ID | 1316 | |
PMID | 2845208 | |
Year | 1988 | |
Sequence | SYS-Nle-EHfRWGKPV | |
Name | [Nle4, D-Phe7]-alpha-MSH | |
Length | 13 | |
N-Terminal Modification | Acetylation | |
C-Terminal Modification | Amidation | |
Linear/ Cyclic | Linear | |
Chirality | Mix | |
Chemical Modification | Nle=Norleucine | |
Origin of Peptide | Derived from α-MSH | |
Nature of Peptide/Cargo | A superpotent(10-1000 times) analogue of alpha-melanocyte stimulating hormone, it causes a very long lasting stimulation of melanocytes in vitro and in vivo, its nonbiodegradeable and it is resistant to enzymatic inactivation by sera, brain enzymes or purified proteolytic enzymes. | |
Mechanism | Topically applied melanotropin could activate cellular processes within follicular melanocytes leading to new eumelanin formation | |
Cargo Sequence/Structure | None | |
Name of cargo | Not applicable | |
Assay | Frog Skin Bioassay, radioimmunoassay and microscopy | |
Enhancer | Propylene glycol was used as carrier | |
Properties of enhancer | Not mentioned | |
Concentration | Dissolved in propylene glycol | |
Incubation time | 24 hours | |
Tissue permeability (value with units) | Transdermal delivery of 0.08% | |
Tissue Sample | Full thickness skin samples (approximately 1 and a half" in diameter) were removed from the trunk area of either black or yellow adult C57BL/6JAy mice killed by cervical dislocation | |
Ex vivo/In vivo/In vitro | in vivo | |
STRUCTURE |
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SMILES | CC(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO) C(=O)N[C@@H](CCCC)C(=O)N[C@H](CCC(=O)O)C(=O)N[C@H](Cc1nc[nH]c1)C (=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=[NH2])N)C(=O) N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCC[NH3]) C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N |