Lodoxamide tromethamine
CAS No. 63610-09-3
Lodoxamide tromethamine ( U-42585E )
产品货号. M26741 CAS No. 63610-09-3
Lodoxamide Tromethamine 是一种具有抗过敏特性的肥大细胞稳定剂,可用于治疗哮喘和过敏性结膜炎的研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥468 | 有现货 |
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| 10MG | ¥710 | 有现货 |
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| 25MG | ¥1135 | 有现货 |
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| 50MG | ¥1609 | 有现货 |
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| 100MG | ¥2241 | 有现货 |
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| 200MG | ¥3312 | 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 | ¥563 | 有现货 |
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生物学信息
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产品名称Lodoxamide tromethamine
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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Lodoxamide Tromethamine 是一种具有抗过敏特性的肥大细胞稳定剂,可用于治疗哮喘和过敏性结膜炎的研究。
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产品描述Lodoxamide tromethamine is a mast cell stabilizer with anti-allergic properties and can be used in studies about the treatment of asthma and allergic conjunctivitis.(In Vitro):In purified rat peritoneal mast cells, Lodoxamide tromethamine inhibits ionophore-induced 45Ca influx with associated histamine release. Lodoxamide tromethamine significantly and dose-dependently inhibits the chemotactic response of eosinophils to fMLP and to IL-5. Lodoxamide tromethamine strongly inhibits the release of eosinophil peroxidase after IgA-dependent activation and inhibits the release of eosinophil cationic protein and eosinophil-derived neurotoxin to a lesser extent.(In Vivo):In Ascaris-sensitized anesthetized rhesus monkeys, Lodoxamide tromethamine significantly inhibits the increased respiratory frequency and decreased tidal volume induced by antigen challenge. The addition of Lodoxamide tromethamine to Euro-Collins or University of Wisconsin solution increases oxygenation, decreases microvascular permeability, and increases compliance thereby decreasing lung reperfusion injury.
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体外实验lodoxamide inhibits compound 48/80-induced histamine release and ionophore-induced 45Ca influx with associated histamine release in purified rat peritoneal mast cells.
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体内实验Lodoxamide has been demonstrated to have cromolyn-like activity when studied in the rat peritoneal mast cell assay (PCA) model3 and in Ascaris antigen-sensitized rhesus monkeys. When given intravenously, orally, or intrabronchially by aerosol, lodoxamide significantly inhibits the increased respiratory frequency and decreased tidal volume induced by antigen challenge in Ascaris-sensitized. anesthetized rhesus monkeys. Addition of lodoxamide tromethamine to Euro-Collins or University of Wisconsin solution results in a marked decrease in lung reperfusion injury as demonstrated by increased oxygenation, decreased microvascular permeability, and increased compliance. Patients treated with lodoxamide tromethamine demonstrate an improvement in daytime breathing difficulty, cough, sputum production, and sleep.
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同义词U-42585E
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通路GPCR/G Protein
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靶点Histamine Receptor
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受体ETV1
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研究领域——
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适应症——
化学信息
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CAS Number63610-09-3
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分子量553.91
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分子式C19H28ClN5O12
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O : ≥ 100 mg/mL (180.54 mM))
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SMILESNC(CO)(CO)CO.NC(CO)(CO)CO.OC(=O)C(=O)Nc1cc(cc(NC(=O)C(O)=O)c1Cl)C#N
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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.Kollareddy M, et al. The small molecule inhibitor YK-4-279 disrupts mitotic progression of neuroblastoma cells, overcomes drug resistance and synergizes with inhibitors of mitosis. Cancer Lett. 2017 Sep 10;403:74-85.
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