CAS 729589-58-6
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5 produits concernés.
N-(2-Furanylcarbonyl)-L-leucyl-L-isoleucylglycyl-L-arginyl-L-leucyl-L-ornithinamide
CAS :Formule :C36H63N11O8Degré de pureté :95%Couleur et forme :SolidMasse moléculaire :777.95432-Furoyl-LIGRLO-amide
CAS :2-Furoyl-LIGRLO-amide TFA is a peptide that acts as a proteinase-activated receptor-2 (PAR2) agonist, and contains a furoyl group addition at its N-terminal.Formule :C36H63N11O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :777.952-Furoyl-LIGRLO-amide trifluoroacetate salt
CAS :Potent agonist of proteinase-activated receptor-2 (PAR2)Formule :C36H63N11O8Couleur et forme :PowderMasse moléculaire :777.96 g/mol2-Furoyl-LIGRLO-amide acetate salt
CAS :2-Furoyl-Leu-Ile-Gly-Arg-Leu-Orn-NH2 is a synthetic peptide that binds to the 5HT3 receptor. It has been shown to have an effect on locomotor activity and growth factor secretion in wild type mice and cell culture, as well as binding to acetylcholine receptors in C57/BL6 mice. 2-Furoyl-Leu-Ile-Gly-Arg-Leu-Orn was synthesized by the reaction of furoic acid with L -alanine, L -glycine, L -arginine and L -ornithine. The product is a white powder.Formule :C36H63N11O8Degré de pureté :Min. 95%Masse moléculaire :777.96 g/mol(2-Furoyl)-PAR-2 (2-6)-Orn amide (mouse, rat)
CAS :<p>2-(2-Furoyl)-PAR-2 (2-6)-Orn amide (mouse, rat) is a potent and selective PAR-2 agonist. In cultured human PAR-2-expressing cells (2-Furoyl)-LIGRLO-amide was equally effective as SLIGRL-amide, in rat PAR-2-expressing cells it was 10 to 25 times more potent than SLIGRLamide in increasing intracellular calcium levels. In bioassays of tissue PAR-2 activity, measured as arterial vasodilation and hyperpolarization this agonist was 10 to 300 times more potent than SLIGRLamide.</p>Formule :C36H63N11O8Degré de pureté :98.0%Couleur et forme :Yellowish LyophilisateMasse moléculaire :777.97
