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Z-PHE-PHE-PHE-OH is a tripeptide compound consisting of three phenylalanine residues, with each phenylalanine being in the Z configuration. Z-PHE-PHE-PHE-OH is characterized by its hydrophobic nature due to the presence of the phenylalanine residues, which are nonpolar amino acids.

57092-52-1

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57092-52-1 Usage

Uses

Used in Pharmaceutical Industry:
Z-PHE-PHE-PHE-OH is used as a hydrophobic modifier for dendritic peptide amphiphiles to enhance their solubility and stability in biological systems. The increased hydrophobic character can improve the interaction of these dendrimers with cell membranes and other biological targets, potentially leading to better drug delivery and therapeutic effects.
Used in Drug Delivery Systems:
In the field of drug delivery, Z-PHE-PHE-PHE-OH can be utilized as a component in the design of novel drug carriers. Its hydrophobic nature can facilitate the encapsulation and release of hydrophobic drugs, improving their bioavailability and targeting efficiency.
Used in Material Science:
Z-PHE-PHE-PHE-OH can also be employed in the development of new materials with specific properties, such as self-assembling systems or hydrogels, where its hydrophobic character can contribute to the formation of stable structures and control the release of encapsulated molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 57092-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57092-52:
(7*5)+(6*7)+(5*0)+(4*9)+(3*2)+(2*5)+(1*2)=131
131 % 10 = 1
So 57092-52-1 is a valid CAS Registry Number.

57092-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Benzyloxy)carbonyl]-L-phenylalanyl-L-phenylalanyl-L-phenylala nine

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyl-L-phenylalanine t-butyl 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:57092-52-1 SDS

57092-52-1Relevant academic research and scientific papers

Tuning the pH-triggered self-assembly of dendritic peptide amphiphiles using fluorinated side chains

Appel, Ralph,Tacke, Sebastian,Klingauf, Jürgen,Besenius, Pol

supporting information, p. 1030 - 1039 (2015/08/03)

We report the synthesis of a series of anionic dendritic peptide amphiphiles of increasing hydrophobic character. By establishing state diagrams we describe their pH and ionic strength triggered self-assembly into supramolecular nanorods in water and highlight the impact of hydrophobic shielding in the supramolecular polymerisation process. Via the incorporation of fluorinated peptide side chains the pH-triggered monomer to polymer transition at physiological ionic strength is shifted from pH 5.0 to pH 7.4. We thereby show that compensating attractive non-covalent interactions and hydrophobic effects with repulsive electrostatic forces, a concept we refer to as frustrated growth, is a sensitive tool in order to manipulate one-dimensional supramolecular polymerisation processes in water.

METHOD OF PREPARING A HYDROGEL

-

Page/Page column 44, (2008/06/13)

A method of preparing a hydrogel comprises : (i) reacting a first molecule comprising a carboxylic acid group and second molecule comprising an amine group or an alcohol group with a hydrolase enzyme to form a product comprising an amide bond or ester bond, wherein the hydrolase enzyme would normally catalyse the production of an amine or an alcohol from an amide or an ester under physiological conditions; and (ii) maintaining the product comprising an amide or ester bond under conditions suitable to allow hydrogel formation.

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