B7-33
Also known as (B7-33)H2, single-chain relaxin analog, H2 relaxin B-chain mimetic
A 24-amino-acid single-chain functional analog of H2 relaxin that acts as a biased RXFP1 agonist with anti-fibrotic activity in preclinical models.
Typical use cases
Dosing guidelines
Titration
Typically flat-dosed in the limited literature; no validated titration scheme.
Reconstitution
6 mg vial: ~2 mL bacteriostatic water yields ~3 mg/mL.
Injection sites
Subcutaneous in research handling (e.g. abdomen), rotate sites.
Storage & handling
Lyophilized: stable months cool/dark, longer frozen. Reconstituted: refrigerate (2–8 °C).
Side effects
- Unknown human safety profile (preclinical only)
- Theoretical vasodilation / blood-pressure effects (relaxin class)
- Injection-site reaction
Research summary
B7-33 is a single-B-chain relaxin mimetic that signals as a biased agonist at the RXFP1 receptor, preferentially activating the ERK1/2–MMP pathway tied to collagen breakdown while largely avoiding the cAMP signaling of native relaxin. Preclinical work reports reduced fibrosis in heart, lung and kidney tissue and cardioprotective effects in animal models, but there are no completed human clinical trials, and native B7-33 has poor serum stability that has prompted lipidated-analog development. Educational only — not medical advice.
Key references
- Hossain et al., Chem. Sci. (2016) — a single-chain relaxin derivative is a functionally selective RXFP1 agonist
- Marshall et al., Pharmacol. Res. (2017) — B7-33 single-chain relaxin mimetic reduces fibrosis
Related compounds
Where to buy
These are affiliate links. Purchasing through them helps support DoseForge at no extra cost to you.
Educational reference only — not medical advice. Dosing figures are commonly-cited ranges, not prescriptions. Consult a qualified clinician.
Log doses, rotate sites, watch your progress — free.