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6PPD-Q (6PPD-Quinone) 是一种环境污染物,可靶向结合 CNR2、CNR1、AA2AR、LCAT 和 TRPA1,其中 CNR2 具有最高结合亲和力,可能作为 CNR2 受体激动剂,激活大麻素受体。6PPD-Q会损害小鼠精子质量并诱发雄性生殖能力的受损。6PPD-Q 可通过破坏线粒体功能,降低神经元糖酵解代谢物和 TCA 循环中间体,以及加剧 α-synuclein (α-syn) 聚集,来诱导肠道炎症和屏障损伤。
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6PPD-Q (6PPD-Quinone) 是一种环境污染物,可靶向结合 CNR2、CNR1、AA2AR、LCAT 和 TRPA1,其中 CNR2 具有最高结合亲和力,可能作为 CNR2 受体激动剂,激活大麻素受体。6PPD-Q会损害小鼠精子质量并诱发雄性生殖能力的受损。6PPD-Q 可通过破坏线粒体功能,降低神经元糖酵解代谢物和 TCA 循环中间体,以及加剧 α-synuclein (α-syn) 聚集,来诱导肠道炎症和屏障损伤。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 542 | In stock | |
5 mg | ¥ 1,290 | In stock | |
10 mg | ¥ 1,930 | In stock | |
25 mg | ¥ 3,280 | In stock | |
50 mg | ¥ 4,790 | In stock | |
100 mg | ¥ 6,820 | In stock |
6PPD-Q 相关产品
产品描述 | 6PPD-Q (6PPD-Quinone) is an environmental pollutant that can target CNR2, CNR1, AA2AR, LCAT and TRPA1. Among them, CNR2 has the highest binding affinity and may act as a CNR2 receptor agonist to activate cannabinoid receptors. 6PPD-Q can damage the sperm quality and induce the impairment of male reproductive ability in mice. 6PPD-Q can induce intestinal inflammation and barrier damage by disrupting mitochondrial function, reducing neuronal glycolytic metabolites and TCA cycle intermediates, and exacerbating α-synuclein (α-syn) aggregation. |
靶点活性 | L02 cells:22.51 µg/L, HEK293 cells (10% FBS):11.78 μM, HEK293 cells (40 g/L HSA):23.96 μM, HEK293 cells (Albumin-free):3.84 μM, ERRγ:6 nM |
体外活性 | 方法:小鼠多巴胺能神经元用6PPD-Q(10 nM、100 nM)处理48小时后检测细胞生长抑制情况。 |
体内活性 | 方法:为研究6PPD-Q对肠道损伤的影响,将6PPD-Q(0.1、 1、10、100 μg/kg)口服给 ICR 小鼠,每日一次,共 21 天。 |
别名 | 6PPD-Quinone |
分子量 | 298.38 |
分子式 | C18H22N2O2 |
CAS No. | 2754428-18-5 |
Smiles | O=C1C=C(NC(C)CC(C)C)C(=O)C=C1NC=2C=CC=CC2 |
存储 | keep away from direct sunlight,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
溶解度信息 | DMSO: 10 mg/mL (33.51 mM), Sonication and heating are recommended. ![]() H2O: < 1 mg/mL (insoluble or slightly soluble) ![]() | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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