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Acetaminophen cysteine is a metabolite of Acetaminophen, an analgesic and antipyretic drug. It is a pain reliever commonly used to treat headache, muscle aches, arthritis, and other acute or chronic painful conditions.

64014-06-8

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64014-06-8 Usage

Uses

Used in Pharmaceutical Industry:
Acetaminophen cysteine is used as an active pharmaceutical ingredient for its analgesic and antipyretic properties, helping to alleviate pain and reduce fever in patients suffering from various conditions such as headache, muscle aches, arthritis, and other acute or chronic painful conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 64014-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,1 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64014-06:
(7*6)+(6*4)+(5*0)+(4*1)+(3*4)+(2*0)+(1*6)=88
88 % 10 = 8
So 64014-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O3S/c1-7(14)13-8-2-4-9(5-3-8)17-6-10(12)11(15)16/h2-5,10H,6,12H2,1H3,(H,13,14)(H,15,16)/t10-/m0/s1

64014-06-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-(4-acetamidophenyl)sulfanyl-2-aminopropanoic acid

1.2 Other means of identification

Product number -
Other names AA-Cysteine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64014-06-8 SDS

64014-06-8Downstream Products

64014-06-8Relevant academic research and scientific papers

Expanding the Structural Diversity of Protein Building Blocks with Noncanonical Amino Acids Biosynthesized from Aromatic Thiols

Wang, Yong,Chen, Xiaoxu,Cai, Wenkang,Tan, Linzhi,Yu, Yutong,Han, Boyang,Li, Yuxuan,Xie, Yuanzhe,Su, Yeyu,Luo, Xiaozhou,Liu, Tao

supporting information, p. 10040 - 10048 (2021/03/26)

Incorporation of structurally novel noncanonical amino acids (ncAAs) into proteins is valuable for both scientific and biomedical applications. To expand the structural diversity of available ncAAs and to reduce the burden of chemically synthesizing them, we have developed a general and simple biosynthetic method for genetically encoding novel ncAAs into recombinant proteins by feeding cells with economical commercially available or synthetically accessible aromatic thiols. We demonstrate that nearly 50 ncAAs with a diverse array of structures can be biosynthesized from these simple small-molecule precursors by hijacking the cysteine biosynthetic enzymes, and the resulting ncAAs can subsequently be incorporated into proteins via an expanded genetic code. Moreover, we demonstrate that bioorthogonal reactive groups such as aromatic azides and aromatic ketones can be incorporated into green fluorescent protein or a therapeutic antibody with high yields, allowing for subsequent chemical conjugation.

Facile Synthesis of S-Substituted L-Cysteines with Nano-sized Immobilized O-Acetylserine Sulfhydrylase

Vahidi, Akbar K.,Wang, Zunsheng,Li, Zhi

, p. 3671 - 3674 (2018/09/12)

Many S-substituted l-cysteines are useful pharmaceutical intermediates but require a simple synthesis method. Here we developed enzymatic synthesis of several S-aryl-l-cysteines and S-benzyl-l-cysteine directly from O-acetylserine (OAS) with immobilized O-acetylserine sulfhydrylase CysM. Novel iron-oxide magnetic nanoparticles (MNPs) with cobalt-nitrilotriacetic acid function were prepared with a diameter of 80 nm in 75 % yield. Direct immobilization of His-tagged CysM in the cell-free extract on the MNPs via affinity attachment afforded stable nanobiocatalyst with 97 % enzyme loading efficiency and 93 % free enzyme activity. The immobilized enzyme catalyzed the biotransformation of benzylthiol and OAS to give S-benzyl-l-cysteine in 88 % yield. The nanobiocatalyst also demonstrated high recyclability, retaining 95 % productivity in the fifth cycle. The immobilized CysM accepts various arylthiols to react with OAS, giving rise to a new synthesis route of several S-substituted l-cysteines in 60–96 % yield.

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