
Retatrutide
Retatrutide es un péptido sintético agonista triple de receptores, sintetizado como agonista de los receptores de GIP, GLP-1 y glucagón, estudiado en la investigación metabólica de fase 2/3 de Eli Lilly por su papel en la activación combinada de los receptores de GIP, GLP-1 y glucagón.
Un péptido agonista triple dirigido a los receptores de GIP, GLP-1 y glucagón — estudiado en contextos avanzados de metabolismo y regulación del peso.
For Research Use Only — Not for Human Consumption.
Investigational compound — no approved therapeutic indication.
Sold strictly for in vitro laboratory research.
- Disponibilidad
- Delivered in 3–7 days (EU)
- Conservación
- Store 2–8 °C. Reconstitute before use.
- Se envía desde
- European fulfilment centre, tracked express
Prueba de laboratorio, por lote
- Analizado de forma independiente, por lote
- Certificado de análisis disponible
- Pureza e identidad documentadas
Investigación en agonistas triples de receptores.
Retatrutide (CAS 2381089-83-2) combina la activación de los receptores de GIP, GLP-1 y glucagón en una sola secuencia. Los ensayos clínicos de fase 2 han descrito reducciones sustanciales del peso corporal y mejoras en los marcadores metabólicos. Fórmula C223H341N57O64S, MW 4858,60 g/mol. Requiere supervisión clínica estricta.
- — Jastreboff et al. — ensayo de fase 2 de Retatrutide: variables de pérdida de peso dependientes de la dosis
- — Coskun et al. — triagonismo GIP/GLP-1/glucagón y marcadores de gasto energético
Solo contexto de investigación. No es consejo médico. Consulta a un profesional sanitario cualificado antes de usarlo.
- 10 mg de polvo liofilizado por vial
- Reconstituir con agua bacteriostática antes de usar
- Conservar liofilizado a 2–8 °C, protegido de la luz
- Una vez reconstituido, refrigerar y usar en 28 días
- Un vial de Retatrutide liofilizado de 10 mg
- Tapón con precinto de seguridad y etiqueta con código de lote
- Tarjeta de conservación y consulta médica
What the research reports about this molecule.
Classic parameters from peer-reviewed literature. Not human dosing guidance — read alongside the PubMed references on /learn.
- Sequence
- Agonista triple de los receptores GIP/GLP-1/glucagón
- Mechanism
- Activa los receptores de GIP, GLP-1 y glucagón
- Research domain
- Metabolismo, regulación del peso (Eli Lilly, fase 2/3)
- Reconstitution
- Agua bacteriostática, USP
- Storage
- Largo plazo -20 °C liofilizado; -80 °C para >12 meses; reconstituido 2–8 °C, ≤4 semanas
Pasos simples y deliberados — no un protocolo.
Estas son notas prácticas de manejo. Las decisiones de dosis quedan entre tu médico y tú.
- 1
Reconstituye bajo supervisión clínica — es esencial titular la dosis desde una dosis inicial baja
- 2
Adminístralo por vía subcutánea según te indiquen; sigue la pauta de escalada de dosis prescrita
- 3
Refrigera el vial reconstituido; úsalo en 28 días
Guía de uso
Lee el protocolo de investigación
Instrucciones breves de reconstitución, dosificación y manejo.
Calculadora de reconstitución
Solo para investigaciónJeringa
Péptido en el vial
Agua bacteriostática
Concentración5 mg/mL
Dosis objetivo
Carga la jeringa hasta
5
unidades · 0.05 mL
Concentración
5
mg/mL
Dosis por vial
40
dosis
U-50 2.5 · U-40 2 unidades
Solo para cálculo de investigación de laboratorio. No es consejo médico ni de dosificación, y no es para uso humano ni veterinario.
Quienes investigan Peso / apoyo metabólico también comparan
- RetatrutideEsta páginaTamaños: 10 mg · 60 mgPrecio / mg: €4.32 / mg
- SemaglutideTamaños: 5 mg · 10 mgPrecio / mg: €5.00 / mg
- TesamorelinTamaños: 5 mg · 10 mgPrecio / mg: €6.90 / mg
- CJC-1295 No DAC + IpamorelinTamaños: 10 mg + 10 mgPrecio / mg: €7.50 / mg
Each release is matched with quality documentation through a documented verification path. Identity, purity, and composition test results sit on the product page before you buy.
Every batch is verified by an ISO/IEC 17025-accredited laboratory before release. Identity, purity, and documentation travel with the product — not behind a form.
Sensitive peptides ship in insulated cold packaging with gel packs sized for a 48-hour transit window, tracked door to door.
Todo lo que vale la pena preguntar antes de pedir.
Envío, conservación, calidad y cuándo hablar con un médico — sin rodeos.
What proof of quality comes with my order?
Every batch ships with a batch code printed on the vial. The matching independent lab report — showing identity, purity, and composition — is linked on the product page and stays on your order page after purchase.
Should I speak to a clinician before using a peptide?
We recommend it — especially if you are pregnant, nursing, managing a medical condition, or combining peptides with prescribed medication. Our product pages are educational. They are not medical advice and they do not replace a conversation with a qualified practitioner.
When will my order ship and arrive?
Orders placed before 14:00 CET Monday–Friday ship the same business day from our European fulfilment centre in The Hague, Netherlands. Standard tracked EU delivery arrives in 2–4 business days; express options are available at checkout.
What does "research only" actually mean on a peptide label?
Research-only means the compound has not been approved by the EMA or any national medicines authority for medical use, and is sold solely for in-vitro and laboratory research. It is not a supplement, a cosmetic, or a medicine, and it carries no claims for human consumption.
Is retatrutide approved or available as a medicine?
No. Retatrutide is a triple agonist of GLP-1, GIP, and glucagon receptors developed by Eli Lilly and currently in Phase 3 trials (TRIUMPH programme). It is not approved by the EMA or FDA, so it cannot be prescribed. Phase 2 data showed up to ~24 percent body-weight reduction at 48 weeks.
What are the most common side effects of GLP-1 peptides specifically?
Across SUSTAIN, SURPASS, SURMOUNT, and TRIUMPH trials, the dominant adverse events for semaglutide, tirzepatide, and retatrutide are gastrointestinal: nausea, vomiting, diarrhoea, constipation, and abdominal discomfort, usually mild-to-moderate and concentrated during dose titration.
What's the difference between a prescription peptide and a research peptide?
A prescription peptide (e.g. Wegovy, Mounjaro, Vyleesi, Zadaxin in the relevant jurisdictions) has been through EMA or national-authority review, carries an authorised indication, and is dispensed by a pharmacy against a script. A research peptide is a reference-grade compound sold for laboratory use only.
How do I reconstitute a lyophilised peptide vial?
Bring both the lyophilised vial and the bacteriostatic water to room temperature, equalise pressure with a sterile vented needle, then inject the solvent slowly down the side of the vial. Swirl gently — never shake — until clear, and refrigerate at 2–8 °C.
How much bacteriostatic water should I add to my peptide vial?
The calculation is peptide mass (mg) ÷ desired concentration (mg/mL) = volume of bacteriostatic water in mL. For example, a 5 mg vial at 1 mg/mL needs 5 mL; at 2 mg/mL, 2.5 mL. Every Peptyds product page carries a suggested reconstitution volume tuned to the vial size.
How long does a reconstituted peptide stay stable in the fridge?
Most lyophilised peptides reconstituted with bacteriostatic water remain stable for 28–30 days at 2–8 °C, protected from light. A handful of short, fragile sequences — Epithalon among them — drop to roughly 14 days. Never freeze a reconstituted vial.
What side effects are most commonly reported across peptide research?
Across published trials and case series, the most frequent reported events are injection-site reactions (redness, induration, transient discomfort), headache, mild nausea, and temporary fatigue. GLP-1 and dual-agonist class peptides add dose-dependent gastrointestinal effects.
Who should not use peptides?
Peptides are not appropriate for anyone who is pregnant, nursing, planning conception, under 18, managing active cancer, or on immunosuppressants — and competitive athletes governed by WADA must avoid every peptide on the prohibited list. Anyone with a personal or family history of melanoma should specifically avoid melanocortin-receptor agonists.