CAS 185379-40-2
:(S)-N-FMOC-(2-Pyridyl)alanine
Description:
(S)-N-FMOC-(2-Pyridyl)alanine is a chiral amino acid derivative commonly used in peptide synthesis and drug development. The "FMOC" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, facilitating the selective coupling of amino acids during synthesis. The presence of the 2-pyridyl group introduces a heterocyclic aromatic ring, which can enhance the compound's solubility and influence its biological activity. This compound is typically characterized by its ability to form stable peptide bonds, making it valuable in the construction of peptides with specific sequences and functionalities. Its chirality is significant in pharmaceutical applications, as the (S) configuration often corresponds to the biologically active form of the amino acid. Additionally, (S)-N-FMOC-(2-Pyridyl)alanine can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, this compound is an important tool in the field of medicinal chemistry and peptide research.
Formula:C23H20N2O4
InChI:InChI=1S/C23H20N2O4/c26-22(27)21(13-15-7-5-6-12-24-15)25-23(28)29-14-20-18-10-3-1-8-16(18)17-9-2-4-11-19(17)20/h1-12,20-21H,13-14H2,(H,25,28)(H,26,27)/t21-/m0/s1
InChI key:InChIKey=DXIVJCDZOMUITR-NRFANRHFSA-N
SMILES:C(OC(N[C@@H](CC1=CC=CC=N1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:- (2S)-2-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)-3-(pyridin-2-yl)propanoic acid
- (αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-pyridinepropanoic acid
- 2-Pyridinepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (S)-
- 2-Pyridinepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-
- Fmoc-2-Pal-OH
- Fmoc-3-(2-Pyridyl)-L-alanine
- Fmoc-L-2-Pyridylalanine
- Fmoc-L-3-(2-Pyridyl)-alanine
- FMOC-BETA-(2-PYRIDYL)-L-ALANINE
- FMOC-(S)-2-AMINO-3-(2'-PYRIDYL)PROPANOIC ACID
- N-(9-FLUORENYLMETHOXYCARBONYL)-2-PYRIDYL-L-ALANINE
- (S)-N-FMOC-(2-PYRIDYL)ALANINE
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-2-PYRIDYLALANINE
- FMOC-2'-PYRIDYL-L-ALA
- (S)-N-FMOC-(2-PYRIDYL)ALANINE 95% (98%E.E.)
- Fmoc-L-2-Pyridylala
- Fmoc-beta-(2-pyridyl)-Ala-OH
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(2-PYRIDYL)-L-ALANINE
- N-Fluorenemethoxycarbonyl-L-3-(2-Pyridyl) Alanine
- FMOC-ALA(2-PYRI)-OH
- (S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-PYRIDIN-2-YL-PROPIONIC ACID
- RARECHEM BK PT 0229
- FMOC-ALA(2'-PYRIDYL)-OH
- See more synonyms
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Found 6 products.
2-Pyridinepropanoic acid,a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (aS)-
CAS:Formula:C23H20N2O4Purity:98%Color and Shape:SolidMolecular weight:388.41593-Pyridin-2-yl-L-alanine, N-FMOC protected
CAS:<p>3-Pyridin-2-yl-L-alanine, N-FMOC protected</p>Purity:99%Molecular weight:388.4159g/molFmoc-3-(2'-pyridyl)-L-alanine
CAS:<p>Fmoc-3-(2'-pyridyl)-L-alanine is an acid molecule that has been shown to have anti-cancer properties. It is a polysaccharide polymer used in the preparation of polyvinyl alcohol and polyvinyl acetate. The phosphatase activity of Fmoc-3-(2'-pyridyl)-L-alanine was first observed in the 1970s, when it was found to be an effective inhibitor of acid phosphatase. This structural study has also revealed the effects of Fmoc-3-(2'-pyridyl)-L-alanine on cancer cells, which may be due to its ability to prevent cell division and genetic control. Fmoc-3-(2'-pyridyl)-L-alanine is also known as a monoclonal antibody that can bind to specific structures on cancer cells, such as antigens and receptors, which may be responsible for these effects.</p>Formula:C23H20N2O4Purity:Min. 95%Color and Shape:SolidMolecular weight:388.42 g/mol(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(pyridin-2-yl)propanoic acid
CAS:Formula:C23H20N2O4Purity:95%Color and Shape:SolidMolecular weight:388.423Fmoc-l-2-pyridylalanine
CAS:Controlled Product<p>Applications Fmoc-l-2-pyridylalanine<br></p>Formula:C23H20N2O4Color and Shape:NeatMolecular weight:388.42





