1562432-09-0 Usage
Description
Fmoc-(S)-2-amino-3-ethoxypropionic acid is a chemical compound belonging to the class of amino acids, with a molecular formula of C17H19NO4. It features an Fmoc group, a protective chemical group used in peptide synthesis to shield the amine group of amino acids, and an (S)-2-amino-3-ethoxypropionic acid derivative with an ethoxypropionic side chain. Fmoc-(S)-2-amino-3-ethoxypropionic acid holds potential for use in peptide synthesis and drug development, offering unique structural properties that can be leveraged in the creation of complex peptides and pharmaceuticals for therapeutic applications.
Uses
Used in Pharmaceutical Development:
Fmoc-(S)-2-amino-3-ethoxypropionic acid is used as a building block in the synthesis of complex peptides for potential therapeutic use. Its unique structure allows for the development of new peptides and pharmaceuticals that can target specific biological pathways or diseases.
Used in Peptide Synthesis:
In the field of peptide synthesis, Fmoc-(S)-2-amino-3-ethoxypropionic acid is utilized as a protected amino acid, enabling the stepwise assembly of peptide chains with controlled selectivity and efficiency. The Fmoc group protects the amine group during synthesis, preventing unwanted side reactions and facilitating the creation of well-defined peptide sequences.
Used in Drug Discovery:
Fmoc-(S)-2-amino-3-ethoxypropionic acid is used as a starting material in drug discovery for the development of new pharmaceuticals. Its incorporation into peptide-based drugs can lead to the discovery of novel therapeutic agents with specific biological activities and potential applications in treating various diseases.
Used in Research Laboratories:
In academic and industrial research settings, Fmoc-(S)-2-amino-3-ethoxypropionic acid is used as a research tool to study the properties and potential applications of novel amino acid derivatives. Its unique structure provides opportunities for investigating new methods in peptide synthesis and exploring its biological effects in various experimental models.
Check Digit Verification of cas no
The CAS Registry Mumber 1562432-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,2,4,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1562432-09:
(9*1)+(8*5)+(7*6)+(6*2)+(5*4)+(4*3)+(3*2)+(2*0)+(1*9)=150
150 % 10 = 0
So 1562432-09-0 is a valid CAS Registry Number.
1562432-09-0Relevant articles and documents
EPHA4 CYCLIC PEPTIDE ANTAGONISTS AND METHODS OF USE THEREOF
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Paragraph 0632-0633; 0639; 0784-0786, (2019/11/19)
Disclosed herein are compounds and methods of use thereof for the modulation of EphA4 receptor activity. In an aspect, is provided a method of treating or preventing a disease or disorder mediated by EphA4, comprising administering to a subject in need thereof a therapeutically effective amount of a compound as described herein, including certain embodiments, or the structural Formula (I), (l-A), (II), (III), (IV), (IV-1), (V), (Vl-A), (Vl-B), (VII-1), (VII-2), (VIII-1), or (VIII-2), or an enantiomer, a mixture of enantiomers, a mixture of two or more diastereomers, or an isotopic variant thereof; or a pharmaceutically acceptable salt, solvate, or hydrate thereof.
