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Tyrosyltyrosine methyl ester, also known as N-(4-hydroxyphenyl)-L-tyrosinyl-N-methylamide, is a synthetic derivative of the amino acid tyrosine. It is a dipeptide consisting of two tyrosine molecules connected by a peptide bond, with a methyl ester group attached to the carboxylic acid group of the second tyrosine. tyrosyltyrosine methyl ester is of interest in the field of chemistry and biochemistry due to its potential applications in the study of protein structure and function, as well as its possible use as a building block for the synthesis of more complex molecules. Tyrosyltyrosine methyl ester is characterized by its ability to mimic the properties of natural peptides and proteins, making it a valuable tool for researchers exploring the interactions between amino acids and their role in biological systems.

13022-41-8

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13022-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13022-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13022-41:
(7*1)+(6*3)+(5*0)+(4*2)+(3*2)+(2*4)+(1*1)=48
48 % 10 = 8
So 13022-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N2O5/c1-26-19(25)17(11-13-4-8-15(23)9-5-13)21-18(24)16(20)10-12-2-6-14(22)7-3-12/h2-9,16-17,22-23H,10-11,20H2,1H3,(H,21,24)/t16-,17-/m0/s1

13022-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]-3-(4-hydroxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names Tyrosyltyrosine methyl ester

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:13022-41-8 SDS

13022-41-8Relevant academic research and scientific papers

Structure-Activity Relationships of cyclo(l -Tyrosyl- l -tyrosine) Derivatives Binding to Mycobacterium tuberculosis CYP121: Iodinated Analogues Promote Shift to High-Spin Adduct

Rajput, Sunnia,McLean, Kirsty J.,Poddar, Harshwardhan,Selvam, Irwin R.,Nagalingam, Gayathri,Triccas, James A.,Levy, Colin W.,Munro, Andrew W.,Hutton, Craig A.

, p. 9792 - 9805 (2019/11/13)

A series of analogues of cyclo(l-tyrosyl-l-tyrosine), the substrate of the Mycobacterium tuberculosis enzyme CYP121, have been synthesized and analyzed by UV-vis and electron paramagnetic resonance spectroscopy and by X-ray crystallography. The introduction of iodine substituents onto cyclo(l-tyrosyl-l-tyrosine) results in sub-μM binding affinity for the CYP121 enzyme and a complete shift to the high-spin state of the heme FeIII. The introduction of halogens that are able to interact with heme groups is thus a feasible approach to the development of next-generation, tight binding inhibitors of the CYP121 enzyme, in the search for novel antitubercular compounds.

Synthesis and biological evaluation of analogue of delavayin-C: A cyclic heptapeptide

Shinde, Nirmala V.,Himaja,Bhosale,Wagh

scheme or table, p. 996 - 1000 (2012/04/10)

The synthesis of N-methylated analogue of delavayin-C, a cyclic heptapeptide was carried out by using solution phase technique. The structure of this compound was confirmed on the basis of analytical IR, 1H NMR and FAB MASS spectral data. The e

Intramolecular Interaction of Porphyrin Moieties in 2,5-Piperazinedione-Bridged Porphyrin Dimers

Tamiaki, Hitoshi,Suzuki, Shinji,Maruyama, Kazuhiro

, p. 2633 - 2637 (2007/10/02)

Diastereomerically pure 2,5-piperazinedione-bridged meso-tetraarylporphyrin dimers were synthesized with easy procedures. 1H NMR, UV-vis, and CD spectra showed that porphyrin moieties in the L,L-molecule interacted more strongly than those in the D,L-isom

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