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CAS RN: 15687-27-1 | 產(chǎn)品編碼: I0415
Ibuprofen
純度/分析方法: >98.0%(GC)(T)
別名:
- 布洛芬
- 2-(4-異丁基苯基)丙酸
- 4-異丁基-α-甲基苯乙酸
- 2-(4-Isobutylphenyl)propionic Acid
- 4-Isobutyl-α-methylphenylacetic Acid
產(chǎn)品文檔:
規(guī)格 | 單價 | 上海 | 天津 | 日本* | 數(shù)量 | 庫存詳情 |
---|---|---|---|---|---|---|
1G |
¥80.00
|
一個工作日后發(fā)貨 | 一個工作日后從上海發(fā)貨 | 請聯(lián)系我們 |
|
|
5G |
¥160.00
|
8 | 17 | 請聯(lián)系我們 |
|
|
25G |
¥260.00
|
18 | 3 | ≥100 |
|
|
100G |
¥460.00
|
9 | 1 | 15 |
|
|
500G |
¥1,890.00
|
2 | 1 | 28 |
|
* 點(diǎn)擊“查詢”可查看預(yù)計(jì)發(fā)貨日期,僅供參考。
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* 更多信息,請聯(lián)系營業(yè)部:021-67121386 / Sales-CN@TCIchemicals.com 。任何貨期、規(guī)格或包裝方面的需求,請聯(lián)系我們 。
* 無具體發(fā)貨日期的情況,如:顯示“8個工作日后發(fā)貨”,將在您訂購日起的8個工作日后發(fā)貨。
* 我們將以最優(yōu)方式從上海/天津兩大倉庫發(fā)貨。國內(nèi)庫存不足,需兩周左右向日本總部調(diào)貨。
* 對于可分裝產(chǎn)品,11:30前的訂單,當(dāng)天發(fā)貨;11:30后的訂單,隔天發(fā)貨。
* 如需大包裝,請點(diǎn)擊“大包裝詢價”按鈕(對于某些產(chǎn)品我們無法提供大包裝)。
* TCI會經(jīng)常復(fù)審儲藏條件以對其進(jìn)行優(yōu)化,請以在線目錄為準(zhǔn),敬請留意。
* 更多信息,請聯(lián)系營業(yè)部:021-67121386 / Sales-CN@TCIchemicals.com 。任何貨期、規(guī)格或包裝方面的需求,請聯(lián)系我們 。
技術(shù)規(guī)格
Appearance | White to Almost white powder to crystal |
Purity(GC) | min. 98.0 % |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 75.0 to 78.0 °C |
Solubility in Methanol | almost transparency |
物性(參考值)
熔點(diǎn) | 76 °C |
沸點(diǎn) | 157 °C/4 mmHg |
水溶性 | 不溶 |
在水中的溶解度 | 21 mg/l 25 °C |
GHS
象形圖 | |
信號詞 | 警告 |
危險性說明 | H302 : 吞咽有害。 H361 : 懷疑對生育能力或胎兒造成傷害。 |
防范說明 | P501 : 將內(nèi)裝物/容器送到批準(zhǔn)的廢物處理廠處理。 P270 : 使用本產(chǎn)品時不要進(jìn)食、飲水或吸煙。 P202 : 在閱讀并明了所有安全措施前切勿搬動。 P201 : 使用前取得專用說明。 P264 : 作業(yè)后徹底清洗皮膚。 P280 : 戴防護(hù)手套/穿防護(hù)服/戴防護(hù)眼罩/戴防護(hù)面具。 P308 + P313 : 如接觸到或有疑慮:求醫(yī)/就診。 P301 + P312 + P330 : 如誤吞咽:如感覺不適,呼叫急救中心/醫(yī)生。漱口。 P405 : 存放處須加鎖。 |
相關(guān)法規(guī)
RTECS# | MU6640000 |
運(yùn)輸信息
監(jiān)管條件代碼(*) |
應(yīng)用
Ibuprofen: A Non-Selective Non-Steroidal Anti-Inflammatory Drug (NSAID)
Ibuprofen is a non-selective non-steroidal anti-inflammatory drug (NSAID) in the propionic acid derivatives group, which possesses analgesic and antipyretic activities. Ibuprofen is a racemic compound and the active enantiomer is (S)-(+)-ibuprofen [I0549] which works by inhibiting both the COX-1 and COX-2 enzymes and prostaglandin synthesis. NSAIDs also include ketoprofen [K0038], loxoprofen [L0244] and naproxen [M1021] among others. Resently, some studies have suggested that NSAIDs may reduce the risk of certain types of cancer and Alzheimer's disease. (The product is for research purpose only.)
References
- Ibuprofen: pharmacology, efficacy and safety (a review)
- Enantioselective pharmacokinetics of ibuprofen and involved mechanisms (a review)
- Cyclo-oxygenase-2: pharmacology, physiology, biochemistry and relevance to NSAID therapy (a review)
- Aspirin, ibuprofen, and other non-steroidal anti-inflammatory drugs in cancer prevention: A critical review of non-selective COX-2 blockade (a review)
- NSAID and antioxidant prevention of Alzheimer's disease: Lessons from in vitro and animal models (a review)
- Resolution of enantiomers of ibuprofen by liquid chromatography: a review
- Ibuprofen (a review on the methods of preparations, physical properties, stability, metabolism and pharmacokinetics and methods for the detection of ibuprofen)
應(yīng)用
Binding of Ibuprofen to Human Serum Albumin
Ibuprofen is known to have affinity for Human Serum Albumin (HSA) and to bind (interact) to drug binding site II on HSA. Those were confirmed using our ibuprofen with Surface Plasmon Resonance (SPR) and a method using fluorescent probes. 【SPR】Dose responses of ibuprofen to HSA were confirmed by SPR. Biacore, as a SPR biosensor, was used for the assay, according to the user’s guide of the instrument.
<Assay condition> Sensor Chip: Series S Sensor Chip CM5, Immobilization: HAS (Amine Coupling method), Buffer : 5%DMSO in PBS. <Result> “Square wave” sensorgrams were exhibited at each concentration, and concentration dependent binding of ibuprofen to HSA was confirmed. 【Method using fluorescent probes】The drug biding site of ibuprofen was confirmed using fluorescent probes which bind to drug binding site on HSA. Dansylamide (DNSA) [D5405] was used as fluorescent probe for site I, and dansylglycine (DNSG) [D5406], BD140 [D4898] were used as fluorescent probes for site II, and then bindings to site I and site II were confirmed.
<Assay condition> Buffer: 1 % DMSO in phosphate buffer (pH 7.2 - 7.5); HSA: 5 µM (DNSA), 20 µM (DNSG, BD140) (50 µL/well) (Fatty acid free HSA is recommended.); Ibuprofen: each concentration (50 µL/well); DNSA: 80 µM, DNSG: 20 µM, BD140: 20 µM (50 µL/well); Incubation: 20-25 °C for 30 min; Measurement: plate-reader with excitation = 365 nm and emission = 480 nm (DNSA, DNSG), with excitation = 365 nm and emission = 585 nm (BD140). <Result> As shown in upper diagram, inhibition against binding of dansylglycine and BD140 which are fluorescent probes for site II by ibuprofen was confirmed. And also, little or extremely weak inhibition against binding of dansylamide which is fluorescent probe for site I was confirmed. In these ways, our ibuprofen can be used for study of interaction with HSA. Also, DNSA [D5405], DNSG [D5406] and BD140 [D4898] can be used for study of drug binding site on HSA.
References
- Fluorescent Dye Cocktail for Multiplex Drug¬Site Mapping on Human Serum Albumin
- High-resolution and high-throughput protocols for measuring drug/human serum albumin interactions using BIACORE
- Biosensor Analysis of the Interaction between Immobilized Human Serum Albumin and Drug Compounds for Prediction of Human Serum Albumin Binding Levels
- Characterizing a drug's primary binding site on albumin
- Structural basis of the drug-binding specificity of human serum albumin
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