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L-Proline, 2-methyl-N-[(phenylmethoxy)carbonyl]alanyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58281-75-7

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58281-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58281-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,8 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58281-75:
(7*5)+(6*8)+(5*2)+(4*8)+(3*1)+(2*7)+(1*5)=147
147 % 10 = 7
So 58281-75-7 is a valid CAS Registry Number.

58281-75-7Relevant academic research and scientific papers

A kinetic method for detecting intramolecular peptide H-bonds

Banerjee, Shreya,Prabhakaran, Erode N.,Reddy, Damodara N.

, p. 15887 - 15891 (2021/09/22)

The current method for the detection of peptide hydrogen bond (PHB) formation places charge donors/acceptors (D/A) at the N-/C-termini of the peptides involved in the putative PHB. The efficiency of the charge transfer influences the kinetics of the first order reaction at A and hence reports on the formation and electronic properties of the PHB.

Impact of Dehydroamino Acids on the Structure and Stability of Incipient 310-Helical Peptides

Joaquin, Daniel,Lee, Michael A.,Kastner, David W.,Singh, Jatinder,Morrill, Shardon T.,Damstedt, Gracie,Castle, Steven L.

, p. 1601 - 1613 (2019/12/02)

A comparative study of the impact of small, medium-sized, and bulky α,β-dehydroamino acids (AAs) on the structure and stability of Balaram's incipient 310-helical peptide (1) is reported. Replacement of the N-terminal Aib residue of 1 with a AA

Synthesis and pharmacological evaluation of glycine-modified analogues of the neuroprotective agent glycyl-L-prolyl-L-glutamic acid (GPE)

Lai, Michelle Y.H.,Brimble, Margaret A.,Callis, David J.,Harris, Paul W.R.,Levi, Mark S.,Sieg, Frank

, p. 533 - 548 (2007/10/03)

The synthesis of 10 G*PE analogues, wherein the glycine residue has been modified, is described by coupling readily accessible dibenzyl-l-prolyl-l- glutamate 2 with various analogues of glycine. Pharmacological evaluation of the novel compounds was undertaken to further understand the role of the glycine residue on the observed neuroprotective properties of the endogenous tripeptide GPE.

SOLUTION PHASE SYNTHESIS OF ALAMETHICIN I

Nagaraj, R.,Balaram, P.

, p. 1263 - 1270 (2007/10/02)

The total synthesis of alamethicin I by solution phase methods is reported.

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