SB 216641 hydrochloride
CAS No. 193611-67-5
SB 216641 hydrochloride ( —— )
产品货号. M33924 CAS No. 193611-67-5
SB-216641A (SB-216641 hydrochloride) 是一种选择性的 5-HT1B/D 受体拮抗剂。SB-216641A 对 h5-HT1B 受体比 h5-HT1D 受体具有高亲和力和选择性。SB-216641A 阻碍 SKF-99101H 在体内的功能。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1501 | 有现货 |
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| 10MG | ¥2233 | 有现货 |
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| 25MG | ¥3608 | 有现货 |
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| 50MG | ¥5180 | 有现货 |
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| 100MG | ¥6804 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称SB 216641 hydrochloride
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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SB-216641A (SB-216641 hydrochloride) 是一种选择性的 5-HT1B/D 受体拮抗剂。SB-216641A 对 h5-HT1B 受体比 h5-HT1D 受体具有高亲和力和选择性。SB-216641A 阻碍 SKF-99101H 在体内的功能。
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产品描述SB-216641A (SB-216641 hydrochloride) is a selective antagonist of 5-HT1B/D receptor. SB-216641A shows high affinity and selectivity for h5-HT1B receptors over h5-HT1D receptors. SB-216641A inhibits the function of SKF-99101H.
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体外实验——
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体内实验Animal Model:Guinea pigs.Dosage:0.6, 2.0, 6.0 and 20.0 mg/kg.Administration:Intraperitoneal injection; single dose.Result:Significantly blocked the effects of SKF-99101H.Animal Model:Dogs.Dosage:559 nmol/kg. Administration:Intravenous injection; single dose.Result:Improved the gastric relaxation.
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同义词——
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通路GPCR/G Protein
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靶点5-HT Receptor
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受体5-HT Receptor
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研究领域——
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适应症——
化学信息
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CAS Number193611-67-5
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分子量523.02
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分子式C28H31ClN4O4
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纯度>98% (HPLC)
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溶解度——
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SMILESCl.O=C(NC1=CC=C(OC)C(OCCN(C)C)=C1)C=2C=CC(=CC2)C=3C=CC(=CC3C)C4=NOC(=N4)C
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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
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Lecozotan HCl
Lecozotan HCl (SRA-333) is a potent and selective 5-HT antagonist that significantly enhances KCl-stimulated glutamate and acetylcholine release from the hippocampal dentate gyrus and has cognitive enhancing properties. Chronic administration of Lecozotan HCl did not induce 5-HT(1A) receptor tolerance or desensitization in a behavioral model demonstrating 5-HT(1A) receptor function.
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Seganserin
Seganserin, a non-selective 5-hydroxytryptamine 2-HT receptor antagonist, reversed the inhibitory effects of fluoxetine and quipazine on luteinizing hormone-induced hyperphagia, depression and nociception, and reversed the antidepressant and analgesic effects induced by fluoxetine and quipazine.
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ML 10302 hydrochlori...
ML 10302 hydrochloride 是一种高效、选择性的 5-HT4 受体 (5-HT4 receptor) 激动剂,其 EC50 值为 4 nM。ML 10302 hydrochloride 对 5-HT4 的选择性结合作用比 5-HT3 至少高出 680 倍。
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