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Z-Thr(But)-Phe-OMe is a synthetic peptide consisting of three amino acid residues: Z-protected threonine (Z-Thr), tert-butyl-protected phenylalanine (But-Phe), and methoxy-protected phenylalanine (Phe-OMe). The Z-group and But-group are protecting groups used in peptide synthesis to prevent unwanted side reactions, while the OMe-group is a protecting group for the phenolic hydroxyl group of phenylalanine. This specific sequence of amino acids is not found in natural proteins, making it a unique synthetic compound with potential applications in drug development, chemical biology, and materials science. The structure and properties of Z-Thr(But)-Phe-OMe can be further explored for its interactions with biological targets or its potential use as a building block in the synthesis of more complex peptides and peptidomimetics.

17115-07-0

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17115-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17115-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17115-07:
(7*1)+(6*7)+(5*1)+(4*1)+(3*5)+(2*0)+(1*7)=80
80 % 10 = 0
So 17115-07-0 is a valid CAS Registry Number.

17115-07-0Relevant academic research and scientific papers

Tritiated Peptides. Part 11. Synthesis of 6>-, 11>-, and 6,11>-Somatostatin and the Metabolite 1>-Somatostatin

Allen, Mark C.,Brundish, Derek E.,Martin, John R.,Wade, Roy

, p. 2040 - 2048 (2007/10/02)

The syntheses are described of somatostatin labelled with tritium singly in the phenylalanine residues at positions 6 and 11 and doubly at residues 6 and 11 to specific radioactivities of 15.5, 13.8 and 14.1 Cim mol-1, respectively, by reductive deiodination of fully-protected precursors.Cysteine residues were proteced by S-trityl groups and the disulphide bridge was formed by iodine oxidation of the tritiated protected precursors.The purity of the products was assessed by acidic hydrolysis, ion-exchange and high-pressure liquid chromatography, and by enzymic digestion of the products modified by reduction and aminoethylation.The synthesis of the metabolite 1>-somatostatin is described.The syntheses of 6>-, 11>- and 6,11>-somatostatin are described.

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