Amino Acids (AA)

<p>N-Boc-pyrroyl-boronic acid is a linker that is used in organic synthesis. It reacts with chloride to form an organochlorine compound, which can be used as an inhibitor of s. aureus or other bacteria. The reaction time for this chemical is shorter than for the corresponding boronic acid, and it does not require the presence of a Lewis acid. This chemical has been shown to have anticancer activity in vitro, and its optimization has been studied using fluorescent carbonyl groups as the active component.</p>

<p>β-(4-Hydroxy-3-methoxyphenyl)propionic acid methyl ester is a fine chemical used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other chemicals. It is also used as a reagent for the detection of alkaloids and for the preparation of valuable speciality chemicals. β-(4-Hydroxy-3-methoxyphenyl)propionic acid methyl ester is an intermediate in organic reactions or can be used to synthesize complex compounds such as antibiotics. It is also an important scaffold that can be modified to produce new drugs with different properties.</p>

<p>6-Methyl-16-dehydropregnenolone acetate (6MDA) is a versatile building block that is used in the synthesis of complex compounds. 6MDA is an intermediate for research chemicals and can be used as a reagent or as a speciality chemical. It has been shown to be useful in the synthesis of many complex compounds, including steroids, nonsteroidal anti-inflammatory drugs, and antibiotics. 6MDA has been shown to have high quality and is a useful scaffold for the synthesis of other compounds.</p>

<p>SB-525334 is a synthetic compound that has been shown to be an inhibitor of the actin molecule. It has been used in cell-based assays to investigate the effects of SB-525334 on renal proximal tubule cells. The compound inhibits the growth and proliferation of carcinoma cells and virus cells, as well as the activity of various types of cell growth factors. SB-525334 is being investigated as a potential diagnostic tool for cancer and other diseases.</p>

<p>Hippuryl-arginine is a peptide hormone that is released by the hypothalamus and stimulates the pituitary gland to release other hormones. It has been shown to increase chemotactic activity in human serum, although it has no effect on carboxypeptidase or soybean trypsin activity. Hippuryl-arginine binds with basic proteins, such as albumin and immunoglobulins, and increases their enzymatic activities. This hormone also inhibits enzymes such as carboxy terminal phosphatases and aminopeptidases that are responsible for degrading amino acids. Activation of hippuryl-arginine may be due to its carboxy terminal group, which is susceptible to cleavage by proteolytic enzymes.</p>

<p>3-Iodo-4-methylbenzamidine is a chemical building block that is used as a reagent for the synthesis of other chemicals. 3-Iodo-4-methylbenzamidine is a versatile building block that can be used to synthesize complex compounds. It can also be used to produce fine chemicals and pharmaceuticals, such as antibiotics, chemotherapeutics, and antivirals. 3-Iodo-4-methylbenzamidine has been shown in preliminary research to have anti-inflammatory properties.</p>

<p>Gamma-Glutamyl-4-methoxy-beta-naphthylamide is a versatile building block that can be used in the synthesis of a variety of complex compounds. It is a high quality chemical that is useful as an intermediate in organic syntheses and as a reagent in research. Gamma-Glutamyl-4-methoxy-beta-naphthylamide has been shown to be an effective scaffold for the preparation of other chemical substances.</p>

<p>N-Boc-D-proline is a lipase inhibitor that is used in the preparation of quinine, aldehyde, and carboxylate. N-Boc-D-proline has been shown to inhibit the activity of the sodium channels, which may be due to its ability to bind to the termini of these channels. The inhibition of sodium channels can lead to a decrease in nerve excitability and seizures. N-Boc-D-proline was synthesized by an organocatalytic method using sodium bicarbonate as the catalyst. It was found that this compound was stereoselective with respect to its activity on different enantiomers of chiral substrates. Preparative methods for N-Boc-D-proline include column chromatography or crystallization with diethyl ether or ethyl acetate. The isolated yield is about 99%.</p>

<p>Please enquire for more information about (5-Chloro-2-methoxyphenyl)(4-(3-nitrophenyl)(2,5-thiazolyl))amine 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 2,3-dimethyl-4-((3-oxo-5-phenylcyclohex-1-enyl)amino)-1-phenyl-3-pyrazolin-5-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>o-Phenanthroline monohydrochloride monohydrate is a ligand that is used in crystallography to study the crystal structure of metal ions. It has been shown to be an efficient catalyst for the ring-opening of chloroformates, and can also be used as an analytical reagent that is capable of detecting chlorine in organic compounds. The hydrate form of o-phenanthroline monohydrochloride has a molecular formula of C12H14ClN3O4·2H2O and a molecular weight of 392.7 g/mol.</p>

<p>Fmoc-D-glu-OtBu is an amide that can be used as a screening reagent for the detection of carbohydrate and periplasmic compounds. It has been shown to inhibit hepatitis in humans, which may be due to its ability to bind with muramyl dipeptide. Fmoc-D-glu-OtBu has also been shown to synergize with other vaccines, such as tetanus and escherichia coli surface antigen.</p>

<p>Please enquire for more information about 2-(2-aza-1-(4-methoxyphenyl)-2-(amino)vinyl)indane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Phenylbutyric acid is a prophylactic antibiotic that has minimal toxicity. It has been shown to significantly up-regulate protein synthesis in kidney cells and to have neural cell protective effects. 4-Phenylbutyric acid also inhibits the production of dextran sulfate, which may be useful for the treatment of liver injury. This compound has been tested as an investigational agent for squamous cell carcinoma and other cancers.</p>

<p>Please enquire for more information about (Des-Gly10,D-Ser4,D-Leu6,Pro-NHEt 9)-LHRH trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methoxycinnamylidene acetaldehyde is a versatile building block with a CAS number of 27394-81-6. It is used in the research and production of fine chemicals, pharmaceuticals, and high quality reagents. 4-Methoxycinnamylidene acetaldehyde can be used as a useful scaffold for the synthesis of complex compounds. This building block is also a useful intermediate in organic chemistry reactions.</p>

<p>4-Bromo-2-methylbenzylamine hydrochloride is a high quality, versatile building block that can be used in the synthesis of many different compounds. It is a reagent that can be used as an intermediate in the production of other compounds. 4-Bromo-2-methylbenzylamine hydrochloride is also a fine chemical and speciality chemical that can be used for research purposes. This compound has been shown to be useful as a reaction component in the synthesis of complex compounds.</p>

<p>6-Amino-7-hydroxy-4-methylcoumarin is an antibacterial agent that has been shown to be effective against a range of Gram-positive and Gram-negative bacteria. It is synthesized from coumarins in nature, but also can be synthesized in the laboratory. This compound has been shown to inhibit bacterial growth by forming a covalent bond with the bacterial enzyme DNA gyrase, preventing the synthesis of DNA. 6-Amino-7-hydroxy-4-methylcoumarin has also been shown to have anti cancer properties.</p>

<p>4-Fluoro-L-tryptophan is an amino acid that is used in the synthesis of proteins. It has a number of uses in molecular biology, including the study of phosphatases, tryptophan synthetase, and mutant strains. 4-Fluoro-L-tryptophan can be used to study the interaction between subunits of these enzymes and to determine kinetic parameters. This compound has been shown to interact with magnetic resonance spectroscopy (NMR) and fluorescence measurements. The biosynthesis of 4-fluoro-L-tryptophan involves two steps: (1) incorporation into protein by tryptophanyl tRNA synthetase; and (2) conversion to tryptamine by phosphatase enzyme.</p>

<p>2-Ethoxy-4-methoxybenzaldehyde is a volatile compound that has been shown to have medicinal properties. It is used to analyze the presence of alcohols and aldehydes in various products. The sensitivity of this compound was optimized by using an analytical method that involved solid phase microextraction (SPME) followed by gas chromatography (GC). The carcinogenicity of this compound was determined by exposing it to rats in a 2 year study, which showed no evidence of carcinogenicity. This compound can also be used as a phenolic or microextraction reagent for the headspace analysis of volatile compounds.</p>

<p>3'-Iodo-4'-methoxyacetophenone is a chemical compound that is used in the synthesis of other organic compounds. It is a byproduct of the reaction between acetophenone and iodomethane. 3'-Iodo-4'-methoxyacetophenone is soluble in most solvents, such as ethanol, ether, chloroform, and acetone. The compound has a CAS number of 79324-77-9.</p>

<p>Perfluoro-2-methylbutane is a pharmaceutical dosage form of a perfluorinated liquid. It is used in clinical practice for the treatment of chronic obstructive pulmonary disease (COPD), asthma, or other respiratory disorders. This drug is also used as an inhalation agent in the treatment of adults with acute bronchitis, emphysema, or other airway obstruction. Perfluoro-2-methylbutane has shown resistance to bacteria that are resistant to natural and synthetic polymers. The diameter of Perfluoro-2-methylbutane particles is between 2 and 10 micrometers and it has a viscosity of about 5 centipoise. It has been shown that the reaction time for this drug can be reduced by adding hexamer, which acts as a surfactant for the gas phase. The active substances in Perfluoro-2-methylbutane are unsaturated ketones such as 3-pentanone, 3-hex</p>

<p>[(4-Methylphenyl)sulfonyl]acetonitrile is a synthetic compound that has been shown to inhibit the enzyme SHP2. This inhibition leads to decreased proliferation of cells and may be useful in the treatment of degenerative diseases. [(4-Methylphenyl)sulfonyl]acetonitrile is an organic solvent and a nucleophilic reagent that reacts with metal carbonates, such as calcium carbonate, to form carbanions. The carbanion intermediate can react with nucleophiles, such as acetonitrile, to form a new compound that is structurally related to the original starting material.</p>

<p>Please enquire for more information about 2-Amino-3-[[[4-(2-methylpropyl)phenyl]methylene]amino]-2-butenedinitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Hydroxy-2-methylbenzyl alcohol is a solvent with a high molecular weight. It is insoluble in water and has good solvency power for organic solvents. 3-Hydroxy-2-methylbenzyl alcohol has anisotropy, which means it can rotate the plane of polarization of light passing through it. 3-Hydroxy-2-methylbenzyl alcohol is used as a reagent to measure the degree of birefringence, which is the property of crystalline materials that causes light passing through them to split into two rays with different polarizations. This property can be used to identify the type and size of chains in crystals. 3HMBAA has been shown to be soluble in organic solvents, but not in water or other nonpolar solvents. The theory behind this is that molecules are generally more soluble in liquids similar to themselves than they are in liquids that are dissimilar from themselves. Hel</p>

<p>Cyclic(glycyl-L-tyrosyl) is a phenolic compound and the main metabolite of the dietary supplement resveratrol. It has been shown to have interactions with cellular transport, as well as the ability to activate a number of proteins that are involved in cellular transport. Cyclic(glycyl-L-tyrosyl) also interacts with hydroxyl groups on proteins and activates them, which may lead to the uptake of these proteins by cells. This interaction between cyclic(glycyl-L-tyrosyl) and hydroxyl groups on proteins may be due to its conformation and affinity for this residue. Cyclic(glycyl-L-tyrosyl) has been reported to inhibit the binding of glucosamine to NUDIX hydrolase, as well as preventing glucosamine from activating NUDIX hydrolase.</p>

<p>D-Ornithine hydrochloride is a synthetic amino acid that is used as a precursor for the synthesis of polyamines in the body. It is also used as an additive in food and animal feed. This amino acid has been shown to inhibit gramicidin production by inhibiting the enzyme acylase. D-Ornithine hydrochloride has also been shown to stimulate the production of ornithine by increasing ATP levels and activating enzymes such as pyruvate kinase, glutamic pyruvate transaminase, and phosphoenolpyruvate carboxykinase. In addition, it has been shown to have chemoenzymatic properties that allow for its use in reactions with fatty acids as substrates. The reaction yield increases with higher substrate concentrations, which can be achieved using immobilized cells or by adding cyclic peptides such as ornithine to the reaction mixture.</p>

<p>N-(2-Chlorobenzyl)-1-phenylpropan-2-amine hydrochloride (CBP) is a potent stimulant drug that is used to treat chronic pain. It has been shown to be effective in the treatment of alopecia areata and inflammatory diseases, such as Crohn's disease, ulcerative colitis, and rheumatoid arthritis. CBP blocks protein synthesis by inhibiting the activity of the enzyme dinucleotide phosphate (DNP). This inhibition leads to the accumulation of adenosine monophosphate (AMP), which inhibits cyclic AMP production and protein synthesis. CBP also prevents the binding of DNP to RNA polymerase II at promoter sites, leading to a decrease in mRNA production. As a result, CBP may inhibit protein synthesis by preventing transcription or translation.</p>

<p>Cbz-L-glutamine is a water soluble compound that is used in the synthesis of pomalidomide. It is synthesized through a stepwise amide formation from methylamine and ethylene diamine. Cbz-L-glutamine has been shown to have an inhibitory effect on cancer cells, which may be due to its ability to break down hydroxamic acids. This chemical reaction causes the release of hydrogen ions, which leads to the disruption of various cellular processes, such as DNA replication and protein synthesis. The uptake of Cbz-L-glutamine by cancer cells has been shown in tissue culture experiments.</p>

<p>H-Cys-Gly-OH is a cyclic peptide that has potent antitumor activity. It was synthesized from glutathione and cysteine, which are naturally occurring amino acids in the human body. The mechanism of action of H-Cys-Gly-OH is not well understood, but it may be due to its ability to bind to α1-acid glycoprotein and other proteins in the blood. The compound also has a redox potential, fluorescence spectra, and structural analysis that can be used for identification purposes. This molecule is stable at acid pH and is easily soluble in water or organic solvents. H-Cys-Gly-OH can be analyzed by titration calorimetry or cyclic voltammetry methods.</p>

<p>N-(2-Oxo-2-phenylethyl)-N-phenylbenzamide is a fine chemical that can be used as a versatile building block and reagent for the synthesis of complex compounds. This compound has been shown to react with both amines and alcohols in the presence of acid to produce useful products. It is also an intermediate for the synthesis of other compounds, such as pharmaceuticals, pesticides, and herbicides. N-(2-Oxo-2-phenylethyl)-N-phenylbenzamide is soluble in organic solvents and can be purified by recrystallization or column chromatography. The purity of this compound can be confirmed by nuclear magnetic resonance spectroscopy (1H NMR) or mass spectrometry (MS).</p>

<p>CCT 241533 is a Chinese herb that has been shown to have anti-cancer properties. It has been demonstrated to inhibit the growth of HL-60 cells and induce apoptosis in these cells. CCT 241533 also inhibits the proliferation of epidermal growth factor (EGF) and induces cell death in response to radiation. This drug also binds to toll-like receptors, which are proteins on the surface of cells that detect pathogens and initiate an immune response. CCT 241533 has been shown to inhibit polymerase chain reactions by competitive inhibition or by binding to DNA, preventing transcription or replication. CCT 241533 may be useful for the treatment of infectious diseases, such as tuberculosis, because it can bind to bacterial 16S ribosomal RNA and inhibit protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division.<br>CCT 241533 has been shown in animal studies to be effective against cervical cancer due to its ability to bind</p>

<p>4-Cyano-L-phenylalanine is an unnatural aminoacid that has been shown to bind to amyloid protein, which is associated with Alzheimer's disease. The binding of 4-Cyano-L-phenylalanine inhibits the synthesis of amyloid protein and prevents the formation of amyloid fibrils. 4-Cyano-L-phenylalanine also irreversibly inhibits the enzyme responsible for the production of hydrochloric acid in bacteria. The x-ray crystal structures of 4-Cyano L-phenylalanine have been determined and show that this compound binds to the active site of the enzyme synthetase, preventing it from forming an amino acid bond. 4-Cyano L-phenylalanine is an analog of 4-L-phenylalanine and, thanks to its cyano (nitrile) group, is a good candidate for use as a fluorescence marker to study the peptide membrane interactions.</p>

<p>(+/-)-6-Chloro-7,8-dihydroxy-3-allyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine HBr is a model system for Parkinson's disease that has been shown to have similar effects on locomotor activity as the dopamine antagonist haloperidol. The drug enhances dopaminergic and cholinergic transmission in the brain by binding to kappa opioid receptors. This leads to an increased release of dopamine and acetylcholine that can be blocked by drugs such as naloxone and atropine respectively. (+/-)-6-Chloro-7,8-dihydroxy 3-(allyl)-1-(phenyl) 2,3,4,5 tetrahydro 1H 3 benzazepine HBr has been shown to decrease camp levels in the caudate putamen region of rats</p>

<p>Fmoc-Lys(Boc)-Wang resin is a synthetic peptide resin that is used in solid-phase peptide synthesis. It is a resin for the synthesis of short, unprotected peptides and has been used to synthesize sequences found in human insulin and other peptide hormones. Fmoc-Lys(Boc)-Wang resin is also used to synthesize peptides with amino acid sequences that are not found in nature, such as those found on the surface of cancer cells. This resin can be used to create antibodies by linking an antigen with the amino acid sequence of interest.</p>

<p>2-Methyl-L-tryptophan is a natural amino acid that is an intermediate in the biosynthesis of tryptophan. It has been used to study protein synthesis and as a potential antibiotic. 2-Methyl-L-tryptophan has been shown to be stereoselective with respect to the enzyme catalysis of its hydroxylation. This active form is converted into the antibiotic thiostrepton by enzymatic reactions.</p>

<p>5-Bromo-2-methoxytoluene is a bromoarene that reacts to form aziridines and phosphotungstic acid. It is used in the synthesis of polyaromatic compounds with steric interactions. 5-Bromo-2-methoxytoluene is also a functional group that can be used as an allosteric modulator. This compound also has stereoisomers that are chiral, meaning they have different structures despite being mirror images of each other. The carbonyl group on the 5-bromo compound is polar, which means it has a charge. The hydrogen bonds between this compound and other molecules are nonpolar, which means they do not have a charge and are more likely to form in a nonpolar solvent.</p>

<p>2-fluoro-5-methoxybenzaldehyde is an asymmetric synthesis that has been shown to inhibit the growth of cancer cells by inhibiting a protein called MT2. 2-Fluoro-5-methoxybenzaldehyde is a nucleophilic compound and reacts with the electrophilic carbon in the enolate to form a sulfoxide, which can be hydrolyzed by acid. This reaction inhibits cancer cell growth as it prevents cellular metabolism and amino acid biosynthesis.</p>

<p>HO-PEG10-OH is a glycol ether that is used as a surfactant in the formulation of intravenous lipid emulsions. It is also used in chromatographic analysis and is capable of reducing the redox potential of biological samples. HO-PEG10-OH has been shown to have pharmacokinetic properties and to be effective against inflammation. HO-PEG10-OH has been shown to inhibit hepcidin, an important regulator of iron metabolism, which may explain its antiinflammatory activity.</p>

<p>Suc-Ala-Ala-Ala-AMC is a fluorogenic substrate that can be used to measure the activity of serine proteases. Suc-Ala-Ala-Ala-AMC has been shown to have high values in mammalian tissue. It also has high activity against many bacteria and fungi, as well as proteolytic enzymes such as collagenase and matrix metalloproteinase. This substrate is activated by phorbol esters and has an optimum pH of 5.5. Suc-Ala-Ala-Ala AMC is a model protein for determining the antibacterial efficacy of various antibiotics.</p>

<p>2-Methylthiopyrimidine-4,6-diamine is a potent inhibitor of the enzyme DNA polymerase. It has shown to be effective against hepg2 cells and other cancer cells. The compound binds covalently to the active site of the enzyme, where it stabilizes the transition state and deshields the electrostatic field around the nucleophilic nitrogen atom. This interaction leads to a decreased affinity for ATP, which is required for DNA synthesis. 2-Methylthiopyrimidine-4,6-diamine also has antimalarial activity and inhibits amide bond formation in hepg2 cells.</p>

<p>Lys(Boc)-OtBu,HCl is a versatile building block and research chemical that can be used for the synthesis of complex compounds. This compound is a useful intermediate and reaction component in organic chemistry. It is also a reagent that can be used to synthesize high-quality chemical products.</p>

<p>Butaphosphan is a drug that has been shown to have clinical relevance for the treatment of metabolic disorders. It is a prodrug that is converted into butaprost-diol, which has been shown to improve insulin sensitivity and reduce aminotransferase activity in rats. Butaphosphan can be used as an alternative to aminotransferase inhibitors such as ursodeoxycholic acid and cholestyramine for the treatment of patients with primary biliary cirrhosis. This drug has also been shown to have a protective effect on fatty acid metabolism, which may be due to its ability to inhibit the activity of enzymes involved in fatty acid synthesis. Butaphosphan is metabolized by cytochrome P450 enzymes and hydroxylases and can be detected using LC-MS/MS methods. The drug has also been shown to have beneficial effects on cortisol concentrations and liver histology when administered orally.</p>

<p>N,N-Dimethylglycine (DMG) is a molecule that inhibits the activity of various enzymes. DMG has been shown to have an inhibitory effect on HIV entry into human cells and can be used in the treatment of HIV infection. DMG has also been found to have an inhibitory effect on energy metabolism and mitochondrial membrane potential, which can lead to increased oxidative stress and inflammation. This molecule is also involved in the synthesis of choline, dimethylglycine, and betaine, which are important for cell signaling and detoxification. DMG has been shown to bind to bile acids and promote bowel motility by increasing peristalsis in patients with chronic constipation. In addition, it has been shown to have anti-inflammatory properties through its inhibition of pro-inflammatory cytokines such as TNF-α and IL-6</p>

<p>H-Hyp-Gly-OH is a dietary supplement that can be used by diabetic patients. It is an amino acid derivative that has been shown to inhibit the production of collagen in cells and help with the prevention of hypertrophy. H-Hyp-Gly-OH has been shown to have upregulated genes for collagen, growth factor, and colony stimulating factor. The use of this product has been tested on mice in which it inhibited the production of type 1 collagen and type 3 collagen by 35%. The use of H-Hyp-Gly-OH also inhibits cell proliferation in human caco2 cells.</p>

<p>4-(Benzyloxy)-3-methoxyphenylacetonitrile is an anti-cancer drug that belongs to the class of dihydroisoquinolines. It is used as a monomer in the synthesis of other drugs and it has been shown to be an effective inhibitor of cancer cells when used with carbamic acid. 4-(Benzyloxy)-3-methoxyphenylacetonitrile is synthesised through the reaction of 2,4-dichloroisonicotinic acid and 3-fluoroacetamide in the presence of a strong acid catalyst. This compound has been shown to have a high level of stereoselectivity, which makes it useful for synthesising other compounds.</p>

<p>2-Methylindole-3-acetic acid is a molecule that has been shown to interact with membrane lipids and induce lipid peroxidation. It also interacts with the molecule creatinine, which is excreted in urine, and has been shown to increase urinary levels of creatinine. 2-Methylindole-3-acetic acid has been shown to have antioxidant activity by scavenging radicals and inhibiting lipid peroxidation. The mechanism for this activity is due to its ability to form hydrogen bonds with radicals and react with them, thereby removing them from the cell membrane. 2-Methylindole-3-acetic acid also interacts with receptor protein within the cell, targeting intracellular targets such as DNA and RNA molecules. This compound is an endogenous hormone that may reduce cholesterol levels in cells.<br>2-Methylindole-3-acetic acid was first isolated from the bark of "Indocalamus latifolius" (</p>

<p>N-Methyldibutylamine is an aliphatic hydrocarbon that has antimicrobial activity. It is a colorless liquid at room temperature and has a boiling point of 78°C. N-Methyldibutylamine can be used as a solvent for polymers and resins, in the manufacture of plastics, and in the production of enamels. It also has potential applications in cancer research due to its ability to inhibit the growth of tumor cells.</p>

<p>D-Alanine amide hydrochloride is a molecule that belongs to the class of organic solvents. It is a chiral compound with high specificity for d-alanine. D-Alanine amide hydrochloride has been shown to block bacterial strains such as Acinetobacter, Ochrobactrum and Stenotrophomonas maltophilia. This drug also inhibits the growth of bacteria by binding to the active site of enzymes, preventing them from catalyzing reactions. The stereoselectivity of this drug is due to its pharmacophore that mimics the three amino acids found in d-alanine: an amide, an aliphatic chain, and a hydroxyl group.</p>

<p>Fmoc-NH-PEG10-propionic acid 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-PEG10-propionic acid 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>