Building Blocks

<p>4-(1,3-Thiazol-4-yl)phenol is a diagnostic marker for bladder cancer. It is expressed in bladder cells and its levels are higher in urine samples of patients with bladder cancer than in controls. 4-(1,3-Thiazol-4-yl)phenol can be used as a biomarker for diagnosis of bladder cancer and to monitor the treatment response. The concentration of this compound can also be used to assess the risk of recurrence or progression to invasive disease. The function of 4-(1,3-thiazol-4-yl)phenol in the body is not known, but it may act as a growth factor or stabilizer for cells. This molecule has been shown to have therapeutic effects on epithelial cancers such as colorectal and pancreatic cancers.</p>

Guanosine is a nucleoside that is metabolized to uridine in the liver. It is a component of RNA and DNA, as well as an intermediate in the synthesis of adenosine triphosphate (ATP) by phosphorylation. Guanosine also has pharmacokinetic properties, including its ability to cross the blood-brain barrier, which make it a promising drug for neurological disorders. Guanosine is used in tissue culture to measure signal transduction pathways and membrane permeability. The tautomers of guanosine are shown in Figure 1 below: Figure 1: Tautomers of Guanosine (1) 5'-O-DMT-Guanosine (2) 5'-O-DMT-2'N3-Guanosine (3) 2'N3-5'-O-DMT-Guanosine (4) 2'N3-5'-

<p>2-(2,6-dimethyl-3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a reagent that is used in the synthesis of other compounds. It is a high quality research chemical and useful scaffold for the preparation of fine chemicals. This versatile building block is also used as an intermediate or building block in the synthesis of complex compounds.</p>

2-[2-(Morpholin-4-yl)ethoxy]ethan-1-amine is a research chemical that is used as a reagent, reaction component, or building block in the synthesis of more complex compounds. It can be used to synthesize fine chemicals such as pharmaceuticals and agrochemicals.

(S)-1-(2-Amino-propan-1-yl)-4-methyl-piperazine is a reagent, reaction component and building block for speciality chemicals. It is a versatile intermediate that has been used in the synthesis of complex compounds. (S)-1-(2-Amino-propan-1-yl)-4-methyl-piperazine is an important building block for the synthesis of a variety of pharmaceuticals and other organic compounds. This compound can be used as an intermediate or reagent to produce high quality research chemicals.

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

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Versatile small molecule scaffold

2-Methoxy-4-aminobenzoic acid is a solute that can be used in the manufacture of pharmaceuticals. It has a high affinity for receptors and is potentially useful in the treatment of hypertension. 2-Methoxy-4-aminobenzoic acid has been shown to exhibit antihypertensive activity in animals by reducing cardiac output, systemic vascular resistance, and total peripheral resistance. The mechanism of action may be due to its ability to inhibit calcium ion influx into myocardial cells and block voltage-gated potassium channels. This drug also has an acidic pH, which makes it soluble in water. 2-Methoxy-4-aminobenzoic acid is insoluble in organic solvents such as hydrochloric acid or ether, which means it cannot be extracted from aqueous solutions by these solvents.

5-Methoxy-2-methylindole is an organic solvent that has been shown to have a wide range of bioactive properties. It is used in the production of acetylcholine, which is an important neurotransmitter. 5-Methoxy-2-methylindole also reacts with chloride ions, which may be an important factor when considering the life cycles and bioactive substances of this molecule. The reaction yield depends on the pH of the solution. 5-Methoxy-2-methylindole can undergo chlorination reactions to form polychlorinated derivatives, which are used as petrochemicals. This molecule also has retinoid properties and can act as a proton donor or acceptor depending on whether it is protonated or deprotonated.

<p>Versatile small molecule scaffold</p>

3,5-Dimethoxy-4-hydroxyphenethylamine hydrochloride is a fine chemical that is used as a building block for other compounds and as a reagent in research. It has been shown to be an effective intermediate in the synthesis of many complex compounds, such as 3,4-methylenedioxyamphetamine (MDA) and 3,4-methylenedioxymethamphetamine (MDMA), which are both psychoactive drugs. This building block can also be used to synthesize speciality chemicals such as psychotropic drugs or pharmaceuticals.

Imidazolyl-4-ethanol is a glycoside derivative that inhibits the synthesis of proteins, fats, and nucleic acids by inhibiting the enzyme phosphofructokinase. The compound has been shown to have anti-inflammatory properties that are similar to those of nonsteroidal antiinflammatory drugs. This drug also has a kinetic energy of -1.2 kcal/mol and it has a ph optimum of 7.5. Imidazolyl-4-ethanol has been shown to be useful in vitro for the synthesis of antibodies against monoclonal antibodies and for radiation protection. It can also be used as a radioactive tracer in vivo.

<p>H-Imidazoleacetic acid is a synthetic compound that can be used to produce other compounds. It is soluble in water and has a hydrophilic interaction with calcium carbonate. H-Imidazoleacetic acid may be recycled, as it is easily synthesized from ethyl bromoacetate by reaction with hydrochloric acid. This substance has shown anticancer activity and may be used to treat blood pressure. The chromatographic method for H-Imidazoleacetic acid involves the use of extracellular medium to remove the organic solvent, followed by reversed phase chromatography on an ion exchange column. H-Imidazoleacetic acid is soluble in water and has a hydrophilic interaction with calcium carbonate. It may be recycled, as it is easily synthesized from ethyl bromoacetate by reaction with hydrochloric acid. This substance has shown anticancer activity and may be used to treat blood pressure. The</p>

5-Iodo-2,4-dimethoxypyrimidine is a chemical compound that can be used as a ligand for palladium. It is selective for alcohols and carbinols. The compound has been shown to catalyze the desilylation of organic halides and oxidized alcohols with high yields. 5-Iodo-2,4-dimethoxypyrimidine can also be used in the synthesis of carbohydrates and vinyl acetate. The yield of dehydrohalogenated products was found to be high when 5-iodo-2,4-dimethoxypyrimidine was used as a catalyst.

<p>Plant hormone; auxin; inducer of root development; used in plant rooting</p>

<p>Indole-3-carboxaldehyde is a chemical compound that is used as an antimicrobial agent. The biological properties of this compound are not well studied, but it has been shown to be effective against bacteria and fungi. Indole-3-carboxaldehyde has been shown to inhibit the enzyme activity of sodium carbonate, which is involved in the production of lactic acid in bacteria. This effect may contribute to its antibacterial activity. Indole-3-carboxaldehyde is also a potential anticancer agent because it can bind to toll-like receptor 4 (TLR4). Indole-3-carboxaldehyde reacts with sulfa drugs through a mechanism similar to the reaction between hydrogen peroxide and potassium permanganate. It has been shown that indole-3-carboxaldehyde can be used as a pesticide for plants and as an electrochemical impedance spectroscopy probe for histological analysis.</p>

<p>3-Indolemethanol is a chemical compound that is used for chemiluminescent reaction. It can be used as an experimental model for studying the effects of 3-indolemethanol on murine hepatoma and human osteosarcoma cells in vitro. This compound has been shown to have oral hypoglycemic activity and to inhibit cancer cell growth. 3-Indolemethanol has also been shown to modulate signal pathways, such as the MAPK pathway, which may lead to pro-apoptotic protein activation or inhibition of physiological effects.</p>

6-Iodopurine is a biologically active substance that belongs to the group of carbinols. It is biosynthesized from 6-chloropurine and an iridoid glucoside, and has been shown to have biochemical properties. 6-Iodopurine can be converted into 6-iodoindoxyl by oxidation with halogens or transfer mechanism with palladium-catalyzed cross-coupling. A high efficiency method for the synthesis of this substance has been developed using a strain of bacteria. The reaction requires an activation energy of 150 kJ/mol.br> 6-Iodopurine inhibits tumor growth by inhibiting DNA synthesis. It also possesses anti-inflammatory activity, which may be due to its inhibitory effects on prostaglandin synthesis.

<p>Isatin is a natural compound that can be found in the bark of the Cinchona tree. It has inhibitory properties against the enzyme polymerase chain reaction (PCR) and has been shown to have antimicrobial activity. Isatin also has an effect on 5-HT concentrations, which may be due to its ability to inhibit platelet aggregation and induce vasoconstriction. Isatin has been shown to have anticancer effects in vitro, and also inhibits cellular transformation by reducing DNA synthesis.</p>

<p>5-Iodoindole is an organic compound that is used as a nematicide. It has been shown to have cytostatic effects on the growth of human pathogens, juveniles, and model systems. 5-Iodoindole inhibits the production of reactive amines and pyridine in vivo. It also inhibits glutamine metabolism by competitive inhibition at the glutamate dehydrogenase enzyme. 5-Iodoindole also has hemolytic activity and is able to induce transcriptomic changes in P. aeruginosa cells.</p>

Indole is a nitrogen-containing heterocyclic aromatic organic compound. Copper chloride in the presence of trifluoroacetic acid and indole gives rise to an indolenine derivative, which reacts with nitrogen atoms to form a copper nitride. This reaction is used as a model system for biological properties of indole. Indolenine has been shown to have bone cancer prevention and treatment effects in mice, and may also be beneficial in autoimmune diseases and metabolic disorders, due to its ability to inhibit toll-like receptor signaling pathways. The wild-type strain has shown resistance to antibiotics, which can be overcome by using mutant strains that are resistant to antibiotic treatments.

<p>4-Imidazoleacetic acid HCl is a fluorescent probe that binds to the α1 subunit of the dinucleotide phosphate (NADH) oxidoreductase. It has been shown to inhibit mitochondrial functions, which may be due to its ability to inhibit the pentose phosphate pathway and reduce reactive oxygen species levels. 4-Imidazoleacetic acid HCl has also shown inhibitory properties against congestive heart failure by acting on the mitochondria and inhibiting energy metabolism. It can also be used as a chemical biology tool for studying protein interactions with NADH dehydrogenase. The x-ray crystal structures have revealed that 4-imidazoleacetic acid HCl binds to the active site of NADH oxidoreductase with an orientation that mimics a substrate molecule. This allows it to bind tightly and disrupt enzyme activity.</p>

L-Homopropargylglycine is a small molecule that inhibits the activity of enzymes involved in fatty acid synthesis. It has been shown to inhibit the activity of enzymes involved in mitochondrial membrane potential and reactive oxygen species production, as well as collagen degradation. L-Homopropargylglycine is used to study the molecular mechanisms of lipid metabolism and mitochondrial function, as well as for wastewater treatment. L-Homopropargylglycine has also been studied as a potential drug for the treatment of metabolic syndrome, diabetes, and cancer.

<p>3-Hydroxy-4-iodobenzaldehyde is a fluorophore that is used in the synthesis of amide compounds, as well as in the production of other synthetic molecules. 3-Hydroxy-4-iodobenzaldehyde has been shown to have pharmacokinetic properties that are similar to those of fluorescein, and can be used to study the distribution and metabolism of this compound. This compound also has an oxidation potential that is higher than that of fluorescein, which makes it more useful for studying drug metabolism. The labile nature of 3-hydroxy-4-iodobenzaldehyde means it will not remain intact for long periods of time.</p>

<p>4-(Hydroxymethyl)phenylacetic acid is an intermediate in the biosynthetic pathway of phenylpropanoids. It is a metabolite of several flavonoids and is found in plants, animals, and humans. 4-(Hydroxymethyl)phenylacetic acid has been shown to have a high concentration in human serum and plasma with low toxicity. This metabolite has been shown to be stable when complexed with collagen or other proteins, which may be due to its insolubility. 4-(Hydroxymethyl)phenylacetic acid can also be biotransformed by microflora into other metabolites such as 4-hydroxybenzoic acid, which is a precursor of salicylic acid.</p>

<p>3-(2-Hydroxyphenyl)propionic acid (HPPA) is an inorganic acid that is found in microbial metabolism. HPPA has been shown to inhibit the growth of bacteria by reacting with the hydroxyl group on the enzyme's active site, thus irreversibly inhibiting enzymatic activity. HPPA can be used as an alternative to other inorganic acids such as p-hydroxybenzoic acid and malonic acid due to its ability to scavenge anion radicals. This inhibition of enzyme activity can be used in wastewater treatment to remove organic compounds from industrial waste streams. It also has been shown to have anti-cancer properties against human breast cancer cells, which may be due to its ability to induce cell death through apoptosis and/or necrosis.</p>

<p>4-Hydroxybenzamide is a fatty acid with the hydroxyl group at the 4 position. It has been shown to inhibit the activity of human protein by interfering with hydrogen bonding and amide formation. The chemical structures of 4-hydroxybenzamide have been studied by electrochemical impedance spectroscopy (EIS) and found to be a competitive inhibitor of 1-hydroxy-2-naphthoic acid, an adenosine receptor antagonist, and p-hydroxybenzoic acid. This compound has also been shown to be acutely toxic in rats at high doses.</p>

<p>4'-Hydroxy-3'-methylacetophenone is a chemical that has been shown to have antimycobacterial activity. This substance is an aldehyde with two hydroxyl groups and one methyl group. It has been shown to inhibit the growth of Mycobacterium tuberculosis in vitro by binding to κ-opioid receptors, which are proteins found on the outside of cells. 4'-Hydroxy-3'-methylacetophenone also inhibits mycobacteria through hydroxide solutions, chemical ionization, and vibrational spectroscopy.</p>

<p>Hexacosanoic acid is a glycol ether that has been shown to have hypoglycemic activity in mice. It was also shown to increase the levels of fatty acids and decrease the levels of glycerides in rats, which may be due to its ability to inhibit the synthesis of phospholipids. Hexacosanoic acid has been used as an analytical reagent for the determination of p-hydroxybenzoic acid and uronic acid. The polymerization of hexacosanoic acid is catalyzed by a polymerase chain reaction (PCR), which can be used for diagnosis. This molecule has also been found to have anti-inflammatory properties and nitrate reductase activity.</p>

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<p>3,4,5,6,7,8-Hexahydro-2,9-benzodioxacyclododecin-1,10-dione is a research chemical that is an important intermediate for the synthesis of many useful compounds. It can be used as a building block for the synthesis of more complex and valuable compounds in the pharmaceutical industry. 3,4,5,6,7,8-Hexahydro-2,9-benzodioxacyclododecin-1,10-dione is also an important reagent for organic chemistry reactions. It has been shown to behave as a good scaffold for the synthesis of other molecules with high purity. This compound has been shown to be useful in many different reactions such as condensations and cyclizations.</p>

2-Hydroxy-6-(methoxymethoxy)benzaldehyde is a chemical intermediate that can be used in the synthesis of a wide range of compounds. It is an aromatic compound which has two hydroxyl groups on the benzene ring. This product is a versatile building block, and is useful in the synthesis of complex compounds with high purity. 2-Hydroxy-6-(methoxymethoxy)benzaldehyde can be obtained as a white solid with a melting point of 57°C.

<p>Please enquire for more information about 4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis[benzaldehyde] including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Only available for delivery in the Europe.  Prohibited for transport by air.  The substantial reactivity and versatility of Hexachlorocyclopentadiene in facilitating multiple synthetic pathways make it indispensable in both agrochemical and industrial sectors.

<p>Purity min. 95%</p>

A building block research chemical

<p>Proline is a non-essential amino acid that is found in the basic structure of collagen. Proline has been shown to have physiological effects, including a protective effect on the myocardium, and can be used as an analytical method for detecting proline residues in biological samples. Trans-4-Hydroxy-L-proline is a proline derivative that has been shown to inhibit collagenase activity in vitro. It was also shown to have an optimum concentration of 1 mM and a matrix effect at pH 6.5. The model system used to study trans-4-hydroxy-l-proline was the enzyme extracted from rat liver.</p>

<p>2-Hydroxy-3-methoxybenzaldehyde is a model compound that is used to study the reaction mechanism of hydrogen bonding. It has been shown to have antioxidative properties and amoebicidal activity. The biological properties of 2-hydroxy-3-methoxybenzaldehyde are still being studied. There are also no reports on its toxicity or carcinogenicity in humans. This compound is a member of the group P2, which includes compounds with two aromatic rings connected by one carbon atom. The molecular geometry around this carbon atom is pyramidal and the molecule can exist in either an axial or equatorial orientation. Synchronous fluorescence experiments have shown that 2-hydroxymethoxybenzaldehyde reacts with Toll-like receptor 4 (TLR4).</p>

<p>2-Hydroxy-4-methoxybenzaldehyde is an antifungal agent that has been shown to have a broad spectrum of activity against filamentous fungi. It is able to inhibit the growth of fungi by inhibiting the enzyme shikimate dehydrogenase, which is involved in the synthesis of aromatic amino acids and other essential metabolites. 2-Hydroxy-4-methoxybenzaldehyde also inhibits xylose reductase and alpha-galactosidase, enzymes that are involved in cell wall biosynthesis. This compound is effective against Candida albicans, Aspergillus niger, and Trichophyton mentagrophytes. 2-Hydroxy-4-methoxybenzaldehyde has also been shown to have bacteriostatic effects on Escherichia coli.</p>

<p>Glycine is the simplest amino acid and is used as a reagent for the synthesis of proteins. It is also a component of buffer solutions to maintain a stable pH in lab applications like electrophoresis and enzyme assays.</p>

<p>Glyceryl-4-aminobenzoate monomer is a fine chemical that is an important building block in the synthesis of a variety of complex compounds. It has been used as a reagent and intermediate in research and development of pharmaceuticals and agrochemicals. Glyceryl-4-aminobenzoate monomer is a versatile building block, which can be used to form polymers, coatings, adhesives, elastomers, polyurethanes, and more. The compound also has been shown to have anticancer activity against human breast cancer cells.</p>

Gallaldehyde hemihydrate is a bioactive phenolic compound that inhibits the tyrosine kinase domain of the epidermal growth factor receptor (EGFR). It has been shown to inhibit tumor cell growth and induce apoptosis in cancer tissues. Gallaldehyde hemihydrate has also been found in lentils, which might be used as a potential biomarker for this compound. The optimum pH for gallaldehyde hemihydrate is between 2.0-4.0, and it can bind to cation channels and act as a potential biomarker for skin cancer cells.

<p>Used with EDC for carboxyl-foot printing studies of proteins</p>

<p>Gallic acid anhydrous is a compound that is found in plants and has antioxidant properties. Gallic acid anhydrous can be used as a model system for the study of electrochemical impedance spectroscopy. It has shown to have anti-cancer activity in vitro, but not in vivo, against squamous carcinoma cells. In addition, gallic acid anhydrous has been shown to inhibit oral pathogens and to scavenge anion radicals. Gallic acid anhydrous may have structural similarities to procyanidin B4, which is important for its antioxidant activity.</p>

<p>5-Fluoro-3-methylindole is a reactive compound that is not soluble in water. It has a molecular weight of 288.5 and an ionization potential of 7.8 eV. 5-Fluoro-3-methylindole can act as a potent antagonist by binding to the pharmacophore, which is the three hydrogen bonding sites on the benzodiazepine receptor. This drug has been shown to be reactive with halides, nitro, and magnesium, as well as with some endogenous compounds such as nitroarenes and amides. 5-Fluoro-3-methylindole also reacts with fluorescence ligands and transfer agents.</p>