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97%
mp
110-112 °C (lit.)
SMILES記法
CC(C(O)=O)c1ccc(c(F)c1)-c2ccccc2
InChI
1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)
InChI Key
SYTBZMRGLBWNTM-UHFFFAOYSA-N
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生物化学的/生理学的作用
シクロオキシゲナーゼ(COX)阻害薬;抗真菌活性を有する非ステロイド性抗炎症薬。 Sエナンチオマーはプロスタグランジン合成を阻害し、抗炎症作用および鎮痛作用の両方を有していますが、Rエナンチオマーはプロスタグランジン合成を阻害せず、鎮痛作用のみ示します。
フルルビプロフェンはシクロオキシゲナーゼ(COX)阻害薬であり、プロスタグランジン合成経路における、アラキドン酸からプロスタグランジンG2(PGG2)へ、PGG2からプロスタグランジンH2(PGH2)への変換に関与する酵素です。本化合物は、炎症、疼痛、腫脹および発熱の原因となるプロスタグランジンを減少させます。フルルビプロフェンはCOX-1および-2両方の活性を阻害します。 Sエナンチオマーはプロスタグランジン合成を阻害し、抗炎症作用および鎮痛作用の両方を有していますが、Rエナンチオマーはプロスタグランジン合成を阻害せず、鎮痛作用のみ示します。
以下による置換
Harish Kumar et al.
European journal of medicinal chemistry, 43(12), 2688-2698 (2008-04-09)
A series of 1,3,4-oxadiazole/thiadiazole and 1,2,4-triazole derivatives of biphenyl-4-yloxy acetic acid were synthesized in order to obtain new compounds with potential anti-inflammatory activity, analgesic activity and lower ulcerogenic potential. All compounds were evaluated for their anti-inflammatory activity by the carrageenan
Mohammad Amir et al.
Bioorganic & medicinal chemistry letters, 18(3), 918-922 (2008-01-10)
A series of 3-(4-biphenyl)-5-substituted phenyl-2-pyrazolines (2a-h) and 1-benzoyl-3-(4-biphenyl)-5-substituted phenyl-2-pyrazolines (3a-h) were synthesized by condensation of chalcones with hydrazine hydrate in solvent system ethanol and DMF. The newly synthesized compounds were screened for their anti-inflammatory and analgesic activity, and were compared
Thomas M Ehrman et al.
Bioorganic & medicinal chemistry, 18(6), 2204-2218 (2010-03-02)
Chinese herbs were screened for compounds which may be active against four targets involved in inflammation, using pharmacophore-assisted docking. Multiple LigandScout (LS) pharmacophores built from ligand-receptor complexes in the protein databank (PDB) were first employed to select compounds. These compounds
Ilaria Peretto et al.
Journal of medicinal chemistry, 48(18), 5705-5720 (2005-09-02)
Flurbiprofen, a nonsteroidal antiinflammatory drug (NSAID), has been recently described to selectively inhibit beta-amyloid(1)(-)(42) (Abeta42) secretion, the most toxic component of the senile plaques present in the brain of Alzheimer patients. The use of this NSAID in Alzheimer's disease (AD)
Mohd Amir et al.
European journal of medicinal chemistry, 43(10), 2056-2066 (2007-11-21)
Several 3,6-disubstituted-1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles were prepared by condensation of 4-amino-5-substituted-3-mercapto-(4H)-1,2,4-triazoles (3a,b) with various substituted aromatic acids and aryl/alkyl isothiocyanates through a one-pot reaction. These compounds were investigated for their anti-inflammatory, analgesic, ulcerogenic, lipid peroxidation, antibacterial and antifungal activities. Some of the synthesized
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