Dermorphin from Super Human Peptides UK is a natural heptapeptide originally isolated from the skin of South American frogs (Phyllomedusa genus). It is a highly potent and selective Mu-opioid receptor agonist. In laboratory research, Dermorphin is utilized as a standard model for examining opioid receptor binding kinetics, pain-signalling modulation, and the physiological effects of potent peptide-based analgesics.
Its unique structure, containing a D-amino acid (D-Alanine), makes it highly resistant to metabolic degradation, providing researchers with a stable tool for long-duration in-vitro and in-vivo studies. Produced under GMP-compliant conditions and verified for 99% purity or higher, Dermorphin is intended strictly for controlled laboratory investigations.
WarningFor laboratory research use only. Not for human consumption.
Key Features
- —High Selectivity: Targeted Mu-opioid receptor agonist.
- —Maximum Purity: 99% purity or higher (verified by HPLC and MS analysis).
- —Metabolic Stability: Natural D-Alanine inclusion for increased resistance to proteolysis.
- —Quality Standard: GMP / ISO certified manufacturing.
Research Focus
- —Opioid Receptor Kinetics: Selective binding and activation of the Mu-opioid receptor.
- —Analgesic Mechanism Studies: Research into peptide-driven pain modulation.
- —Blood-Brain Barrier (BBB) Permeability: Studies on peptide transport across biological membranes.
- —Respiratory and Cardiovascular Impact: Preclinical modeling of opioid-induced physiological responses.
- —Metabolic Resistance: Investigation of D-amino acid influence on peptide longevity.
Published Research and Study Findings
Dermorphin has been extensively studied for its superior potency compared to morphine and other endogenous opioid peptides like enkephalins. Research indicates that its high affinity for the Mu-receptor is attributed to its specific 7-amino acid sequence, specifically the presence of D-Ala in the second position. Laboratory models utilize Dermorphin to study the decoupling of analgesic effects from respiratory depression and potential tolerance mechanisms.
It remains one of the most cited peptides for exploring the pharmacodynamics of the opioid system in animal models.
NoteAll research applications are limited to controlled laboratory and preclinical settings.
Representative Scientific References
- 1.Monteiro-Siqueira, M. et al., "Dermorphin: A potent Mu-opioid receptor agonist," Journal of Peptide Science, 2012.
- 2.Negri, L. et al., "Pharmacological profile of dermorphin and its analogues," British Journal of Pharmacology, 1991.
- 3.Amiche, M. et al., "The Dermorphin family: Structure-activity relationship studies," European Journal of Biochemistry, 1998.
- 4.Broccardo, M. et al., "Relative potency of dermorphin on opioid receptors," British Journal of Pharmacology, 1981.