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2-(butylsulfonyl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57076-15-0

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57076-15-0 Usage

Purpose

Non-steroidal anti-inflammatory drug (NSAID)

Analgesic

Reduces pain

Anti-inflammatory

Decreases inflammation

Usage

Topical formulations for inflammatory skin conditions
Treatment of musculoskeletal injuries

Chemical Structure

Benzoic acid backbone
Butylsulfonyl group attached to the para position

Mechanism of Action

Inhibits the production of prostaglandins responsible for inflammation, pain, and fever

Precautions

Adverse effects on the gastrointestinal system
Potential impact on kidneys
Cardiovascular system risks

Check Digit Verification of cas no

The CAS Registry Mumber 57076-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,7 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57076-15:
(7*5)+(6*7)+(5*0)+(4*7)+(3*6)+(2*1)+(1*5)=130
130 % 10 = 0
So 57076-15-0 is a valid CAS Registry Number.

57076-15-0Downstream Products

57076-15-0Relevant academic research and scientific papers

PIPERAZINYL METHANONE NAAA INHIBITORS

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Paragraph 0215; 0304; 0308, (2017/12/16)

Disclosed herein, inter alia, are compositions and methods for modulating the activity of N-acylethanolamine acid amidase for the treatment of a pathological state, including pain, an inflammatory condition, or a neurodegenerative disorder.

Second-Generation Non-Covalent NAAA Inhibitors are Protective in a Model of Multiple Sclerosis

Migliore, Marco,Pontis, Silvia,Fuentes de Arriba, Angel Luis,Realini, Natalia,Torrente, Esther,Armirotti, Andrea,Romeo, Elisa,Di Martino, Simona,Russo, Debora,Pizzirani, Daniela,Summa, Maria,Lanfranco, Massimiliano,Ottonello, Giuliana,Busquet, Perrine,Jung, Kwang -Mook,Garcia-Guzman, Miguel,Heim, Roger,Scarpelli, Rita,Piomelli, Daniele

supporting information, p. 11193 - 11197 (2016/10/13)

Palmitoylethanolamide (PEA) and oleoylethanolamide (OEA) are endogenous lipid mediators that suppress inflammation. Their actions are terminated by the intracellular cysteine amidase, N-acylethanolamine acid amidase (NAAA). Even though NAAA may offer a new target for anti-inflammatory therapy, the lipid-like structures and reactive warheads of current NAAA inhibitors limit the use of these agents as oral drugs. A series of novel benzothiazole–piperazine derivatives that inhibit NAAA in a potent and selective manner by a non-covalent mechanism are described. A prototype member of this class (8) displays high oral bioavailability, access to the central nervous system (CNS), and strong activity in a mouse model of multiple sclerosis (MS). This compound exemplifies a second generation of non-covalent NAAA inhibitors that may be useful in the treatment of MS and other chronic CNS disorders.

Pharmaceutical compositions comprising azapurinones useful in treating allergic respiratory disorders

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, (2008/06/13)

8-Azapurin-6-ones substituted in the 2-position by an unsubstituted or substituted phenyl or naphthyl group, or by an alkenyl or alkynyl group, a cycloalkyl group, an alkyl group contaning 2 to 10 carbon atoms, or an alkyl group containing 1 to 10 carbon

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