S89199 |
BIBO3304 TFA |
源叶(MedMol) | 98% |
- 产品描述:
BIBO3304 TFA is a potent, orally active, and selective neuropeptide Y (NPY) Y1 receptor antagonist, with subnanomolar affinity for both the human and the rat Y1 receptor (IC50=0.38 and 0.72 nM, respectively)
- 靶点: Neuropeptide Y Receptor;NeuropeptideYReceptor
- 体外研究:
BIBO3304 TFA (30 μg; bilateral paraventricular nucleus injection) attenuates the hyperphagia following fasting. BIBO3304 TFA (15-60 μg) dose-dependently inhibits the feeding reponse mediated by 1 μg NPY. BIBO3304 TFA (0.5 μM; p.o.) significantly increases serum insulin levels. Animal Model: Adult male Chbb:Thom rats weighing between 300 and 340g Dosage: 30 μg Administration: bilateral paraventricular nucleus injection Result: Attenuated the hyperphagia following fasting, especially during the first 2 h of refeeding. Animal Model: 7-week-old C57BL/6JAusb mice Dosage: 0.5 μM Administration: p.o. Result: Significantly increased serum insulin levels.
- 参考文献:
1. Wieland HA, et al. Subtype selectivity of the novel nonpeptide neuropeptide Y Y1 receptor antagonist BIBO 3304 and its effect on feeding in rodents. Br J Pharmacol. 1998 Oct;125(3):549-55. 2. Loh K, et al. Inhibition of Y1 receptor signaling improves islet transplant outcome. Nat Commun. 2017 Sep 8;8(1):490.
- 溶解性: Soluble in DMSO
- 保存条件: -20℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 1.554 ml 7.768 ml 15.536 ml 5 mM 0.311 ml 1.554 ml 3.107 ml 10 mM 0.155 ml 0.777 ml 1.554 ml 50 mM 0.031 ml 0.155 ml 0.311 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)