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- CAS号:
22071-15-4
- 规格:
1mLx10mM(inDMSO)/1g/5g/500mg
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥306.0 |
|---|---|---|---|
| 规格: | 1g | 产品价格: | ¥334.0 |
| 规格: | 5g | 产品价格: | ¥536.0 |
| 规格: | 500mg | 产品价格: | ¥282.0 |
Product Introduction
Bioactivity
| 名称 | Ketoprofen |
| 描述 | Ketoprofen (RP-19583) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic and antipyretic effects. Ketoprofen inhibits the activity of the enzymes cyclo-oxygenase I and II, resulting in a decreased formation of precursors of prostaglandins and thromboxanes. The resulting decrease in prostaglandin synthesis, by prostaglandin synthase, is responsible for the therapeutic effects of ibuprofen. Ketoprofen also causes a decrease in the formation of thromboxane A2 synthesis, by thromboxane synthase, thereby inhibiting platelet aggregation. |
| 体外活性 | Ketoprofen联合UVB照射在浓度依赖的方式内对HaCaT细胞产生细胞毒性作用并抑制DNA合成,抑制细胞增长。Ketoprofen通过调节cdc2、cyclin B1、Chk1、Tyr15磷酸化的cdc2和p21的水平,诱导G2/M细胞周期阻滞。Ketoprofen和UVB的联合照射还促使cyclin B1-cdc2-p21复合物显著积累,同时伴随着Tyr15磷酸化cdc2和p21蛋白水平的升高。Ketoprofen联合UVB照射,通过DAPI染色增强HaCaT细胞对UVB辐射的凋亡反应。[1] |
| 体内活性 | Ketoprofen以1%浓度于适宜的局部应用载体中,可有效抑制猕猴牙周炎模型中的GCF-LTB4与GCF-PGE2,改变齿槽骨活性。[2] Ketoprofen(3.63 mg/kg )在减轻蹄痛和跛行方面,效果超过2.2 mg/kg Ketoprofen和phenylbutazone。[3] Ketoprofen比局部麻醉(LA)或尾部硬膜外麻醉(EPI)更能有效降低皮质酮水平,并部分逆转去势后平均日增重(ADG)的下降。[4] Ketoprofen以40和80 mg/kg饮食剂量,可将饮食小鼠的尿路移行细胞癌发生率降低70%以上。[5] |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | Ethanol : 48 mg/mL (188.77 mM), Sonication is recommended. 10% DMSO+90% Saline : < 10 mg/mL (39.33 mM), Lower concentrations may be soluble, but exact solubility limit is unknown. DMSO : 250 mg/mL (983.17 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 10 mg/mL (39.33 mM), Solution. |
| 关键字 | white adipocytes | RP19583 | RP 19583 | obesity | MRAP4 | Ketoprofen | Inhibitor | inhibit | HFD-induced obese mice | Cyclooxygenase | COX-2 | COX-1 | COX inhibitor | COX | Apoptosis | Anti-inflammatory agents | 3T3-L1 cell |
| 相关产品 | Trometamol | Formamide | Urea | Dimethyl phthalate | Aceglutamide | Alginic acid | Cysteamine hydrochloride | Metronidazole | Sildenafil citrate | Citric Acid Triammonium | Stavudine | Tamoxifen |
| 相关库 | Inhibitor Library | Bioactive Compound Library | Anti-Cancer Approved Drug Library | Bioactive Compounds Library Max | Anti-Aging Compound Library | Anti-Neurodegenerative Disease Compound Library | Membrane Protein-targeted Compound Library | Immunology/Inflammation Compound Library | Drug Repurposing Compound Library | Pain-Related Compound Library | Anti-Cancer Clinical Compound Library | Anti-Cancer Drug Library |
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停药。 本类药物中的萘普生(naproxen)及酮洛芬(ketoprofen)的作用及用途均相似,但t 1/2 分别为12~15小时和2小时。 吡罗昔康 吡罗昔康(piroxicam,炎痛喜康)属苯噻嗪类。口服吸收完全,2~4小时血药浓度达峰值。在体外抑制PG合成酶的效力与吲哚美辛相等。对风湿性及类风湿性关节炎的疗效与乙酰水杨酸、吲哚美辛及萘普生相同而不良反应少,患者耐受良好。其主要优点是血浆t
水杨酸,但主要特点是胃肠反应较轻,易耐受。 不良反应有轻度消化不良、皮疹;胃肠出血不常见,但长期服用者仍应注意;偶见视力模糊及中毒性弱视,出现视力障碍者应立即停药。 本类药物中的萘普生(naproxen)及酮洛芬(ketoprofen)的作用及用途均相似,但t 1/2 分别为12~15小时和2小时。 吡罗昔康 吡罗昔康(piroxicam,炎痛喜康)属苯
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酮洛芬【22071-15-4】
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