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Ibuprofen structure

FIGURE 25.29 (a) The structures of several commou analgesic agents. Acetaminophen is marketed under the tradename Tylenol. Ibuprofen is sold as Motrin, Nuprin, and Advil, (b) Acetylsalicylate (aspirin) inhibits the cyclooxygenase activity of endoperoxide synthase via acetylation (covalent modification) of Ser ... [Pg.832]

NSAIDs are of diverse chemical structures salicylates (aspirin, sulphasalazine), indole acetic acids (indomethacin, etodolac), heteroaryl acetic acids (diclofenac), arylpropionic acids (ibuprofen, naproxen), anthranilic acids (mefenamic acid) and enolic acids (piroxicam, meloxicam). [Pg.405]

Observing and Inferring What structural shape do aspirin, acetaminophen, and ibuprofen have in common ... [Pg.68]

Predicting Predict the possibility of other medicines that might have the same common structural shape as aspirin, acetaminophen, and ibuprofen. [Pg.68]

Elements of the structure of ibuprofen and its congeners are clearly visible in cicloprofen. [Pg.218]

Structural changes of MCM-41 spheres during ibuprofen release to SBF... [Pg.249]

Ordered mesoporous silica have already been studied as carriers for drug delivery [1,2] recently, their use has also been proposed in bone tissue engineering [3,4], in combination with bioactive glass-ceramic scaffolds [5,6]. The kinetics of ibuprofen release in SBF [7] from MCM-41 silica with similar pore diameter has shown puzzling discontinuities [3,6,8] aim of the present work is to assess whether these anomalies may be related to structural changes in the MCM-41 mesoporous spheres under the adopted conditions. [Pg.249]

Changes in the releasing properties of MCM-41 spheres loaded with ibuprofen are not ascribable either to the morphology, as SEM pictures show the same spherical shape before and after the contact with the SBF solution, or to structural phenomena, because XRD patterns are the same even after 170 hours of contact with SBF. [Pg.252]

The structures of luminol derivatives used for HPLC-CL detection are shown in Figure 7A. Analytes labeled with luminol derivatives can be detected using hydrogen peroxide and potassium hexacyanoferrate(III) under alkaline conditions after HPLC separation (Table 1). For example, ibuprofen in saliva [34], saturated... [Pg.404]

The above problem becomes an NLP problem when we fix the integer variables. Since we have only 6 feasible pairs, 6-NLP problems were solved by fixing the binary variables representing the solvent and anti-solvent in the 6 pairs. The molecular structures of the optimal solvent and anti-solvent mixture giving a maximum potential recovery of 69% ibuprofen is shown in Table 2. The properties of solvent and anti-solvent are shown in Table 3 and Table 4 respectively. [Pg.141]

Ibuprofen has good analgesic and anti-inflammatory action. Ibuprofen is made at approximately 16 million Ib/yr in the U.S. Its price is higher than aspirin or acetaminophen and is usually around 9.30/lb. Its common name does tell us something about its structure. There are a number of profens, ... [Pg.452]

This study also suggests that molecular size and structure play a role in this interaction. The binding behaviors of dextrin oligomers for four different pharmaceuticals (ibuprofen, ketoprofen, furosemide, and warfarin) were observed under the same experimental conditions. Ibuprofen and ketoprofen, two compounds that are similar in chemical structure and pharmaceutical use, showed obvious differences in interaction patterns (Fig. 13A and B). Ketoprofen, having an extra aromatic ring, required an octa-saccharide (DP = 8) for binding, whereas ibuprofen required a heptasac-... [Pg.305]

For example, in a general screen for acidic drugs, which includes most of the NSAIDs (Fig. 13.5), three mobile phases may be used. Table 13.3 shows the Rf values obtained for three NSAIDs in three different mobile phases. It can be seen from the data in Table 13.3 that even for closely related structures slight differences in polarity and lipophilicity can be exploited to produce separation. For instance, ibuprofen is the least polar drug in system 1 but is the most polar drug in system 3, where the carboxyl groups in the structures will be ionised due to the ammonia in the mobile phase. It can also be seen that the polarity of a mobile phase containing a mixture of chloroform and acetone is similar to that of pure ethyl acetate. [Pg.282]

Ibuprofen works by inhibiting the enzyme cyclooxygenase (COX), which in turn interferes with the synthesis of prostaglandins. COX exists as several coenzyme forms that are similar in structure COX-1, COX-2, COX-3 ibuprofen is a nonselective inhibitor of both COX-1... [Pg.150]


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See also in sourсe #XX -- [ Pg.479 ]

See also in sourсe #XX -- [ Pg.315 ]

See also in sourсe #XX -- [ Pg.57 ]




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Ibuprofen

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Ibuprofen enantiomer structure

Ibuprofen molecular structure

Ibuprofen, chirality and structure

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