N-[2-[[(六氢-2-氧代-1H-氮杂卓-3-基)氨基]羰基]苯基]苯并[b]噻吩-2-甲酰胺结构式
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常用名 | N-[2-[[(六氢-2-氧代-1H-氮杂卓-3-基)氨基]羰基]苯基]苯并[b]噻吩-2-甲酰胺 | 英文名 | ANA-12 |
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CAS号 | 219766-25-3 | 分子量 | 407.48500 | |
密度 | N/A | 沸点 | N/A | |
分子式 | C22H21N3O3S | 熔点 | N/A | |
MSDS | 中文版 美版 | 闪点 | N/A | |
符号 |
GHS07 |
信号词 | Warning |
用途ANA-12是有效,选择性的 TrkB 拮抗剂,对高亲和力和低亲和力位点的IC50 分别为45.6 nM和41.1 μM。 |
中文名 | N-[2-[[(六氢-2-氧代-1H-氮杂卓-3-基)氨基]羰基]苯基]苯并[b]噻吩-2-甲酰胺 |
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英文名 | N-{2-[(2-Oxo-3-azepanyl)carbamoyl]phenyl}-1-benzothiophene-2-carb oxamide |
英文别名 | 更多 |
描述 | ANA-12是有效,选择性的 TrkB 拮抗剂,对高亲和力和低亲和力位点的IC50 分别为45.6 nM和41.1 μM。 |
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相关类别 | |
体外研究 | ANA-12(10 nM)可阻止BDNF诱导的TrkB表达细胞中神经突向外生长,并在浓度高达10-100μM时完全消除BDNF的作用[1]。 |
体内研究 | ANA-12(0.5mg/kg,ip)部分抑制小鼠全脑中的内源性TrkB活性。注射到小鼠体内的ANA-12表现出0.5mg/kg的抗焦虑和抗抑郁活性。 ANA-12(0.5,1.0和2.0 mg/kg)不影响神经元存活[1]。 ANA-12(0.5mg/kg)在脂多糖(LPS)诱导的抑郁样行为中显示出抗抑郁作用。 ANA-12(0.5mg/kg)显着减弱抑郁小鼠的不动时间增加。在TST,FST和SPT中,ANA-12(0.5mg/kg)在对照小鼠中不显示抗抑郁样作用[2]。 ANA-12(0.5 mg/kg,ip)可逆转CocSired大鼠中可卡因自我给药的减少[3]。 |
动物实验 | 在注射当天,氯胺酮(氯胺酮盐酸盐,10 mg / kg),7,8-二羟基黄酮(7,8-DHF; 10 mg / kg)和ANA-12,N2-(2 - {[(2-在磷酸盐缓冲盐水中的17%二甲基亚砜(DMSO)载体中制备氧代氮杂环庚烷-3-基)氨基]羰基}苯基)苯并[b]噻吩-2-甲酰胺(0.5mg / kg)。选择氯胺酮(10mg / kg),7,8-DHF(10mg / kg)和ANA-12(0.5mg / kg)的剂量。将所有化合物腹膜内(ip)给予小鼠。 |
参考文献 |
分子式 | C22H21N3O3S |
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分子量 | 407.48500 |
精确质量 | 407.13000 |
PSA | 126.01000 |
LogP | 4.78680 |
外观性状 | white to beige |
储存条件 | 2-8°C |
水溶解性 | DMSO: ≥5mg/mL at 60°C |
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ANA-12 |