Oxatomide
CAS No. 60607-34-3
Oxatomide ( —— )
产品货号. M33637 CAS No. 60607-34-3
Oxatomide 是一种有效的具有口服活性的双重 H1 组胺受体 (H1-histamine receptor) 和 P2X7 受体拮抗剂,具有抗组胺和抗过敏活性。Oxatomide 几乎完全阻断人 P2X7 受体中 ATP 诱导的电流 (IC50 为 0.95 μM)。Oxatomide 可抑制 ATP 诱导的 Ca2+ 内流,IC50 值为 0.43 μM,并且还抑制 5-羟色胺 (serotonin)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥708 | 有现货 |
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| 10MG | ¥1169 | 有现货 |
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| 25MG | ¥2306 | 有现货 |
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| 50MG | ¥3692 | 有现货 |
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| 100MG | ¥5211 | 有现货 |
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| 200MG | ¥7038 | 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 |
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| 1 mL x 10 mM in DMSO | ¥777 | 有现货 |
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生物学信息
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产品名称Oxatomide
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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Oxatomide 是一种有效的具有口服活性的双重 H1 组胺受体 (H1-histamine receptor) 和 P2X7 受体拮抗剂,具有抗组胺和抗过敏活性。Oxatomide 几乎完全阻断人 P2X7 受体中 ATP 诱导的电流 (IC50 为 0.95 μM)。Oxatomide 可抑制 ATP 诱导的 Ca2+ 内流,IC50 值为 0.43 μM,并且还抑制 5-羟色胺 (serotonin)。
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产品描述Oxatomide is a potent and orally active dual H1-histamine receptor and P2X7 receptor antagonist with antihistamine and anti-allergic activity. Oxatomide almost completely blocks the ATP-induced current in human P2X7 receptors (IC50 of 0.95 μM). Oxatomide inhibits ATP-induced Ca2+ influx with an IC50 value of 0.43 μM and also inhibits serotonin.
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体外实验——
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体内实验——
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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 | Calcium Channel | P2X Receptor | Histamine 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 Number60607-34-3
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分子量426.55
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分子式C27H30N4O
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 250 mg/mL (586.10 mM; 超声助溶 )
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SMILESO=C1NC2=C(C=CC=C2)N1CCCN1CCN(CC1)C(C1=CC=CC=C1)C1=CC=CC=C1
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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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DA-6886
DA-6886 is an agonist 5-Hydroxytryptamine receptor 4 (5-HT4). DA-6886 induced relaxation of the rat oesophagus preparation in a 5-HT4 receptor antagonist-sensitive manner. The evaluation of DA-6886 in CHO cells expressing hERG channels revealed that it inhibited hERG channel current with an pIC50 value of 4.3, indicating that the compound was 1000-fold more selective for the 5-HT4 receptor over hERG channels.
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NAN-190 hydrobromide
NAN-190 是一种 5-HT1A 受体拮抗剂,Ki 为 0.6 nM;还有效阻断 α2-肾上腺素能受体。
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