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其他生物化学试剂

安吡昔康 T6387

英文名称:Ampiroxicam
品牌 厂商性质 产地 货期
TargetMol 生产商 美国 现货

性能特点

生化试剂,可用于动物细胞实验

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产品参数
规格 CAS号 价格 操作
200 mg 99464-64-9 ¥2,790.00 询底价
10 mg 99464-64-9 ¥467.00 询底价
1 mL 99464-64-9 ¥483.00 询底价
100 mg 99464-64-9 ¥1,880.00 询底价
5 mg 99464-64-9 ¥259.00 询底价
50 mg 99464-64-9 ¥1,210.00 询底价
25 mg 99464-64-9 ¥828.00 询底价
产品介绍

Product Introduction
Bioactivity


英文名: Ampiroxicam

描述: Ampiroxicam (Flucam) 是一种非选择性的环氧化酶抑制剂,有抗炎活性。

细胞实验: Panc-1 cells are plated in DME/F12 medium with 5% fetal bovine serum and treated on the next day with vehicle (0.1% DMSO) or various concentrations of Ampiroxicam. Cells are counted at the indicated times with a Coulter Z1 cell counter. Each experiment is done in triplicate, and results are expressed as means, with error bars representing 95% confidence intervals (CIs).(Only for Reference)

体外活性: Ampiroxicam (<150 μM) dose-dependently decreases the proliferation of Panc-1 cells. [1] Ampiroxicam (50 μM) results in decreased expression of Sp1, Sp3, Sp4, and VEGFR1 proteins in Panc-1 cells and L3.6pl cells as determined by Western blot analysis. Ampiroxicam (50 μM) results in increased phosphorylation of MAPK1/2 in Panc-1 cells and L3.6pl cells. [2]

体内活性: Ampiroxicam inhibits the stretching response in mice induced by phenylbenzoquinone (PBQ) with maximum protective effect (MPE) of 2 mg/kg. Ampiroxicam inhibits swelling in a dose-responsive manner in the rat foot edema (RFE) assay with ED50 of 28 mg/kg at single oral dose and 7.8 mg/kg at 5 daily oral dose. Ampiroxicam blocks primary and secondary lesion development in rat adjuvant arthritis with ED50 of 2.2 mg/kg and 0.5 mg/kg, respectively. Ampiroxicam (3.2 mg/kg) leads to a plasma concentration of 12 μg/mL at a Tmax of 2 hours for piroxicam derived from ampiroxicam in rats. [3] Ultraviolet-A (UVA)-irradiated 1% Ampiroxicam sensitized in guinea pigs shows positive reaction in the patch testing to UVA-irradiated 1% Ampiroxicam and 1% thiosalicylate (TOS). Concentration of Ampiroxicam is easily reduced by the increase in UVA irradiation doses, as compared with that of piroxicam. [4]

存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度: Ethanol : < 1 mg/mL (insoluble or slightly soluble)
H2O : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 83 mg/mL (185.5 mM)


关键字: COX | inhibit | CP65703 | Cyclooxygenase | Ampiroxicam | Inhibitor | CP-65703

相关产品: Sulfasalazine | Timegadine | Tolmetin | Desmethyl Celecoxib | (-)-Catechin gallate | SC-560 | Quercimeritrin | Indomethacin heptyl ester | Sulindac sulfone | FR 122047

相关库: Drug Repurposing Compound Library | ReFRAME Related Library | Anti-Cancer Compound Library | FDA-Approved & Pharmacopeia Drug Library | Anti-Cancer Drug Library | Neuronal Signaling Compound Library | Inhibitor Library | Anti-Cancer Approved Drug Library | Anti-Fibrosis Compound Library | NO PAINS Compound Library

安吡昔康 T6387信息由TargetMol中国为您提供,如您想了解更多关于安吡昔康 T6387报价、型号、参数等信息,欢迎来电或留言咨询。

注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途

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