Amino Acids (AA)

<p>Applications 3,5-Diiodo-DL-tyrosine is used for diagnosis of hypothyroidism caused by DEHAL1 gene defects.<br>References Encinas, S., et al.: Chem. Res. Toxicol., 11, 946 (1998), Daneshvar, A., et al.: Chemosphere, 80, 301 (2010), Eriksson, J., et al.: Photochem. Photobiol., 86, 528 (2010),<br></p>

<p>Applications 3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide is used in the novel synthesis of benzoin catalyzed by thiazolium salts.<br></p>

<p>Applications 1,2-Bismethylphenidate is an impurity of methylphenidate (M325880), an CNS stimulant.<br>References Greenblatt, E.N., et al.: J. Pharmacol. Exp. Ther., 131, 115 (1961), Padmanabhan, G.R., Anal. Profiles Drug Subs., 10, 473 (1981), Srinivas, N.R., et al.: Pharm. Res., 10, 14 (1993),<br></p>

<p>Stability Hygroscopic<br>Applications Used in the manufacturing of L-tryptophan by enzymic reaction.<br>References Franke, L., et al.: J. Med. Chem., 48, 6997 (2005), Fox, T., et al.: Curr. Top Med. Chem., 6, 1579 (2006),<br></p>

<p>Applications Ethyl 2-chloro-2-(2-(4-methoxyphenyl)hydrazono)acetate (cas# 27143-07-3) is a useful research chemical.<br></p>

<p>Applications DL-glutamine<br></p>

<p>Applications 2-Methoxy-1-[4-(oxiranylmethoxy)phenyl]ethanone (cas# 110458-44-1) is a compound useful in organic synthesis.<br></p>

<p>Applications L-Lysine-3,3,4,4,5,5,6,6-d8 Dihydrochloride, is the labelled L-Lysine, a naturally occurring amino acid which is used in the labelling of human bone marrow mesenchymal stem cells for analysis.<br>References Rocha, B. et al.: J. Prot. Res., 11, 5350 (2012); Kumar, D. et al.: Polym. J., 45, 160 (2013);<br></p>

<p>Stability Hygroscopic<br>Applications Hexanoyl-L-carnitine-(N-methyl-d3) Chloride, is the labeled analogue of Hexanoyl-L-carnitine Hydrochloride (H294440), which is used as reactant in the synthesis of carnitine benzyl esters as prodrugs.<br>References Gong, X., et. al.: J. Chem. Res., 6, 327 (2008)<br></p>

<p>Stability Moisture Sensitive<br>Applications N-Methyl-1H-imidazole-1-carboxamide is a useful Methyl Isocyanate (MIC) substitute.<br></p>

<p>Applications 2,3-Dihydroxy-2-methylbutanoic Acid Sodium Salt is a useful research chemical.<br></p>

<p>Applications L-Leucic Acid is a reagent in the synthesis of cryptophycins based macrocyclic depsipeptides which are used as tubulin inhibitors.<br>References Kumar, A., et al.: Eur. J. Med. Chem., 93, 55 (2015)<br></p>

<p>2,4-Dichloro-6-phenyl-1,3,5-triazine is a triazine that has been synthesized and characterized by gel permeation chromatography and powder diffraction analysis. This compound is insoluble in organic solvents due to its high molecular weight. 2,4-Dichloro-6-phenyl-1,3,5-triazine has a number of different applications in the field of polymer science as an acceptor for activated polymers. It can also be used for thermally or photophysically activated polymers. The molecular structure of this compound was determined using x-ray crystallography and molecular modelling techniques.</p>

<p>Sex pheromone inhibitor IPD1 is an antibody that inhibits the production of sex pheromones by Streptococcus faecalis. It is used to diagnose and treat allergic diseases, such as atopic dermatitis or bronchial asthma. This antibody binds to a protein called polypide, which is involved in the synthesis of sex pheromones, and inhibits its activity. It has been shown to inhibit the production of sex pheromones by Streptococcus faecalis when analyzed using an SDS-polyacrylamide gel electrophoresis method. Sex pheromone inhibitor IPD1 also binds to antibodies against streptococcus, acari, and other bacteria.</p>

<p>D-Thiaproline is a pro-inflammatory cytokine that belongs to the group of tnf-α. It has been shown to have depressant activity on mitochondria and can be used as a sample preparation agent. D-Thiaproline has also been shown to inhibit the uptake of various neurotransmitters, such as serotonin and dopamine, in rat brain synaptosomes. This compound also has functional groups, such as hydroxyl, carboxyl, and amino acid groups, which are necessary for reactions with other molecules. D-Thiaproline is an isomer of L-thiaproline and can be differentiated from this form by its protonated amine group at pH 7.0 and by its zwitterionic nature.</p>

<p>4-(4'-Formyl-3'-methoxyphenoxy)butanoic acid is a carboxylate that can be used as a preloaded reagent for the synthesis of peptides, proteins, and other organic molecules. 4-(4'-Formyl-3'-methoxyphenoxy)butanoic acid has been shown to be an efficient linker for solid-phase peptide synthesis. 4-(4'-Formyl-3'-methoxyphenoxy)butanoic acid is labile to hydrolysis and so should be stored in an organic solvent such as dimethylsulfoxide. The carboxylate group is readily available in the form of its sodium salt, which can be synthesized by reacting sodium acetate with formaldehyde.</p>

<p>Suc-Gly-Pro-Leu-Gly-Pro-AMC (SGLP) is a synthetic substrate that is hydrolyzed by proteases and has been used as a model substrate in protease studies. It has been shown to be cleaved by a number of enzymes, including chymotrypsin, trypsin, elastase, and cathepsin D. The hydrolysis products are sucrose glycolate, glycerol phosphate, leucine amino acid ester, and proline amino acid ester. SGLP has been shown to have low bioavailability in human liver cells and heart tissue. Studies have also shown that SGLP can stimulate the production of myelocytic cells in vitro. This activity may be due to its ability to act as an immunomodulator or by targeting tissue enzyme activities.</p>

<p>4,6-Dihydroxy-5-methoxypyrimidine is a white crystalline solid. It is soluble in alkali, acid ethyl, and alcohol. This compound can be used as a solvent for organic substances and has been shown to methylate phosphorus oxychloride. 4,6-Dihydroxy-5-methoxypyrimidine is also used in the synthesis of nucleosides.</p>

<p>Ponazuril is a veterinary drug that belongs to the group of chemotherapeutics. It is used in the treatment of endoparasites, such as nematodes and cestodes, which are parasites that live inside the human body. Ponazuril is administered orally or by injection and has been shown to have minimal toxicity in CD-1 mice. Ponazuril binds to DNA polymerase, inhibiting RNA synthesis and protein synthesis. This leads to cell death by apoptosis and necrosis. The drug also inhibits DNA replication in the parasite and blocks parasite growth.</p>

<p>Prednisolone is a steroid hormone that has been used for the treatment of inflammatory bowel disease. It has been shown to be effective in the treatment of bowel diseases and is also used as a replacement therapy for adrenal insufficiency. Prednisolone has an excellent safety profile and does not cause insulin resistance or weight gain, unlike some other steroids. It can be used to treat inflammatory diseases such as rheumatoid arthritis and psoriasis. The anti-inflammatory properties of prednisolone are due to its ability to bind to the mineralocorticoid receptor, which prevents the binding of cortisol. This blocks the conversion of cholesterol into pregnenolone, which is required for the production of glucocorticoids and mineralocorticoids. 16a-Methyl-9,11-dehydro prednisolone (16D) is a metabolite that can be found in blood plasma after oral administration of prednisolone. 16D binds</p>

<p>Ac-Phe-Arg-AMC hydrochloride is a versatile building block that is used in the synthesis of complex compounds and research chemicals.<br>It is a fine chemical with CAS No. 177028-04-5. Ac-Phe-Arg-AMC hydrochloride is soluble in water, ethanol, and acetone, and insoluble in ether. This compound can be used as an intermediate for the synthesis of research chemicals with high quality or as a reagent. Ac-Phe-Arg-AMC hydrochloride can be used to produce a variety of useful scaffolds for medicinal chemistry or organic chemistry applications.</p>

<p>Cyclo(-Pro-Val) is a type of natural product that has been shown to inhibit the growth of tumor cells. Cyclo(-Pro-Val) is a metabolite produced by the fungus Cryptococcus neoformans and may serve as a potential anti-cancer drug. The compound blocks mitochondrial membrane potential, which prevents cancer cells from multiplying. Cyclo(-Pro-Val) has also been shown to inhibit the growth of bacteria such as Pseudomonas aeruginosa and Burkholderia cepacia complex, although it has little or no effect on other types of bacteria and fungi.</p>

<p>Sar-Gly-OH is a high quality, reagent chemical that is a useful intermediate in the production of complex compounds. It has CAS No. 38082-72-3 and can be used as a fine chemical, speciality chemical, or research chemical. Sar-Gly-OH is also a versatile building block that can be used in the production of many different types of compounds. It has been shown to be an important reaction component in the synthesis of several types of pharmaceuticals and other organic materials.</p>

<p>L-Methionine 4-nitroanilide is a polymerase chain reaction (PCR) substrate. It has been shown to bind to DNA with calcium and to have protease activity. L-Methionine 4-nitroanilide is a synthetic substrate used in the biochemical study of serine proteases. L-Methionine 4-nitroanilide has been found to be active against P. aeruginosa and thermococcus, but not against mosquitoes. The optimum pH for this compound is 7 and it can be found at a concentration of 10mM in the range of pH 5 - 8.</p>

<p>N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide is a serotonin analog that has been shown to inhibit the production of tryptophan decarboxylase in organisms. This compound has also been shown to be an inhibitor of the biosynthesis of p-coumaric acid, which is involved in the synthesis of lignin, phytoalexins, and other phenolic compounds. N-(2-indol-3-ylethyl)-3-phenylprop-2-enamide may be useful as a fungicide against pyricularia or as an antimicrobial against microbial infections.</p>

<p>Ethyl 5-methylindole-2-carboxylate is an antioxidant that is used as a reagent in the synthesis of other compounds. It has been shown to inhibit cancer cell growth in vitro via its ability to inhibit the metabolic activity of human hepatoma cells. Ethyl 5-methylindole-2-carboxylate has also been shown to have cytotoxic activity against human hepatoma cells in vitro, and may be a potential anticancer drug candidate.</p>

<p>3-Methoxy-4-nitrobenzoic acid methyl ester is a dianellidin, a type of natural product. It is an ionizing acid that catalyzes the reaction between carboxylic acids and hydroxyl compounds. This compound is used to produce some drugs, such as methyldopate, which is an antiarrhythmic drug that slows heart rate. The catalytic rate of 3-methoxy-4-nitrobenzoic acid methyl ester can be increased by buffers and solvents (e.g., methanol). These compounds increase the concentration of the reactants in solution and reduce the activation energy required for the reaction to take place. Uncatalyzed reactions are slow because there are no molecules to act as intermediates in the process.</p>

<p>Please enquire for more information about L-γ-Glutamyl-3-(1-propenylsulfinyl)-L-alanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Valine tert-butyl ester hydrochloride is a chiral diastereomeric, stereocontrolled acid ester. This product is a kinetically controlled reaction of L-valine and toluene that produces a racemic mixture of the cis and trans isomers in the ratio of 1:1. The cis isomer has been shown to be more effective than the trans isomer as a peptidomimetic. This product also exhibits stereogenic properties when reacted with acid anhydrides.</p>

<p>2-Amino-6-bromo-4-methoxyphenol (2ABMP) is a benzyl compound that can be used as a substitute for 2,4-diaminophenol. It has been shown to have estrogenic activity and may function as an estrogen receptor agonist. 2ABMP has also been shown to inhibit the growth of breast cancer cells in culture. The role of this drug in the treatment of breast cancer is not yet clear, but it may be useful in combination therapy with other drugs.</p>

<p>Glutamic acid is a non-essential amino acid that is present in all cells. It is one of the most abundant amino acids and plays an important role in the biochemical properties and biological properties of living organisms. Glutamic acid has been found to be an important neurotransmitter and is involved in neuronal activity, which can lead to death. It also has been shown to be a potent inhibitor of DNA polymerase, which may explain the structural analysis of glutamic acid as a divalent cation coordination-activator molecule. Glutamate can be used as a model system for studying glutamate receptor function and its optimum concentration is determined using vitro assays. The dinucleotide phosphate (NADPH) oxidase pathway may be involved in the toxicity of glutamic acid as it produces reactive oxygen species.</p>

<p>1,4-Phenylenediacrylic acid is a yellow crystalline solid that has been shown to be carcinogenic in rodents. It is structurally similar to benzene and may have the same carcinogenic properties. 1,4-Phenylenediacrylic acid has been found to cause genetic damage in mammalian cells, which may lead to cancer. There are databases for carcinogenicity, mutagenicity, and toxicology of 1,4-Phenylenediacrylic acid. 1,4-Phenylenediacrylic acid also belongs to the subset of organic chemicals that are classified as carcinogens by IARC or NTP.</p>

<p>2-[4-(4-Chloro-a-phenylbenzyl)-1-piperazinyl]-ethoxyacetic acid hydrochloride is a chemical compound that has been used to investigate the possible neuroprotective effects of cetirizine, an antihistamine. This drug was developed as a prodrug of cetirizine, which is converted in vivo to its active form. The main mechanism of action for this drug is inhibition of histamine release from mast cells and basophils by blocking H1 receptors. 2-[4-(4-Chloro-a-phenylbenzyl)-1-piperazinyl]-ethoxyacetic acid hydrochloride has also been shown to have beneficial effects on allergic symptoms and bowel disease in experimental models and clinical properties.</p>

<p>FA-Leu-Gly-Pro-Ala-OH is a gelatinase inhibitor that inhibits the action of collagenase, an enzyme that breaks down collagen. It has been shown to inhibit the growth of cancer cells in vitro and may be useful as a therapeutic agent against skin cancer. FA-Leu-Gly-Pro-Ala-OH binds to the active site of the enzyme and blocks its catalytic activity by preventing proton transfer during the hydrolysis of peptide bonds. This inhibitor also has proteolytic properties, which are due to its ability to cleave proteins with basic amino acids such as arginine and lysine. The inhibitory effects of FA-Leu-Gly-Pro-Ala-OH on histological analysis were also tested on fibroblast cells with collagenase activity, which showed a significant reduction in enzyme activity after incubation with this inhibitor.</p>

<p>N-Boc-2-bromoethylamine is a chemical compound that is used as a gadolinium chelate. This molecule has been shown to be chemically stable and can be easily synthesized in high yield, which makes it an ideal candidate for use in cell culture experiments. The reaction solution of N-Boc-2-bromoethylamine with serine proteases, such as trypsin and chymotrypsin, has been shown to result in the formation of peptides with amide bonds at the C terminus. This process is called a "Michael addition." The 2-nitroimidazole group of N-Boc-2-bromoethylamine is potent inhibitor of protein kinases and has been shown to inhibit hypoxic tumor growth by inhibiting the uptake of glucose by cancer cells. It also has antimicrobial properties, acting as an affinity ligand for binding to bacterial or fungal cells.</p>

<p>N-Boc-L-prolinol is a chiral proline derivative that has been modified with an allyl group. It is a potent nicotinic acetylcholine antagonist, and it has been shown to have immune functions in vitro. The synthesis of N-Boc-L-prolinol occurs through a three-step process involving the use of organocatalysts, asymmetric synthesis, and stereoselective reactions. This molecule is also useful for the study of apoptotic signaling pathways in cells.</p>

<p>H-Trp-Pro-OH is an amide that can be used as a model system in the preparation of collagen. It has been shown to inhibit the linker between collagen molecules, which may lead to the formation of proline-rich peptides. H-Trp-Pro-OH has also been found to have anticancer properties, and inhibits cancer cell growth by inhibiting protein synthesis and promoting apoptosis. H-Trp-Pro-OH was found to inhibit cancer cells through a mechanism that is not yet fully understood, but it may involve both competitive inhibition of amino acids and activation of apoptosis through reactive oxygen species.</p>

<p>N2-Phenoxyacetyl guanine is a labile nucleoside that can be synthesized by the aminoacylation of guanosine with phenoxyacetic acid. It has been shown to have an important role in oxidative DNA damage, which may lead to mutagenesis and cancer. N2-Phenoxyacetyl guanine is stereoselective and binds preferentially to the GGC sequence, and it is also aminopropylated at its 2′ position. This nucleoside is not ionizing but can be degraded by radiation or enzymes such as deaminases.</p>

<p>N-Methyl-4-pyridone-3-carboxamide is a nonnutritive sweetener that has been shown to have no effect on peroxisome proliferation. It also had no effect on the levels of fatty acids in rat cardiomyocytes and did not affect uv absorption. N-Methyl-4-pyridone-3-carboxamide binds to the receptor α subunit of the taste receptor and inhibits adenosine uptake, which may be responsible for its effects on depression. This compound also alters energy metabolism by inhibiting mitochondrial ATP production and glycolysis.</p>

<p>2-Boc-6-Chloro-3,4-dihydro-1H-isoquinoline-1-carboxylic acid is a useful scaffold for the production of various chemical compounds. It is a versatile building block that can be used as an intermediate in various chemical reactions or as a speciality chemical. 2-Boc-6-Chloro-3,4-dihydro-1H-isoquinoline-1 carboxylic acid has been shown to be a high quality and reliable reagent for use in research and development.</p>

<p>4-Methylpyrazole is a competitive inhibitor of alcohol dehydrogenase, which can be used to treat methanol and ethylene glycol poisoning. It is also used to inhibit the metabolism of ethanol by blocking the conversion of ethanol to acetaldehyde. 4-Methylpyrazole is metabolized into 4-methylpyridinium ion (4MP) by alcohol dehydrogenase, which prevents the conversion of acetaldehyde to acetic acid. This results in an increase in blood levels of acetaldehyde and a decrease in blood levels of acetic acid, leading to an accumulation of toxic metabolites such as formic acid. In addition, 4-methylpyrazole inhibits the enzyme glycol dehydrogenase that breaks down glycols into their harmless components. This leads to an accumulation of toxic intermediate products that are converted back into glycols.</p>

<p>Fmoc-a-Me-Glu(OtBu)-OH is a versatile chemical that can be used to synthesize complex compounds in the laboratory. It is a useful building block for organic synthesis and can be used as a reagent, speciality chemical, or useful scaffold. It has been shown to be of high quality and is often used as an intermediate for other compounds. Fmoc-a-Me-Glu(OtBu)-OH is also listed by CAS number 1072845-48-7.</p>

<p>H-Asp(Lys-OH)-OH is a metabolite that is an intermediate in the fatty acid oxidation pathway. It may be involved in the progression of colorectal carcinoma by inhibition of fatty acid synthesis, leading to the accumulation of fatty acids and subsequent death. This metabolite can also be used to identify potential biomarkers for colorectal cancer. H-Asp(Lys-OH)-OH can be detected using liquid chromatography coupled with mass spectrometry (LC/MS).</p>

<p>2-Bromo-4'-phenylacetophenone is a methanol solvent that is used as an intermediate in the synthesis of phenacyl. It is also used as a reagent for the titration of fatty acids and for the determination of terminal alkynes. 2-Bromo-4'-phenylacetophenone has been shown to have antibacterial activity against Mycobacterium tuberculosis, which may be due to its ability to inhibit protein biosynthesis. This compound can also be used as an analytical tool for determining the mass of organic acids. The solubility properties of 2-bromo-4'-phenylacetophenone are similar to those of ethyl acetate and ethanol, making it useful as a solvent in analytical methods.</p>

<p>Hydrochloride salt</p>

<p>3-(4-Fluorobenzoyl)-6-Methoxy-2-Methyl-1H-Indole-1-Acetic Acid is a prodrug that is metabolized to 6-fluoro-3,4 dioxo tamoxifen in the liver. It has been shown to have anticholinergic, cytosolic calcium and c1-4 alkyl properties. 3-(4-Fluorobenzoyl)-6-Methoxy-2-Methylindole Acetic Acid also has a basic group, cyclopentane ring, and pyridine ring.</p>

<p>2-Fluoro-3-methylaniline is a reactive, biomolecular, research chemical that belongs to the class of allosteric modulators. It has been shown to have muscarinic M1 receptor antagonist activity and can be used as a pharmacophore for the development of cholinergic drugs. 2-Fluoro-3-methylaniline also has carbonylation and formylation properties. It forms 1-bromo-2-iodobenzene through reductive amination with benzyne. This reaction is both intramolecular and allosteric, thus making it a useful tool for studying these types of reactions.</p>

<p>4-Fluoro-2-methoxybenzoic acid is a versatile building block that is used in the synthesis of many complex compounds. It is a reagent, which means it can be used as an intermediate in the synthesis of other compounds. 4-Fluoro-2-methoxybenzoic acid is also a useful scaffold for the preparation of new chemical entities with specific pharmaceutical properties. The CAS number for this compound is 395-82-4.</p>

<p>5-Methylindole-2-carboxylic acid (5MICA) is a synthetic compound that has been shown to be cytotoxic in vitro. It has been shown to inhibit the growth of multiple cancer cell lines, including hepatoma cells, and is currently being studied as a potential anticancer drug. 5MICA inhibits the synthesis of protein and RNA by binding to the ribosome. This inhibition leads to cell death by apoptosis. 5MICA also exhibits an antimicrobial effect against opportunistic fungal pathogens such as Candida albicans, Aspergillus fumigatus, and Cryptococcus neoformans. The mechanism for this inhibition is unknown but may involve inhibition of protein synthesis or other cellular processes.</p>

<p>6-Chloro-7-methylchromone-2-carboxylic acid is a fine chemical that has been used as a versatile building block for the synthesis of complex compounds. It has been shown to be an effective reaction component in the synthesis of 1,4-benzoquinones and N'-acylhydrazones. 6-Chloro-7-methylchromone-2-carboxylic acid is also a useful intermediate in the preparation of other chemicals, such as pharmaceuticals and pesticides. This compound can be used as an additive to improve the quality of high purity reagents.</p>

<p>D-His(Bzl)-OH is a chromatographic ligand that has been used in the preparation of recombinant proteins and vaccines. D-His(Bzl)-OH is an amphipathic molecule with a hydrophilic head group and hydrophobic tail group. It has been shown to be an effective inhibitor of papillomavirus, as well as other viruses such as HIV, herpes simplex virus, poliovirus, and vesicular stomatitis virus. D-His(Bzl)-OH has also been shown to induce antibody production in micelles when conjugated to antigens. The binding of D-His(Bzl)-OH to the viral envelope protein can be increased by increasing pH or by adding ammonium sulfate or chloride ions. Increasing the flow rate during chromatography will also increase the progressions of D-His(Bzl)-OH through the column.</p>

<p>Fmoc-Cys(Trt)-OH is a cyclic peptide that has potent antitumor activity. It binds to albumin and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. Fmoc-Cys(Trt)-OH has been shown to be effective against cancer cells in vitro and in vivo. Fmoc-Cys(Trt)-OH also binds the plasma glucose, which may be due to its ability to impede insulin release from the pancreas. This compound is synthesized by a stepwise light-induced solid-phase synthesis with trifluoroacetic acid as a solvent.</p>

<p>Fmoc-12-amino-4,7,10-trioxadodecanoic 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-12-amino-4,7,10-trioxadodecanoic 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>

<p>H-Arg-AMC hydrochloride is a denaturing agent that is used to prevent the proteolytic degradation of proteins in muscle and other tissues. It has been shown to inhibit the activity of lipase, myofibrillar, and endoplasmic enzymes. H-Arg-AMC hydrochloride also has cancer preventive effects by inhibiting the growth of tumor cells. H-Arg-AMC hydrochloride has been shown to have high values in notochord markers, supplementing cytosolic markers, and endogenous markers.</p>

<p>2-Nitro-p-phenylenediamine is a chemical substance that can be used as a predictive biomarker for allergic reactions. It is an amine with the chemical formula C6H5CH2N2O2. It is soluble in water, ethanol, and ether, but insoluble in acetone and diethylether. 2-Nitro-p-phenylenediamine has been shown to cause cutaneous lesions in animal studies and has been classified as a possible human carcinogen by the International Agency for Research on Cancer (IARC). This compound was not mutagenic to bacteria or yeast strains tested, but it did cause chromosome aberrations in cultured human lymphocytes. The metabolite profile of 2-nitro-p-phenylenediamine has been studied in rats treated with this compound at different doses. When administered orally to rats at a dose of 50 mg/kg body weight per day, 2 nitro p phenylened</p>

<p>Reference material for food analysis</p>

<p>L-Leucine 4-nitroanilide serves as a substrate for the colorimetric determination of leucine aminopeptidase. The application of L-Leucine-p-nitroanilide includes its utilization as a substrate in studies assessing the intestinal leucine aminopeptidase activity of juvenile rainbow trout (Oncorhynchus mykiss). Additionally, it plays a role in insulin-regulated aminopeptidase inhibition assays and is employed to determine exopeptidase activity.</p>

<p>3'-Methoxypropiophenone is an acylating agent that is used in the synthesis of racemic and optically active phenylacetic acids. It can be prepared by the reaction of ketones with methoxypropiolic acid, which is catalyzed by a base such as sodium ethoxide. 3'-Methoxypropiophenone also has been shown to undergo transformation reactions with hydrogenolysis and salt formation. The deprotection step involves removal of a protective group such as dimethylamine or diastereomer.</p>

<p>4-Methylindole-3-carboxaldehyde is a lipophilic extract that inhibits the growth of fungi. It has been shown to be effective against phytopathogenic fungi, and it has been used as an antibiotic in the treatment of bacterial infections. 4-Methylindole-3-carboxaldehyde is an analog of streptochlorin, which inhibits protein synthesis by binding to the ribosome. This leads to cell death by inhibiting the production of proteins vital for cell division. 4-Methylindole-3-carboxaldehyde also has antifungal activity against Candida albicans and Trichophyton mentagrophytes.</p>

<p>3-Amino-2-chloro-6-methylphenol is a chemical substance that has been shown to have potential as a therapeutic agent for treating human cancers. 3-Amino-2-chloro-6-methylphenol has been shown to express in humans and is sensitive to the human body, which may be due to its ability to react with DNA and damage it. 3-Amino-2-chloro-6-methylphenol has also been shown to have an inhibitory effect on other chemical substances that are responsible for allergic reactions. This chemical substance has not yet been validated in animal models or clinical trials.</p>

<p>Please enquire for more information about ent-(14S)-3-Methoxy-17-methylmorphinan including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Pyroglutamyl-L-histidyl-L-prolinamide (PGC) is a pyrrolidine that is used for the treatment of neurologic disorders. It has been shown to be effective in treating depression and a number of other neurologic disorders, including Parkinson's disease, Alzheimer's disease, and epilepsy. PGC has also been shown to have an antidepressant effect in women with depression who are pregnant or have recently given birth. In addition, it has been found to be clinically effective in the treatment of symptoms associated with Parkinson’s Disease. PGC is not absorbed into the bloodstream and must be injected directly into muscle tissue or fat cells in order to produce its therapeutic effects.</p>

<p>D-Alanine benzyl ester p-toluenesulfonate salt is a fine chemical that is used in research and development. It is a versatile building block that can be used as an intermediate or a reaction component. D-Alanine benzyl ester p-toluenesulfonate salt has been shown to have high quality, which makes it useful for the production of complex compounds. This compound can be used as a speciality chemical or as a reagent in research.</p>

<p>Z-Val-Met-OH is a high purity synthetic compound that can be used as a research tool in cell biology, ion channels and peptides. This compound is an activator of the receptor for bradykinin and has been shown to inhibit the activity of protein kinase C. Z-Val-Met-OH is also a ligand for the acetylcholine receptor and has been shown to inhibit acetylcholinesterase, leading to an increase in acetylcholine levels. Z-Val-Met-OH binds to the receptor for insulin and can be used as an inhibitor of insulin release from pancreatic beta cells.</p>

<p>4-Amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide is an amide that is used to treat HIV infections. It has been shown to have potent anti-viral activity against HIV infected cells in the laboratory and can inhibit the replication of HIV by interfering with the virus's ability to use the reverse transcriptase enzyme. 4ABAB has been shown to bind to the enzyme ribonuclease H (crth2), which is responsible for breaking down viral RNA. This binding prevents crth2 from cleaving viral RNA, thus inhibiting DNA synthesis and preventing cell death. 4ABAB also interferes with a hydrogen bond between ethyl group and the hydroxyl group on crth2, leading to a decrease in activity.</p>

<p>Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic 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-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic 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>

<p>Please enquire for more information about 4-Chloro-1-(2-methyl(8-quinolyloxy))-2-nitrobenzene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>O-tert-Butyl-L-tyrosine is a biostable, low molecular weight, hydrophobic, and diffraction active compound. It can be used as a solvent for chiral and non-chiral compounds. O-tert-Butyl-L-tyrosine has been shown to have biological function in the synthesis of peptides, proteins, and amides. This compound also has an effect on gelation and is often used in organic solvents.</p>

<p>1-Phenyl-piperazin-2-one is a versatile chemical that can be used as a building block in the synthesis of complex compounds. This compound is also used as a reagent and speciality chemical. It is an important intermediate in organic synthesis and has been used in the preparation of pharmaceuticals, pesticides, and herbicides. 1-Phenyl-piperazin-2-one can be prepared by reacting phenylacetonitrile with nitrous acid to form the nitrile followed by hydrolysis to produce the corresponding carboxylic acid.</p>

<p>4-Methoxy-3-nitrobenzoic acid is a hydroxybenzoic acid, and belongs to the group of heterocyclic compounds. It is a preactivated hydroxybenzoate that can be used in the synthesis of griseoluteic acid with chloride as an electron donor. Griseoluteic acid has inhibitory activities on isolated yield. This compound also has potent antitumor activity, which may be due to its ability to inhibit DNA synthesis and protein synthesis by binding to DNA polymerase and ribosomes respectively. Preparative high performance liquid chromatography (HPLC) using this compound is possible with marine microorganisms as the stationary phase. The x-ray absorption spectrum shows that 4-methoxy-3-nitrobenzoic acid has potential for use as a contrast agent for x-rays in imaging tissues.</p>

<p>H-Lys-Asp-OH is a molecule that binds to the receptor binding molecule for the colony stimulating factor. It has been shown to be effective in protecting against experimental models of hepatic steatosis and monoclonal antibody induced liver injury. The therapeutic potential of H-Lys-Asp-OH is being investigated as a treatment for human hepatic steatosis, which is a condition characterized by high levels of fat in the liver. This drug also has pharmacokinetic properties that are important in its use as an experimental model for studying the effects of antibiotics on bacterial DNA synthesis, and as a diagnostic tool for detecting antibiotic resistant bacteria.</p>

<p>Butenafine hydrochloride is a mycological agent that is used to treat tinea. It has been shown to have an antifungal activity in vitro against wild-type strains of c. glabrata. Butenafine hydrochloride inhibits the synthesis of ergosterol, which is a vital component of fungal cell membranes, by blocking the conversion of squalene to lanosterol through inhibition of 14alpha-demethylase. It also has antimicrobial properties, which may be due to its ability to inhibit bacterial growth.</p>

<p>Quinazolinones are a class of chemicals that inhibit the enzyme acetylcholinesterase. 3-Fluorophenyl-2-methylquinazolin-4(3H)-one (3FPMQ) is a connector molecule that has been shown to be an inhibitor of acetylcholinesterase, the enzyme responsible for the breakdown of the neurotransmitter acetylcholine. It is also an antenna molecule that can be used in ethyl esters and enzymatic assays. The high resistance of this molecule has been shown by chemical treatments and chemical analyses. Amplitudes generated by 3FPMQ have been shown to be effective at positioning it next to naphthalene, which is a ring structure with two c1-c6 alkoxy groups on either side. This molecule has also shown muscle relaxant properties.</p>

<p>Z-O-4-Toluenesulfonyl-L-serine methyl ester is a new chemical substance that has been synthesized as a potential pharmaceutical formulation. It has been shown to have protective effects against ischemia reperfusion injury in rats, reducing the damage to muscle and other tissues caused by ischemia reperfusion. The mechanism of action may be due to glyceride release and creatine production, which can maintain perfusion during periods of ischemia. Z-O-4-Toluenesulfonyl-L-serine methyl ester has also been shown to be effective in preventing damage to platelets during induction of ischemia.</p>

<p>3-(3-Methyl-3H-diazirine-3-yl)propionic acid (3MDZ) is a fluorophore that can be used in cancer research. It has been shown to bind to the active site of human SIRT1 and inhibit its activity, which leads to cell death by deacylating histone H3. 3MDZ is also able to bind to carbenes, which are highly reactive molecules that have been implicated in aging and cancer. 3MDZ has shown chemopreventive effects against tumor formation and growth by binding to the carbenes and preventing them from forming reactive oxygen species. It can be used as a fluorescent probe for studying the interactions between carbenes and nucleic acids.</p>

<p>MeOSuc-Ala-Phe-Lys-AMC is a compound that has a destabilizing effect on the vascular wall, due to its ability to inhibit proteolytic activity. It is also able to reduce the level of angiogenic factors, and thus has an anti-angiogenic effect. MeOSuc-Ala-Phe-Lys-AMC has been shown to have a macroscopic effect on vessels in tissue culture, and this can be observed through leucocyte migration. MeOSuc-Ala-Phe-Lys-AMC has also been shown to cause haemorrhagic changes in microvessels and muscle cells. This compound is also able to inhibit placental growth factor and muscle cell proliferation, as well as reducing the number of microvessels in the placenta.</p>

<p>1-Palmitoyl-2-oleoyl-rac-glycerol is a fatty acid that is made in the mitochondria and is an intermediate in the production of diacylglycerol. It has been shown to have a linear response with cellular protein levels, and it has been shown to be involved in the genetic mechanisms of cells. 1-Palmitoyl-2-oleoyl-rac-glycerol has been found to have a number of protein targets, including phosphatidylinositide 3 kinase, PKC, and Akt. This molecule also has been used as an analytical method for measuring fatty acids in tissue samples and has been shown to alter enzyme levels, such as those found in prostaglandin synthase 2. 1-Palmitoyl-2-oleoyl-rac-glycerol can be synthesized by laser ablation or chromatographic science methods.</p>

<p>Deamino-histidine (DAH) is a diagnostic marker that can be used to measure the disease activity of inflammatory bowel disease. It is also a marker for tissue damage, as it accumulates in mammalian tissues during inflammation or necrosis. DAH is formed by the hydrolysis of histidine catalyzed by bacterial enzyme arginase, and it can be detected in blood plasma and urine samples. The concentration of DAH correlates with the degree of intestinal inflammation and has been found to be elevated in patients with Crohn's disease or ulcerative colitis.</p>

<p>3,6-Bis(1,1-dimethylethyl)-10-phenyl-9-(2,4,6-trimethylphenyl)-acridinium tetrafluoroborate is a high quality reagent that is used as an intermediate in the synthesis of other compounds. It has CAS No. 1810004-87-5 and a molecular weight of 345.7 g/mol. This compound is useful for the synthesis of complex compounds and can be used in fine chemicals. 3,6-Bis(1,1-dimethylethyl)-10-phenyl-9-(2,4,6-trimethylphenyl)-acridinium tetrafluoroborate is also useful for research purposes and can be used as a scaffold for drug discovery. It is also a versatile building block that can be used in reactions to produce speciality chemicals and reaction components such as esters or amides.</p>

<p>1-O-Hexadecyl-sn-glycero-3-phosphocholine (1OHDGPC) is a compound that inhibits the uptake of oxidized LDL in neuronal cells and reduces neuronal death. 1OHDGPC also has antihypertensive activity, as it decreases systolic blood pressure. This compound is an antioxidant because it prevents the oxidation of LDL cholesterol, which is the main cause of atherosclerosis. 1OHDGPC has been shown to reduce the incidence of allergic reactions in animal studies. It also has been shown to have hydroxyl groups and fatty acid chains, which may contribute to its antioxidant properties.</p>

<p>Fmoc-3-(3'-pyridyl)-D-alanine is a building block for the synthesis of a wide variety of compounds. This compound has been shown to be an excellent and versatile starting material for the synthesis of complex compounds. Fmoc-3-(3'-pyridyl)-D-alanine is also a useful intermediate in organic synthesis and can be used as a reagent or in research. It has CAS number 142994-45-4.</p>

<p>Please enquire for more information about 4-(4-Ethoxyphenyl)-2-(1-methylindol-3-yl)-4-oxobutanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-(2-Methyl-1,3-oxazol-5-yl)phenyl]amine is a versatile building block that is widely used in the research and development of complex compounds. This compound can be used as a reagent, speciality chemical, or useful intermediate as it has high reactivity and good solubility. 4-(2-Methyl-1,3-oxazol-5-yl)phenyl]amine is also a useful scaffold for producing other compounds.</p>

<p>2,3-Diphospho-D-glyceric acid pentasodium salt is a pyridine complex that is found in nature as a constant. It is also synthesized by humans and can be formed in the laboratory. 2,3-Diphospho-D-glyceric acid pentasodium salt is reactive and has been shown to be useful for producing radical species. This compound has been analysed in the human body at physiological concentrations and has been shown to interact with endogenous molecules such as lipids. The interaction of this compound with lipids could be due to its ability to form emulsions.</p>