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BIBO3304 TFA

    
98.20%

BIBO3304 TFA

源叶(MedMol)
S89199 一键复制产品信息
191868-14-1
C31H36F3N7O5
643.66
BIBO-3304; BIBO 3304; BIBO3304; BIBO-3304 TFA; (R)-2-(2,2-diphenylacetamido)-5-guanidino-N-(4-(ureidomethyl)benzyl)pentanamide bis(2,2,2-trifluoroacetate)
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89199-5mg买3赠1
98.20%

¥1000.00

3 - - - -
S89199-10mg买3赠1
98.20%

¥1500.00

4 - - - -
S89199-25mg买3赠1
98.20%

¥2800.00

5 - - - -
S89199-100mg
≥98%

¥6150.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
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
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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