Fmoc-L-Dap(Poc)-OH - CAS 2250437-44-4

Fmoc-L-Dap(Poc)-OH - CAS 2250437-44-4 Catalog number: BADC-01816

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Fmoc-L-Dap(Poc)-OH is a click chemistry reagent containing an azide group.

Category
ADCs Linker
Product Name
Fmoc-L-Dap(Poc)-OH
CAS
2250437-44-4
Catalog Number
BADC-01816
Molecular Formula
C22H20N2O6
Molecular Weight
408.40

Ordering Information

Catalog Number Size Price Quantity
BADC-01816 -- $-- Inquiry
Description
Fmoc-L-Dap(Poc)-OH is a click chemistry reagent containing an azide group.
Synonyms
(S)-1-(9H-Fluoren-9-yl)-3,8-dioxo-2,9-dioxa-4,7-diazadodec-11-yne-5-carboxylic acid
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(prop-2-ynoxycarbonylamino)propanoic acid
Canonical SMILES
C#CCOC(=O)NCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChI
InChI=1S/C22H20N2O6/c1-2-11-29-21(27)23-12-19(20(25)26)24-22(28)30-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h1,3-10,18-19H,11-13H2,(H,23,27)(H,24,28)(H,25,26)/t19-/m0/s1
InChIKey
SUBBTJIFFMPNNY-IBGZPJMESA-N

Fmoc-L-Dap(Poc)-OH, a protected amino acid derivative widely utilized in peptide synthesis, plays a pivotal role in various applications. Here are four key applications of Fmoc-L-Dap(Poc)-OH:

Peptide Synthesis: Acting as a cornerstone in solid-phase peptide synthesis, Fmoc-L-Dap(Poc)-OH enables the incorporation of diaminopropionic acid residues into peptide chains. This compound facilitates selective deprotection steps, allowing for the construction of intricate peptide sequences with utmost purity and specificity. Its utilization ensures the production of functional peptides crucial for both research endeavors and therapeutic interventions.

Drug Design: Positioned at the forefront of pharmaceutical innovation, Fmoc-L-Dap(Poc)-OH facilitates the development of peptide-based drugs by enabling the strategic introduction of functional groups at specific locations along the peptide chain. This adaptability enhances the stability, bioavailability, and efficacy of peptide drugs. Researchers harness this derivative to engineer peptides tailored to target distinct receptors or pathways.

Bioconjugation: Embraced in the realm of bioconjugation, Fmoc-L-Dap(Poc)-OH serves as a linchpin in linking peptides to diverse biomolecules such as proteins, nucleic acids, or polymers. The protected amine group offers a platform for selective modification and attachment, culminating in the creation of bioconjugates essential for designing diagnostic tools, vaccines, and targeted delivery systems.

Structural Studies: Introducing Fmoc-L-Dap(Poc)-OH into peptide sequences unlocks opportunities for delving into the structural and functional aspects of peptides. Researchers leverage this derivative to explore how specific residues influence peptide folding, stability, and interactions with other molecules, shedding light on peptide dynamics.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Historical Records: DAPOA | Fmoc-L-Dap(Poc)-OH
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