Aminoácidos com Grupos Protectores

Fmoc-OSu is a matrix that can be used as an absorption enhancer in biological and biochemical studies. The ester hydrochloride form of Fmoc-OSu is soluble in water and methanol, but not in organic solvents such as chloroform or ether. Fmoc-OSu is also a fluorescent derivative that can be used to label glycan structures in primary cells. The reaction solution with anhydrous sodium carbonate and glycan produces a cyclic peptide. This reaction is carried out at room temperature with analytical methods using a spectrophotometer or high performance liquid chromatography (HPLC).

Fmoc-Asp(OtBu)-OH is a fluorescent probe that binds to the integrin receptor. This protein is a cell-surface receptor that binds to collagen, fibronectin and other extracellular matrix proteins. Fmoc-Asp(OtBu)-OH has been shown to inhibit the binding of human cells to collagen in a homogenous assay. The chemical ligation of this amino acid with an amine results in an isopeptide bond, which can be cleaved by trifluoroacetic acid. Fmoc-Asp(OtBu)-OH can be used for the detection of integrin receptors in mammalian cells and sectioned tissues.

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Fmoc-D-Arg(Pbf)-OH is a synthetic peptide that can inhibit the growth of cancer cells. It has been shown to inhibit protease activity in mitochondria and inhibit mitochondrial membrane potential. The uptake of Fmoc-D-Arg(Pbf)-OH by neutrophils is dependent on the presence of superparamagnetic iron nanoparticles, which are taken up by phagocytic cells and used for oxidative burst. Fmoc-D-Arg(Pbf)-OH has a high affinity for mammalian cells but not for bacterial or fungal cells.

Fmoc-Glu-OMe is a small molecule that is synthesized by N-Fmoc chemistry. It has been shown to have synergistic effects with nitrate and antimicrobial agents, such as chloramphenicol, in the inhibition of bacterial growth. Fmoc-Glu-OMe also has strong antibacterial activity against Gram-positive bacteria such as Staphylococcus aureus and Streptococcus pyogenes. In addition, this compound is soluble in water and can be used for the delivery of hydrophobic drugs. This compound may be prepared using natural products or other chemical reactions.

Fmoc-Trp(5-OH)-OH is a molecule that has been shown to have anticancer activity. It inhibits the proliferation of cancer cells and inhibits the production of fatty acids. It also has antiinflammatory properties and inhibits the growth of bacteria by inhibiting chloride channels. Fmoc-Trp(5-OH)-OH has been shown to inhibit the binding of 4-methylumbelliferone (4MU) to human erythrocytes, which is an indicator of its capability as a coumarin derivative. Fmoc-Trp(5-OH)-OH has also been found to be effective against tuberculosis through hydrogen bond interactions with the enzyme mycobacterium tuberculosis DNA polymerase.

Fmoc-4,4-difluoro-L-proline is an antibacterial that binds to the bacterial cell wall by competitive inhibition. Fmoc-4,4-difluoro-L-proline has been shown to be effective in treating inflammatory bowel disease and other inflammatory diseases, such as traumatic brain injury and Alzheimer's disease. Fmoc-4,4-difluoro-L-proline also has inhibitory effects on a number of enzymes, including dehydrogenase and caspases. This drug may also have therapeutic potential for degenerative diseases and autoimmune diseases such as infectious diseases. 6 Fluoro 3 indoxyl beta D galactopyranoside Rifapentine is an anti tuberculosis drug that belongs to the class of rifamycins. It is the most active of the rifamycins for the treatment of tuberculosis. Rifapentine inhibits bacterial growth by binding

Fmoc-Ala-OH-3-13C is a versatile building block that can be used to synthesize a variety of compounds. It is an intermediate in the synthesis of more complex compounds and has been shown to possess high reactivity in peptide coupling reactions. Fmoc-Ala-OH-3-13C has a CAS number of 201489-21-6 and is a fine chemical that can be used for research, development, and other purposes.

Fmoc-Tyr-OH is a peptide that can be used as an agent for the treatment of epidermal growth factor receptor (EGFR) related diseases. It has been shown to be effective in inhibiting the replication of RNA and DNA, which may contribute to the inhibition of tumor growth. Fmoc-Tyr-OH is synthesized through solid phase synthesis where it is reacted with trifluoroacetic acid and particle. This reaction is enhanced by adding an iodination reaction and phosphatase. The polymerase chain reaction then occurs in order to produce more Fmoc-Tyr-OH peptides. Fmoc-Tyr-OH also has a high affinity for acidic ph, making it suitable for use in acidic environments such as tumors.

N-Fmoc-4-methanesulfonylamino-L-phenylalanine is a versatile building block that is used in the synthesis of complex compounds. It can be used as a reagent or speciality chemical, and has been shown to be an effective building block for the synthesis of high quality compounds. N-Fmoc-4-methanesulfonylamino-L-phenylalanine is soluble in water and meets USP requirements for purity. This compound can be used as an intermediate, scaffold, or reaction component.