Thymulen 4

Thymulen 4 - Names and Identifiers

Name	N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine
Synonyms	Uplevity Thymulen 4 Ac-KDVY-OH Ac-Lys-Asp-Val-Tyr L-Tyrosine, N2-acetyl-L-lysyl-L-α-aspartyl-L-valyl- N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine (2S,5S,8S,11S)-11-(4-Aminobutyl)-8-(carboxymethyl)-2-(4-hydroxybenzyl)-5-isopropyl-4,7,10,13-tetraoxo-3,6,9,12-tetraazatetradecan-1-oic acid
CAS	757942-88-4

Thymulen 4 - Physico-chemical Properties

Molecular Formula	C26H39N5O9
Molar Mass	565.62
Storage Condition	Keep in dark place,Inert atmosphere,Room temperature

Thymulen 4 - Introduction

N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine, also known as N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine, is a polypeptide compound.

Nature:
N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine is a white crystal or crystalline powder that dissolves in water.

Use:
N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine is a bioactive peptide molecule commonly used in biochemical research and drug development. It can be used in the synthesis of new drugs, fluorescent probes and protein engineering.

Method:
N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine can be synthesized by chemical synthesis. The specific preparation method is relatively complex, and generally requires steps such as peptide synthesis, removal of protecting groups, and activation.

Safety Information:
There are no clear data and research results on the safety of N2-Acetyl-L-lysyl-L-alpha-aspartyl-L-valyl-L-tyrosine. In the use and handling of the compound, the relevant laboratory safety practices should be followed and appropriate precautions should be taken. Further toxicity studies and assessments can be conducted if needed.

Last Update：2024-04-09 21:54:55