Fmoc-3-(3'-pyridyl)-L-alanine
Need Assistance?
  • US & Canada:
    +
  • UK: +

Fmoc-3-(3'-pyridyl)-L-alanine

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
Fmoc-Amino Acids
Catalog number
BAT-007320
CAS number
175453-07-3
Molecular Formula
C23H20N2O4
Molecular Weight
388.42
Fmoc-3-(3'-pyridyl)-L-alanine
IUPAC Name
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-pyridin-3-ylpropanoic acid
Synonyms
Fmoc-β-(3'-pyridyl)-Ala-OH; Fmoc-(S)-2-amino-3-(3'-pyridyl)propanoic acid
Related CAS
142994-45-4 (D-isomer)
Appearance
White powder
Purity
≥ 99.5% (Chiral HPLC)
Density
1.309 g/cm3
Melting Point
150-170 °C
Boiling Point
645.6°C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C23H20N2O4/c26-22(27)21(12-15-6-5-11-24-13-15)25-23(28)29-14-20-18-9-3-1-7-16(18)17-8-2-4-10-19(17)20/h1-11,13,20-21H,12,14H2,(H,25,28)(H,26,27)/t21-/m0/s1
InChI Key
JQLPMTXRCLXOJO-NRFANRHFSA-N
Canonical SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CN=CC=C4)C(=O)O

Fmoc-3-(3'-pyridyl)-L-alanine, an amino acid derivative extensively utilized in peptide synthesis and biological research, finds diverse applications. Here are the key applications presented with high perplexity and burstiness:

Peptide Synthesis: Integral to solid-phase peptide synthesis, Fmoc-3-(3'-pyridyl)-L-alanine plays a pivotal role in crafting complex peptides. Its pyridyl group fosters unique chemical interactions, enabling the formation of peptides endowed with specific structural and functional properties. This compound is indispensable for generating peptides with a myriad of biological activities, essential for both research endeavors and therapeutic interventions.

Protein Engineering: By integrating Fmoc-3-(3'-pyridyl)-L-alanine into protein sequences, researchers can imbue proteins with novel functionalities. This allows for the exploration of intricate protein structure-function relationships and the development of engineered proteins exhibiting enhanced or entirely new properties. Such modifications are critical for the creation of biocatalysts, biosensors, or therapeutic proteins, pushing the boundaries of protein engineering.

Bioconjugation: Serving as a versatile linker in bioconjugation strategies, Fmoc-3-(3'-pyridyl)-L-alanine offers a myriad of possibilities. Its reactive groups facilitate the attachment of diverse molecules, including drugs, fluorescent tags, or other biomolecules. This feature enables the design of targeted drug delivery systems, imaging agents, and multifunctional bioconjugates tailored for various biomedical applications, showcasing the versatility and potential of this compound.

Pharmaceutical Development: Within the realm of drug discovery, derivatives of Fmoc-3-(3'-pyridyl)-L-alanine are explored for their pharmacological activities. Through structural modifications, researchers can tailor new compounds to interact with specific biological targets, aiding in the identification of lead compounds and the development of novel therapeutic agents across a spectrum of diseases. This avenue of exploration holds immense promise for advancing pharmaceutical development and enhancing treatment options.

Online Inquiry
Verification code
Inquiry Basket