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Structure

Fmoc-4-amino-(1-carboxymethyl) piperidine

CAS
221352-82-5
Catalog Number
ACM221352825-1
Category
Amino Acids
Molecular Weight
380.4
Molecular Formula
C22H24N2O4

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Specification

Description
2-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidin-1-yl)acetic acid is a synthetic compound designed as a scaffold for drug discovery. It is commonly referred to as Fmoc-Lys(Dde)-OH in the research community. The compound contains one Lysine (Lys) residue, and the abbreviation Dde stands for the protection group used to prevent the Lysine side chain from reacting during peptide synthesis.
Synonyms
2-(4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)piperidin-1-yl)acetic acid, Fmoc-Lys(Dde)-OH
IUPAC Name
2-[4-(9H-fluoren-9-ylmethoxycarbonylamino)piperidin-1-yl]acetic acid
Canonical SMILES
C1CN(CCC1NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)CC(=O)O
InChI
1S/C22H24N2O4/c25-21(26)13-24-11-9-15(10-12-24)23-22(27)28-14-20-18-7-3-1-5-16(18)17-6-2-4-8-19(17)20/h1-8,15,20H,9-14H2,(H,23,27)(H,25,26)
InChI Key
VLQJIWJYRZIBMP-UHFFFAOYSA-N
Boiling Point
604.151℃at 760 mmHg
Flash Point
319.179℃
Density
1.323 g/cm3
Application
The versatility of Fmoc-Lys(Dde)-OH has led to its use in various scientific experiments, including peptide synthesis, drug discovery, and chemical biology. Peptides and peptidomimetics containing Fmoc-Lys(Dde)-OH have been used as probes for studying protein-protein interactions, enzyme kinetics, and receptor-ligand binding.
Exact Mass
380.174
Functional Group
Fmoc
LogP
3.4029
MDL Number
MFCD01321021
PSA
78.87
Refractive Index
1.649
Storage Temperature
4 ℃
Type
Unusual Amino Acids, Heterocyclic Amino Acids
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