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This compound is a synthetic molecule that has been shown to have growth factor activity and may be useful in cancer research. The molecule is a nucleophile and reacts with epidermal growth factor (EGF) to form the corresponding adduct. This adduct can then react with chloride to form the corresponding chloro-adduct. It also binds to cellular proteins, such as antigen and factor receptors. The piperazine ring of this molecule is responsible for its binding affinity for these receptors.
The compound was expressed from a plasmid under normoxic conditions, but was not expressed under hypoxic conditions.

2,4-Dimethoxy-3-methylbenzyl alcohol is a syntheses and deuterium analogue of orsellinic acid. It has been shown to inhibit bacterial growth in the presence of an oxygen atmosphere.

1-(3,4,5-Trimethoxyphenyl)-2-nitropropene is a high quality chemical that is a reagent and useful intermediate. It has been shown to be a useful scaffold for the synthesis of various compounds and as a building block for the synthesis of speciality chemicals. This compound can be used in research and as a versatile building block in organic chemistry.

6-Methoxyindole is an acetate extract of the plant 5-methoxyindole. It has been shown to be a 5-HT1A receptor agonist in animals, and has been shown to have cardiac effects in rats. 6-Methoxyindole is also used as a precursor for the synthesis of diphenylacetylindoles. 6-Methoxyindole is one of the molecules that can be recombined to form a batcho-leimgruber indole (BLI).

2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical & Laboratory Equipment.

Methyl 6-bromo-3,4-dimethoxybenzoate is a potent compound that inhibits topoisomerase. It is not as selective as other topoisomerase inhibitors, but it is more reactive and has been shown to be effective in the synthesis of lactones. This compound can also be used as an intermediate for the synthesis of more potent inhibitors of topoisomerase. Methyl 6-bromo-3,4-dimethoxybenzoate has been shown to react with aliphatic aldehydes and nitro compounds to form zinc powder. The reaction proceeds via a catalytic mechanism involving an initial complexation of the methyl group with the carbonyl oxygen atom followed by nucleophilic attack by zinc.

(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide is a reagent and research chemical that can be used as a building block in the synthesis of other compounds. It is also a versatile building block in organic chemistry. (E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide has been shown to be an effective intermediate for the synthesis of various complex compounds, such as pharmaceuticals and pesticides. This compound is also a useful scaffold for the synthesis of other fine chemicals.

7-Methoxy-2-tetralone is an organic compound that is synthesised from the chlorination of phenol. It inhibits cancer cells by binding to their receptors and inhibiting the growth of new blood vessels, which are necessary for tumour growth. 7-Methoxy-2-tetralone also inhibits the synthesis of DNA, RNA, and protein in a cell-free system. It binds to chloride ions in solution and has a potent inhibitory activity against dehydrogenase and hydrochloric acid. 7-Methoxy-2-tetralone is used as a reagent for water treatment studies because it can be broken down to produce harmless products, such as chloride ion and cyanogen.

3-Methoxy-5-nitrobenzoic acid is an organic compound that has mesomorphic and switchable properties. It is a chalcone derivative, with homologues such as 3-hydroxybenzoic acid. It is synthesized from the reaction of nitrous acid and 3-methoxybenzoic acid. The synthesis of this compound can be achieved by two different routes: peroxide oxidation or fluorine substitution. Both routes produce the same product, but offer different advantages. The first route involves the addition of hydrogen peroxide to 3-methoxybenzoic acid, which produces a mixture of products containing 3-methoxy-5-nitrobenzoic acid. This route is advantageous in that it can be conducted at room temperature with high yields, but the disadvantage is that this method produces a mixture of products which may contain undesired byproducts. The second route involves the use of sodium hypofluorite and potassium

2,2'-Dimethoxybiphenyl is a thermoplastic that is exothermic, making it useful in the production of polyketones. It can be used as a linker to form covalent bonds with monomers and polymers. 2,2'-Dimethoxybiphenyl has been used as a monomer to produce polyethers and polyesters. This compound has many chemical stability properties, which makes it suitable for use in polymer synthesis. It also can react with nucleophiles such as amines to form ether linkages. 2,2'-Dimethoxybiphenyl has kinetic properties that are faster than those of other ketones but slower than those of other ether-linked compounds. The activation energy for its reaction is low, making it an effective monomer for polymerization reactions.

4-Amino-5-chloro-2-ethoxybenzoic acid is a phenoxy compound that is synthesized in the laboratory. The chemical structure of this compound has been studied using high performance liquid chromatography and it was found to have pharmacokinetic properties that are consistent with those of other drugs in its class. This drug is being developed as an anti-depressant, targeting the 5HT4 receptor. The bioactive metabolite of 4-amino-5-chloro-2-ethoxybenzoic acid is 4-(4′ hydroxybutyl)phenol, which has been shown to be a potent inhibitor of phosphodiesterase activity.

3-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)propanoic acid HCI 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. 3-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)propanoic acid HCI 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.

3-Methoxy-5-(trifluoromethyl)aniline is a chemical building block that is used in the preparation of pharmaceuticals, agrochemicals, dyes, and other chemicals. 3-Methoxy-5-(trifluoromethyl)aniline is also a versatile intermediate that can be used to produce heterocyclic compounds. 3-Methoxy-5-(trifluoromethyl)aniline has been found to be high quality and useful for many reactions. It is an important compound for research use because it can be used as a reagent or scaffold for complex compounds.

6,7-Dimethoxycarbostyril is a small molecule that has been shown to induce cell death in cancer cells by inhibiting the chaperone function of heat shock protein 90 (HSP90). HSP90 is a multifunctional molecular chaperone that affects many cellular processes including cell growth, apoptosis and tumorigenesis. 6,7-Dimethoxycarbostyril binds to the ATP binding site of HSP90, preventing it from performing its chaperone role. This leads to inhibition of cell growth and induction of apoptosis. 6,7-Dimethoxycarbostyril has also been shown to inhibit tumor growth in vivo in mouse models and has successfully completed phase I clinical trials at doses up to 2000 mg/day.

2,2,3,3-Tetrafluoro-3-(trifluoromethoxy)propanoic acid (TFMP) is a fluorine-containing monomer that can be synthesized in an efficient method. TFMP is a resistant strain and has been shown to react with amines, carbonyls, and carboxylic groups. It can be copolymerized with other monomers to form polymeric materials. TFMP is a fluoride monomer that exhibits properties similar to perfluoroalkyl methacrylate monomers.

5-Methoxy-L-tryptophan is a nonsteroidal anti-inflammatory drug that acts by inhibiting the synthesis of prostaglandins. It has been shown to have a clinical relevance in the treatment of cancer and ischemia reperfusion injury. 5-Methoxy-L-tryptophan has also been shown to be effective in the treatment of inflammatory diseases such as rheumatoid arthritis, ulcerative colitis, and Crohn disease. 5-Methoxy-L-tryptophan is a precursor for serotonin, which regulates many physiological functions including pain perception. Tryptophan has also been found to increase epithelial mesenchymal transition (EMT) and repair mechanisms in fibroblasts. X-ray crystal structures have revealed that 5-methoxy tryptophan binds at the active site of xanthine oxidase, which is an enzyme involved in purine metabolism.

cis-3,4-Dihydroxy-2,5-dimethoxytetrahydrofuran is a tetrahydrofuran derivative that has been shown to have neuroprotective effects. It has been shown to inhibit the formation of crosslinks in rat spinal cord neurons and to inhibit the release of reactive oxygen species (ROS) and nitric oxide (NO), which are known to be neurotoxic. In addition, cis-3,4-dihydroxy-2,5-dimethoxytetrahydrofuran has antibacterial activity against Staphylococcus aureus and Dasycarpus sp. This compound is also a precursor for limonoids and glyceraldehyde.

Please enquire for more information about 4-[(2,3,4Trimethoxyphenyl)methyl]piperazine-1-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Desmethoxy-4-chloro omeprazole sulfide is a versatile building block in the synthesis of new chemical compounds. The compound can be used as a reagent, speciality chemical, or reaction component and is suitable for use in research or as a building block. 4-Desmethoxy-4-chloro omeprazole sulfide is a valuable intermediate that can be used in the synthesis of many useful scaffolds. CAS No. 220757-74-4

Please enquire for more information about 2-amino-4-(3,4-dimethoxyphenyl)-5-oxo-4,6,7,8-tetrahydro2H-chromene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page