16637-59-5 Usage
Description
N-ACETYL-S-METHYL-L-CYSTEINE, also known as a metabolite of Acetaminophen (A161220), is a chemical compound derived from the metabolism of the widely used analgesic and antipyretic agent, Acetaminophen. It is characterized by its white crystalline appearance and plays a significant role in the body's detoxification process after the consumption of Acetaminophen.
Uses
Used in Pharmaceutical Industry:
N-ACETYL-S-METHYL-L-CYSTEINE is used as a metabolite for the detoxification process in the body after the consumption of Acetaminophen (A161220). This metabolite plays a crucial role in the body's ability to eliminate the potentially harmful effects of Acetaminophen, which is commonly used as a pain reliever to treat headache, muscle aches, and arthritis.
Used in Research and Development:
N-ACETYL-S-METHYL-L-CYSTEINE is used as a research compound for studying the metabolism and detoxification pathways of Acetaminophen. This knowledge can be applied to develop safer and more effective pain management strategies, as well as to understand the potential side effects and risks associated with the use of Acetaminophen.
Used in Quality Control and Analysis:
N-ACETYL-S-METHYL-L-CYSTEINE is used as a reference compound in the quality control and analysis of pharmaceutical products containing Acetaminophen. This ensures the safety, efficacy, and proper dosage of the medication, protecting consumers from potential harm and ensuring the effectiveness of the treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 16637-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,3 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16637-59:
(7*1)+(6*6)+(5*6)+(4*3)+(3*7)+(2*5)+(1*9)=125
125 % 10 = 5
So 16637-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3S/c1-4(8)7-5(3-11-2)6(9)10/h5H,3H2,1-2H3,(H,7,8)(H,9,10)/t5-/m0/s1
16637-59-5Relevant articles and documents
Direct monitoring of biocatalytic deacetylation of amino acid substrates by1H NMR reveals fine details of substrate specificity
De Cesare, Silvia,McKenna, Catherine A.,Mulholland, Nicholas,Murray, Lorna,Bella, Juraj,Campopiano, Dominic J.
supporting information, p. 4904 - 4909 (2021/06/16)
Amino acids are key synthetic building blocks that can be prepared in an enantiopure form by biocatalytic methods. We show that thel-selective ornithine deacetylase ArgE catalyses hydrolysis of a wide-range ofN-acyl-amino acid substrates. This activity was revealed by1H NMR spectroscopy that monitored the appearance of the well resolved signal of the acetate product. Furthermore, the assay was used to probe the subtle structural selectivity of the biocatalyst using a substrate that could adopt different rotameric conformations.
Carvacrol codrugs: A new approach in the antimicrobial plan
Cacciatore, Ivana,Di Giulio, Mara,Fornasari, Erika,Di Stefano, Antonio,Cerasa, Laura Serafina,Marinelli, Lisa,Turkez, Hasan,Di Campli, Emanuela,Di Bartolomeo, Soraya,Robuffo, Iole,Cellini, Luigina
, (2015/06/02)
Objective: The increasing prevalence of antibiotic-resistant bacterial infections led to identify alternative strategies for a novel therapeutic approach. In this study, we synthesized ten carvacrol codrugs - obtained linking the carvacrol hydroxyl group
Palatability of aquaculture feed
-
, (2008/06/13)
A method for enhancing the palatability of aquaculture food, the method comprising treating the food with a compound of Formula I: wherein R1, R2, R3, and n are as defined herein, are disclosed.
