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Specimen Atlas of Research Peptides81 plates · MIT
← CataloguePlate XVIII of 81
XVIIIPlate XVIIIReviewed 2026-04-27

Dermorphin

Opioid Peptide

also known as H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2, TAPS, dermorphin heptapeptide

Heptapeptide opioid (H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2) originally isolated from Phyllomedusa frog skin. Highly selective μ-opioid receptor agonist with ~30× potency of morphine. Contains naturally occurring D-alanine at position 2, conferring exceptional receptor selectivity and biostability. Research use only; controlled substance in many jurisdictions.

§ I

At a glance

Morphine potency
~30×
Receptor type
μ-selective
Unique feature
D-Ala²
Route

Research only · ICV / SC (animal models)

§ II

Mechanism

Edit ↗

Primary target — μ-opioid receptors (central and peripheral) [negri-1992][steel-2014].

Pathway — μ-receptor activation → G-protein coupling → adenylyl cyclase inhibition → neuronal hyperpolarization.

Downstream effect — Potent analgesia, reduced nociceptive signaling, opioid-mediated CNS and peripheral effects.

Origin — Phyllomedusa sauvagei and P. bicolor frog skin — gene-encoded with natural D-amino acid incorporation [amiche-1998][mignogna-1992].

Feedback intact — N/A — exogenous opioid agonist.

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Legal statusControlled substance in many jurisdictions · Research onlyNot approved for human use.
Animal research (ICV)Low nanomolar to picomolar rangeIntracerebroventricular administration in rodent models.
Detection limit (doping)5 pg/mL in equine plasma/urine [steel-2014]High-throughput LC-MS/MS screen developed for racing industry.
Duration of action10–120 minutes (dose-dependent, intrathecal)
Evidence basisAnimal studies · In vitro assays
Human toxicityKambô ritual (P. bicolor skin) — violent emesis, vasodilation, fluid shifts, ADH dysregulation [tran-2025]
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to Dermorphin's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Edit ↗
Opioid effectssevere
Respiratory depression, sedation, euphoria, tolerance, dependence risk
CNS effectsmoderate
Analgesia (high-affinity sites), catalepsy (low-affinity sites) [negri-1992]
Kambô ritual toxicitysevere
Violent emesis, vasodilation, profound fluid shifts, hyponatremia, ADH dysregulation, brain death (case report) [tran-2025]
Peripheral effectsmoderate
GI motility inhibition (ileum > vas deferens in vitro) [negri-1992]
Receptor selectivity caveat
Two μ-receptor subtypes — differential behavioral effects (analgesia vs. catalepsy) [negri-1992]
Proteolytic stability
Tyr³-Pro⁶ bond relatively unstable; endogenous enzymes may produce tetrapeptide fragments [cucumel-1996]
Absolute contraindications
  • Human use — not approved by any regulatory authority
  • Controlled substance status — possession illegal in many jurisdictions
  • Known opioid hypersensitivity or respiratory compromise
Relative contraindications
  • Any context outside approved animal research protocols
  • CNS depressant co-administration
§ VI

Administration

Edit ↗
  1. 01
    Legal and ethical framework

    Dermorphin is a controlled substance in many jurisdictions and is not approved for human use. Possession, synthesis, or distribution may be illegal. Use is restricted to licensed research settings under institutional review.

  2. 02
    Animal research protocols

    In rodent models, intracerebroventricular (ICV) or intrathecal injection is used at nanomolar to picomolar concentrations. Subcutaneous administration also documented. All protocols require IACUC approval.

  3. 03
    Analytical detection

    High-throughput LC-MS/MS screens developed for anti-doping programs detect dermorphin and 17 related peptides in equine and human urine/plasma at limits as low as 5 pg/mL. [steel-2014]

  4. 04
    Kambô ritual (traditional use)

    Application of Phyllomedusa bicolor skin secretions to superficial burns. Not recommended — associated with severe toxicity including violent emesis, hyponatremia, and documented case of brain death. [tran-2025]

Appendix

Sources

43%

of 47 rendered claims carry a resolvable citation.

  1. [amiche-1998]
    Amiche 1998Opioid peptides from frog skin.
    journal, 1998
  2. [cucumel-1996]
    Cucumel 1996Production and characterization of site-directed antibodies against dermorphin and dermorphin-related peptides.
    journal, 1996
  3. [lazarus-1999]
    Lazarus 1999What peptides these deltorphins be.
    journal, 1999
  4. [mignogna-1992]
    Mignogna 1992Identification and characterization of two dermorphins from skin extracts of the Amazonian frog Phyllomedusa bicolor.
    journal, 1992
  5. [negri-1992]
    Negri 1992Dermorphin-related peptides from the skin of Phyllomedusa bicolor and their amidated analogs activate two mu opioid receptor subtypes that modulate antinociception and catalepsy in the rat.
    journal, 1992
  6. [steel-2014]
    Steel 2014A high throughput screen for 17 Dermorphin peptides in equine and human urine and equine plasma.
    journal, 2014
  7. [tran-2025]
    Tran 2025Shamanic Kambô Frog Hyponatremic Toxicity Leading to Brain Death: A Case Report.
    journal, 2025
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · Contributors: peptidesdb-core · 27 fields uncited — open contributions