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Cognitive & Neuropeptides · Source-reviewed dossier

Dermorphin

Source-Reviewed Research Dossier

Dermorphin is a short peptide first found in frog skin. It binds the mu-opioid receptor, the same target as morphine, and produces strong pain relief in animal experiments. Researchers study it to understand how peptides activate this receptor and to design analogues with different stability or effect profiles. Reports describe potent, long-lasting pain relief in animals and some entry into the brain after dosing outside the central nervous system. Rodents given dermorphin repeatedly showed less tolerance and dependence than those given morphine. These are mostly receptor and animal findings. Opioid-class risks such as breathing depression and dependence remain important limits. This material is for research use only.

Research use only Lot documents on request
Dermorphin research product family with 1 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
Dermorphin
Research category
Cognitive & Neuropeptides
Catalog CAS RN
77614-16-5
Catalog molecular formula
C40H50N8O10
Catalog molecular weight
802.88 g/mol
Catalog sequence
Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2
Evidence status
Receptor and animal analgesia research; no approved human product
Intended use
Research, development and manufacturing use only

Literature reference parameters

Compound or material class
Frog-skin-derived μ-opioid peptideCatalog-family identity
Evidence scope
Receptor and animal analgesia research; no approved human productDo 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 Dermorphin is studied

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

Why frog-skin peptides interest opioid researchers

Dermorphin has an unusual D-alanine near its start, which helps it fit the mu-opioid receptor tightly and selectively. This lets it trigger pain-relief signalling at low amounts in laboratory tests. Because many natural opioid peptides break down quickly, this stable structure became a template for designing analogues. Reviewers treat dermorphin as the founding member of a peptide family that now includes several natural and many synthetic versions. It serves as a standard reference for receptor pharmacology and peptide design.

Shortened analogues and enzymatic stability

Structure-activity work suggests the first four amino acids are the minimum needed to activate the mu-opioid receptor. Replacing the second residue with D-arginine makes these short tetrapeptides harder for enzymes to break down, which can lengthen their effects. In experimental systems, several analogues produced pain relief at least as strong as morphine by various injection routes. Some behaved differently from classic mu agonists, for example by triggering dynorphin release. These findings are specific to each sequence and largely from animal or cell studies.

Pain research and important safety limits

The receptor-level story is convincing but is not a health claim. Reviews describe pain relief in rodents and primates, sometimes after dosing outside the central nervous system, and less tolerance or dependence in chronically treated animals than with morphine. These are model-bound observations. Opioid-class risks, including breathing depression and dependence, remain key interpretive limits. A research catalogue peptide, its salt form, a modified analogue, and a finished medicine are different materials; findings for one do not automatically apply to another. Lot identity and quality are governed by the product specification and lot documents, not by potency in animal assays.

Reported research findings

What published studies report about Dermorphin

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

Peptide-family review

Dermorphin analogues show strong μ-opioid activity

A review summarized sequences, receptor pharmacology and biological activity across the dermorphin peptide family.

Family-level potency data do not define human safety.

Read the primary study
Analogue review

Short dermorphin analogues were studied for prolonged analgesia

A review described tetrapeptide analogues with potent, long-lasting analgesic activity in experimental systems.

Analogue findings are sequence-specific and predominantly preclinical.

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.DR5
Pack size5 mg × 10 vials
Current variant
Specification & documents for DR5

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.

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.

Peptide-family review

Dermorphin analogues show strong μ-opioid activity

Family-level potency data do not define human safety.

View primary record
Analogue review

Short dermorphin analogues were studied for prolonged analgesia

Analogue findings are sequence-specific and predominantly preclinical.

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

    The dermorphin peptide family

    Review. 1996. PMID 8981054.

    Peptide-family review
  2. 02 Analogue review

Research FAQ

Dermorphin questions

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

What effects are studied for Dermorphin?

The main reported effect is strong activation of the mu-opioid receptor, which in animal and receptor models leads to powerful pain relief, often described as stronger than morphine. Reviewers also note that some family members can reach the brain after dosing outside the central nervous system, and that rodents given dermorphin repeatedly showed less tolerance and dependence than those given morphine. These are experimental findings tied to specific sequences, models, and routes. They do not establish safe or effective human use, and opioid-class risks such as breathing depression and dependence remain serious limits.

How should the Dermorphin research findings be understood?

The receptor-level story is convincing but is not a health claim. Reviews describe pain relief in rodents and primates, sometimes after dosing outside the central nervous system, and less tolerance or dependence in chronically treated animals than with morphine. These are model-bound observations. Opioid-class risks, including breathing depression and dependence, remain key interpretive limits. A research catalogue peptide, its salt form, a modified analogue, and a finished medicine are different materials; findings for one do not automatically apply to another. Lot identity and quality are governed by the product specification and lot documents, not by potency in animal assays.

What evidence is available for Dermorphin?

The literature is preclinical and review-based, without an approved dermorphin medicine.

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 Dermorphin 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

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Selected: DR5 · 5 mg × 10 vials