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洛草氨酸 /Lodoxamide {[allProObj[0].p_purity_real_show]}

货号:A370864 同义名: U-42585E free acid Ambeed 开学季,买赠积分,赢豪礼

Lodoxamide is an agonist of GPR35.

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Lodoxamide 化学结构 CAS号:53882-12-5
Lodoxamide 化学结构
CAS号:53882-12-5
Lodoxamide 3D分子结构
CAS号:53882-12-5
Lodoxamide 化学结构 CAS号:53882-12-5
Lodoxamide 3D分子结构 CAS号:53882-12-5
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Lodoxamide 纯度/质量文件 产品仅供科研

货号:A370864 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 H1 receptor H2 receptor H3 receptor H4 receptor Histamine receptor 其他靶点 纯度
Hydroxyzine 2HCl {[allProObj[0].p_purity_real_show]}
Cyclizine {[allProObj[0].p_purity_real_show]}
Loratadine +

B(0)AT2, IC50: 4 μM

{[allProObj[0].p_purity_real_show]}
Desloratadine ++

Histamine H1 receptor, IC50: 51 nM

{[allProObj[0].p_purity_real_show]}
Doxylamine succinate {[allProObj[0].p_purity_real_show]}
Ebastine {[allProObj[0].p_purity_real_show]}
Tripelennamine HCl +

H1 receptor, IC50: 30 μM

{[allProObj[0].p_purity_real_show]}
Meclizine dihydrochloride {[allProObj[0].p_purity_real_show]}
Chlorpheniramine maleate +++

Histamine H1 receptor, IC50: 12 nM

{[allProObj[0].p_purity_real_show]}
Diphenhydramine HCl {[allProObj[0].p_purity_real_show]}
Alcaftadine ++++

H1 receptor, pKi: 8.5

++

H2 receptor, pKi: 7.2

{[allProObj[0].p_purity_real_show]}
Fexofenadine HCl ++

Histamine H1 receptor, IC50: 246 nM

{[allProObj[0].p_purity_real_show]}
Bilastine +++

H1 receptor, Ki: 44.15 nM

{[allProObj[0].p_purity_real_show]}
Pemirolast potassium {[allProObj[0].p_purity_real_show]}
Bepotastine besilate +

Histamine H1 receptor, pIC50: 5.7

{[allProObj[0].p_purity_real_show]}
Mizolastine +++

Histamine H1 receptor, IC50: 47 nM

{[allProObj[0].p_purity_real_show]}
Brompheniramine maleate {[allProObj[0].p_purity_real_show]}
Carbinoxamine maleate salt {[allProObj[0].p_purity_real_show]}
Clemastine fumarate ++++

Histamine H1 receptor, IC50: 3 nM

{[allProObj[0].p_purity_real_show]}
Ketotifen fumarate salt {[allProObj[0].p_purity_real_show]}
Rupatadine Fumarate ++

Histamine H1 receptor, Ki: 102 nM

PAFR {[allProObj[0].p_purity_real_show]}
Famotidine {[allProObj[0].p_purity_real_show]}
Roxatidine Acetate HCl +

Histamine H2 receptor, IC50: 3.2 μM

{[allProObj[0].p_purity_real_show]}
Lafutidine {[allProObj[0].p_purity_real_show]}
Cimetidine {[allProObj[0].p_purity_real_show]}
Nizatidine ++++

Histamine H2 receptor, IC50: 0.9 nM

AChE {[allProObj[0].p_purity_real_show]}
Ranitidine {[allProObj[0].p_purity_real_show]}
Betahistine +

Histamine H3 receptor, IC50: 1.9 μM

{[allProObj[0].p_purity_real_show]}
Ciproxifan maleate +++

Histamine H3 receptor, IC50: 9.2 nM

{[allProObj[0].p_purity_real_show]}
S 38093 ++

rat H3 receptor, Ki: 1.44 μM

human H3 receptor, Ki: 1.2 μM

{[allProObj[0].p_purity_real_show]}
JNJ-7777120 ++++

Histamine H4 receptor, Ki: 4.5 nM

{[allProObj[0].p_purity_real_show]}
Azelastine HCl {[allProObj[0].p_purity_real_show]}
Epinastine HCl {[allProObj[0].p_purity_real_show]}
Levodropropizine {[allProObj[0].p_purity_real_show]}
Cyproheptadine hydrochloride {[allProObj[0].p_purity_real_show]}
Hesperetin {[allProObj[0].p_purity_real_show]}
Olopatadine HCl {[allProObj[0].p_purity_real_show]}
Mianserin hydrochloride {[allProObj[0].p_purity_real_show]}
Buclizine 2HCl {[allProObj[0].p_purity_real_show]}
Latrepirdine 2HCl GluR {[allProObj[0].p_purity_real_show]}
Cetirizine 2HCl {[allProObj[0].p_purity_real_show]}
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Lodoxamide 生物活性

描述 Lodoxamide blocks histamine release induced by compound 48/80 and inhibits ionophore-induced 45Ca influx along with associated histamine release in purified rat peritoneal mast cells[1]. Lodoxamide significantly and dose-dependently reduces the chemotactic response of eosinophils to fMLP and IL-5. It also strongly inhibits the release of eosinophil peroxidase following IgA-dependent activation and, to a lesser extent, inhibits the release of eosinophil cationic protein and eosinophil-derived neurotoxin[2].
体内研究

Lodoxamide exhibits cromolyn-like effects in rat peritoneal mast cell assay (PCA) models and in Ascaris antigen-sensitized anesthetized rhesus monkeys. When administered intravenously, orally, or by aerosol intrabronchially, lodoxamide significantly mitigates the increased respiratory rate and reduced tidal volume triggered by antigen exposure in these monkeys[1].

Adding lodoxamide tromethamine to Euro-Collins or University of Wisconsin solution significantly reduces lung reperfusion injury, evidenced by improved oxygenation, reduced microvascular permeability, and enhanced compliance[3].

Patients receiving lodoxamide tromethamine show improvements in daytime breathing difficulties, cough, sputum production, and sleep[4].

体外研究

Lodoxamide blocks histamine release induced by compound 48/80 and inhibits ionophore-induced 45Ca influx along with associated histamine release in purified rat peritoneal mast cells[1].

Lodoxamide significantly and dose-dependently reduces the chemotactic response of eosinophils to fMLP and IL-5. It also strongly inhibits the release of eosinophil peroxidase following IgA-dependent activation and, to a lesser extent, inhibits the release of eosinophil cationic protein and eosinophil-derived neurotoxin[2].

Lodoxamide 参考文献

[1]Watt GD, et al. Protective effect opf lodoxamide tromethamine on allergen inhalation challenge. J Allergy Clin Immunol. 1980 Oct;66(4):286-94.

[2]Capron M,et al. Inhibitory effects of lodoxamide on eosinophil activation. Int Arch Allergy Immunol. 1998 Jun;116(2):140-6.

[3]Barr ML, et al. Addition of a mast cell stabilizing compound to organ preservation solutions decreases lung reperfusion injury. J Thorac Cardiovasc Surg. 1998 Mar;115(3):631-6; discussion 636-7.

[4]Mann JS, et al. Inhaled lodoxamide tromethamine in the treatment of perennial asthma: a double-blind placebo-controlled study. J Allergy Clin Immunol. 1985 Jul;76(1):83-90.

Lodoxamide 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.21mL

0.64mL

0.32mL

16.04mL

3.21mL

1.60mL

32.09mL

6.42mL

3.21mL

Lodoxamide 技术信息

CAS号53882-12-5
分子式C11H6ClN3O6
分子量 311.635
别名 U-42585E free acid
运输蓝冰
存储条件

粉末 Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 50 mg/mL(160.44 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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