Description
99% Purity Dermorphin Peptide Vials Supplement 10mg CAS 77614-16-5
Description
Product Name: | Dermorphin | CAS No: | 77614-16-5 |
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HPLC: | Available | MS: | Available |
Grade: | Medicine Grade | Shelf Life: | 2years |
High Light: |
99% Purity Dermorphin Peptide, Dermorphin Peptide CAS 77614-16-5, Peptide Vials CAS 77614-16-5 |
99% purity Peptide vials Supplement 10mg Vial CAS No 77614-16-5 Dermorphin Powder
Product Name | Dermorphin |
Other name | DERMORPHIN ACETATE |
Appearance | White frozen Powder |
MF | C40H50N8O10 |
MW | 802.87300 |
Purity | 99%MIN |
Product Description:
Dermorphin is a hepta-peptide first isolated from the skin of South American frogs belonging to the genus Phyllomedusa. The peptide is a natural opioid that binds as an agonist with high potency and selectivity to mu Opioid receptors. Dermorphin is about 30–40 times more potent than morphine but theoretically may be less likely to produce drug tolerance and addiction (due to its high potency). The amino acid sequence of dermorphin is H-Tyr-D-Ala-Phe-Gly-Tyr-Pro-Ser-NH2. Dermorphin is not found in humans or other mammals and similar D-amino acid peptides have only been found in bacteria, amphibians and molluscs. Dermorphin appears to be made in these through an unusual posttranslational modification carried out by an amino acid isomerase. This unusual process is needed because the D-alanine in this peptide is not among the 20 amino acids coded for in the genetic code and thus the peptide cannot be synthesized in the usual way from the encodings in the genome of an organism.
Function:
Dermorphin, a peptide isolated from the skin of Phyllomedusa frogs and the peptide receptor (NOP) component by the endogenous agonist nociceptin/orphanin FQ (N/OFQ). In displacement binding studies at CHOhMu, Dermorphin and DeNo displac the binding of [3H]-DPN in a concentration dependent and saturable manner. Dermorphin displays an affinity of 7.17, while N/OFQ fails to displace [3H]-DPN at the Delta receptor. Dermorphin and DeNo stimulate the binding of GTPγ[35S] in a concentration dependent and saturable manner at the Mu receptor[2].
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