Aldehídos

<p>Ac-Tyr-Val-Lys-Asp-aldehyde is a synthetic compound that can be used to study the apoptotic process. It is an aldehyde and has been found to activate caspases, aspartyl proteases, at high concentrations. This pseudo acid also has a significant activation of n-terminal protein kinase (SB203580) when irradiated with UV light. Ac-Tyr-Val-Lys-Asp-aldehyde can be used as a marker for the apoptotic process because it is synthesized by cells during this process. In addition, it has been shown to produce a red color during staining and can be detected using immunohistochemical techniques.</p>

20% by weight in water. 98 atom % 13C

3-Bromo-5-chlorobenzaldehyde is a fine chemical that is used as a building block in the synthesis of other chemicals. It is also a reagent and speciality chemical with high quality and versatility. 3-Bromo-5-chlorobenzaldehyde has been shown to be useful in the preparation of complex compounds, such as heterocyclic aromatic compounds, which are versatile scaffolds for drug discovery. 3-Bromo-5-chlorobenzaldehyde has a CAS No. 188813-05-0.

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5-Bromo-2-(trifluoromethoxy)benzaldehyde is a chemical that is used as a reactant in organic chemistry. It can be used as a building block for the synthesis of complex compounds, or as an intermediate in the preparation of fine chemicals. 5-Bromo-2-(trifluoromethoxy)benzaldehyde is also useful in research and development. It has been used to synthesize pharmaceuticals, pesticides, and other organic compounds.

Boc-Asn-Phe-Pro-aldehyde is a cytosolic proteolytic target enzyme that hydrolyzes peptides with an aliphatic amino acid residue at the carboxy terminus. It is localized in the cytoplasm, where it is activated by serine proteases. Boc-Asn-Phe-Pro-aldehyde has been shown to be effective in cell culture and supernatant. This enzyme can also be used to demonstrate the presence of a particular peptide by releasing a reactive chloride, which can be detected using tetrazolium chloride. This protease has been shown to exacerbate inflammation when administered in vivo.

<p>4-Chloro-2-nitrobenzaldehyde is a reactive intermediate that has been used to investigate the reaction mechanism of protonation. It is an n-oxide and has been shown to react with calcium carbonate under acidic conditions, forming a stable product. 4-Chloro-2-nitrobenzaldehyde has also been used in the synthesis of amides and nitro compounds. This compound possesses two functional groups, which are a nitro group and a chloro group on the aromatic ring.</p>

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<p>Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde, also known as ZILEAL, is a potent immunosuppressant that binds to the Toll-like receptor (TLR) and inhibits NF-κB binding activity. It has been shown to reduce the activation of macrophages by inhibiting the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα), IL-1β, and IL-6. This drug has been shown to inhibit HIV replication in vitro and was also found to have an antiviral effect against herpes simplex virus type 1 in vivo. ZILEAL also inhibits dsDNA binding activity, which may have potential applications in cancer treatment.</p>

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Ac-Val-Glu-Ile-Asp-aldehyde is a pseudo acid that has been shown to induce apoptotic cell death in cultured cells. It is localized in the cerebellar granule and mitochondria of HL-60 cells and HK-2 cells. Ac-Val-Glu-Ile-Asp-aldehyde induces necrotic cell death when it binds to the serine protease zymogen, which is localized in the mitochondrial membrane. It also induces apoptosis by disrupting the mitochondrial membrane potential, leading to a release of cytochrome c into the cytosol. Ac-Val-Glu-Ile-Asp-aldehyde can bind to annexin and tubule cells, which are important for β cell function.

<p>2-Methyl-5-nitrobenzaldehyde is a nitro compound that is used in the synthesis of dobutamine. It has been shown to undergo rearrangements, with the formation of 2-methyl-5-nitrophenol. Kinetic studies have shown that chlorine can be substituted for hydrogen at the 2 position, and this substitution leads to an increase in reactivity. 2-methyl-5-nitrobenzaldehyde also reacts with dopamine to form a ketone. The hydroxy group on this molecule is nucleophilic and can attack electrophiles, making it useful as an active site for synthetic reactions. This compound is also pyrophoric, which means it will spontaneously ignite in air and burn until all its fuel is consumed.</p>

<p>1H-Pyrazole-4-carbaldehyde is a chemical compound that inhibits the growth of bacteria by binding to the enzyme ribonucleotide reductase. It has been shown to have significant antifungal activity against Candida albicans and Saccharomyces cerevisiae, as well as in vitro antifungal activity against other fungi. The 1H-pyrazole-4-carbaldehyde has also been found to inhibit xanthine oxidase and nitric oxide synthase (NOS) in vitro and in vivo, which may be due to its ability to reduce oxidative stress. This chemical compound is a coumarin derivative and contains a pyrazole ring.</p>

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N-Boc-(3S)-3-phenyl-3-aminopropionaldehyde is a synthetic chiral ligand that can be used as a building block in the synthesis of other compounds. It has been used to optimize the synthetic process, and it can be used in buffers, ammonium formate, metal chelate, and other additives to synthesize new compounds. N-Boc-(3S)-3-phenyl-3-aminopropionaldehyde is an optical isomer that can be used for supercritical fluid chromatography (SCFC) or liquid chromatography (LC). This compound has been shown to have a high affinity for ligands with a phenol group.

2-Thiophenecarboxaldehyde is a synthetic compound that has been shown to have in vitro antifungal activity. It has also been shown to inhibit the growth of bacteria and fungi, such as Candida albicans. The antimicrobial activity of 2-thiophenecarboxaldehyde has been demonstrated by in vitro studies using human serum, metal carbonyl complexes, and sodium salts. In addition, this compound inhibits the synthesis of proteins in animal cells infected with viruses or bacteria. It also has amoebicidal activity against Entamoeba histolytica and Leishmania donovani. This compound is used for the treatment of autoimmune diseases such as rheumatoid arthritis and multiple sclerosis.

<p>2-Hydroxy-4-fluorobenzaldehyde is a chemical used as a diagnosis agent to detect radiation exposure. It reacts with magnesium and water molecules to form an amination reaction that produces hydrogen fluoride gas. 2-Hydoxy-4-fluorobenzaldehyde has been shown to have the ability to penetrate into mitochondria, which may be related to its use in the treatment of hepatitis. The chemical structure of this compound is similar to salicylaldehyde, which is used as a reagent for formylation reactions and optical properties. It has also been shown that 2-hydroxy-4-fluorobenzaldehyde can act as a fluorescence probe for the detection of hydrophobic regions on proteins.</p>

<p>4-Chloro-3-fluorobenzaldehyde is an atypical molecule that has a deuterium atom. It is classified as a group p2 functional theory reuptake inhibitor, which blocks the reuptake of noradrenaline at the synapse. The vibrational and spectroscopic properties of this molecule are similar to those of other molecules in its class. 4-Chloro-3-fluorobenzaldehyde was shown to inhibit the production of noradrenaline in rat brain tissue and is used as a model for studying genetic polymorphism. Techniques such as nuclear magnetic resonance spectroscopy, infrared spectroscopy, and X-ray crystallography have been used to investigate the structure and reactivity of 4-chloro-3-fluorobenzaldehyde.</p>

Cis-3-hexenal is a fatty acid that is found in various foods, including soybean and corn oils. It can be used as a chemical substrate to measure the activity of lipoxygenases, enzymes that catalyze the formation of hydroperoxides from polyunsaturated fatty acids. Cis-3-hexenal is also an insect attractant and has been shown to have antifungal properties against plant pathogens such as Phytophthora infestans. This chemical compound has also been shown to inhibit protein synthesis in cells and to be able to react with DNA. Cis-3-hexenal - stabilised: 50% in triacetin

N-Ethylcarbazole-3-carboxaldehyde is an organic compound that has been shown to have anti-cancer properties. It activates the enzyme dioxygenase, which in turn generates reactive oxygen species (ROS) that induce DNA damage and apoptosis in mammalian cells. The photophysical and fluorescence spectrometry of N-ethylcarbazole-3-carboxaldehyde were studied as a function of pH and found to be sensitive to acidic environments. N-Ethylcarbazole-3-carboxaldehyde is also able to form covalent bonds with DNA bases, leading to irreversible oxidation.

<p>4-Fluorobenzaldehyde oxime is a phenylhydrazine derivative that reacts with an aromatic amine to form a ternary complex. The reaction time for this process is short, and the yield of the product is high. 4-Fluorobenzaldehyde oxime also reacts with an aromatic amine to form an ion-pair. It can react with acidic hydrogen donors such as peracids and it also has high hydrogen bonding interactions. 4-Fluorobenzaldehyde oxime is used in pharmacological agents as well as other chemical reactions, including halogenation.</p>

4,6-Dimethoxysalicylaldehyde is a protonated molecule with a cyclohexane ring and 4 hydroxyl groups. Its chemical formula is C6H8O3. The compound has low bioavailability due to the presence of an intramolecular hydrogen bond that causes high redox potential. There are two amines on the aromatic ring which can coordinate with metal ions to form a complex. This compound's structural analysis has been conducted using X-ray crystallography, NMR spectroscopy, and IR spectroscopy. The structure of 4,6-dimethoxysalicylaldehyde is unsymmetrical due to the presence of two asymmetric carbon atoms in the molecule. It forms hydrogen bonds with other molecules due to its hydroxyl group and intramolecular hydrogen bond. Hydrogen bonding interactions occur between this compound and other molecules including water, alcohols, ammonia, amines, and carboxylic acids.

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<p>Perillaldehyde is a natural compound that has been used in food and medicine for centuries. It is an antimicrobial agent with dextran sulfate, which is a sugar polymer that inhibits the growth of fungi and bacteria. Perillaldehyde also has been shown to inhibit the energy metabolism of microorganisms by decreasing ATP production. Perillaldehyde has also been shown to have genotoxic activity, as it can cause DNA strand breaks. This compound also causes oxidative stress in cells by reducing mitochondrial membrane potential and inducing reactive oxygen species (ROS). Perillaldehyde has acute toxicities, as it causes electrochemical impedance spectroscopy changes that indicate cell death.</p>

<p>3-Nitroisonicotinaldehyde is a kinase inhibitor that binds to the ATP binding site of receptor tyrosine kinases. It inhibits the activation of these receptors and prevents the phosphorylation of tyrosine residues on the receptor. 3-Nitroisonicotinaldehyde has been shown to inhibit VEGFR-2, ABCG2, and efflux in human cancer cells. This drug has been shown to inhibit tumor growth in mice by inhibiting angiogenesis, which is a process that involves the formation of new blood vessels from pre-existing ones. 3-Nitroisonicotinaldehyde also inhibits tumor growth by blocking the production of vascular endothelial growth factor (VEGF) from angiogenic cells.</p>

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Trans,cis-2,6-Nonadienal is a fatty acid derivative with an unsaturated 2,6-nonadiene structure. It is an inhibitor of the enzyme fatty acid synthase, which catalyzes the formation of long-chain polyunsaturated fatty acids. Trans,cis-2,6-Nonadienal has been shown to inhibit v79 cells and ester compounds that are used in analytical methods for measuring fatty acids. It is also able to inhibit lysine residues and it can be used as a reactive antioxidant system in mammalian cells. Trans,cis-2,6-Nonadienal has shown a profile of activities that includes inhibition at multiple endpoints involving noncompetitive inhibition as well as antioxidant activity.

<p>2,3,5-Trichlorobenzaldehyde is a chemical compound that has been shown to have anticancer and apoptotic effects. It inhibits the growth of bacteria by chelating iron ions and inhibiting bacterial dna synthesis. 2,3,5-Trichlorobenzaldehyde has also been shown to inhibit the growth of cancer cells in culture in an experimental study. This chemical has been used as a substrate for nmr spectroscopy to study its functional groups and radical scavenging activities. 2,3,5-Trichlorobenzaldehyde can be synthesized from phenacyl chloride and benzaldehyde in the presence of hydrogen chloride gas. The carbonyl group in 2,3,5-trichlorobenzaldehyde may cause metabolic disorders such as diabetes mellitus or hyperglycemia.</p>

<p>Benzaldehyde semicarbazone is a hydrogen bond acceptor and donor, which can be used for the synthesis of pharmaceuticals. It is also known to have significant biological activity, including anticonvulsant activity. Benzaldehyde semicarbazone has been shown to be an inhibitor of pyrazole ring formation in the reaction between 4-chlorobenzaldehyde oxime and hydrochloric acid. This inhibition may be due to its ability to act as a hydrogen bond acceptor, forming hydrogen bonds with both the carbonyl group of 4-chlorobenzaldehyde oxime and the protonated chloride ion. The mechanism is supported by kinetic studies which show that benzaldehyde semicarbazone has a much lower activation energy than the other reactants involved in the reaction.</p>

2-Propyl valeraldehyde is a solvent that is used in pharmaceutical preparations and has been shown to inhibit the activity of aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of alcohols and aldehydes. 2-Propyl valeraldehyde also inhibits the formation of carboxylic acids by competitive inhibition with metal ions such as zinc. The deuterium isotope effect has been used to show that 2-propyl valeraldehyde is metabolized by deuterium exchange. Mass spectrometric detection has shown that this compound contains a carbonyl group (C=O). This compound can be used as an intermediate in organic synthesis reactions, but it also has convulsant effects.

<p>Doebner-Miller reaction the 4- nitrocinnamaldehyde and 2-methylaniline in concentrated HC1 give the corresponding 8-methyl-2-phenylquinoline (3: R = 4'-N02) directly. The asymmetric Friedel-Crafts-type alkylation in aqueous media reaction of 4-Nitrocinnamaldehydr with N-methyl indole using trifluoro</p>

<p>Enalaprilat is an angiotensin-converting enzyme (ACE) inhibitor that prevents the formation of angiotensin II, a potent vasoconstrictor. It is used to treat high blood pressure and congestive heart failure. Enalaprilat is metabolized to enalapril, which has been found to act as an active inhibitor of DNA polymerase. This drug is also capable of inhibiting the synthesis of other proteins, such as those involved in protein transport and cell wall biogenesis.</p>

<p>2-Bromo-4,5-difluorobenzaldehyde is a chemical intermediate and speciality chemical. It is an important building block for the synthesis of organic compounds, such as pharmaceuticals and agrochemicals. This product is a versatile building block, which can be used in a wide range of reactions and is suitable for use as an intermediate or scaffold. It has high quality and complex structure that can be used to synthesize a number of different compounds.</p>

<p>5-Fluoro-2-methylbenzaldehyde is a fine chemical that is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic molecules. It is also useful in the preparation of synthetic resins, dyes, and flavors. 5-Fluoro-2-methylbenzaldehyde has been shown to be a versatile building block with many potential applications. This molecule can be used as a reaction component or as a speciality chemical to produce high quality reagents.</p>

<p>2,4-Dimethoxybenzaldehyde is a synthetic compound that has been shown to have activity against pancreatic lipase. It has been suggested as a potential drug for the treatment of metabolic disorders such as obesity or diabetes. 2,4-Dimethoxybenzaldehyde can be synthesized by reacting ethyl diazoacetate with an aldehyde in the presence of ammonium acetate. This chemical can also be used to produce ethyl esters and compounds belonging to the group of phlorotannins. 2,4-Dimethoxybenzaldehyde has been shown to have antioxidative activity and inhibitory effects on pancreatic lipase.</p>

<p>3-Nitrobenzaldehyde is an organic compound that is used in the synthesis of monoclonal antibodies for use in cancer research. It has been shown to have genotoxic and carcinogenic effects, as it binds to nucleic acids and inhibits DNA replication. 3-Nitrobenzaldehyde has been shown to be effective against a variety of bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. This compound also inhibits protein synthesis by binding with amines and hydrogen bonding with the amino acid residues of proteins.</p>

<p>3,4-Dihydroxybenzaldehyde is an active compound that is a protocatechuic aldehyde. It has been shown to inhibit protein oxidation and kidney injury. 3,4-Dihydroxybenzaldehyde also inhibits the production of bcl-2 protein and growth factor-β in rat urine. This compound has been used in Chinese medicinal preparations as well as in control methods for oxidizing agents.</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>3-Fluoropyridine-4-carboxaldehyde is a reactivator that can be used in the treatment of bladder cancer. It binds to pyridinium and oxime derivatives, which are present in proteins, to form a reactive intermediate. This intermediate reacts with aldehyde groups on hemoglobin, restoring the oxygen binding capacity of hemoglobin to levels seen in healthy individuals. 3-Fluoropyridine-4-carboxaldehyde has been shown to have anticancer activity against bladder cancer cells and also has potential use as an additive for the treatment of red blood cells.</p>

<p>3-Ethynylbenzaldehyde is a tryptic, nitro compound that contains terminal alkynes and has functional groups. The functional theory of this compound suggests that it may be used as a chemosensor for the detection of acidic compounds. 3-Ethynylbenzaldehyde reacts with sodium trifluoroacetate to form an aldehyde, which is then oxidized to an acid by the addition of water. This acid can be detected using NMR spectroscopy. 3-Ethynylbenzaldehyde has been shown to react with sodium trifluoroacetate in solid form at room temperature and above. The resulting product is a yellow crystalline solid that can be identified by its UV spectrum.</p>

<p>(E)-2-Hexadecenal is an asymmetric molecule that is a reactive and carcinogenic compound. It has been shown to induce c-Jun phosphorylation in the human carcinoma cell lines, leading to physiological changes. (E)-2-Hexadecenal has also been used to induce chemiluminescence in vitro, which can be used for analytical chemistry. It is made by a hydroxyl group on a fatty acid with a biofuel reaction. This molecule may also have pro-apoptotic properties due to its chemical biology and ability to affect mitochondrial membrane potentials.</p>

<p>Applications 8-Nonenal is used as a reactant in the preparation of macrocyclic Z-enoates and (E,Z)- or (Z,E)-dienoates through catalytic stereoselective ring-closing metathesis.<br>References Zhang, H., et al.: JACS., 136, 16493 (2014)<br></p>

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<p>3-Chloro-1H-indole-2-carbaldehyde is a bifunctional reagent that can be used to form amides. It reacts with primary and secondary amines, as well as dialkyl and methylene amines, to produce the corresponding chloro-, phenylhydrazine-, or nitrosoaminoureas. This reaction is intramolecular and yields the desired product in high yield. The reactant can also be used as a chloride source. 3-Chloro-1H-indole-2-carbaldehyde is manufactured by reacting phenylhydrazine with chloroacetic acid in an organic solvent at room temperature (25°C).</p>

<p>5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%.</p>

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<p>4-Acetoxybenzaldehyde is a compound with an acetyl group attached to the benzene ring. It is potentially toxic to cells and has been shown to produce reactive oxygen species (ROS) in v79 cells, which can lead to cell death. The biological properties of 4-acetoxybenzaldehyde are not well understood, but it has been shown to have antioxidant properties in other studies. This compound also reacts with amines, forming acetamides and amides. 4-Acetoxybenzaldehyde is found in environmental pollution as a result of its presence in the atmosphere and its use as a solvent. It was first synthesized by the reaction of coumaric acid and acetyl chloride with formaldehyde at reflux temperature. The compound can be purified by chromatographic methods or mass spectrometric analysis.</p>