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Nα-(tert-butoxycarbonyl)-L-tyrosyl-L-tyrosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

881887-95-2

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881887-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881887-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,8,8 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 881887-95:
(8*8)+(7*8)+(6*1)+(5*8)+(4*8)+(3*7)+(2*9)+(1*5)=242
242 % 10 = 2
So 881887-95-2 is a valid CAS Registry Number.

881887-95-2Downstream Products

881887-95-2Relevant academic research and scientific papers

Sulfotyrosine dipeptide: Synthesis and evaluation as HIV-entry inhibitor

Ju, Tong,Hu, Duoyi,Xiang, Shi-Hua,Guo, Jiantao

, p. 105 - 111 (2016)

Human immunodeficiency virus type 1 (HIV-1) is responsible for the worldwide AIDS pandemic. Due to the lack of prophylactic HIV-1 vaccine, drug treatment of the infected patients becomes essential to reduce the viral load and to slow down progression of the disease. Because of drug resistance, finding new antiviral agents is necessary for AIDS drug therapies. The interaction of gp120 and co-receptor (CCR5/CXCR4) mediates the entry of HIV-1 into host cells, which has been increasingly exploited in recent years as the target for new antiviral agents. A conserved co-receptor binding site on gp120 that recognizes sulfotyrosine (sTyr) residues represents a structural target to design novel HIV entry inhibitors. In this work, we developed an efficient synthesis of sulfotyrosine dipeptide and evaluated it as an HIV-1 entry inhibitor.

A mechanistic and kinetic study of the formation of metal nanoparticles by using synthetic tyrosine-based oligopeptides

Si, Satyabrata,Bhattacharjee, Rama Ranjan,Banerjee, Arindam,Mandal, Tarun K.

, p. 1256 - 1265 (2008/09/18)

Synthetic oligopeptides containing redox-active tyrosine residues have been employed to prepare gold and silver nanoparticles. In this reduction process an electron from the tyrosinate ion of the peptide is transferred to the metal ion at basic pH through the formation of a tyrosyl radical, which is eventually converted to its dityrosine form during the reaction. This reaction mechanism was confirmed from UV-visible, fluorescence, and EPR spectroscopy and was found to be pH-dependent. Transmission electron microscopy measurement shows that the average size and the monodispersity of gold nanoparticles increase as the number of tyrosine residues in the peptide increases. The kinetic study, based on spectrophotometric measurements of the surface plasmon resonance optical property, shows that the rate of formation of gold nanoparticles was much faster at higher pH than at lower pH and was also dependent on the number of tyrosine residues present in the peptide. The dityrosine form of the peptide was found to retain reducing properties like those of tyrosine in basic medium.

Smart oligopeptide gels: In situ formation and stabilization of gold and silver nanoparticles within supramolecular organogel networks

Ray, Sudipta,Das, Apurba Kumar,Banerjee, Arindam

, p. 2816 - 2818 (2008/09/19)

Tripeptide with redox active chemical entities based smart organogels have been used for in situ formation and stabilization of gold and silver nanoparticles within the supramolecular gel networks and the gold nanoparticles are aligned in arrays along the gel nanofibers of peptide 1-toluene gels. The Royal Society of Chemistry 2006.

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