16864-90-7

Usage

Explanation

This is the chemical name of the compound, which is also known as fenoprofen.

Explanation

Fenoprofen belongs to a class of drugs called NSAIDs, which are commonly used to relieve pain and reduce inflammation.

Explanation

Fenoprofen is often prescribed to treat various conditions that involve pain and inflammation, such as arthritis and menstrual cramps.

Explanation

The medication is available in different forms, including tablets and capsules, for oral administration.

Explanation

Although fenoprofen can be effective in managing pain and inflammation, it may also cause some side effects, including gastrointestinal irritation, dizziness, and changes in blood pressure.

Explanation

It is important to use fenoprofen as directed by a healthcare professional to ensure its effectiveness and minimize potential risks. Patients should also be aware of the potential benefits and risks associated with its use.

Classification

Non-steroidal anti-inflammatory drug (NSAID)

Mechanism of action

Inhibition of chemical production in the body involved in the inflammatory response

Common uses

Treatment of arthritis, menstrual cramps, and mild to moderate pain

Available forms

Tablets and capsules

Side effects

Gastrointestinal irritation, dizziness, and changes in blood pressure

Usage

Directed by a healthcare professional

Upstream product

• 1878-66-6 4-chlorophenylacetic Acid 
• 50-00-0 formaldehyd 
• 109135-06-0 methyl 2-(4-chlorophenyl)-3-hydroxypropanoate 
• 52449-43-1 (4-chloro-phenyl)-acetic acid methyl ester 
• 14062-24-9 4-chloro-benzeneacetic acid, ethyl ester 
• 86762-37-0 2-(4-Chloro-phenyl)-3-hydroxy-propionic acid ethyl ester 

Downstream Products

• 86762-37-0 2-(4-Chloro-phenyl)-3-hydroxy-propionic acid ethyl ester 
• 63978-23-4 2-(4-chloro-phenyl)-3-hydroxy-propionic acid tropan-3-yl ester 
• 1025804-17-4 (S)-3-Acetoxy-2-(4-chloro-phenyl)-propionic acid 
• 83055-26-9 3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-chloro-phenyl)-propionic acid; compound with cyclohexylamine 
• 83055-21-4 3-{2-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetoxy}-2-(4-chloro-phenyl)-propionic acid 

Relevant academic research and scientific papers

“Solvent-induced chirality switching” in the enantioseparation of chlorine-substituted tropic acids via diastereomeric salt formation by (1R,2S)-(?)-2-amino-1,2-diphenylethanol (ADPE)

The optical resolution of chlorine-substituted tropic acids (TAs) by diastereomeric salt formation with (1R,2S)-(?)-2-amino-1,2-diphenylethanol ((?)-ADPE) has been demonstrated. Efficient solvent-induced chirality switching was observed in the case of racemic 2-chlorotropic acid (rac-2-Cl-TA). The recrystallization of the diastereomeric salts of rac-2-Cl-TA from branched alcohols such as i-PrOH and s-BuOH afforded (R)-2-Cl-TA, whereas (S)-2-Cl-TA was obtained from linear alcohols such as MeOH, EtOH, and n-PrOH. The chirality switching mechanism was elucidated from the crystal structures of the diastereomeric salts, which revealed that the incorporation of solvent in the (S)-2-Cl-TA salt crystals played a key role in chirality switching by reinforcing the supramolecular structure of the salt. However, no chirality switching was achieved for racemic 3-chlorotropic acid and 4-chlorotropic acid. The position of the chlorine substituent plays an important role in the solvent-induced chirality switching effect.

ESTERS OF 1-p-CHLOROBENZOYL-5-METHOXY-2-METHYL-3-INDOLYLACETIC ACID

Reactions of imidazolide of 1-p-chlorobenzoyl-5-methoxy-2-methyl-3-indolylacetic acid, prepared from the acid and N,N'-carbonyldiimidazole, with the optically active forms of 2-phenyl-3-hydroxypropane acid and with the inactive forms of p-chloro-, p-isopropyl- and p-isobutyl-2-phenyl-3-hydroxypropane acids gave the corresponding esters.The compounds were tested for antiinflammatory activity.