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Metabolic & Weight Loss · Source-reviewed dossier

Adipotide

Source-Reviewed Research Dossier

Adipotide is studied for a strategy that targets blood vessels supporting fat tissue. It links a targeting part to a cell-death signal. A small experiment in obese rhesus monkeys reported lower body weight, less white fat and improved insulin-resistance measures. The same report described reversible kidney-tubule changes, so the safety findings matter alongside weight loss. Later mouse work compared delivery formats. These are animal findings, not established benefits or safety in people, and they do not validate NHD research material.

Research use only Lot documents on request
Adipotide research product family with 3 catalog variants
AI-generated packaging mockup for catalog navigation. It is not a photograph of an actual supplied lot; container, label and presentation may vary.

Product family

Compound overview

Shared values below are consolidated from the current catalog record. They are not independent verification or lot results; request the applicable product specification and ask which lot records are available before ordering.

Product identity

Product type
Peptide research compound
Catalog family
Adipotide
Research category
Metabolic & Weight Loss
Catalog CAS RN
859216-15-2
Catalog sequence
Cys-Lys-Gly-Gly-Arg-Ala-Lys-Asp-Cys-Gly-Gly-D(Lys-Leu-Ala-Lys-Leu-Ala-Lys)2
Evidence status
Non-human primate and preclinical evidence; no approved human use
Intended use
Research, development and manufacturing use only

Literature reference parameters

Compound or material class
Prohibitin-targeting peptidomimeticCatalog-family identity
Evidence scope
Non-human primate and preclinical evidence; no approved human useDo not generalize beyond the cited model
Source review
Primary or authoritative records linked belowChecked 2026-09-01

Identity safeguard Reference identifiers above describe the literature compound record. Confirm the supplied form, formula, molecular weight, purity and storage conditions against the applicable product specification and any available lot records.

Mechanism of action

How Adipotide is studied

A target-to-pathway view grounded in the linked research records.

Aim: blood vessels in fat

The compound has a targeting part and a cell-death-triggering part. The targeting part is meant to find a marker on the endothelial cells that line blood vessels inside white fat. The idea is indirect: if those vessels are damaged, the fat they support may shrink. This is a proposed delivery strategy, not a confirmed human mechanism.

Monkey study needs careful reading

In obese rhesus monkeys, a defined research version was reported to trigger cell death in fat blood vessels. Monkeys lost weight, white fat shrank on imaging, and insulin-resistance measures improved. Reversible changes in kidney proximal tubules were also seen at tested doses. This was a small non-human experiment, so it cannot indicate human benefit, dose, or safety.

Delivery format changes results

A later mouse comparison tested a nanoparticle carrying the same cell-death peptide against a linked peptide version. The nanoparticle was reported to lower body weight and leptin, reduce fat in liver and muscle, raise adiponectin, and show no detectable liver toxicity in that model. This informs delivery strategy, not human effectiveness or catalog quality.

Reported research findings

What published studies report about Adipotide

Reported outcomes are paired with their experimental model and evidence boundary.

Non-human primate

Obese-monkey study reported weight and insulin-resistance changes

The published study reported loss of white adipose tissue, body-weight reduction and improved insulin-resistance measures in obese rhesus monkeys.

This was a small non-human-primate experiment with a defined research construct; it was not a human treatment trial.

Read the primary study
Preclinical comparison

Targeted therapeutic formats were compared in obesity models

A later preclinical study compared nanoparticle-targeted therapeutics and peptide bioconjugates as adipose-vascular targeting approaches.

The experiment informs delivery strategy rather than human effectiveness or catalog-lot quality.

Read the primary study
Translation boundary: findings are limited to the evidence level stated on each card. Experimental protocol quantities are research details, not usage instructions.

Catalog options

Variant specifications

Pack-level catalog data; lot-level controls remain document-specific.

Catalog no.AP2
Pack size2 mg × 10 vials
Specification & documents for AP2

Product specification

Single-component peptide · 2 mg/vial nominal · 10-vial pack · supplied form and release limits controlled by lot specification.

Lot documentation

Document availability and scope must be confirmed for this variant and lot in the written quotation. A catalog description is not a lot-specific test result.

Catalog no.AP5
Pack size5 mg × 10 vials
Specification & documents for AP5

Product specification

Single-component peptide · 5 mg/vial nominal · 10-vial pack · supplied form and release limits controlled by lot specification.

Lot documentation

Document availability and scope must be confirmed for this variant and lot in the written quotation. A catalog description is not a lot-specific test result.

Catalog no.AP10
Pack size10 mg × 10 vials
Specification & documents for AP10

Product specification

Single-component peptide · 10 mg/vial nominal · 10-vial pack · supplied form and release limits controlled by lot specification.

Lot documentation

Document availability and scope must be confirmed for this variant and lot in the written quotation. A catalog description is not a lot-specific test result.

Quality system

Quality documentation

A listed document is not proof of availability for this lot. Ask the team to confirm the current COA status and the scope of any other records before ordering.

Lot-specific Certificate of AnalysisAvailability and scope must be confirmed for the selected catalog variant and lot
COA availability unconfirmed Ask about availability
Product Specification SheetAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request
Analytical Method SummaryAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request

Analytical interpretation

Interpret the documents, not just the headline number.

Use the source-reviewed guide to separate chromatographic area purity, quantitative assay, LC-MS identity, composition and stability evidence before comparing variants or requesting a lot record.

Open the Quality & Documentation Hub

HPLC area ≠ assayA dominant peak does not establish target mass fraction.

Intact mass ≠ full sequenceIdentity strength depends on resolution and orthogonal evidence.

Counterions affect contentWater, salt form and solvents change the as-is composition.

Storage needs a data basisShipping practice is not the same as stability evidence.

Evidence map

Research context

Published studies and regulatory records, not customer testimonials or usage guidance.

Non-human primate

Obese-monkey study reported weight and insulin-resistance changes

This was a small non-human-primate experiment with a defined research construct; it was not a human treatment trial.

View primary record
Preclinical comparison

Targeted therapeutic formats were compared in obesity models

The experiment informs delivery strategy rather than human effectiveness or catalog-lot quality.

View primary record
Evidence boundary: each card states its evidence type. Human trials and regulatory records describe the studied or regulated intervention; preclinical records remain model-specific. None verifies the identity, quality, safety or efficacy of this catalog lot or provides usage instructions.

Literature basis

Curated references

Third-party publications selected for direct relevance.

  1. 01

    A peptidomimetic targeting white fat causes weight loss and improved insulin resistance in obese monkeys

    Barnhart KF, et al. Science Translational Medicine. 2011. PMID 22072637.

    Non-human primate
  2. 02

    Comparative study of nanoparticle-targeted therapeutics and bioconjugates

    Daquinag AC, et al. Molecular Pharmaceutics. 2013. PMID 23871959.

    Preclinical comparison

Research FAQ

Adipotide questions

Concise answers for researchers comparing identity, evidence and catalog variants.

What effects are studied for Adipotide?

In obese monkeys, a defined research version was reported to cause cell death in fat blood vessels and produce weight loss, reduced white fat on imaging, and improved insulin-resistance measures. Reversible kidney tubule changes were also seen at tested doses. A separate mouse study compared delivery formats. These are early non-human findings, not demonstrated human outcomes.

How should the Adipotide research findings be understood?

A later mouse comparison tested a nanoparticle carrying the same cell-death peptide against a linked peptide version. The nanoparticle was reported to lower body weight and leptin, reduce fat in liver and muscle, raise adiponectin, and show no detectable liver toxicity in that model. This informs delivery strategy, not human effectiveness or catalog quality.

What evidence is available for Adipotide?

One directly relevant non-human-primate study and additional preclinical delivery research are available.

Does the cited research validate this catalog material?

No. The cited records describe their own intervention, formulation, model and controls. They do not verify the identity, purity, sterility, safety or efficacy of a catalog lot.

Which quality documents can be requested?

A lot-specific COA, product specification sheet and analytical method summary can be requested where applicable.

How should Adipotide be stored?

Store at -20 °C, protected from light and moisture. After reconstitution, aliquot and avoid repeated freeze-thaw cycles. Confirm the applicable storage statement on the product-specific specification and lot documentation.

Knowledge tools

Continue with structured evidence

Move from this dossier into canonical evidence maps, verified status records, analytical interpretation and laboratory calculations.

Internal technical source review

Claims were checked against the linked primary publication, regulatory label or authoritative compound record. Published findings stay attached to their study model, formulation and route. Catalog identity and lot quality remain controlled by the applicable specification and lot-specific documents.

Editorial status: NHD evidence editorial workflow · 2026-09-01 · Not independent medical review · Review policy

Technical procurement

Ready to request a quote?

Selected: AP2 · 2 mg × 10 vials