(S)-(+)-4-Isobutyl-a-methylphenylacetic acid

CAS: 51146-56-6

Rif. 3D-FI24528

Informazioni sul prodotto

• Nome: (S)-(+)-4-Isobutyl-a-methylphenylacetic acid
• Sinonimi: (S)-(+)-Ibuprofen(2S)-2-[4-(2-Methylpropyl)phenyl]propionic acidDEXIBUPROFEN, (+)-(S)-Ibuprofen, (+)-(S)-p-Isobutylhydratropic acid, (+)-Ibuprofen, (+)-Ibuprophen, (+)-α-Methyl-4-(2-methylpropyl)benzeneacetic acid, (S)-(+)-2-(4-Isobutylphenyl)propionic acid, (S)-(+)-4-Isobutyl-α-methylphenylacetic acid, (S)-2-(4-Isobutylphenyl)propanoic acid, (S)-2-(p-Isobutylphenyl)propionic acid, (αS)-α-Methyl-4-(2-methylpropyl)benzeneacetic acid, Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (S)-, Dexibuprofen, Nyfen, Propanoic Acid, 2-(4-Isobutylphenyl)-, S(+)-, S-Optifen, Seractil, Ultraprofen, d-Ibuprofen, (2S)-2-[4-(2-methylpropyl)phenyl]propanoic acid, (2S)-2-[4-(2-Methylpropyl)phenyl]propionic acid, Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (αS)-

Descrizione

Ibuprofen is a non-steroidal anti-inflammatory drug (NSAID) that inhibits the production of prostaglandins and has been shown to be effective in the treatment of pain, fever, and inflammation. Ibuprofen binds to and blocks cyclooxygenase enzymes COX-1 and COX-2, which are responsible for the production of prostaglandins. It also inhibits leukocyte migration, which may reduce symptoms associated with infectious diseases. The molecular docking analysis has shown that ibuprofen interacts with crystalline cellulose through hydrogen bonding interactions. Ibuprofen can be used in conjunction with sodium citrate as an anticoagulant during blood sampling procedures to prevent clotting. This medication can cause side effects such as nausea, stomach upset, heartburn, dizziness, headache, or increased risk of bleeding.>

• Marchio: Biosynth

Proprietà chimiche

• Peso molecolare: 206.28 g/mol
• Formula: C₁₃H₁₈O₂
• Purezza: Min. 95%
• Colore/Forma: White Powder