201016-22-0

Basic information

• Product Name: N-ME-LYS(Z)-OH
• Synonyms: N-ALPHA-METHYL-EPSILON-CARBOBENZOXY-L-LYSINE HYDROCHLORIDE;N-ALPHA-METHYL-N-EPSILON-BENZYLOXYCARBONYL-L-LYSINE HYDROCHLORIDE;N-ALPHA-METHYL-N-EPSILON-CARBOBENZOXY-L-LYSINE HYDROCHLORIDE;N-ALPHA-METHYL-N-EPSILON-Z-L-LYSINE;N-ME-LYSINE(Z)-OH;N-ME-LYS(Z)-OH;H-MELYS(Z)-OH;H-L-MELYS(Z)-OH HCL
• CAS NO: 201016-22-0
• Molecular Formula: C15H22N2O4
• Molecular Weight: 294.35
• Product Categories: amino acids
• Mol File: 201016-22-0.mol

Chemical Properties

• Boiling Point: 498.7±45.0 °C(Predicted)
• Appearance: /
• Density: 1.159±0.06 g/cm3(Predicted)
• Storage Temp.: Store at RT.
• PKA: 2.46±0.24(Predicted)
• CAS DataBase Reference: N-ME-LYS(Z)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: N-ME-LYS(Z)-OH(201016-22-0)
• EPA Substance Registry System: N-ME-LYS(Z)-OH(201016-22-0)

Safety Data

• Hazardous Substances Data: 201016-22-0(Hazardous Substances Data)

Usage

Uses

Used in Biochemical Research:
N-ME-LYS(Z)-OH is used as a research molecule for understanding the role of protein methylation in biological processes. Its ability to modify proteins and influence cellular function is vital for studying the mechanisms of gene expression and chromatin remodeling.
Used in Drug Development:
N-ME-LYS(Z)-OH is utilized as a potential therapeutic target in drug development, particularly for conditions related to abnormal protein methylation and chromatin remodeling. Its implication in the development of certain diseases, such as cancer, makes it a promising candidate for the creation of new treatment strategies.
Used in Diagnostics:
N-ME-LYS(Z)-OH can be employed as a biomarker in diagnostics to identify and monitor diseases associated with altered protein methylation patterns, providing insights into disease progression and treatment response.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-ME-LYS(Z)-OH is used as a key component in the development of drugs targeting protein methylation pathways. Its role in gene expression regulation and cellular activity makes it a valuable asset in creating medications that can modulate these processes for therapeutic benefit.
Used in Academic Research:
N-ME-LYS(Z)-OH is used as a subject of study in academic research to explore its effects on cellular processes and its potential as a therapeutic agent. Understanding its mechanisms of action can lead to advancements in the fields of molecular biology and medicine.

Upstream product

• 63628-63-7 Nε-benzyloxycarbonyl-L-lysine tert-butyl ester 

Relevant articles and documents

Pmc-protected amino acid esters as substrates in N-alkylamino acid synthesis

N-alkylamino acids may be synthesised via Mitsunobu reaction of N-(2,2,5,7,8-pentamethylchroman-6-sulphonyl-)-amino acid esters with various alcohols and subsequent deprotection.