777952-61-1

Upstream product

• 124-30-1 1-aminooctadecane 
• 24424-99-5 di-tert-butyl dicarbonate 
• 60-18-4 L-tyrosine 
• 2130-96-3 O-benzyl-N-tert-butoxycarbonyl-L-tyrosine 
• 777952-60-0 N-[N-(tert-butyloxycarbonyl)-O-(benzyl)-tyrosyl]-octadecylamine 
• 3978-80-1 Boc-Tyr-OH 

Downstream Products

• 1407512-86-0 (S)-N-(2-{3,5-bis[((bis(pyridin-2-ylmethyl)amino)methyl)]-4-hydroxyphenyl}-1-(octadecylcarbamoyl)ethyl)carbamic acid tert-butyl ester 
• 1407512-87-1 (S)-2-amino-3-{3,5-bis[((bis(pyridin-2-ylmethyl)amino)methyl)]-4-hydroxyphenyl}-N-octadecylpropionamide 

Relevant academic research and scientific papers

Method to improve antiviral activity of nucleotide analogue drugs

An amino acid conjugate of a cyclic or acyclic nucleoside phosphonate is provided. In some cases, the amino acid conjugate is a tyrosine alkyl amide phosphonate ester conjugate of a cyclic or acyclic nucleoside phosphonate, and is useful as an antiviral c

Dynamic interface imprinting: High-affinity peptide binding sites assembled by analyte-induced recruiting of membrane receptors

Come together: Dynamic molecular recognition events at biological membrane receptors play a key role in cell signaling. Artificial membranes have been prepared with embedded synthetic receptors which dynamically arrange and selectively respond to external stimuli, such as, small peptide ligands. Copyright

Dynamic interface imprinting: High-affinity peptide binding sites assembled by analyte-induced recruiting of membrane receptors

Come together: Dynamic molecular recognition events at biological membrane receptors play a key role in cell signaling. Artificial membranes have been prepared with embedded synthetic receptors which dynamically arrange and selectively respond to external stimuli, such as, small peptide ligands. Copyright

Variation in morphology of gold nanoparticles synthesized by the spontaneous reduction of aqueous chloroaurate ions by alkylated tyrosine at a liquid-liquid and air-water interface

We demonstrate the formation of gold nanocrystals of different morphologies using alkylated tyrosine (AT) as a reducing agent at a liquid-liquid and air-water interface. The reduction of aqueous chloroaurate ions occurs in a single step wherein the AT mol

Lyotropic Lipo-Amino-Acids: Synthesis and Structural Study

Lyotropic lipo-amino-acids Cn(AA) where AA is one of the following amino-acids: glycine, alanine, sarcosine, serine, tyrosine, lysine, hydroxyethylglutamine, hydroxypropylglutamine, hydroxypentylglutamine and glutamic acid, and Cn is a paraffinic chain with 12 or 18 carbon atoms have been synthesized.The study by X-ray diffraction of the lipo-amino-acids in concentrated water solution and in the anhydrous state has shown the existence of two types of mesophases: lamellar and hexagonal.The respective influence of the water concentration, the nature of the amino-acid and the length of the paraffinic chain on the domain of stability of the mesophases and on the values of their structural parameters has been established.