Fmoc Amino Acids

<p>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.</p>

<p>N-alpha-Fmoc-Nepsilon-dansyl-L-lysine is a fluorescent molecule that is synthesized by attaching an allyl group to the amino acid lysine. This fluorescence can be used as a probe for specific interactions with proteins. N-alpha-Fmoc-Nepsilon-dansyl-L-lysine has been shown to interact with copolymers of poly(ethylene glycol) and poly(allylamine). The interaction results in a supramolecular, or self assembling, structure. The molecule's fluorescence can be activated by irradiation and this makes it useful for studying protein target binding.</p>

<p>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.</p>

<p>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</p>

<p>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.</p>

<p>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.</p>

<p>Please enquire for more information about Fmoc-(R)-3-amino-3-(3-trifluoromethyl-phenyl)-propionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-5-hydroxy-L-Nva-OH is a useful building block and reagent that belongs to the group of speciality chemicals. It is a versatile compound that can be used as a reaction component, useful intermediate, or useful scaffold. Fmoc-5-hydroxy-L-Nva-OH is an important building block for organic synthesis. It has been shown to be a good substitute for expensive natural products in the synthesis of pharmaceuticals and other organic compounds.</p>

<p>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.</p>

<p>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).</p>

<p>Fmoc-L-norleucine is a non-natural amino acid that can be used to study the interactions of proteins with cellular receptors. It is synthesized from methylandrostenediol and caproic acid, which are then reacted with sodium salt. The resultant product contains a tertiary amine group that interacts with the surface receptor. Fmoc-L-norleucine has shown affinity for endogenous ligands such as nucleobases and phospholipids on cell membranes. In addition, it has been shown to interact with other proteins through its side chain, including erythrocyte band 3 protein. Fmoc-L-norleucine also has a high affinity for binding to divalent metal ions such as calcium and magnesium in aqueous solution, giving it potential applications in the field of analytical chemistry.</p>

<p>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.</p>

<p>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.</p>

<p>M06246 - Fmoc-Gly-OPfp</p>

<p>M03391 - Fmoc-Thr(Trt)-OH</p>

<p>Applications Fmoc-Lys(5-FAM)-OH (CAS# 1242933-88-5) is a useful research chemical compound.<br></p>

<p>Applications Fmoc-Cit-OPfp (CAS# 1356537-03-5) is a useful research chemical compound. It is an anti-heparin compound.<br>References Scott, R. W., et al.: PCT Int. Appl. (2011), WO 2011084970 A1 20110714;<br></p>

<p>Applications Fmoc-L-Leu-OH-d10 is the labeled analogue of Fmoc-L-Leu-OH (F625015), an amino acid derivative, used in peptide chemistry. It is also one of the novel PPARγ ligands that can activate PPARγ in different ways, that reduces osteoclasts differentiation, and thus are better therapeutic targets in diabetes than traditional antidiabetic drugs.<br>References Haochen, W., et al.: J. Cell. Biochem., 114, 1969 (2013)<br></p>

<p>Applications 8-(Fmoc-amino)-3,6-dioxaoctanoic Acid is a hydrophilic, heterobifunctional spacer.<br>References Koskinen, A., et al.: Bioorg. Med. Chem. Lett., 5, 573 (1995)<br></p>

<p>Versatile small molecule scaffold</p>

<p>N-Fmoc-L-homoserine is a carbohydrate molecule that has been synthesised using solid-phase methodology. It is glycosylated and glycolic, with a carboxy chain. N-Fmoc-L-homoserine is expressed in E. coli cells and purified by acetylation. This compound has been synthesised as part of the carbohydrate antigens project, which aims to produce synthetic glycan structures for use as vaccine adjuvants.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about Fmoc-D-Dab(N3) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about rac Fmoc-trifluoromethylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-Val-Cit-PAB-MMAE including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Fmoc-N-(propargyl)-glycine (Fmoc-PG) is a synthesized and modified amino acid that can be used in the treatment of cancer. Fmoc-PG has been shown to inhibit the growth of tumor cells when conjugated with positron emission radiotracers, such as 18F-Fluorodeoxyglucose, for use in positron emission tomography. Fmoc-PG also inhibits the glucose analogue, which may lead to an improvement of neurological function. Fmoc-PG has been shown to be metabolized by acid conjugates and conjugates, resulting in increased stability and reduced toxicity.</p>

<p>Please enquire for more information about Fmoc-[D10]Leu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about N2-[1-(4,4-Dimethyl-2,6-dioxocyclohexylidene)ethyl]-N6-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-lysine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about Fmoc-L-3-aminomethylphe(boc) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Fmoc-PEG4-NHS ester is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Fmoc-PEG4-NHS ester is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>Fmoc-Glu-OH is a carboxylate that is used in the synthesis of acidic, disulfide bond containing, conjugates. It has been shown to be an effective anticancer agent against MDA-MB-231 cells and other cancer cells. Fmoc-Glu-OH is an antimicrobial agent that inhibits the growth of bacteria by targeting intracellular targets. This drug also binds to bacterial 16S ribosomal RNA and prevents protein synthesis, leading to cell death in the target organism.</p>

<p>Fmoc-D-Hyp(tBu)-OH is a carbonyl compound that belongs to the class of glycopeptide. It has been shown to have anti-cancer activity against thp-1 cells, which are derived from human acute promyelocytic leukemia cells. Fmoc-D-Hyp(tBu)-OH inhibits cell proliferation and induces apoptosis in thp-1 cells. This chemical has also been shown to inhibit the production of collagen, an important component of blood vessel walls, by inhibiting the activity of lysyl hydroxylase. The biological function of this drug is not fully understood but it may be related to autophagy and asymmetric synthesis.</p>

<p>N-alpha-Fmoc-Nepsilon-Boc-D-lysine is a synthetic amino acid that is used for the treatment of bacterial, fungal, and cancer cells. It has been shown to induce apoptosis in cancer cells by increasing the mitochondrial membrane potential and reducing the cellular uptake of glucose. This drug also increases the production of reactive oxygen species in cancer cells, which can lead to cancer cell death. N-alpha-Fmoc-Nepsilon-Boc-D-lysine has been shown to have synergistic anticancer effects when combined with other drugs, such as antibiotics or antimicrobial peptides. NAPBODA has a high affinity for bacterial membranes and can be used as an antimicrobial agent.</p>

<p>Please enquire for more information about Fmoc-O-sulfo-L-tyrosine sodium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fmoc-NH-(PEG)2-COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Fmoc-NH-(PEG)2-COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>