![N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanyl-L-phenylalanine](https://static.cymitquimica.com/cas-image/thumb-webp/339190-fmoc-phe-phe-oh.webp)
CAS 84889-09-8
:N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanyl-L-phenylalanine
Description:
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanyl-L-phenylalanine, commonly referred to as Fmoc-L-Phe-L-Phe, is a synthetic compound primarily used in peptide synthesis and research. It features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The compound consists of two phenylalanine residues, which contribute to its hydrophobic characteristics and potential interactions in biological systems. Its molecular structure includes aromatic rings, which can enhance π-π stacking interactions, making it relevant in studies of protein folding and stability. The presence of the Fmoc group allows for selective protection of the amino group, facilitating the stepwise assembly of peptides. This compound is typically handled under standard laboratory conditions, and its applications extend to drug development, biochemistry, and materials science, where understanding peptide interactions is crucial. As with all chemical substances, proper safety protocols should be followed when handling this compound.
Formula:C33H30N2O5
InChI:InChI=1S/C33H30N2O5/c36-31(34-30(32(37)38)20-23-13-5-2-6-14-23)29(19-22-11-3-1-4-12-22)35-33(39)40-21-28-26-17-9-7-15-24(26)25-16-8-10-18-27(25)28/h1-18,28-30H,19-21H2,(H,34,36)(H,35,39)(H,37,38)/t29-,30-/m0/s1
InChI key:InChIKey=KZPTXQVSHOISSL-KYJUHHDHSA-N
SMILES:C(OC(N[C@@H](CC1=CC=CC=C1)C(N[C@@H](CC2=CC=CC=C2)C(O)=O)=O)=O)C3C=4C(C=5C3=CC=CC5)=CC=CC4
Synonyms:- 2: PN: WO2023003984 SEQID: 2 claimed sequence
- Fmoc-Phe-Phe-OH
- L-Phenylalanine, N-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanyl]-
- L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanyl-
- N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanyl-L-phenylalanine
- Fmoc-FF-OH
- (2S)-2-[[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-phenylpropanoyl]amino]-3-phenylpropanoicacid
- Fmoc-Phe-Phe
- (S)-2-((S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-3-phenylpropanaMido)-3-phenylpropanoic acid
- Fmoc-L-Phe-L-Phe-OH
- FMOC- phenylalanyl-phenylalanine
- See more synonyms
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Fmoc-Phe-Phe-OH
CAS:The nanotube formation of Fmoc-FF has been studied by Gazit and Reches. Jayawarna et al. found that this self-assembling dipeptide forms fibrous hydrogels at pH<8. Such hydrogels are excellently suited for 3D cell microculture formation, they can be modified by addition of Fmoc-amino acids as Fmoc-Lys-OH.Formula:C33H30N2O5Purity:99.67%Color and Shape:White PowderMolecular weight:534.61Fmoc-FF
CAS:Fmoc-FF is a molecular building block. Hydrogels and nanogels made from Fmoc-FF are used for the selective delivery of Dexamethasone to leukemia cells.Formula:C33H30N2O5Molecular weight:534.6017(S)-2-((S)-2-((((9H-Fluoren-9-yl)Methoxy)Carbonyl)Amino)-3-Phenylpropanamido)-3-Phenylpropanoic Acid
CAS:(S)-2-((S)-2-((((9H-Fluoren-9-yl)Methoxy)Carbonyl)Amino)-3-Phenylpropanamido)-3-Phenylpropanoic AcidFormula:C33H30N2O5Purity:0.98Color and Shape:SolidMolecular weight:534.6(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acid
CAS:Formula:C33H30N2O5Purity:97%Color and Shape:SolidMolecular weight:534.6017(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acid
CAS:(S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanamido)-3-phenylpropanoic acidFormula:C33H30N2O5Purity:95%Molecular weight:534.6Fmoc-Phe-Phe-OH
CAS:Fmoc-Phe-Phe-OH is a supramolecular compound that has been synthesized and characterized. It is a carboxylic acid with an amino group at the end of the side chain. Fmoc-Phe-Phe-OH has been shown to be an effective antioxidant, which is due to its ability to regenerate other antioxidants in the body. It also has regenerative properties, as it can be used for cell culture, skin cells, and optical properties. Fmoc-Phe-Phe-OH also has antidiabetic effects, as it can inhibit glucose production by pancreatic beta cells.Formula:C33H30N2O5Purity:Min. 95%Color and Shape:PowderMolecular weight:534.6 g/mol
