Aldéhydes

<p>3,4-Dimethylbenzaldehyde oxime is a reactive oxygen species (ROS) that is produced by the oxidation of 3,4-dimethylbenzaldehyde. It has been shown to be an efficient oxidant in aerobic oxidation reactions. The active species generated by this reaction is the aldehyde or ketone form of 3,4-dimethylbenzaldehyde oxime, which can then react with another substrate to generate an oxidized product. This reaction is catalyzed by metal ions and is activated by molecular oxygen.</p>

<p>4-Ethoxy-3-hydroxybenzaldehyde (4EHB) is a thioacetal that has been shown to be an effective precursor for the synthesis of many other molecules, such as combretastatin a-4. It is prepared by reaction of ethylmagnesium bromide and acetone. 4EHB has been shown to have antifungal properties in vitro, and can be used in the treatment of cancer cells. This compound is volatile and can be easily detected with headspace techniques. The functional group of this molecule is an alcohol group, which is found on the ring structure. Spectroscopic analysis shows that it has a carbonyl group with an OH group attached to it.</p>

<p>3-Bromo-4,5-dimethoxybenzaldehyde is a molecule that is acidic in nature. It inhibits phosphatases and has shown cytotoxic activity against cancer cells in vitro. This compound also has antibacterial properties and can be used to treat bacterial infections. 3-Bromo-4,5-dimethoxybenzaldehyde is also a synthetic compound that can be found in the bisbenzylisoquinoline alkaloids family. It has been shown to have anti-tumor activity as well as an interaction with aldehydes and chalcones, which may lead to anti-inflammatory effects.</p>

<p>2,3-Dihydroxy-4-methoxybenzaldehyde is the oxidized form of 2,3-dihydroxybenzaldehyde. It has been used in biological studies to investigate the biosynthetic pathways of reductoisomerase and analytical methods for detecting hydrogen bonds in samples. This chemical can also be found in urine samples as a metabolite of adenine nucleotide and polypeptides. The chemical has been shown to have health benefits, such as being a recombinant that helps cell culture.</p>

<p>Vegetable, nutty and floral flavour/fragrance</p>

<p>(E)-2-Octenal is a reactive compound that is produced by the degradation of unsaturated fatty acids. It has been shown to have antioxidant properties, which may be due to its ability to inhibit the activity of lipoxygenase and cyclooxygenase enzymes. (E)-2-Octenal also inhibits bacterial growth through genotoxic effects, such as DNA damage and mutations. The chemical ionization mass spectrometry method has been used for identification and quantification of (E)-2-octenal in a variety of natural products, including ethyl decanoate, caproic acid, and galacturonic acid.</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>3-Hydroxybenzaldehyde (3HBA) is an organic molecule that belongs to the group of substituted benzaldehydes. It has been shown to induce muscle cell proliferation in vitro and in vivo, as well as increased levels of activated caspase-3 in vitro. 3HBA also has a high resistance to hydrochloric acid, hydrogen bond, and chemical structures. It also shows properties of intramolecular hydrogen bonding and aldehyde groups. 3HBA has been shown to be active against malonic acid-induced pulmonary edema in rats, which may be due to its ability to inhibit the release of erythrocytes from the bone marrow into the circulation.</p>

<p>1-Methyl-1H-imidazole-4-carbaldehyde is an Imidazole derivative. Imidazoles are the most prominent heterocyclic scaffolds found in medical molecules and natural products. Due to the peculiar structural characteristics of imidazole, it is advantageous for imidazole groups to combine with various receptors and enzymes in biological systems, through diverse weak interactions. 1-Methyl-1H-imidazole-4-carbaldehyde is one of many imidazole derivatives that are used as building blocks for a wide variety of target compounds.</p>

<p>Glyceraldehyde is a monosaccharide that is an important intermediate in the glycolytic pathway. It is also classified as a hydroxyl group donor and has been shown to have cytotoxic effects on mammalian cells. Glyceraldehyde has been implicated in many biological processes, including fatty acid synthesis and dinucleotide phosphate synthesis. This molecule has been shown to bind to proteins through its hydroxyl groups, which are found on its carbonyl carbon atoms. The enzyme cytosolic protein kinase (PK) has been shown to phosphorylate glyceraldehyde, which may be involved in transcriptional regulation. In addition, glyceraldehyde may be involved in human serum glucose levels and plant metabolism.</p>

<p>5-Methoxyindole-3-carboxaldehyde is a molecule that belongs to the genus of indolequinones. It has been shown to have potent inhibitory activity against prostate cancer cells, and also has anti-cancer properties. 5-Methoxyindole-3-carboxaldehyde inhibits the proliferation of cancer cells by inducing apoptosis in prostate cancer cells. 5-Methoxyindole-3-carboxaldehyde also suppresses the growth of cervical cancer cells and breast cancer cells. This molecule binds to the hydrogen bond sites on DNA, which may be one reason for its anti-cancer properties. The molecule is fluorescent and can be used as a marker for detecting cancers or other diseases in living tissue.</p>

<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>

<p>2,6-Dimethyl-4-hydroxybenzaldehyde is a synthetic compound that belongs to the class of aminoguanidines. It has been shown to be a potent vasoprotective agent and is used in the treatment of cardiovascular diseases. 2,6-Dimethyl-4-hydroxybenzaldehyde reverses the effects of formate on the jejunum by inhibiting secretion and intestinal motility. The activity of this drug has been shown to be due to its inhibitory effect on histamine release from mast cells.</p>

<p>Trifluoroacetaldehyde is a chemical with aqueous solubility of 0.2 g/L at 25 °C. It has been used in the preparation of insoluble polymers, such as phosphonates and polyurethanes. Trifluoroacetaldehyde can be prepared by reacting anhydrous hydrogen fluoride with trifluoroacetic acid in the presence of amines and an oxidizing agent, such as phosphorus pentoxide. The reaction mechanism is believed to involve a cationic polymerization involving hydrolysis of the amine to give an ammonium ion that reacts with hydrogen fluoride to form trifluoroacetyl fluoride and ammonium chloride. Trifluoroacetaldehyde has also been used in asymmetric synthesis, hydroxyl group reactions, pharmaceutical preparations, and monoclonal antibody production.</p>

<p>2-Phenoxybenzaldehyde is an organic compound that belongs to the heterocyclic aldehyde family. It is a white solid with a strong, pleasant odor. 2-Phenoxybenzaldehyde is used as an intermediate in organic synthesis, and has been shown to inhibit the receptor activity of human leukocyte antigen (HLA) class II molecules. The reaction mechanism for this inhibition is not known. The reaction of 2-phenoxybenzaldehyde with hydrochloric acid produces phenylhydroxylamine, which can be oxidized by inorganic acids to form phenyloxalic acid. This compound also inhibits the production of inflammatory cytokines such as TNFα and IL-1β in vitro and in vivo.</p>

<p>3,5-Di-tert-butyl-4-hydroxybenzylaldehyde is a compound that can be used as an extraction solvent for solid phase microextraction (SPME) in analytical methods. This sample preparation technique is used to measure the amount of malonic acid in kidney bean samples, as well as to detect growth factors in cell cultures. 3,5-Di-tert-butyl-4-hydroxybenzylaldehyde has been shown to be effective in wastewater treatment and has also been found to have anti-inflammatory properties. In addition, this compound was detected at low levels in urine samples from patients with inflammatory diseases. The mechanism of 3,5-Di-tert-butyl-4-hydroxybenzylaldehyde's antiinflammatory activity may be due to its ability to inhibit oxidative DNA damage by reacting with hydrogen bonds.</p>

<p>2-Benzyloxy-3-methoxybenzaldehyde is an enantiopure compound that has been shown to have antiproliferative effects on cancer cells. It was also found to have a strong binding affinity for DNA and protein. The antiproliferative effects of 2-Benzyloxy-3-methoxybenzaldehyde were found to be due to its ability to bind to dna and inhibit the enzyme activity of pyrazine-2-carboxylic acid, leading to a decrease in the production of proteins vital for cell division. 2-Benzyloxy-3-methoxybenzaldehyde has been shown to have anticancer activity against colorectal cancer cells and may serve as a lead compound for future drug development.</p>

<p>2,6-Dimethoxy-4-methylbenzaldehyde (DMMB) is a useful chemical that is used as a building block in the synthesis of complex compounds. It has been shown to be an effective chemical intermediate and can be used in the synthesis of various products, such as pharmaceuticals and pesticides. DMMB can also be used to produce high quality research chemicals.</p>

<p>5-Bromo-2-methoxybenzaldehyde is a benzodiazepine receptor ligand that has been shown to have antiviral, antibacterial and anticancer properties. 5-Bromo-2-methoxybenzaldehyde is an inhibitor of the enzyme benzyl alcohol dehydrogenase (BAHD). BAHD plays an important role in the production of reactive oxygen species (ROS) by converting benzoic acid to benzoate, which is then converted to ROS. The inhibitory concentration values for 5-bromo-2-methoxybenzaldehyde are not yet known.</p>

<p>2-Phenylindole-3-carboxaldehyde is an organic compound that belongs to the class of bioactive molecules. It is a nitrogen heterocycle that has been shown to inhibit the growth of cancer cells in culture. 2-Phenylindole-3-carboxaldehyde has also been shown to have anti-inflammatory and antimicrobial properties. This molecule can be used in the treatment of cancer, as it inhibits the growth of tumor cells by inhibiting DNA synthesis, which leads to cell death. The molecular structure can be altered by allylation or replacement with other functional groups. The 2-phenylindole moiety can be modified at its C2 position, altering its pharmacological properties and may lead to new anticancer drugs.</p>

<p>4-Iodobenzaldehyde is a chemical compound with the molecular formula C6H5IO. It is an aromatic compound that can be used in cancer therapy. 4-Iodobenzaldehyde reacts with trifluoroacetic acid to form an intramolecular hydrogen, which is detected using a low-energy monomer and high detection sensitivity. 4-Iodobenzaldehyde has two phenyl substituents and a serine protease functional group, which are required for its interaction with other molecules. The presence of these functional groups allows analytical methods to be used to identify 4-iodobenzaldehyde in various samples. Using analytical methods, it can be determined that 4-iodobenzaldehyde interacts with an acceptor molecule at the reaction vessel thermally or by irradiation.</p>

<p>2-Fluoro-6-nitrobenzaldehyde is an electron donor that reduces a range of electron acceptors including piperazine. This compound has been shown to have antitumor effects. 2-Fluoro-6-nitrobenzaldehyde has also been shown to inhibit the growth of cancer cells in vitro and in vivo. The mechanism of action is not yet known, but it is thought that 2-fluoro-6-nitrobenzaldehyde may be a potential chemotherapeutic agent for pancreatic cancer therapy.</p>

<p>3,4-Dihydroxy-5-methoxybenzaldehyde is a synthetic compound that has shown to have inhibitory effects on the replication of DNA and RNA. It also inhibits the growth of bacteria in culture by binding to the nucleic acid. The chemical structure of 3,4-Dihydroxy-5-methoxybenzaldehyde is similar to that of bisbenzylisoquinoline alkaloids, which are found in plants such as opium poppy. This similarity may explain its ability to inhibit bacterial growth. 3,4-Dihydroxy-5-methoxybenzaldehyde may be used as a drug candidate for treating bacterial infections.</p>

<p>Cyclooctanecarbaldehyde is a reactive chemical that contains a hydroxyl group and hydroxy group. It is used for the production of polymers such as cyclooctyne-1,4-diol. Cyclooctanecarbaldehyde is also used to synthesize acyl halides. The compound has been shown to be cytotoxic in cancer cells. It can inhibit the production of nucleic acids, proteins and lipids in cancer cells, leading to cell death. Cyclooctanecarbaldehyde also has depression and cardiac arrhythmia effects due to its κ-opioid receptor agonist properties.</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>Polydialdehyde starch is a cross-linking agent that is used to form hydrophobic polymers, which are prodrugs. It is a polymer of dialdehydes and can be used as an additive for restenosis prevention. Polydialdehyde starch has been shown to reduce platelet adhesion and aggregation in vitro and in vivo. The mechanism of action may be related to the ability of polydialdehyde starch to bind collagen and promote its degradation by hydrolysis. This also results in an increase in the rate of dilation of blood vessels, which may contribute to the antiplatelet effect. Polydialdehyde starch has been shown to be biodegradable, with a half-life of about two weeks in vivo after injection into rats.</p>

<p>Isoquinoline-4-carbaldehyde is an aldehyde chemical that has been synthesized in the laboratory. It is a chiral molecule with one asymmetric carbonyl group. Isoquinoline-4-carbaldehyde is a potential precursor to naphthyridine, which can be used as a building block for the synthesis of natural products. Isoquinoline-4-carbaldehyde has been shown to have phosphine properties, and it can be used as a ligand in transition metal complexes. The molecule has been shown to exist in two forms, which coexist in equilibrium and can undergo interconversion.</p>

<p>4-Methoxy-2-methylbenzaldehyde (4MMBA) is a synthetic chemical that is used as an antifungal agent. It interacts with the cellular membranes of fungi and disrupts their ability to maintain homeostasis. 4MMBA inhibits the growth of invasive aspergillosis by inhibiting protein synthesis, which leads to cell death. The mechanism of action for 4MMBA is not well understood, but it has been shown to inhibit the growth of fungi in a model system. It also inhibits the production of pyrylium, which may be responsible for its activity against fungi.</p>

<p>5-Fluoro-2-methoxybenzaldehyde is an inhibitor that blocks the enzyme acetylcholinesterase. It has been shown to be useful in the synthesis of a variety of drugs, including anticancer agents and antibiotics. 5-Fluoro-2-methoxybenzaldehyde is used in the industrial production of acetonitrile and can also be found in small quantities as a natural component of many fruits and vegetables. It is also used as a precursor for other chemicals, such as pharmaceuticals and pesticides. The compound is generally synthesized by condensation reactions involving benzaldehyde, acetamide, and formaldehyde. This chemical has been studied in medicinal chemistry because it can inhibit bacterial growth by binding to DNA gyrase.</p>

<p>3-Chloro-4-nitrobenzaldehyde is an aldehyde that is produced by the oxidation of 2-chloro-4-nitrobenzaldehyde. This chemical has been shown to have antitubercular activity in human erythrocytes, and it can be recycled from its reaction product with sodium hypochlorite. 3-Chloro-4-nitrobenzaldehyde has been shown to interact with acidic heterocycles such as oxadiazoles and triazoles. 3-Chloro-4-nitrobenzaldehyde has also been shown to alter the morphology of bacteria, such as subtilis, when exposed to ionic liquids. It is also known to inhibit the growth of Gram positive bacteria and show cytotoxic effects on mammalian cells.</p>

<p>β2-adrenergic receptor agonist</p>

<p>Ureaformaldehyde is a synthetic slow-release fertilizer that contains urea and formaldehyde. It has been shown to be highly active as a slow-release fertilizer in Langmuir adsorption isotherm studies. Ureaformaldehyde also has the ability to mineralize chloride and hydrogen bond to soil particles, increasing the availability of these ions for plant uptake. Ureaformaldehyde is also used in analytical methods such as chromatographic determination of fatty acids, which are an important component of animal and vegetable oils. !--</p>

<p>6,6'-Dihydroxy-5,5'-dimethoxy-[1,1'-biphenyl]-3,3'-dicarboxaldehyde (DDM) is a molecule that belongs to the class of organic compounds known as phenols. DDM has been shown to be an inhibitor of the enzyme activity of lysine residues and protocatechuic acid production. DDM also inhibits 5-carboxyvanillic acid production by competitively binding to the enzyme's active site. DDM has been shown to have antibacterial activity against wild-type strains of Staphylococcus aureus and Escherichia coli.</p>

<p>3-Fluoro-4-methoxybenzaldehyde is a chemical compound that is used in the synthesis of natural products. It has been shown to have inhibitory properties against cancer cells, and has been synthesized as an analog of 3-fluoro-4-hydroxybenzaldehyde. The biological function of 3-fluoro-4-methoxybenzaldehyde is not yet known. Hydrochloric acid may be used to react with 3-fluoro-4-methoxybenzaldehyde to form a salt. This chemical also has anti-tumor effects and can be synthesized using cryogenic techniques.</p>

<p>2-Bromobenzaldehyde ethylene acetal is a reactive intermediate that can be used to form allyl ethers. It is prepared by the Grignard reaction of 2-bromobenzaldehyde with an ethylene acetal. This molecule may be useful for the synthesis of dioxolanes and amines, as well as for other applications such as supramolecular chemistry and emulsions.</p>

<p>2-Ethoxybenzaldehyde is an organic compound that has been found to be a potential anticancer agent. It inhibits the growth of tumor cells in vitro, by inhibiting the PI3K/Akt signaling pathway. 2-Ethoxybenzaldehyde also has antibacterial activity against Gram-positive bacteria, such as P. aeruginosa, by binding to the nitrogen atoms on the cell wall and disrupting their function. The molecule has a functional group that reacts with metal cations, which helps to explain its chemical nature and its reaction mechanism. The molecule is soluble in water but not in organic solvents. 2-Ethoxybenzaldehyde crystallizes as a white solid with a monoclinic crystal system and can react with salicylaldehyde to produce benzalmalonic acid.</p>

<p>3-[(Dimethylamino)methyl]benzaldehyde is a fine chemical that is used as a versatile building block in the synthesis of pharmaceuticals. It is also a useful intermediate in the synthesis of complex compounds and research chemicals. This product has been shown to be high quality and can be used as a reagent for many reactions.</p>

<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>

<p>4-Acetoxy-3-methoxybenzaldehyde is an antimicrobial agent that is used specifically for the treatment of lemongrass oil and eugenol. It has been shown to be effective against a wide range of microorganisms, such as Escherichia coli, Pseudomonas aeruginosa, Salmonella enterica, Staphylococcus aureus, and Streptococcus pneumoniae. 4-Acetoxy-3-methoxybenzaldehyde has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. The molecule also has hydroxyl group which can react with potassium dichromate and sodium carbonate. This reaction results in the formation of 4-acetoxy-3-hydroxybenzaldehyde through an S N 2 substitution mechanism.</p>

<p>(Z)-9-Hexadecenal is an organic compound that is used as a pheromone in the species of bark beetles. It has been shown to inhibit the growth of other fungi, including opportunistic fungal pathogens. This activity may be due to its ability to bind and activate specific receptors on the surface of inflammatory cells, leading to an increase in cytokine production and expression of proinflammatory genes. (Z)-9-Hexadecenal also has anti-inflammatory properties against physiological activities such as growth factor binding experiments and solid phase microextraction studies. (Z)-9-Hexadecenal binds to lysine residues, inhibiting hydrogen bonding between amino acid residues and promoting population growth inhibition.</p>

<p>7-Methoxy-1-naphthaldehyde is an aldehyde that is synthesized from acetaldehyde and 7-methoxy-1-naphthol. It has been shown to inhibit the cytosolic aldehyde dehydrogenase, which converts acetaldehyde to acetate. This reaction is one of the major routes for the metabolism of alcohol in humans. 7-Methoxy-1-naphthaldehyde can be used as a substrate in immunochemical assays, and its synthetic scheme has been published. 7MNA was also found to have cytotoxic effects on human liver cells in vitro.</p>

<p>3-Fluoro-4-hydroxybenzaldehyde is a hydroxyl group with an activation energy of 87.7 kJ/mol. The molecule can be synthesized by the reaction of salicylaldehyde and 3,4-dihydroxybenzaldehyde in the presence of an organic solvent such as chloroform or methylene chloride. This compound has been shown to cause cell death in ht-29 cells and cancer cell lines, as well as human ovarian carcinoma cells. It causes apoptosis by inhibiting mitochondrial membrane potential, which leads to decreased intracellular ATP levels. 3-Fluoro-4-hydroxybenzaldehyde is most commonly used in molecular modeling studies to represent the hydroxyl group due to its simplicity in comparison to other hydroxyl groups like methanol or ethanol.</p>

<p>4-Dimethylamino-2-methoxybenzaldehyde is a chemical used as a research reagent and intermediate. It can be used to synthesize other compounds, such as pharmaceuticals, pesticides, and agrochemicals. It is also useful in the production of various dyes, pigments, and fragrances, representing effective staining under anaerobic conditions. CAS No. 84562-48-1</p>

<p>4-Nitrobenzaldehyde oxime is a phenylhydrazone derivative that is a potent cytotoxic agent. The 1,2-nitration of the benzene ring in 4-nitrobenzaldehyde oxime produces a reactive intermediate that reacts with nucleophilic groups on cellular macromolecules to produce DNA strand breaks and other types of damage. 4-Nitrobenzaldehyde oxime has been shown to have significant anticancer activity against leukemia cells in culture, as well as antibacterial and anticancer activity against Staphylococcus aureus and Escherichia coli.</p>

<p>3-Ethoxy-4-hydroxybenzaldehyde is an active analogue of p-hydroxybenzoic acid that can be used in the synthesis of vanillin. 3-Ethoxy-4-hydroxybenzaldehyde is extracted from a reaction solution using solid phase microextraction, and can then be analyzed by gas chromatography/mass spectrometry to determine the concentration of vanillin. This compound has been shown to have a solubility in water, but not in organic solvents. 3-Ethoxy-4-hydroxybenzaldehyde has been found to inhibit cytochrome P450 activity and polyvinyl chloride production. This chemical compound has also been found to be toxic when inhaled or ingested, with no known toxicity studies for skin contact or eye contact.</p>

<p>2-Hydroxy-4-methoxybenzaldehyde is an organic chemical that is used as a versatile building block for complex compounds, research chemicals, and reagents. It is also used as a speciality chemical and as a useful intermediate in the synthesis of other chemicals. 2-Hydroxy-4-methoxybenzaldehyde has CAS No. 673-22-3 and can be used to make many different types of compounds. This compound is a useful scaffold for the synthesis of diverse compounds with biological activity such as pharmaceuticals, agrochemicals, dyes, perfumes, fragrances, flavors and fragrances.</p>

<p>4'-Chloro-[1,1'-biphenyl]-4-carbaldehyde (CBA) is an intermediate in the synthesis of oritavancin. CBA is obtained by condensation of benzyl chloride and aldehydes. It is also used as a precursor to other compounds. In the laboratory, it can be obtained by heating an ether with chloroform in the presence of acid. 4'-Chloro-[1,1'-biphenyl]-4-carbaldehyde has been shown to be toxic, selective and efficient for certain reactions.</p>

<p>1-Acetyl-3-indolecarboxaldehyde is a ligand that binds to the cannabinoid receptor 1 (CB1). It has been shown to bind to the CB1 receptor with high affinity and selectivity. In addition, it has been demonstrated to inhibit the proliferation of human breast cancer cells in vitro. The compound is used as a fluorescent probe for cb1 receptor binding. Data obtained from molecular modelling studies have suggested that the hydroxyl group might be involved in binding to the CB1 receptor. 1-Acetyl-3-indolecarboxaldehyde also binds carotenoids, which are molecules responsible for giving plants and other photosynthetic organisms their coloration. This compound can be found in many different plants, such as carrots and bananas, where it acts as an antioxidant.</p>

<p>4-Benzyloxy-3-methoxybenzaldehyde is a deuterium isotope analog of the natural compound benzaldehyde. This molecule has been shown to inhibit the growth of cancer cells in tissue culture by binding to DNA. The molecular mechanism of this inhibition is believed to involve an enzymatic process that results in the substitution of chloride for chlorine, thereby inhibiting DNA synthesis and preventing cell division. 4-Benzyloxy-3-methoxybenzaldehyde also inhibits the production of growth factors and thus has anticancer activity.</p>

<p>Please enquire for more information about 2-(4-Fluorophenyl)thiazole-4-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>