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(S)-(+)-Ibuprofen

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纯度: 99.86%

货号 T0448Cas号 51146-56-6

别名 Dexibuprofen, (S)-Ibuprofen, (S)-(+)-布洛芬

(S)-(+)-Ibuprofen (Dexibuprofen) 是 Ibuprofen 的 S(+)-对映异构体,能够有效的抑制COX-1(IC50:2.1 μM)和COX-2(IC50:1.6 μM),。它具有抗癌、退热、止痛,抗炎的效果。

(S)-(+)-Ibuprofen

(S)-(+)-Ibuprofen

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Rating icon 很棒

纯度: 99.86%

货号 T0448 别名 Dexibuprofen, (S)-Ibuprofen, (S)-(+)-布洛芬Cas号 51146-56-6

(S)-(+)-Ibuprofen (Dexibuprofen) 是 Ibuprofen 的 S(+)-对映异构体,能够有效的抑制COX-1(IC50:2.1 μM)和COX-2(IC50:1.6 μM),。它具有抗癌、退热、止痛,抗炎的效果。

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1 g
¥ 123
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2 g
¥ 152
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5 g
¥ 198
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10 g
¥ 297
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纯度: 99.86%
颜色: 白色
性状: Solid
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产品介绍


(S)-(+)-Ibuprofen AI Summary
(S)-(+)-Ibuprofen exhibits diverse bioactivities, including anti-inflammatory, antiviral, and enzyme inhibitory properties. It demonstrates significant anti-inflammatory activity, as evidenced by its effective dose (ED50) of 7.08 mg/kg in a rat hind paw edema model and notable selectivity toward cyclooxygenase II (COX-2) over cyclooxygenase I (COX-1) with a selectivity ratio of 117.5. The compound inhibits pro-inflammatory enzymes such as COX-1 (IC50 of 105.0 nM) and COX-2 (IC50 of 1,500.0 nM), and shows a selectivity index of 1.83 for COX-2 over COX-1. In addition to its anti-inflammatory effects, (S)-(+)-Ibuprofen inhibits CXCL8-induced chemotaxis of human polymorphonuclear cells (IC50 100.0 nM) and lipopolysaccharide-induced PGE-2 production (>99% at 10µM). In terms of enzyme inhibition, (S)-(+)-Ibuprofen affects acetylcholine esterase, various aldo-keto reductases (AKRs), and ASIC channels. It inhibits Fischer 344 rat brain acetylcholine esterase (20% inhibition at 0.6 mM) and AKR1C2, AKR1C3 with IC50 values of 42400.0 nM and 32700.0 nM respectively, while showing moderate activity against ASIC3 and ASIC1a receptors. The compound also demonstrates antiviral activities, including modest inhibition of SARS-CoV-2 in Vero E6 and Caco-2 cell assays. It exhibits an inhibition percentage of 9.369% on the SARS-CoV-2 3CL-Pro protease at a concentration of 20µM. Pharmacokinetic properties of (S)-(+)-Ibuprofen show an oral bioavailability of 80% in humans and good plasma concentration (96% at 30 µg/mL). It has acceptable lipid solubility with a LogD of 1.07 at pH 7.4 and a dissociation constant (pKa) of 5.2. Overall, (S)-(+)-Ibuprofen's profile suggests potential applications in therapeutic areas requiring anti-inflammatory, antiviral, and enzyme inhibitory actions..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
(S)-(+)-Ibuprofen (Dexibuprofen) , is a non-steroidal anti-inflammatory drug (NSAID), inhibiting cyclooxygenase (COX).
靶点活性
COX-2:370 μM, COX-1:13 μM
别名Dexibuprofen, (S)-Ibuprofen, (S)-(+)-布洛芬
化学信息
分子量206.28
分子式C13H18O2
CAS No.51146-56-6
SmilesCC(C)CC1=CC=C(C=C1)[C@H](C)C(O)=O
密度1.029 g/cm3
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 25 mg/mL (121.19 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (9.7 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM4.8478 mL24.2389 mL48.4778 mL242.3890 mL
5 mM0.9696 mL4.8478 mL9.6956 mL48.4778 mL
10 mM0.4848 mL2.4239 mL4.8478 mL24.2389 mL
20 mM0.2424 mL1.2119 mL2.4239 mL12.1194 mL
50 mM0.0970 mL0.4848 mL0.9696 mL4.8478 mL
100 mM0.0485 mL0.2424 mL0.4848 mL2.4239 mL

计算器

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  • 配液 计算器
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体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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