MEN10207 is a peptide neurokinin-2 (NK2) receptor antagonist. It inhibits contractions induced by neurokinin A (NKA) in endothelium-deprived isolated rabbit pulmonary artery (pA2 = 7.89), which is endogenously enriched in NK2 receptors. It is selective for NK2 receptors in isolated rabbit pulmonary artery over NK2 receptors in isolated hamster trachea (pA2 = 5.9 using NKA as an agonist) and NK1 receptors in isolated guinea pig ileum (pA2 = 5.52 using substance P metl ester as an agonist), tissues that highly express these respective receptors, as well as NK3 receptors in isolated guinea pig cerebral cortex membranes (Ki = >10 μM). In vivo, MEN10207 (1 μmol/kg) inhibits increases in bladder motility induced by the NK2 receptor agonist [β-Ala8]-NKA (4-10) in anesthetized rats, as well as [β-Ala8]-NKA (4-10)-induced increases in bronchoconstriction in anesthetized guinea pigs. However, MEN10207 also induces bladder motility in anesthetized rats and bronchoconstriction in anesthetized guinea pigs when administered alone.
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Produktdokumente (Product Documents)
Purity:>98.00%Appearance:A solid
Chemische Eigenschaften (Chemical Properties)
Synonyme
Asp-Tyr-D-Trp-Val-D-Trp-D-Trp-Arg-NH2; [Tyr5,D-Trp6,8,9,Arg10]-Neurokinin A (4-10); [Tyr5,D-Trp6,8,9,Arg10]-NKA (4-10)
Chemischer Name
L-α-aspartyl-L-tyrosyl-D-tryptophyl-L-valyl-D-tryptophyl-D-tryptophyl-L-argininamide, acetate
SMILES
N=C(N)NCCC[C@@H](C(N)=O)NC([C@@H](CC1=CNC2=CC=CC=C12)NC([C@H](NC([C@H](C(C)C)NC([C@H](NC([C@@H](NC([C@@H](N)CC(O)=O)=O)CC3=CC=C(C=C3)O)=O)CC4=CNC5=CC=CC=C45)=O)=O)CC6=CNC7=CC=CC=C67)=O)=O.OC(C)=O
Summenformel
C57H68N14O10 • XC2H4O2
Molekulargewicht
1109.259
Löslichkeit
DMSO: Soluble: ≥10 mg/ml; Ethanol: Slightly soluble: 0.1-1 mg/ml
Lagerung
-20°C
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.
Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit
g/mol
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