| CAS: | 146362-70-1 | |
| 分子式: | C32H31ClN4O5 | |
| 分子量: | 587.07 | |
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||
| S921333 | MACKLIN | SR 48692 | ≥98% (HPLC) | 426元/1mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||
储存:-20°C | |||||||||||||||||||||||||||||||||||||||||||
| SML0278 | Sigma-Aldrich | SR 48692 | ≥98% (HPLC) | 1567.12元/5 MG; 6335.57元/25 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||
产品说明 应用 SR 48692 has been used as a neurotensin high-affinity receptor 1 (NTSR1) antagonist:
包装 5, 25 mg in glass bottle 生化/生理作用 SR 48692 is a high affinity, orally bioavailable and selective nonpeptide NT1 neurotensin receptor antagonist that antagonizes neurotensin-induced calcium mobilization with a pA2 of 8.13 in HT-29 human colon carcinoma cell line, and blocks the ability of neurotensin to increase GABA levels in the prefrontal cortex. 特点和优势 This compound is featured on the Neurotensin Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here. 基本信息
产品性质
安全信息
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