodents or implanted materials do not establish a human outcome, dose, formulation or commercial-sample identity.

Sources

  • 01
    Design and preclinical characterization of B7-33PubMed
    Shows
    Receptor-signaling work and several rodent fibrosis models
    Does not show
    Preclinical evidence; does not establish human pharmacology or a supplier lot
  • 02
    B7-33 controlled-release coating studyPubMed
    Shows
    In-vitro RXFP1 activity and mouse implant-capsule findings for a defined delivery system
    Does not show
    Device-coating and animal model; not evidence for another route or formulation

External database index

LIVE DATABASE INDEX / SEPARATE FROM CURATED EVIDENCE

Records below come directly from public scientific databases. They help find relevant material, but do not affect the evidence grade until they are matched to the molecule and added to the curated source list.

PUBMED / FOUND RECORDS

  1. B7-33 replicates the vasoprotective functions of human relaxin-2 (serelaxin).European journal of pharmacology / 2017 Jul 15PMID 28478069 / DOI 10.1016/j.ejphar.2017.05.005
  2. Coatings Releasing the Relaxin Peptide Analogue B7-33 Reduce Fibrotic Encapsulation.ACS applied materials & interfaces / 2019 Dec 11PMID 31713411 / DOI 10.1021/acsami.9b17859
  3. B7-33, a Functionally Selective Relaxin Receptor 1 Agonist, Attenuates Myocardial Infarction-Related Adverse Cardiac Remodeling in Mice.Journal of the American Heart Association / 2020 Apr 21PMID 32295457 / DOI 10.1161/JAHA.119.015748
  4. The single-chain relaxin mimetic, B7-33, maintains the cardioprotective effects of relaxin and more rapidly reduces left ventricular fibrosis compared to perindopril in an experimental model of cardiomyopathy.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie / 2023 AprPMID 36753958 / DOI 10.1016/j.biopha.2023.114370
  5. Single chain peptide agonists of relaxin receptors.Molecular and cellular endocrinology / 2019 May 1PMID 30641102 / DOI 10.1016/j.mce.2019.01.008

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