
Aldeidi
Trovati 8576 prodotti di "Aldeidi"
6-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxaldehyde
CAS:Please enquire for more information about 6-Chloro-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C9H8ClN3OPurezza:Min. 95%Peso molecolare:209.63 g/mol5-Bromo-2-furaldehyde
CAS:5-Bromo-2-furaldehyde is a chemical compound that belongs to the class of heterocycles. It is used in industry as a precursor for the synthesis of other organic compounds. 5-Bromo-2-furaldehyde has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. The use of this chemical has been linked with autoimmune diseases and cancer development in animal models. 5-Bromo-2-furaldehyde is an environmental pollutant that can enter the body by ingestion or inhalation, and it can cause irritation of the skin, eyes, nose, throat, and lungs. This chemical is also known as amide or suzuki coupling reaction (SCR).
Formula:C5H3BrO2Purezza:Min. 98%Colore e forma:Off-White To Yellow To Light Brown SolidPeso molecolare:174.98 g/molButyraldehyde
CAS:Butyraldehyde is a colorless to yellowish liquid with a strong, pungent odor. It is soluble in water and has an acidic pH of 2.6-3.0. Butyraldehyde is used as a chemical intermediate for the production of polyvinyl acetate and can be made by reacting acetic acid with butanol or butyl acetate. This chemical reacts with human serum albumin at low concentrations and may have biological properties such as catalyzing the conversion of picolinic acid to nicotinic acid, which aids in the prevention against infectious diseases. Butyraldehyde also has synergistic effects when used with picolinic acid, increasing its effectiveness in combating infection.Formula:C4H8OPurezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:72.11 g/mol4-Cinnolinecarboxaldehyde
CAS:4-Cinnolinecarboxaldehyde is an organic compound that belongs to the group of cinnoline. It is a colorless liquid that can be used as a precursor in the production of aluminum metal. 4-Cinnolinecarboxaldehyde reacts with lithium aluminum hydride to form a compound that can be used as a reducing agent in organic chemistry. 4-Cinnolinecarboxaldehyde is also used as a precursor for preparing other compounds, such as lithium aluminum hydride and lithium aluminum trihydride.
Formula:C9H6N2OPurezza:Min. 95%Peso molecolare:158.16 g/mol4-Iodo-2-methoxypyridine-3-carboxaldehyde
CAS:4-Iodo-2-methoxypyridine-3-carboxaldehyde is a disubstituted compound that has insulin-like properties. It inhibits the activity of the insulin receptor, which may contribute to its insulin-like growth factor effects. This inhibitor also targets the protein kinase, which is responsible for the response of cells to insulin. 4-Iodo-2-methoxypyridine 3 carboxaldehyde has been shown to inhibit IGF1R and malonate ion, and it may have potential as an oral treatment for diabetes.Formula:C7H6INO2Purezza:Min. 95%Peso molecolare:263.03 g/mol4-(Dimethylamino)-2-hydroxybenzaldehyde
CAS:4-(Dimethylamino)-2-hydroxybenzaldehyde (DMAA) is an anticancer agent that has been shown to enhance the antitumor effect of sodium succinate. DMAA binds to the tetradentate site of the DNA and prevents it from binding with a transcription factor, which may lead to cancer cell death. DMAA has low detection in urine and blood, making it difficult to detect its presence in patients. DMAA also has no known complexation partners, making it difficult for the body to excrete this drug. DMAA is not carcinogenic or mutagenic. It is used as a fluorescent probe for detecting hydroxy groups in organic compounds and as an environmental pollutant when mixed with other chemicals such as benzene and methylene chloride.Purezza:Min. 95%2-Furaldehyde diethylacetal
CAS:2-Furaldehyde diethylacetal is a synthetic compound that has been used in the synthesis of calcium carbonate. It is also a potent inhibitor of p. aeruginosa and other bacteria, as well as organic acids and halogen compounds. It reacts with hydroxy groups to form aldehydes, which are then oxidized to form carboxylic acid derivatives. The reaction mechanism for this compound is not well understood, but it is thought that the activation energy for the reaction may be low due to the presence of a furfural functional group.Formula:C9H14O3Purezza:Min. 95%Peso molecolare:170.21 g/mol2-Hydroxy-3-(Trifluoromethoxy)Benzaldehyde
CAS:2-Hydroxy-3-(trifluoromethoxy)benzaldehyde is a coordination compound that is used as a ligand. It has two-dimensional and crystal structures. The ligated molecule is usually coordinated to the metal ion, forming a dimer.Formula:C8H5F3O3Purezza:Min. 95%Peso molecolare:206.12 g/molp-Anisaldehyde dimethyl acetal
CAS:p-Anisaldehyde dimethyl acetal is a broad-spectrum antimicrobial that can be synthesized from anisaldehyde and dimethoxyacetal. It has been shown to have anticancer properties in vitro. p-Anisaldehyde dimethyl acetal has also been shown to inhibit the growth of HL60 cells, which are specialized white blood cells. This compound was found to increase neuronal death and induce cachexia in mice. The molecular weight of p-Anisaldehyde dimethyl acetal is 244.24 g/mol, with a melting point of -14 °C and a boiling point of 156 °C. The molecule contains one asymmetric center, one hydrogen bond, one non-bonding electron pair, and no double bonds. This compound has acidic properties and it reacts with vitamin D3 in a cationic polymerization process at alkaline pH levels.
Formula:C10H14O3Purezza:Min. 95%Colore e forma:Colourless To Pale Yellow Clear LiquidPeso molecolare:182.22 g/mol4-Bromofuran-2-carbaldehyde
CAS:4-Bromofuran-2-carbaldehyde is a synthetic compound that has been shown to have antioxidant properties. It contains an electron-donating carbonyl group and an electron-withdrawing bromine atom. 4-Bromofuran-2-carbaldehyde is useful in the treatment of endophytic fungi infections, as it inhibits the synthesis of ergosterol, which is an important component of the fungal cell membrane. The molecule's conformational properties are also important for its biological activity, as they enable it to act as a chiral ligand by binding to proteins in a way that will inhibit their function. In addition, 4-bromofuran-2-carbaldehyde has been shown to be effective against cancer cells in vitro, particularly against MMCF7 cells. This may be due to its ability to bind to DNA and prevent transcription or replication of DNA strands.
Formula:C5H3BrO2Purezza:Min. 95%Peso molecolare:174.98 g/mol5-Bromopyridine-2-carbaldehyde
CAS: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%.
Formula:C6H4BrNOPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:186.01 g/mol1-Allyl-1H-benzimidazole-2-carbaldehyde
CAS:1-Allyl-1H-benzimidazole-2-carbaldehyde is a dipolar compound that can be synthesized from the reaction of 1,3-diphenylazomethine and allyl bromide. It is an orange solid that has been shown to form cycloadducts with alkenes. The selectivity of this reaction depends on the substituents on both reactants, with electron withdrawing groups increasing the rate of substitution. Dipolar cycloaddition theory predicts that 1-allyl-1H-benzimidazole-2-carbaldehyde undergoes intramolecular cycloaddition to form a six membered ring in which one carbon atom is shared between two adjacent atoms.Formula:C11H10N2OPurezza:Min. 95%Colore e forma:SolidPeso molecolare:186.21 g/mol5-(Methoxymethyl)-2-furancarboxaldehyde
CAS:5-hydroxymethylfurfural (5-hmf) is an organic compound that is produced when a carbohydrate or sugar undergoes oxidation. It is used as an additive in animal feed and as an industrial chemical. 5-hmf is a solid catalyst that can be used at high temperatures, making it suitable for use in the production of 2,6-dihydroxybenzoic acid. The reaction mechanism of 5-hmf involves the dehydration of furfural to form 5-hydroxymethylfurfural. This process occurs when a molecule of water reacts with furfural to produce two molecules of 5-hmf. The reaction may be accelerated by introducing heat, which breaks down the hydrogen bonds between the molecules of furfural and water.Formula:C7H8O3Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:140.14 g/molTacrolimus methyl acryl aldehyde
CAS:Please enquire for more information about Tacrolimus methyl acryl aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C11H18O3Purezza:Min. 95%Peso molecolare:198.26 g/mol3-(Difluoromethoxy)benzaldehyde
CAS:Please enquire for more information about 3-(Difluoromethoxy)benzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C8H6F2O2Purezza:Min. 95%Peso molecolare:172.13 g/mol3,4-Dichlorobenzaldehyde
CAS:3,4-Dichlorobenzaldehyde is a monosubstituted aromatic organic compound with inhibitory effects. 3,4-Dichlorobenzaldehyde has shown significant antifungal activity against Candida albicans and Saccharomyces cerevisiae. It also inhibits the growth of certain cancer cells in cell culture studies. 3,4-Dichlorobenzaldehyde has been found to have anti-inflammatory properties and would be effective in treating inflammatory diseases such as asthma or arthritis. This compound has been shown to have significant effects on energy metabolism and fatty acid synthesis by inhibiting enzymes that are involved in these processes. 3,4-Dichlorobenzaldehyde can also be used to treat metabolic disorders such as diabetes mellitus type II and hyperlipidemia by inhibiting enzymes that are involved in these processes.Formula:C7H4Cl2OPurezza:Min. 95%Colore e forma:White To Off-White SolidPeso molecolare:175.01 g/molN-Methyl-N-hydroxyethyl-4-aminobenzaldehyde
CAS:N-Methyl-N-hydroxyethyl-4-aminobenzaldehyde (NHABA) is a bathochromic molecule that absorbs light at wavelengths of 400 to 500 nm. It is reactive and reacts with metal cations to form chromophores. NHABA has been shown to be a fluorescent probe for the detection of tyrosinase and autophagy in human serum. It also has inhibitory properties against tyrosinase, which may be due to its ability to inhibit the formation of melanin. NHABA is used as an analytical chemistry reagent for the determination of ammonia, nitrite, and nitrate ions in water samples. This molecule can also be used as a chemosensor for the detection of phenolic compounds in water samples.Formula:C10H13NO2Purezza:Min. 95%Peso molecolare:179.22 g/mol5-Bromo-3-methoxybenzaldehyde
CAS:5-Bromo-3-methoxybenzaldehyde is a type of growth factor that is synthesized by cancer cells. It has been shown to have anticancer activity when used in conjunction with other drugs. 5-Bromo-3-methoxybenzaldehyde has been shown to inhibit tumor growth in mice, which may be due to its ability to prevent the activation of PD-L1. This compound interacts with a tetranuclear ligand and can be activated by light.Formula:C8H7BrO2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:215.04 g/molBoc-Tyr(Bzl)-aldehyde
CAS:Please enquire for more information about Boc-Tyr(Bzl)-aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C21H25NO4Purezza:Min. 95%Peso molecolare:355.43 g/mol2-Chloro-3-methoxybenzaldehyde
CAS:Please enquire for more information about 2-Chloro-3-methoxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C8H7ClO2Purezza:Min. 95%Peso molecolare:170.59 g/molN-Boc-4-piperidineacetaldehyde
CAS:N-Boc-4-piperidineacetaldehyde is a chiral, stable, and readily available aldehyde. It has been used in the synthesis of various biologically active molecules including imidazolidinones, which are important for their use as catalysts in organic chemistry. The synthesis of this molecule by the condensation of 4-piperidineacetic acid with acetaldehyde followed by reduction with sodium borohydride is an example of this type of reaction. N-Boc-4-piperidineacetaldehyde can be used to synthesize imines and linkers that are covalently bonded to the protein backbone. This molecule also has conformational stability and is not susceptible to oxidation or radiation damage.
Formula:C12H21NO3Purezza:Min. 95%Peso molecolare:227.3 g/molAc-Glu-Ser-Met-Asp-aldehyde (pseudo acid)
CAS:Ac-Glu-Ser-Met-Asp-aldehyde is a molecule that is naturally produced by the human body. It has been shown to be an endogenous caspase activator, which may lead to apoptosis. Ac-Glu-Ser-Met-Asp-aldehyde can also bind to cholesterol and influence its synthesis, thus affecting the production of other proteins. This molecule has a protease activity and can cleave peptides at specific sites. The sequences of this molecule have been determined and it has been found that these sequences are similar to those found in other proteases such as serine proteases.Formula:C19H30N4O10SPurezza:Min. 95%Peso molecolare:506.53 g/mol4-Bromobenzaldehyde
CAS:4-Bromobenzaldehyde is a chemical compound that belongs to the group of aromatic compounds. It has been shown to have a potent stimulatory effect on locomotor activity in mice, which may be due to its ability to increase levels of epidermal growth factor and gamma-aminobutyric acid in the brain. 4-Bromobenzaldehyde can be synthesized from 2,4-dibromophenol and anhydrous copper chloride in the presence of sodium hydroxide. The reaction mechanism for this synthesis is believed to involve an intermediate enamine form of 4-bromobenzaldehyde, which can then undergo hydrolysis into 2,4-dibromophenol and benzaldehyde. This product is used as a reagent in organic synthesis because it can be used to form esters with trifluoroacetic acid or hydrochloric acid in high yield.
Formula:C7H5BrOPurezza:Min. 90 Area-%Colore e forma:White PowderPeso molecolare:185.02 g/mol1-Methyl-1H-indazole-7-carbaldehyde
CAS:1-Methyl-1H-indazole-7-carbaldehyde is a 1,3,5-substituted indazole derivative that can be used as a building block for the synthesis of complex compounds. It is an intermediate in the synthesis of various pharmaceuticals and it has been shown to have potential applications in research chemicals. 1-Methyl-1H-indazole-7-carbaldehyde can be used as a versatile building block after conversion to other derivatives. This chemical is also being investigated as a possible treatment for Parkinson's disease and Alzheimer's disease.Formula:C9H8N2OPurezza:Min. 95%Colore e forma:Yellow PowderPeso molecolare:160.17 g/molBenzimidazole-5-aldehyde
CAS:Please enquire for more information about Benzimidazole-5-aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C8H6N2OPurezza:Min. 95%Colore e forma:PowderPeso molecolare:146.15 g/mol1H-Indole-2-carbaldehyde
CAS:1H-Indole-2-carbaldehyde is a solvent that has been used in the protein data and molecular modeling study. The 1H NMR spectrum of this compound showed an intense signal at δ 4.8 ppm, corresponding to the hydroxyl proton. This solvent also has fluorescence properties, as shown by its photophysical and structural analysis. The 1H-indole-2-carbaldehyde molecule has an active methylene group and an oxindole ring with amine substituents.
Formula:C9H7NOPurezza:Min. 98%Colore e forma:PowderPeso molecolare:145.16 g/molPropionaldehyde
CAS:Propionaldehyde is a simple aliphatic aldehyde that is used in the synthesis of other compounds. It can be synthesized by oxidizing propylene with an oxidation catalyst such as manganese dioxide or platinum metal under pressure. Propionaldehyde can also be formed by the direct oxidation of propanol using ferric chloride, but this reaction has been shown to produce a mixture of products. Propionaldehyde can be produced by the oxidation of acetaldehyde with hydrogen peroxide, which produces formaldehyde and acetone. In addition to its use as a chemical reagent, propionaldehyde has been used as an additive in nutrient solutions for experiments in plant physiology and microbiology. The kinetic data for reactions involving propionaldehyde have been determined using methyl ethyl ketone (MEK) as the solvent and copper(II) sulfate pentahydrate as the catalyst. The redox potential for this molecule is -0.034 volts at pH 7,Formula:C3H6OPurezza:Min. 95%Colore e forma:Colorless Clear LiquidPeso molecolare:58.08 g/mol2-(Dimethylamino)acetaldehyde sulfite
CAS:2-(Dimethylamino)acetaldehyde sulfite is a white crystalline solid with a melting point of around 100°C. It is soluble in water and slightly soluble in organic solvents. 2-(Dimethylamino)acetaldehyde sulfite can be used as a reagent to prepare alkali solutions and acid hydrochlorides. It can also be used as an intermediate for the synthesis of methacrylic acid, methyl acetate, and other organic compounds. 2-(Dimethylamino)acetaldehyde sulfite can be synthesized using a high-yield synthetic method involving lithium, acidification, and an organic solvent.
Purezza:Min. 95%Caspase-3/7 Inhibitor II Ac-Asp-Asn-Leu-Asp-aldehyde (pseudo acid)
CAS:Caspase-3/7 Inhibitor II Ac-Asp-Asn-Leu-Asp-aldehyde (pseudo acid) is a peptide inhibitor of caspases. It blocks the activation of these proteases and their subsequent cleavage of substrates in the apoptotic pathway. This drug has potent inhibitory activity against caspases 3, 7, 8, 9, and 10. Caspase-3/7 Inhibitor II Ac-Asp-Asn-Leu-Asp-aldehyde (pseudo acid) specifically interacts with the active site and inhibits the enzyme by binding to an aspartic acid residue at position D197 in human caspase 3. Caspase 3/7 Inhibitor II Ac-Asp-Asn-Leu-Asp-aldehyde (pseudo acid) is localized to mitochondria and binds to acetyldeviceine (acDEV), a substrate for caspasesFormula:C20H31N5O10Purezza:Min. 95%Peso molecolare:501.49 g/molAc-Ile-Glu-Thr-Asp-aldehyde (pseudo acid)
CAS:Ac-Ile-Glu-Thr-Asp-aldehyde (pseudo acid) is a neurotrophic factor that plays an important role in the development and function of the nervous system. It stimulates the production of other neurotrophic factors such as NGF, BDNF, and GDNF. This protein has been shown to be involved in a number of autoimmune diseases, including multiple sclerosis and rheumatoid arthritis. Ac-Ile-Glu-Thr-Asp-aldehyde (pseudo acid) is also known to reduce neuronal death by binding to toll receptors on neurons and activating mitogen activated protein kinases. Acetylcholine esterase activity can also be inhibited by this protein. Acetylcholine esterase is responsible for breaking down acetylcholine, which is a neurotransmitter that transmits nerve impulses across the synapses between neurons. The inhibition of this enzyme leads to an increase in acetylcholine levels and increased transmission of
Formula:C21H34N4O10Purezza:Min. 95%Peso molecolare:502.52 g/mol3-Thien-2-yl-1H-pyrazole-4-carbaldehyde
CAS:3-Thien-2-yl-1H-pyrazole-4-carbaldehyde is a ligand that can be used to inhibit the activity of nicotine in the human liver. It has been shown to reduce chemical inhibitor activity globally and systematically, and it may have therapeutic potential for preventing death from tobacco use. 3-Thien-2-yl-1H-pyrazole-4-carbaldehyde binds to nicotine receptors by forming hydrogen bonds with the receptor's nicotinic acetylcholine binding sites. This prevents nicotine from binding to those sites, resulting in a reduction of the addictive properties of tobacco. 3TPCA is being developed as a drug candidate for treating tobacco use disorders.Formula:C8H6N2OSPurezza:Min. 95%Colore e forma:PowderPeso molecolare:178.21 g/molAc-Tyr-Val-Ala-Asp-aldehyde (pseudo acid)
CAS:Ac-Tyr-Val-Ala-Asp-aldehyde is a sesquiterpene lactone that has been shown to have anti-inflammatory properties. It inhibits the inflammatory response by inhibiting the production of pro-inflammatory cytokines and chemokines, such as IL1β, IL6, and TNFα. Ac-Tyr-Val-Ala-Asp-aldehyde also inhibits the activity of cyclooxygenase 2 (COX2) and lipoxygenase (LOX), which are enzymes that produce prostaglandins from arachidonic acid. Acetylsalicylic acid is an example of a drug with similar properties. Acetylsalicylic acid has been shown to inhibit the growth of cancer cells in tissue culture studies and in animal models. This compound may also be used to treat bowel disease, congestive heart failure, or other diseases that are characterized by increased apoptosis.Formula:C23H32N4O8Purezza:Min. 95%Peso molecolare:492.52 g/molCell-permeable Caspase-3 Inhibitor I trifluoroacetate salt
CAS:Please enquire for more information about Cell-permeable Caspase-3 Inhibitor I trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C94H158N20O27Purezza:Min. 95%Peso molecolare:2,000.38 g/mol3,5-Bis(trifluoromethyl)benzaldehyde
CAS:3,5-Bis(trifluoromethyl)benzaldehyde is a synthetic compound that has been shown to inhibit cancer cell growth. It is a chromatographic reagent and an intermediate in the production of pharmaceuticals. 3,5-Bis(trifluoromethyl)benzaldehyde was shown to bind to the amino group of proteins and inhibit the synthesis of protein inhibitors. This compound also binds to cholesterol esters and causes lipid peroxidation, leading to cell death in cancer cells.
Formula:C9H4F6OPurezza:Min. 95%Colore e forma:PowderPeso molecolare:242.12 g/mol5-Bromo-2-hydroxybenzaldehyde
CAS:5-Bromo-2-hydroxybenzaldehyde (5BHB) is an organic compound that has been shown to have a coordination geometry of group p2. This compound binds to DNA and RNA, inhibiting the transcription process. 5BHB also has the ability to form a copper complex with malonic acid. This redox potential is reduced by one electron when copper is added in order to form the copper complex, which allows for the reactivity of 5BHB to be increased. 5BHB binds to nucleic acids through hydrogen bonding interactions with nitrogen atoms and lone pairs on oxygen atoms. The reaction mechanism for 5BHB involves intramolecular hydrogen transfer from one molecule of 5BHB to another, forming an intermediate that then reacts with nucleic acid.
Formula:C7H5BrO2Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:201.02 g/mol3-Bromobenzaldehyde
CAS:3-Bromobenzaldehyde is an organic compound with the formula CHBrCHO. It is a colorless liquid that is soluble in many organic solvents. 3-Bromobenzaldehyde can be synthesized by the reaction of ethyl acetoacetate and anhydrous sodium in methanol, and can be purified by distillation or recrystallization from ethanol. This compound has been used as a solvent for analytical methods, such as GC-MS analysis, due to its high boiling point and low volatility. 3-Bromobenzaldehyde also reacts with hydrogen chloride to form benzoyl chloride, which can then be reacted with alcohols to produce esters. 3-Bromobenzaldehyde has been shown to react with chalcones to form optical active compounds, such as curcumin analogues. These reactions are typically carried out in solution using acetic acid or sulfuric acid as a catalyst.br>br>Formula:C7H5BrOPurezza:Min. 95%Peso molecolare:185.02 g/mol3,5-Dibenzyloxybenzaldehyde
CAS:3,5-Dibenzyloxybenzaldehyde is a molecule that has been shown to induce apoptosis in prostate cancer cells. It binds to the survivin protein and prevents its function. 3,5-Dibenzyloxybenzaldehyde also has anti-cancer properties due to its ability to inhibit the growth of cultured prostate cancer cells in vitro. This compound can be used as a photophysical probe for radiation studies or as a fatty acid monomer for metathesis reactions. The molecule is also active against cox-2 inhibitory activity and has been shown to have clinical efficacy in diazepine synthesis.Formula:C21H18O3Purezza:Min. 95%Peso molecolare:318.37 g/molAc-Leu-Glu-His-Asp-aldehyde (pseudo acid) trifluoroacetate salt
CAS:Ac-Leu-Glu-His-Asp-aldehyde (pseudo acid) trifluoroacetate salt is a chemical compound that belongs to the group of apoptosis proteins. It has been shown to have anti-inflammatory and neuroprotective effects in primary cells, as well as to induce apoptosis in HL60 cells. Ac-Leu-Glu-His-Asp-aldehyde (pseudo acid) trifluoroacetate salt is also able to inhibit the activation of the caspase pathway by preventing the release of cytochrome c from mitochondria and decreasing the mitochondrial membrane potential. The protein may be used as an agent for skin cancer treatment.Formula:C23H34N6O9Purezza:Min. 95%Peso molecolare:538.55 g/moltrans-2-Hexenal
CAS:Trans-2-hexenal is a natural compound that has been used as a model system for studying the toxicity of sodium salts. It is also used in studies on the enzyme activities of leaves and its carcinogenic potential. Trans-2-hexenal exhibits genotoxic effects, which may be due to its reaction with DNA or by inhibiting the polymerase chain reaction. In addition, this compound can inhibit enzymes involved in the synthesis of fatty acids, leading to cell death. Trans-2-hexenal is also found in plants and fruits such as apples, bananas, and pineapples.Formula:C6H10OPurezza:Min. 97 Area-%Colore e forma:Clear LiquidPeso molecolare:98.14 g/mol5-(2-Methyl-4-nitrophenyl)-2-furaldehyde
CAS:Please enquire for more information about 5-(2-Methyl-4-nitrophenyl)-2-furaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C12H9NO4Purezza:Min. 95%Peso molecolare:231.2 g/mol3-Acetoxybenzaldehyde
CAS:3-Acetoxybenzaldehyde is a chemical compound that has been used as a photosensitiser for the production of hydrogen peroxide. When irradiated with light, it undergoes a series of reactions, including the removal of an electron from the molecule and the formation of a reactive oxygen species (ROS). This ROS then reacts with chloride ions to form chlorine radicals. These chlorine radicals can react with acetyl groups to form 3-acetoxybenzoic acid. 3-Acetoxybenzaldehyde is also used in organic synthesis to produce ketones and aldehydes. The functional groups on this compound are an acetyl group and a carbonyl group. 3-Acetoxybenzaldehyde is produced by the dehydrogenation of trimethyl acetate, which is catalyzed by palladium on charcoal or platinum oxide.Formula:C9H8O3Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:164.16 g/molAc-N-Me-Tyr-Val-Ala-Asp-aldehyde (pseudo acid)
CAS:Please enquire for more information about Ac-N-Me-Tyr-Val-Ala-Asp-aldehyde (pseudo acid) including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C24H34N4O8Purezza:Min. 95%Peso molecolare:506.55 g/molMethoxyacetaldehyde diethyl acetal
CAS:Methoxyacetaldehyde diethyl acetal is a viscous liquid with a low vapor pressure. This substance is stable at high temperatures and has a high resistance to chemical interactions. It is also hydrophobic in nature. Methoxyacetaldehyde diethyl acetal has been shown to interact with the aminoglycoside antibiotics, erythromycin, streptomycin, and neomycin. The interaction of this substance with these antibiotics may be due to the fact that it has proton resonances similar to those of amino acids, as well as its ability to form hydrogen bonds with the antibiotic molecules. Methoxyacetaldehyde diethyl acetal also interacts with triethyl orthoformate, which can lead to the formation of an ester bond between them.Formula:C7H16O3Purezza:Min. 95%Colore e forma:Colorless Clear LiquidPeso molecolare:148.2 g/mol3-Hydroxyisonicotinaldehyde
CAS:3-Hydroxyisonicotinaldehyde is a disulfide bond that plays an important role in enzyme catalysis. The active site of the enzyme, which contains a nucleophilic attack on the electrophilic carbon atom, is composed of two cysteine residues with their sulfhydryl group (-SH) bonded to each other through a disulfide bond. This bond can be broken by either an acidic environment or protonation. In the absence of these conditions, the -SH groups are coordinated to metal ions and form a complex. The hydroxyl group (-OH) on one cysteine residue can coordinate to the nitrogen atom on the other cysteine residue and form tautomers. These tautomers correspond to two different configurations of the molecule: one where both sulfur atoms are in a trans configuration (tautomer A), and one where they are in a cis configuration (tautomer B). The biological properties of 3-hydroxyisonFormula:C6H5NO2Purezza:Min. 95%Peso molecolare:123.11 g/mol(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde
CAS:(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde is an epoxide. It is a colorless liquid with a pleasant odor and taste that can be used as a flavoring agent. This compound is biosynthesized by bacteria from the alpha-terpineol or 2,2,3-trimethylcyclopentanone. The biological activity of (2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde has been investigated in cultures and in vitro studies on acid bacteria. The production of this compound was found to be stimulated by the presence of other terpenoids such as limonene and alpha pinene.Formula:C10H16OPurezza:Min. 95%Peso molecolare:152.23 g/molN-Ethylcarbazole-3-carboxaldehyde
CAS: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.Formula:C15H13NOPurezza:Min. 95%Peso molecolare:223.27 g/molZ-Leu-Leu-4,5-dehydro-Leu-aldehyde
CAS:Please enquire for more information about Z-Leu-Leu-4,5-dehydro-Leu-aldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C26H39N3O5Purezza:Min. 95%Peso molecolare:473.61 g/mol3-Fluoro-2-hydroxybenzaldehyde
CAS:3-Fluoro-2-hydroxybenzaldehyde is a colorless liquid with a sweet, aromatic odor. It has been shown to be an antibacterial agent against Gram positive bacteria and may have potential as a drug for the treatment of MRSA. 3-Fluoro-2-hydroxybenzaldehyde is used in the production of cellulose acetate and sodium sulfide. It is also used in the chemical reactions that form amines, hydroxyl groups, and chloride ions. It has been shown to inhibit mitochondrial respiration by chelating ring complexes in the respiratory chain. It also inhibits biological processes such as DNA synthesis, protein synthesis, and hydrogen bond formation.Formula:C7H5FO2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:140.11 g/mol3-(3-Chlorophenyl)propionaldehyde
CAS:Please enquire for more information about 3-(3-Chlorophenyl)propionaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C9H9ClOPurezza:Min. 95%Peso molecolare:168.62 g/molZ-Pro-Pro-aldehyde-dimethyl acetal
CAS:Z-Pro-Pro-aldehyde-dimethyl acetal is a neurotoxin that can be used to label lysosomal enzymes in cells. The labeling is stable and does not interfere with the enzymatic activity of the enzyme. It has been shown to exacerbate neurological disease in mice, including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. Z-Pro-pro-aldehyde-dimethyl acetal binds to microglia cells and induces reactive oxygen species production, which may contribute to cell damage. This toxin also diffracts light at a wavelength of 630 nm when exposed to X-rays, making it useful for labeling lysosomal enzymes in tissue sections or cell supernatants.Formula:C20H28N2O5Purezza:Min. 95%Peso molecolare:376.45 g/mol
