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The peptide 2-furoyl-LIGRLO-NH2 showed higher potency and receptor selectivity for in vitro assays than other PAR-2-activating peptides. 2-Furoyl-LIGRLO-NH2 peptide was equally or more potent than SLIGRL-NH2 for increasing intracellular calcium in cultured human and rat PAR-2-expressing cells and significantly more potent than SLIGRL-NH2 in assays of tissue PAR-2 activity.
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M.W/Mr. | 778 |
Sequence | One Letter Code: 2-Furoyl-LIGRLO-NH2 Three Letter Code: 2-Furoyl-Leu-Ile-Gly-Arg-Leu-Orn-NH2 |
References | McGuire, JJ. et al. J Pharmacol Exp Ther 309, 1124 (2004). |
2. SERS spectrum of the peptide thymosin‐β4 obtained with Ag nanorod substrate
5. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function
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