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Z-Aib-Pro-Aib-Ala-OH is a synthetic peptide composed of five amino acids: Z-Aib (N-benzyloxycarbonyl-α-aminoisobutyric acid), Pro (proline), Aib (α-aminoisobutyric acid), Aib (α-aminoisobutyric acid), and Ala (alanine), with a hydroxyl group (OH) at the C-terminus. This peptide is characterized by its unique structure, featuring two Aib residues, which are non-natural amino acids that can induce β-turns in peptide chains. The presence of Z-Aib at the N-terminus provides protection against enzymatic degradation, while the Pro and Ala residues contribute to the overall stability and conformation of the peptide. Z-Aib-Pro-Aib-Aib-Ala-OH has potential applications in drug design, as it can mimic natural peptide sequences and exhibit specific biological activities.

79755-77-4

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79755-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79755-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,5 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79755-77:
(7*7)+(6*9)+(5*7)+(4*5)+(3*5)+(2*7)+(1*7)=194
194 % 10 = 4
So 79755-77-4 is a valid CAS Registry Number.

79755-77-4Downstream Products

79755-77-4Relevant academic research and scientific papers

RACEMIZATION AT PROLINE RESIDUES DURING PEPTIDE BOND FORMATION A STUDY OF DIASTEREOMERIC MIXTURES OF SYNTHETIC ALAMETHICIN FRAGMENTS BY 270 MHz 1H NMR

Nagaraj, R.,Balaram, P.

, p. 2001 - 2006 (2007/10/02)

The stepwise synthesis of amino terminal pentapeptide of alamethicin, Z-Aib-Pro-Aib-Ala-Aib-OMe, by the dicyclohexylcarbodiimide mediated couplings leads to extensive racemization at the Ala and Pro residues.Racemization is largely suppressed by the use o

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