
Tepoxalin
CAS No. 103475-41-8
Tepoxalin ( ORF-20485 | ORF20485 | ORF 20485 | RWJ-20485 | RWJ 20485 | RWJ20485 )
产品货号. M28562 CAS No. 103475-41-8
Tepoxalin 是一种 5-脂氧合酶抑制剂,可用于治疗哮喘、骨关节炎。替泊沙林抑制 COX-1、COX-2 和 5-LOX。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥988 | 有现货 |
![]() ![]() |
10MG | ¥1442 | 有现货 |
![]() ![]() |
25MG | ¥3345 | 有现货 |
![]() ![]() |
50MG | ¥5006 | 有现货 |
![]() ![]() |
100MG | ¥7120 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Tepoxalin
-
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
-
产品简述Tepoxalin 是一种 5-脂氧合酶抑制剂,可用于治疗哮喘、骨关节炎。替泊沙林抑制 COX-1、COX-2 和 5-LOX。
-
产品描述Tepoxalin is a 5-lipoxygenase inhibitor potentially for the treatment of asthma, osteoarthritis. Tepoxalin inhibits COX-1, COX-2, and 5-LOX. Tepoxalin is a potent inhibitor of sheep seminal vesicle cyclooxygenase (COX) (IC50 = 4.6 microM), rat basophilic leukemia cell (RBL-1) lysate COX (IC50 = 2.85 microM) and COX from intact RBL-1 cells (IC50 = 4.2 microM).(In Vitro):Tepoxalin inhibits the production of thromboxane B2 (TxB2) in Ca++ ionophore A-23187-stimulated human peripheral blood leukocytes (HPBL; IC50 = 0.01 microM) and human whole blood (IC50 = 0.08 microM) and is a potent inhibitor of epinephrine-induced human platelet aggregation (IC50 = 0.045 microM). Tepoxalin inhibits lipoxygenase (LOX) in RBL-1 lysates (IC50 = 0.15 microM) and intact RBL-1 cells (IC50 = 1.7 microM) and inhibits the generation of leukotriene B4 (LTB4) in calcium ionophore A-23187-stimulated HPBL (IC50 = 0.07 microM) and human whole blood (IC50 = 1.57 microM). Human platelet 12-LOX (IC50 = 3.0 microM) is inhibited, but 15-LOX is only weakly so (IC50 = 157 microM). (In Vivo):Tepoxalin inhibits inflammation and microvascular dysfunction induced by abdominal irradiation in rats.In vivo, tepoxalin, administered orally, demonstrated potent anti-inflammatory activity in the established adjuvant arthritic rat (ED50 = 3.5 mg/kg) and potent analgesic activity in the acetic acid abdominal construction assay in mice (ED50 = 0.45 mg/kg). In an ex vivo whole blood eicosanoid production assay, tepoxalin produces a dose-related inhibition of prostaglandin (PG) and LT production in dogs (PGF2 alpha - ED50 = 0.015 mg/kg; LTB4 - ED50 = 2.37 mg/kg) and adjuvant arthritic rats following oral administration. In adjuvant arthritic rats, tepoxalin is devoid of ulcerogenic activity within its anti-inflammatory therapeutic range (1-33 mg/kg p.o.) and does not exhibit ulcerogenic activity in normal rats at doses lower than 100 mg/kg (UD50 = 173 mg/kg p.o.).
-
体外实验——
-
体内实验——
-
同义词ORF-20485 | ORF20485 | ORF 20485 | RWJ-20485 | RWJ 20485 | RWJ20485
-
通路Immunology/Inflammation
-
靶点Lipoxygenase
-
受体GABAA
-
研究领域——
-
适应症——
化学信息
-
CAS Number103475-41-8
-
分子量385.85
-
分子式C20H20ClN3O3
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (259.17 mM)
-
SMILESCOc1ccc(cc1)-n1nc(CCC(=O)N(C)O)cc1-c1ccc(Cl)cc1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.N Zheleznova, et al. alpha1beta2delta, a silent GABAA?receptor: recruitment by tracazolate and neurosteroids. Br J Pharmacol. 2008 Mar;153(5):1062-71.
产品手册




关联产品
-
ALOX15-IN-2
ALOX15-IN-2 (compound 8a) 是一种有效的兔和人 ALOX15 亚油酸加氧酶 (linoleate oxygenase) 活性抑制剂,对 ALOX15 直系同源物亚油酸 (LA) 和花生四烯酸 (AA) 的 IC50 分别为 1.55 和 2.79 μM。
-
NNK
NNK 是一种致癌物质,也是一种主要的烟草特异性毒物。它抑制赖氨酰氧化酶的表达,赖氨酰氧化酶是一种肿瘤抑制因子。
-
ER-34122
ER-34122, a novel orally available dual 5-lipoxygenase/cyclooxygenase inhibitor, exhibits potent anti-inflammatory activity in an arachidonic acid-induced ear inflammation model.