中文名 | 2-FUROYL-LEU-ILE-GLY-ARG-LEU-ORN-NH2 |
英文名 | 2-(2-FUROYL)-LEU-ILE-GLY-ARG-LEU-ORN-NH2 |
别名 | 呋喃甲酸-亮氨酸-异亮氨酸-甘氨酸-精氨酸-亮氨酸-鸟氨酸-NH2 N-(2-呋喃基羰基)-L-亮氨酰-L-异亮氨酰甘氨酰-L-精氨酰基-L-亮氨酰-L-鸟氨酸酰胺 |
英文别名 | 2F-LIGRLO-AMIDE PAR-2 AGONIST II 2-FUROYL-LIGRLO-AMIDE 2-(2-FUROYL)-LIGRLOAMIDE 2-FUROYL-LEU-ILE-GLY-ARG-LEU-ORN-NH2 2-(2-FUROYL)-LEU-ILE-GLY-ARG-LEU-ORN-NH2 PROTEINASE ACTIVATED RECEPTOR-2 AGONIST II 2-(2-FUROYL)-PAR-2 (2-6)-ORN AMIDE (MOUSE, RAT) |
CAS | 729589-58-6 |
化学式 | C36H63N11O8 |
分子量 | 777.95 |
存储条件 | -20°C |
外观 | 粉末 |
颜色 | white |
体外研究 | 2-Furoyl-LIGRLO-amide (2-Furoyl-LIGRLO-NH 2 ) is equally effective to and 10 to 25 times more potent than SLIGRLNH 2 for increasing intracellular calcium in cultured human and rat PAR2-expressing cells, respectively. In bioassays of tissue PAR2 activity, measured as arterial vasodilation and hyperpolarization, 2-Furoyl-LIGRLO-amide (2-Furoyl-LIGRLO-NH 2 ) is 10 to 300 times more potent than SLIGRL-NH 2 . Unlike trans-cinnamoyl-LIGRLO-NH 2 , 2-Furoyl-LIGRLO-amide do not cause a prominent non-PAR2-mediated contraction of murine femoral arteries. |
体内研究 | Furoyl-LIGRLO-amide (injected intradermally at the nape of the neck; 10 μg; pre-injected) exhibits fewer scratches in response to 2-Furoyl-LIGRLO-amide but not to histamine in Trpv3 -/- mice. But it decreases significantly the number of scratches in WT mice. Animal Model: Adult male (2/3-month-old) Trpv3 -/- and WT mice Dosage: 10 μg Administration: Injected intradermally at the nape of the neck Result: Was involved in PAR2- induced acute itch. |
危险品标志 | Xi - 刺激性物品![]() |
风险术语 | 36/37/38 - 刺激眼睛、呼吸系统和皮肤。 |
安全术语 | 26 - 不慎与眼睛接触后,请立即用大量清水冲洗并征求医生意见。 |
WGK Germany | 3 |
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