
Progabide
CAS No. 62666-20-0
Progabide ( SL 76002 | Halogabide | Gabren | Gabrene )
产品货号. M26795 CAS No. 62666-20-0
Progabide 是 γ-氨基丁酸受体的激动剂。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥381 | 有现货 |
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10MG | ¥648 | 有现货 |
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25MG | ¥1320 | 有现货 |
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50MG | ¥2130 | 有现货 |
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100MG | ¥3345 | 有现货 |
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200MG | ¥4779 | 有现货 |
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500MG | ¥7638 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Progabide
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Progabide 是 γ-氨基丁酸受体的激动剂。
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产品描述Progabide is an agonist of the gamma-aminobutyric acid receptor.(In Vivo):Progabide ( 50, 100 and 200 mg/kg) given IP to male Wistar rats enhance the plasma corticosterone levels by 244, 365, and 476% respectively (t=6.44 to12.55, p<0.01). Progabide (10 mg/kg) fails to change the concentration of corticosterone in plasma (t=0.76, N.S.). The increased plasma corticosterone level induced by administration of 200 mg/kg Progabide is evident 30 (t=2.625, p<0.05), 60 (t=13.13, p<0.001) and 120 min (t=4.07, p<0.01) after drug injection, but returns to the control value 240 min after drug injection (t=0.86, N.S.). Compare with the corresponding control, The greatest corticosterone rise is reached 60 min following the administration of Progabide.
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体外实验——
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体内实验Progabide is a gamma-aminobutyric acid receptor (GABA) agonist. Doses of 50, 100 and 200 mg/kg Progabide given IP to male Wistar rats increase the plasma corticosterone levels by 244, 365 and 476% respectively (t=6.44 to12.55, p<0.01). 10 mg/kg of Progabide fails to change the concentration of corticosterone in plasma (t=0.76, N.S.). The increased plasma corticosterone level induced by administration of 200 mg/kg Progabide is evident 30 (t=2.625, p<0.05), 60 (t=13.13, p<0.001) and 120 min (t=4.07, p<0.01) after drug injection, but returns to the control value 240 min after drug injection (t=0.86, N.S.). The greatest corticosterone rise (compare with the corresponding control) is reached 60 min following the administration of Progabide.
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同义词SL 76002 | Halogabide | Gabren | Gabrene
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通路Others
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靶点Other Targets
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受体Kv2.2
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研究领域——
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适应症——
化学信息
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CAS Number62666-20-0
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分子量334.78
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分子式C17H16ClFN2O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 250 mg/mL (746.78 mM)
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SMILESNC(=O)CCC\N=C(\c1ccc(Cl)cc1)c1cc(F)ccc1O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Herrington J, et al. Identification of novel and selective Kv2 channel inhibitors. Mol Pharmacol. 2011 Dec;80(6):959-64.
产品手册




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