2370-57-2 Usage
Description
Methyl-3-tyrosine, also known as L-3-methyltyrosine, is a tyrosine derivative in which the hydrogen at position 3 on the phenyl ring of L-tyrosine is replaced by a methyl group. This modification of the tyrosine molecule may result in altered properties and potential applications in various fields.
Uses
Used in Pharmaceutical Applications:
Methyl-3-tyrosine is used as an intermediate in the synthesis of pharmaceutical compounds. The presence of the methyl group at position 3 on the phenyl ring can influence the reactivity and selectivity of the molecule, making it a valuable building block for the development of new drugs.
Used in Research and Development:
Methyl-3-tyrosine can be utilized as a research tool in the study of tyrosine metabolism and its role in various biological processes. It may also be used to investigate the effects of tyrosine derivatives on enzyme activity and protein function.
Used in Chemical Synthesis:
Methyl-3-tyrosine can be employed as a starting material or a reagent in the chemical synthesis of various organic compounds, including specialty chemicals, dyes, and other fine chemicals.
Used in Analytical Chemistry:
Methyl-3-tyrosine may be used as a reference compound or a standard in analytical chemistry for the development and validation of analytical methods, such as high-performance liquid chromatography (HPLC), mass spectrometry (MS), and other techniques for the analysis of tyrosine and its derivatives.
Used in Nutritional Supplements:
Methyl-3-tyrosine could potentially be used as an ingredient in nutritional supplements, particularly those aimed at supporting cognitive function or athletic performance. However, further research would be required to establish its safety and efficacy in this context.
Check Digit Verification of cas no
The CAS Registry Mumber 2370-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2370-57:
(6*2)+(5*3)+(4*7)+(3*0)+(2*5)+(1*7)=72
72 % 10 = 2
So 2370-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-6-4-7(2-3-9(6)12)5-8(11)10(13)14/h2-4,8,12H,5,11H2,1H3,(H,13,14)/t8-/m0/s1
2370-57-2Relevant articles and documents
Biocascade Synthesis of L-Tyrosine Derivatives by Coupling a Thermophilic Tyrosine Phenol-Lyase and L-Lactate Oxidase
Jiang, Yiqi,Ju, Shuyun,Li, Guosi,Lian, Jiazhang,Lin, Jianping,Wu, Mianbin,Xue, Hailong,Yang, Lirong
supporting information, (2020/02/25)
A one-pot biocascade of two enzymatic steps catalyzed by an l-lactate oxidase and a tyrosine phenol-lyase has been successfully developed in the present study. The reaction provides an efficient method for the synthesis of l-tyrosine derivatives, which exhibits readily available starting materials and excellent yields. In the first step, an in situ generation of pyruvate from readily available bio-based l-lactate catalyzed by a highly active l-lactate oxidase from Aerococcus viridans (AvLOX) was developed (using oxygen as oxidant and catalase as hydrogen peroxide removing reagent). Pyruvate thus produced underwent C–C coupling with phenol derivatives as acceptor substrate using specially designed thermophilic tyrosine phenol-lyase mutants from Symbiobacterium toebii (TTPL). Overall, this cascade avoids the high cost and easy decomposition of pyruvate and offered an efficient and environmentally friendly procedure for l-tyrosine derivatives synthesis.
Incorporation of 3'-methyltyrosine and 5'-methyl-DOPA into naphthyridinomycin
Palaniswamy,Gould
, p. 5651 - 5652 (2007/10/02)
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