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    Eloralintide

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    Lab-direct quality — full packs or single-vial samples

    Every batch ships straight from the lab that synthesises it — sealed, tamper-evident, and HPLC-verified to >99% purity with a batch-linked Certificate of Analysis. Buying direct means you pay the lab-direct rate on every vial, with nothing stacked on top.

    Order a full sealed 10-vial research pack for a complete study supply, or add a single-vial sample alongside your pack to trial a new compound first. Same lab, same batch, same verified purity — scaled to whatever your research needs.

    What It's Researched For

    In plain terms, eloralintide is an appetite-focused compound that works through the amylin hunger pathway rather than the GLP-1 pathway, and is designed to be selective for the amylin receptor. It is still investigational. Here is what that looks like across the research.

    Appetite & fullness

    In clinical research, studied for reducing food intake through the amylin pathway — a satiety signal separate from the GLP-1 compounds.

    Weight research

    Human proof-of-concept and Phase 2 studies investigate meaningful body-weight reduction with once-weekly dosing.

    Receptor selectivity

    Research explores its preference for the amylin AMY1R receptor over the calcitonin receptor, distinguishing it from non-selective amylin analogues.

    Pairing with GLP-1

    Studied as a complement to incretin (GLP-1) therapy, where amylin and GLP-1 satiety pathways may add together.

    Once-a-week convenience

    Engineered with an albumin-binding lipid tail so research uses a single weekly subcutaneous injection.

    Overview

    Eloralintide (LY3841136) is a selective, long-acting amylin receptor agonist engineered for once-weekly dosing, with an amylin-pathway appetite mechanism complementary to GLP-1 receptor agonists.

    Eloralintide is an engineered agonist of the amylin receptor, built on the 37-amino-acid amylin scaffold. Native human amylin is unstable, forms amyloid fibrils, and has a half-life of only minutes, which made it impractical as a research tool. Eloralintide is stabilised by an intramolecular Cys2–Cys7 methylene-thioacetal bridge and protracted by acylation at Lys26 with a lipid side chain (two γ-glutamate residues plus a saturated C20 fatty diacid) that reversibly binds serum albumin for sustained circulation.

    Its defining feature is receptor selectivity. Where the earlier amylin analogue cagrilintide is a non-selective agonist across the amylin receptor family and the calcitonin receptor, in-vitro characterisation reports that eloralintide preferentially activates the human AMY1R receptor over both the calcitonin receptor and the AMY3R subtype. Amylin-pathway agonism engages hindbrain and hypothalamic satiety circuits to reduce caloric intake.

    Published Phase 1 proof-of-concept research reported that once-weekly eloralintide was well tolerated with minimal gastrointestinal adverse events, and a subsequently reported Phase 2 obesity programme described clinically meaningful body-weight reduction with favourable tolerability. It is being studied both as monotherapy and alongside incretin (GLP-1) therapy. Supplied here as sterile lyophilised powder for research use only.

    Mechanism of Action

    Eloralintide is a selective amylin receptor agonist that preferentially activates AMY1R to engage satiety circuits and reduce food intake — a mechanism complementary to, but distinct from, GLP-1.

    Pathway Effect Why it matters AMY1R agonism Preferential activation of the human AMY1R amylin receptor Selectivity over CTR/AMY3R distinguishes it from non-selective amylin analogues Satiety signalling Engages hindbrain (area postrema / nucleus tractus solitarius) and hypothalamic appetite circuits Reduces caloric intake via enhanced satiety and fullness Gastric emptying Amylin-class delay of gastric emptying Prolongs satiety and flattens postprandial glucose excursions Complement to GLP-1 Acts on the amylin pathway, distinct from incretin receptors Rationale for studying it alongside GLP-1 receptor agonists C20 albumin anchor Reversible serum-albumin binding via the di-γ-Glu / C20 diacid side chain Extends duration of action to support once-weekly dosing Deeper dive for scientific readers

    Eloralintide (LY3841136) was designed to be a selective, long-acting amylin receptor agonist. In-vitro pharmacology reports preferential activation of the human AMY1R receptor over the calcitonin receptor and the AMY3R subtype — a selectivity profile intended to isolate amylin-pathway satiety signalling. Structurally, the peptide combines a stabilising Cys2–Cys7 methylene-thioacetal bridge with a Lys26 lipid acylation (two γ-glutamate spacers and a C20 fatty diacid) that binds albumin for protraction, analogous to the acylation strategy used for other once-weekly metabolic peptides. Because the amylin pathway is mechanistically distinct from the incretin pathway, eloralintide has been investigated both as a standalone agent and in combination with GLP-1 receptor agonists.

    Common Questions People Are Asking

    What is eloralintide and how does it work?

    Eloralintide (LY3841136) is a selective, long-acting amylin receptor agonist. It engages the amylin satiety pathway — hindbrain and hypothalamic appetite circuits — to reduce caloric intake, and in vitro it preferentially activates the human AMY1R receptor over the calcitonin receptor and AMY3R subtype. A lipid side chain at Lys26 (two γ-glutamate residues plus a C20 fatty diacid) binds serum albumin to extend its duration of action for once-weekly research dosing.

    How is eloralintide different from cagrilintide?

    Both are long-acting amylin analogues, but cagrilintide is a non-selective agonist across the amylin receptor family and the calcitonin receptor, whereas eloralintide is reported to be selective — preferentially activating the AMY1R amylin receptor. That selectivity is the main design difference between the two research peptides.

    How is eloralintide different from a GLP-1 agonist?

    GLP-1 agonists such as semaglutide activate the GLP-1 (incretin) receptor. Eloralintide activates the amylin receptor pathway. The two systems are distinct satiety circuits, which is why eloralintide has been studied both on its own and as a complement to incretin therapy.

    What does the research on eloralintide actually show?

    Published Phase 1 proof-of-concept research reported that once-weekly eloralintide was well tolerated with minimal gastrointestinal adverse events, and a subsequently reported Phase 2 obesity programme described clinically meaningful body-weight reduction with favourable tolerability. These are descriptive research findings for an investigational compound, not outcomes promised for any use of this research-grade material.

    Is eloralintide approved or legal?

    Eloralintide is an investigational compound (LY3841136) and is not an approved medicine in any jurisdiction. The material supplied here is unapproved, research-grade laboratory material sold strictly for in-vitro and preclinical research use only — not for human use.

    How is eloralintide reconstituted and stored?

    Keep the lyophilised powder at −20 °C in the freezer. Reconstitute with bacteriostatic water by directing it down the vial wall rather than onto the powder, then swirl gently — do not shake. After reconstitution, refrigerate at 1–6 °C and protect from light. Avoid repeated freeze–thaw cycles, which can damage the fatty-acid tail.

    Where can I buy Eloralintide?

    Right here — Eloralintide is supplied directly by New-U Research Compounds on this page. Every batch is independently third-party tested to >99% HPLC purity with a batch-linked Certificate of Analysis, supplied as lyophilised research-grade material, and shipped direct from source worldwide in discreet, tracked packaging. Strictly for laboratory research use only — not for human use.

    How much does Eloralintide cost?

    Eloralintide pricing is shown live on this page, per pack size — 10-vial research packs as standard, with single-vial sample options on selected compounds. Larger vial strengths lower the per-mg cost, every order includes the batch Certificate of Analysis, and shipping is free on orders over $300.

    Is Eloralintide third-party tested?

    Yes. Every Eloralintide batch is verified by independent laboratories (Janoshik Analytics and Freedom Diagnostics) for identity and purity, with a batch-linked Certificate of Analysis confirming >99% purity by HPLC. Every order ships with its COA, and current batch certificates are published on our COA page.

    How do I buy Eloralintide?

    Add the Eloralintide pack size you need to your cart and check out: enter your shipping details, then choose your payment method — cryptocurrency or card — on the next step. Every order ships with its batch Certificate of Analysis (COA). Eloralintide is supplied strictly for laboratory research use only, not for human or veterinary use.

    What payment methods can I use to buy Eloralintide?

    At checkout you can pay by cryptocurrency (BTC, ETH, SOL, LTC, USDC, USDT and more) or by card, each handled by a dedicated secure payment provider. You choose your method after confirming your order.

    How fast is shipping, and do you ship worldwide?

    Yes — we ship worldwide in discreet, unmarked, temperature-stable, tracked packaging. Delivery typically takes 6–14 business days, and shipping is free on orders over $300.

    Pharmacokinetics

    Half-life Long-acting — engineered for once-weekly subcutaneous dosing via albumin binding Absorption route Subcutaneous injection; sustained exposure through reversible albumin binding Bioavailability Protracted subcutaneous exposure via the di-γ-Glu / C20 fatty-diacid albumin anchor Metabolism / clearance Proteolytic cleavage of the peptide backbone plus β-oxidation of the C20 fatty-diacid chain Stability Lyophilised: −20 °C. Reconstituted: 1–6 °C, protect from light; avoid repeated freeze–thaw Notes The C20 fatty-diacid / albumin interaction is the protraction mechanism enabling once-weekly research administration. Precise human half-life and Tmax values are study-specific and reported in the published clinical programme.

    Research-Observed Effects

  • Clinically meaningful body-weight reduction with once-weekly dosing reported in the Phase 2 obesity programme
  • Well tolerated with minimal gastrointestinal adverse events in Phase 1 proof-of-concept research
  • Appetite / caloric-intake reduction via amylin-pathway satiety signalling
  • Selective AMY1R agonism reported in vitro (preference over CTR and AMY3R)
  • Amylin-pathway agonism that is mechanistically distinct from, and studied alongside, incretin (GLP-1) therapy
  • Published Research Context

    In the published clinical programme, once-weekly subcutaneous eloralintide was introduced at low doses and titrated upward over several weeks. These figures describe the escalation schedules reported in published research and are recorded here as research context only.

    Stacking Compatibility

    Compatible compounds

  • Semaglutide: Amylin and GLP-1 pathways are distinct satiety circuits; eloralintide is studied as a complement to incretin therapy
  • Tirzepatide: Incretin agonism is mechanistically distinct from amylin signalling and studied as a complementary partner
  • Avoid combinations

  • Other amylin analogues (e.g. cagrilintide, pramlintide): Redundant amylin-receptor occupancy; no additive research rationale
  • Side Effects (Observed in Literature)

    Common

  • Nausea (amylin-class, escalation-related and typically transient)
  • Decreased appetite
  • Vomiting
  • Gastrointestinal effects generally reported as minimal in the Phase 1 programme
  • Rare

  • Injection-site reactions
  • Hypersensitivity reactions
  • Dose-dependent

  • Gastrointestinal effects may increase with dose and during up-titration
  • Evidence Tier

    Overall: Mixed (human + animal)

    Eloralintide has human Phase 1 proof-of-concept data and a reported Phase 2 obesity programme, but it remains investigational with no approved indication in any jurisdiction. The research-grade material supplied here is unapproved laboratory material for research use only.

    Tier 1 · Human clinical

  • Eloralintide Phase 1 proof-of-concept study — well tolerated, minimal GI adverse events (PMID 41559929)
  • Reported Phase 2 obesity programme — clinically meaningful weight reduction with favourable tolerability
  • Source References & Further Reading

    Last reviewed: 13 July 2026 · New-U Research Compounds

  • Eloralintide (LY3841136), a novel amylin receptor agonist for the treatment of obesity: from discovery to clinical proof of concept. Mol Metab. · 2025 · PMID: 41109426
  • Eloralintide, a selective, long-acting amylin receptor agonist for treatment of obesity: Phase 1 proof of concept. Diabetes Obes Metab. · 2025 · PMID: 41559929
  • PubMed: peer-reviewed literature on Eloralintide
  • ClinicalTrials.gov: registered studies on Eloralintide
  • Eloralintide: Wikipedia (search)
  • WebMD: consumer health reference
  • BBC News: Health
  • CNN Health: “Peptides: what to know about the wellness trend”
  • Sky News: “Can peptides make America healthy again?”
  • Sky News: “Inside the exploding US peptides craze” (video)
  • Sky News Australia: “Black market peptide trade explodes as influencers fuel uptick in use”
  • Sky News Australia: “Backyard peptide boom sparks alarm” (video)
  • Sky News Australia: “Oprah reveals struggle with shame of weight-loss drugs”
  • Key Characteristics

  • Selective amylin receptor agonist (AMY1R-preferring)
  • 37-amino-acid amylin-scaffold linear peptide, C-terminally amidated
  • Cys2–Cys7 methylene-thioacetal stabilising bridge
  • Lys26 acylation: two γ-glutamate residues + C20 fatty diacid (albumin anchor)
  • Long-acting: engineered for once-weekly subcutaneous dosing
  • Investigational (LY3841136); studied as monotherapy and with GLP-1 therapy
  • Research-grade purity: >99% HPLC
  • Specifications

    Identifier LY3841136 Class Selective long-acting amylin receptor agonist Scaffold 37-amino-acid amylin-based linear peptide, C-terminally amidated Key modifications Cys2–Cys7 methylene-thioacetal bridge; Lys26 di-γ-Glu / C20 fatty-diacid acylation Receptor selectivity Preferential human AMY1R activation (over CTR and AMY3R) Purity >99% (HPLC) Form Lyophilised powder Route Once-weekly subcutaneous in published research Storage Lyophilised: −20 °C freezer. Reconstituted: 1–6 °C, away from light.

    About Eloralintide (LY3841136): Selective Long-Acting Amylin Receptor Agonist Research Guide

    Eloralintide (LY3841136) is a selective, long-acting amylin receptor agonist studied for obesity research. It belongs to the amylin class — a satiety pathway that is distinct from the GLP-1 (incretin) system that most metabolic research peptides target. Native human amylin forms amyloid fibrils and has a circulating half-life of minutes; eloralintide addresses this with a stabilising Cys2–Cys7 methylene-thioacetal bridge and a Lys26 lipid acylation (two γ-glutamate residues plus a C20 fatty diacid) that reversibly binds serum albumin to extend its duration of action for once-weekly research use.

    The molecule's distinguishing feature is receptor selectivity. In-vitro characterisation reports that eloralintide preferentially activates the human AMY1R amylin receptor over the calcitonin receptor and the AMY3R subtype, in contrast to the non-selective amylin analogue cagrilintide. Published Phase 1 proof-of-concept research reported that once-weekly eloralintide was well tolerated with minimal gastrointestinal adverse events, and a subsequently reported Phase 2 obesity programme described clinically meaningful body-weight reduction, with the compound studied both as monotherapy and as a complement to incretin therapy.

    Supplied here as a sterile lyophilised powder for in-vitro and preclinical laboratory research only. Eloralintide is an investigational compound, is not a licensed pharmaceutical product, and is not a substitute for any prescribed medication — research use only, not for human use.

  • Eloralintide discovery to clinical proof of concept, Mol Metab (PubMed)
  • Eloralintide Phase 1 proof of concept, Diabetes Obes Metab (PubMed)
  • Amylin — Wikipedia
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  • More on Eloralintide

  • Eloralintide research guide
  • Research use only — not for human consumption. All products are supplied strictly for laboratory research purposes.

    © 2026 New-U Research Compounds · new-u.io — Copyright held with Hilxera Distribution Services LLC. All rights reserved.