Developed at the Florey Institute. Preclinical studies show potent anti-fibrotic effects in cardiac and renal fibrosis models with reduced hypotensive side effects vs native relaxin-2.
Selectively activates RXFP1 as a biased agonist, engaging anti-fibrotic pERK1/2 signaling while minimizing cAMP-mediated vasodilation. Single B-chain design retains therapeutic anti-fibrotic activity.
Biased RXFP1 agonist; reduces cardiac and renal fibrosis; less hypotension than relaxin-2; investigational.
Research data is not a treatment plan. If you are considering B7-33, the questions that matter are whether it suits your history, your labs and your goals. That is a conversation with a licensed physician, not a lookup.
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Reconstitution calculator · Full deep dive · Peptide fundamentals