| CAS: | 686347-12-6 | |||||
| 分子式: | C25H25Cl2N7O · HCl | |||||
| 分子量: | 546.88 | |||||
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||
| C794834 | MACKLIN | CP-945598 HCl | 2mM in DMSO | 390元/1ml; | 展开 | ||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||
| C864593 | MACKLIN | CP-945598 HCl | ≥98% | 768元/10mg; | 展开 | ||||||||||||||||||||||||||||||
储存:室温 状态:固体 | |||||||||||||||||||||||||||||||||||
| PZ0019 | Sigma-Aldrich | CP-945,598 | ≥98% (HPLC) | 1116.07元/5 MG; 4498.97元/25 MG; | 展开 | ||||||||||||||||||||||||||||||
产品说明 生化/生理作用 CP-945,598 is a potent, selective, high affinity and competitive cannabinoid type 1 (CB1) receptor antagonist. CP-945,598 inhibits both basal and cannabinoid agonist-mediated CB1 receptor signaling in vitro and in vivo. CP-945,598 exhibits anorectic activity in two models of acute food intake in rodents, fast-induced re-feeding and spontaneous, nocturnal feeding. 特点和优势 This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm. 其他说明 This compound was developed by Pfizer for Neuroscience research. To learn more about Sigma′s partnership with Pfizer and view other authentic, high-quality Pfizer compounds, visit sigma.com/bsm-pfizer. 法律信息 Sold for research purposes under agreement from Pfizer Inc. 基本信息
产品性质
安全信息
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