At human MC3 and MC5 receptors, the cyclic analogue MTII had lower binding affinity than linear NDP-MSH.
In plain wordsIn cells, MTII bound two human melanocortin receptors less strongly than NDP-MSH did.
- Peptide
- Melanotan II
- Outcome
- DecreaseBinding affinity at hMC3R and hMC5R versus NDP-MSH
- Study
humann: not reported in source
Human melanocortin receptors hMC1R, hMC3R, hMC4R and hMC5R- Comparator
- NDP-MSH
- Outcome group
- Receptor activity and mechanism · Pharmacology
- Studied dose
- Dose not stated
Source sentences
Interestingly, the linear NDP-MSH possessed greater binding affinity for the hMC3R and hMC5R than did the cyclic analogue MTII.
1 context sentence(design, population, supporting numbers)
MTII (Ac-Nle4-c[Asp5,D-Phe7,Lys10]-alpha-MSH(4-10)-NH2) were also examined at each of these melanocortin receptors.