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Z-GLY-PRO-ALA-OH is a chemical compound composed of four amino acids: glycine (Gly), proline (Pro), alanine (Ala), and an acetyl group (Z) attached to the amino terminus. It serves as a model peptide in research laboratories for investigating the structure-function relationships of proteins. Known for its capacity to form stable secondary structures like helices and beta-sheets, Z-GLY-PRO-ALA-OH is instrumental in protein folding and stability studies. Furthermore, its role as a substrate for enzymes that cleave peptide bonds highlights its significance in enzymatic research. Z-GLY-PRO-ALA-OH is a multifaceted tool for elucidating the behavior and function of proteins within biological systems.

5891-41-8

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5891-41-8 Usage

Uses

Used in Research Laboratories:
Z-GLY-PRO-ALA-OH is used as a model peptide for studying the structure-function relationships of proteins due to its ability to form stable secondary structures, which aids in understanding protein folding and stability.
Used in Enzymatic Studies:
Z-GLY-PRO-ALA-OH is used as a substrate for enzymes that cleave peptide bonds, making it crucial for research into enzymatic processes and their mechanisms.
Used in Pharmaceutical and Biochemical Industries:
While the provided materials do not explicitly mention pharmaceutical or biochemical applications, the compound's role in studying protein folding and enzymatic activity suggests potential uses in these industries for drug development and understanding biochemical pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 5891-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5891-41:
(6*5)+(5*8)+(4*9)+(3*1)+(2*4)+(1*1)=118
118 % 10 = 8
So 5891-41-8 is a valid CAS Registry Number.

5891-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Alanine,N-[(phenylmethoxy)carbonyl]glycyl-L-prolyl- (9CI)

1.2 Other means of identification

Product number -
Other names benzyloxycarbonylglycylproline N-hydroxysuccinimide 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:5891-41-8 SDS

5891-41-8Relevant academic research and scientific papers

LINEAR TRI- AND TETRAPEPTIDES ACTING AS PRODRUGS

Kasafirek, Evzen,Sturc, Antonin,Roubalova, Alena

, p. 179 - 187 (2007/10/02)

Tri- and tetrapeptides with C-terminal 1-amino-1-cycloalkanecarboxylic acid of the general formula X-Ala-Y-OR, where X is Ala, Leu, Phe, Ac-Tyr, Gly-Pro, Ac-Leu-lys or Ac-Leu-Arg.Y is Acb, Acp or Ach, and R is methyl or ethyl, have been prepared.These pep

Examination of a New Cross-Linker in Monoclonal Antibody Reaction Against the C-Terminus of Tobacco Mosaic Virus Coat Protein

Dietzgen, Ralf G.,Sander, Evamarie,Christner, Juergen,Jung, Guenther

, p. 441 - 453 (2007/10/02)

The C-terminal tetrapeptide Gly-Pro-Ala-Thr of TMV coat protein was linked to poly(L-lysine) of 37,300 and 80,000 daltons and to human serum albumin using different ratios of tetrapeptide to carrier.The new hydrazidosuccinyl HSc cross-linker effected the

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