Amides

<p>Inhibits carbonic anhydrase; diuretic</p>

<p>2-[(2,6-Dichlorophenyl)amino]-N,N-dimethylbenzeneacetamide is a reagent, complex compound and useful intermediate with a CAS number of 21789-06-0. It is a fine chemical that can be used as a building block in the synthesis of other compounds. It has been shown to be useful in the production of speciality chemicals and research chemicals. The versatility of this compound makes it an excellent scaffold for the synthesis of other compounds. This product is not intended for human or animal use.</p>

<p>Lacosamide is a drug that is used for the treatment of epilepsy. It has been shown to inhibit neuronal death in vitro and in animal models, and has been extensively studied for its potential benefits in the treatment of bowel disease. The mechanism of action for lacosamide involves inhibition of the transport of neurotransmitters from the synaptic cleft by binding to the neuronal sodium channels and increasing their recovery rate. Lacosamide has also been found to affect energy metabolism by inhibiting the activity of mitochondrial enzymes such as matrix effect and complex I/III.</p>

<p>4-Aminothiobenzamide (4ATB) is a chemical compound that is used as an anticancer agent and an antimicrobial agent. It has been shown to have antitumor activity against human liver cancer cells and anticancer activity against human adrenergic receptor-positive lung cancer cells. 4ATB binds to the chloride ion present in the cell membrane, which prevents the influx of chloride ions into the cell. This leads to an increase in intracellular pH and disruption of cellular functions. 4ATB has also been shown to inhibit methicillin-resistant Staphylococcus aureus (MRSA) infections by inhibiting bacterial growth and reducing the production of proteins vital for cell division.</p>

<p>2-(5-Bromo-1H-indol-3-yl)acetamide is a high quality, reagent, complex compound, useful intermediate and fine chemical. It is also a useful scaffold or building block for the synthesis of speciality chemicals. 2-(5-Bromo-1H-indol-3-yl)acetamide is used in research and development as a versatile building block for the synthesis of new compounds. The CAS number for this compound is 196081-79-5.</p>

<p>Please enquire for more information about 1-Methylindole-3-acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-[(3S)-2,5-Dioxotetrahydro-3-furanyl]-2,2,2-trifluoroacetamide is a boronic acid that has been used to synthesize polymers. This compound is of interest for the synthesis of hydrophobic amino acids such as threonine and lysine. The high yield and functionalisation of this molecule make it deserving of further investigation.</p>

<p>Hydroxyflutamide is an anti-androgen drug that belongs to the group of nonsteroidal anti-androgens. It has been shown to bind to the androgen receptor with high affinity and inhibit the growth of cancer cells in vitro. Hydroxyflutamide also has a strong antitumor response in vivo, which is due to its ability to inhibit cellular proliferation by binding to DNA polymerase during replication. The drug may also have some activity as an antineoplastic agent because it inhibits the growth of prostate cancer cells. However, hydroxyflutamide has never been tested on humans or animals, so its effects are unknown.</p>

<p>Oxyclozanide is an antimicrobial agent that inhibits the enzyme activity of chitin synthase in the nematode, which is necessary for the production of chitin. This inhibition leads to disruption of the nematode's cell membrane and death. Oxyclozanide has been shown to be effective against resistant mutants, as well as synergistic with other antimicrobial agents. It is also a specific antidote for oxyclozanide poisoning.</p>

<p>3-Bromobenzamide is an amide compound, which is a functional group. It has a molecular weight of 273.3 g/mol and three amine groups. The 3-methoxybenzamide moiety in the molecule can be protonated, which provides the hydration of the molecule and increases its solubility in water. This molecule also has a dipole moment due to the presence of two amide groups.<br>The synthesis of 3-bromobenzamide starts with the reaction between 3-aminobenzoic acid and benzoyl chloride to form 3-benzoyloxybenzoic acid. This is then reacted with ammonia to form 3-aminobenzamide. Finally this is converted into 3-bromobenzamide by reacting it with bromine in the presence of potassium carbonate as a catalyst. <br>This molecule is used as an inhibitory compound for mammalian cell proliferation, specifically for cancer cells</p>

<p>2,2'-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride (BPDC) is a synthetic compound that is used as an analytical reagent and a model system for oxidative injury. It has significant cytotoxicity on human cells in cell culture. BPDC induces oxidative damage to proteins and DNA by increasing the production of reactive oxygen species such as hydrogen peroxide, superoxide, and hydroxyl radicals. The mechanism of action is not well understood but may be due to Toll-like receptor signalling pathways. This compound has been shown to inhibit the activity of antioxidant enzymes such as glutathione peroxidase and catalase. It also inhibits the activity of proinflammatory cytokines such as IL-6 and IL-8. BPDC is being investigated for its potential use in bowel disease treatment.</p>

<p>N-[2-(p-Cinnamylamino)ethyl]-5-isoquinolone sulfonamide is a high quality chemical that can be used as a reagent, complex compound, and useful intermediate. N-[2-(p-Cinnamylamino)ethyl]-5-isoquinolone sulfonamide is a fine chemical that is useful in the production of speciality chemicals. It can be used as a versatile building block and reaction component to produce various compounds.</p>

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<p>Dimethylphosphonoacetamide (DMPPA) is a phosphorus-containing compound that is used as an intermediate in the synthesis of fatty acids. DMPPA can be synthesized by the reaction of ethylene diamine and phosphorus pentoxide, which is a common reagent for preparing phosphorus compounds. The reaction mechanism has been studied using electrochemical impedance spectroscopy. This study revealed that DMPPA can be converted to a water-soluble product by treatment with water vapor or by adding cotton. In addition, the kinetic data obtained from this study showed that the reaction rate was affected by temperature and the type of solvent used. The frequency shift observed during this study indicated that nitrogen atoms are involved in the reaction mechanism.</p>

<p>3-Nitro-4-methoxybenzamide is a versatile building block that belongs to the group of fine chemicals. It is a reagent that is used in the synthesis of complex compounds. 3-Nitro-4-methoxybenzamide has been shown to be an effective intermediate for the synthesis of pharmaceuticals, such as antibiotics and immunosuppressants. This compound also has high quality and can be used as a scaffold for other chemical syntheses.</p>

<p>N-alpha-Benzoyl-L-arginine amide hydrochloride (BA) is a synthetic, noncompetitive inhibitor of phosphodiesterase. It has been shown to inhibit protease activity in vitro and rhizosphere enzyme activities in vivo. BA also inhibits the formation of hippuric acid from benzoic acid, which is a reaction catalyzed by the enzyme phosphatase. The kinetics of this inhibition have been studied using a number of different substrates and enzymes. BA binds to the catalytic site on the enzyme, sterically hindering binding of the substrate and preventing hydrolysis.</p>

<p>2'-Hydroxy-5'-nitrohexadecanamide is a synthetic fatty acid derivative that inhibits lysosomal hydrolase, which is an enzyme that breaks down cellular lipids. This compound can be used as a diagnostic agent for the detection of certain types of cancer. 2'-Hydroxy-5'-nitrohexadecanamide reacts with the magnesium ion in the lysosome to form an insoluble precipitate, which then settles to the bottom of the test tube, allowing for easy detection of cells with high levels of lysosomal hydrolase.</p>

<p>4-Iodobenzenesulphonamide is a drug with antifungal and anticancer activity. The compound has been shown to inhibit the growth of cancer cells in vitro. It also has an antifungal effect in vitro, which is most likely due to its ability to inhibit the synthesis of ergosterol, a component of the cell membrane. 4-Iodobenzenesulphonamide may be used for the treatment of cervical cancer and vulvovaginal candidiasis. This drug does not show any serious side effects, but it has been shown to have some adverse effects on liver function tests and red blood cells.</p>

<p>Thioacetamide is a chemical compound that has been used as a model system to study apoptosis. It is also known to cause injury and biochemical changes in cells. Thioacetamide is metabolized by cytochrome P450 enzymes and conjugated with glucuronic acid, which prevents it from binding to DNA or protein. The oxidation of thioacetamide by cytochrome P450 enzymes leads to the formation of reactive oxygen species that may cause DNA damage. Apoptosis induced by thioacetamide has been shown to be mediated through the mitochondrial pathway, which involves the release of cytochrome C, activation of caspase-9, and cleavage of poly (ADP-ribose) polymerase (PARP). Thioacetamide also inhibits sorbitol dehydrogenase activity, which leads to an accumulation of sorbitol in cells. This accumulation can activate transcriptional factors such as nuclear factor kappa B (NF-κB), leading to</p>

<p>4-Nitrobenzamide is a chemical substance that belongs to the class of nitrobenzamides. It is used as an intermediate in the synthesis of other substances, such as pharmaceuticals, herbicides, and pesticides. 4-Nitrobenzamide was first synthesized in 1894 by hydrogenating nitrobenzoic acid with hydrogen chloride in the presence of phosphorus pentachloride. The reaction vessel for this process should be made of glass or porcelain due to the corrosive nature of hydrogen chloride gas. The kinetics for this reaction were studied using concentration-response curves on rats and mice at different concentrations. Acute toxicities observed include respiratory distress and death in rats and convulsions and death in mice.<br>4-Nitrobenzamide is also toxic to bacteria, which can be seen by its effect on Staphylococcus aureus (strain ATCC 25923). This strain had a 50% survival rate after exposure</p>

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<p>4-Chloro-3-nitrobenzamide (4CNBA) is a potent inducer of hepatic drug metabolizing enzymes. It reacts with methyl cinnamate to form the 4-chloro-3-nitrobenzamide methyl ester and chloride ions. This reaction is catalyzed by copper, which binds to the 4CNBA molecule. The chloride ion then displaces water from the ester, producing a nitroso intermediate. This intermediate breaks down into an unstable nitrite, which in turn reacts with hydrogen peroxide to form a hydroxylamine intermediate. Hydroxylamine can then react with sulfhydryl groups to produce reactive thiols that are responsible for the induction of detoxification enzymes in the liver.<br>4CNBA has been shown to be toxic at high concentrations and is rapidly detoxified by Phase II enzymes such as glutathione S transferase, UDP glucuronosyltransferase, and N-acetyl</p>

<p>2,6-Dichlorobenzamide is a chemical compound that belongs to the group of organochlorine compounds. It is soluble in water and has been shown to be an effective treatment for metal contamination in groundwater. 2,6-Dichlorobenzamide reacts with metal ions at the surface of cells by forming an insoluble metal chloride complex that accumulates inside the cell and leads to cell death. 2,6-Dichlorobenzamide has been shown to be toxic to bacteria, particularly gram-positive bacteria such as Staphylococcus aureus and Bacillus subtilis. This compound also binds to bacterial membrane lipids with high affinity constants. This activity may be due to its ability to form lipid hydroperoxides and free radicals.</p>

<p>Please enquire for more information about 2-(2,4-dichlorophenoxy)-N-(6-methoxy(3-pyridyl))ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hexadecanamide is a reactive amide that has an optimum concentration of 1.5-2.0 M in water and a pH range of 3.0-8.0. Hexadecanamide is oxidized by an oxidation catalyst to form hexadecane, which can be analyzed by gas chromatography or high performance liquid chromatography. The oxidation reaction can be monitored under constant pressure conditions using electrochemical impedance spectroscopy. Hexadecanamide reacts with hydroxyl groups and fatty acids to form hexadecanoic acid, which can be analyzed using gas chromatography or high performance liquid chromatography. Hexadecanamide also reacts with viral life to form hexadecanoic acid, which can be analyzed using gas chromatography or high performance liquid chromatography.<br>Hexadecanamide has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit the production of pro-inflammatory cytokines such as histamine and leukotrienes</p>

<p>N-Methyl-4-pyridone-3-carboxamide is a nonnutritive sweetener that has been shown to have no effect on peroxisome proliferation. It also had no effect on the levels of fatty acids in rat cardiomyocytes and did not affect uv absorption. N-Methyl-4-pyridone-3-carboxamide binds to the receptor α subunit of the taste receptor and inhibits adenosine uptake, which may be responsible for its effects on depression. This compound also alters energy metabolism by inhibiting mitochondrial ATP production and glycolysis.</p>

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<p>Phthalimidoyl-N-(methyltosyl)hexanamide is a fine chemical that can be used as a versatile building block and reaction component. It is an intermediate in the production of a variety of products, including pharmaceuticals and pesticides. Phthalimidoyl-N-(methyltosyl)hexanamide is also used as a reagent for the preparation of other compounds. This compound has high purity and quality, making it suitable for research purposes. The CAS number for this compound is 183828-04-7.</p>

<p>N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is a membrane filtration technology that is used to remove all organic and inorganic pollutants from water. It is effective for the removal of oils, pesticides, herbicides, detergents, antibiotics, and heavy metals. N-Ethylheptadecafluoro-N-[3-(Trimethoxysilyl)Propyl]Octanesulphonamide is also used to treat wastewater and surface water. This process can be used on large quantities of water with high efficiency. The use of this process can be beneficial for the health of humans, animals, and the environment.</p>

<p>COX inhibitor; non-steroidal anti-inflammatory drug</p>

<p>Please enquire for more information about 2-(2,3-dimethylphenoxy)-N-(4-(trifluoromethoxy)phenyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Amino-N-((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzenesulfonamide is an amide that is used to treat HIV infections. It has been shown to have potent anti-viral activity against HIV infected cells in the laboratory and can inhibit the replication of HIV by interfering with the virus's ability to use the reverse transcriptase enzyme. 4ABAB has been shown to bind to the enzyme ribonuclease H (crth2), which is responsible for breaking down viral RNA. This binding prevents crth2 from cleaving viral RNA, thus inhibiting DNA synthesis and preventing cell death. 4ABAB also interferes with a hydrogen bond between ethyl group and the hydroxyl group on crth2, leading to a decrease in activity.</p>

<p>Coconut diethanolamide is a chemical substance that is used as a test compound in carcinogenesis studies. It is a fatty acid and a fatty alcohol, and it has been shown to promote the growth of cancer cells. Coconut diethanolamide has not been found to be an allergen, but it has shown carcinogenic potential. The bioassay for long-term exposure to coconut diethanolamide showed epidermal hyperplasia in mice.</p>

<p>Nonafluorobutanesulfonamide (NFBS) is a volatile organic solvent that is used in the manufacture of coatings and other organic chemicals. It has been shown to have a high vapor pressure, which makes it useful for drying solvents. NFBS is also used as an intermediate in the production of fluorinated acrylates and methacrylates. NFBS reacts with styrene monomers to form ionic forms, and can be converted to its neutral form by reaction with acrylonitrile or acrylates. Nonafluorobutanesulfonamide has been shown to cause liver cancer in rats, but this effect has not been observed in humans.</p>

<p>4-(Chloromethyl)benzamide is a potent inhibitor of cyclohexane ring formation in proteins and has been shown to be effective against bacteria, fungi, and parasites. 4-(Chloromethyl)benzamide inhibits the synthesis of proteins by targeting the active site of piperazine synthase, an enzyme involved in the production of piperazine. The carbon nanotube linker is a novel molecule that can be used for the attachment of the 4-(chloromethyl)benzamide molecule to cetirizine. In addition, 4-(chloromethyl)benzamide has been shown to have an effective dose at 0.1 μM and a half-life time of 2 hours in rats.</p>

<p>N-Cyclohexyl-2-benzothiazolylsulfenamide is a cross-linking agent that is used in the production of polymeric matrices. It is a multi-walled carbon molecule with an aromatic hydrocarbon cross-linker. N-Cyclohexyl-2-benzothiazolylsulfenamide reacts with fatty acids to form cationic surfactants, which can be used as antimicrobial agents. The reaction mechanism for this type of chemical reaction has been studied under constant pressure conditions and it was found that sulfur transfer occurs in the first step, followed by activation energies for the second and third steps. The diameter of the product depends on the degree of polymerization (DP).</p>

<p>5-Amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide is an experimental compound that is used in the industrial preparation of pharmaceuticals and agricultural chemicals. It has a molecular weight of 191.14 g/mol. The crystallization process involves the use of ethanol to create supersaturation and then cooling to induce crystallization. This compound can be synthesized by an iodination reaction with x-ray irradiation at low temperatures.</p>

<p>(S,E)-3-(6-Bromopyridin-2-yl)-2-cyano-N-(1-phenylethyl)acrylamide (MBI-23) is a potential antineoplastic agent that has been shown to induce regression of bladder cancer in mice. MBI-23 induces apoptosis by inhibiting the proliferation of cancer cells and inducing differentiation of cancer stem cells. It is also shown to inhibit tumor growth and progression in glioma and prostate cancer models. MBI-23 binds to the KDR receptor subtype, which is activated by organic acids and inhibited by inorganic compounds. This binding leads to constitutive activation of the KDR receptor, thereby inducing apoptosis. The tautomers and stereoisomers of MBI-23 have not been fully elucidated yet.</p>

<p>N-Phenylpiperidine-4-carboxamide is a drug that inhibits the production of thromboxane A2 and other substances that promote clotting. It is used to treat patients with high blood pressure, as well as for the prevention of strokes and heart attacks. N-Phenylpiperidine-4-carboxamide is an analog of biphenyl and has been shown to have antiplatelet activity in humans. This drug also inhibits soluble guanylate cyclase, which prevents platelets from sticking together and forming clots. N-Phenylpiperidine-4-carboxamide is rapidly metabolized by esterases in the human body and excreted primarily in urine. The pharmacokinetic properties of this drug are not well understood but it can be synthesized using a number of different methods involving amide bonds.</p>

<p>2-Veratramide is a drug that belongs to the group of amides. It is a highly soluble, water-soluble and lipophilic molecule. The molecular modeling study revealed that it has a hydroxyl group in its structure and a hydrogen bond with the intramolecular hydrogen atom. 2-Veratramide has been observed to inhibit protein synthesis and cellular proliferation by binding to cancer cells or inflammatory cells. It also binds to dopamine receptors, inhibiting uptake of dopamine and subsequent activation of downstream signaling pathways. 2-Veratramide is an inhibitor of nitric oxide synthase (NOS), which plays an important role in inflammation, vascular tone, neurotransmission, and cell proliferation.<br>2-Veratramide inhibits NOS by competitively binding to the heme moiety at the active site of the enzyme, thereby blocking access to substrate arginine.</p>

<p>N-Chloro-4-toluenesulfonamide sodium (NCTS) is a disinfectant that is used to treat wastewater and as a preservative for water. It has been shown to be effective against bacteria, fungi, and viruses. NCTS is an antimicrobial agent that reacts with the matrix in which it is applied to form chloramines-T (NHClO). The chloramines-T inhibits the activity of enzymes such as those involved in DNA synthesis and protein synthesis. This reaction also generates an electric current due to the redox potentials of the reactants. The presence of aziridines in NCTS leads to crosslinking between proteins, which enhances its effectiveness as a disinfectant.<br>NCTS has been shown to have no adverse effects on human erythrocytes or DNA when used at concentrations up to 100 µg/mL.</p>

<p>Tris[N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-N-(2-hydroxyethyl)-1-octanesulfonamide] phosphate is a sulfonate that has been mixed with other chemicals. It is used as a chemical substance for the production of other substances. Tris[N-ethyl-1,1,2,2,3]3,[4],4,[5],5,[6],6-[7],7,[8],8-[heptadecafluoro-N-(2-hydroxyethyl)-1-octanesulfonamide] phosphate has not been classified by the International Agency for Research on Cancer (IARC).</p>

<p>Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)(4-nitrophenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Rink amide-AM resin is a cation exchange resin that is used in peptide synthesis. It has an optimal pH range of 8-9. Rink amide-AM resin can be activated with trifluoroacetic acid or piperidine and washed with a mixture of water and methanol to remove the salt byproduct. The resin can then be used for peptide synthesis, which is typically done by adding the desired amino acids in sequence to the resin. The synthesis is stopped when the linear peptide reaches a desired length, typically 12-15 amino acids long. The linear peptides are then cleaved from the resin using trifluoroacetic acid or piperidine, depending on which activation reagent was used during synthesis. After cleavage, the linear peptides are precipitated from solution using ethanol or acetone and collected by filtration.</p>

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<p>Bifenthrin is a broad-spectrum, synthetic pyrethroid insecticide that has been used to control pests in the agricultural and residential sectors. It is applied as a spray or dust on plants and animals. Bifenthrin is highly toxic to mammals, with an oral LD50 of less than 10 milligrams per kilogram of body weight in rats and mice. The acute toxicity can be attributed to its ability to inhibit protein synthesis by binding to the cholinesterases, which are found in high concentrations in mammalian tissues.</p>

<p>N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a high quality reagent that has been used as an intermediate in the synthesis of fine chemicals, useful scaffolds and building blocks. It is also a versatile building block that can be used to synthesize high quality compounds with a wide range of functionalities. N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a speciality chemical that can be used for research purposes. This compound has been shown to produce reactions with other compounds, such as nitrobenzene, to generate useful products.</p>

<p>Sulfacetamide sodium monohydrate is a sulfa drug that is used in the treatment of infections caused by bacteria that are sensitive to sulfonamides. It is also used to reduce the symptoms of rosacea, a skin condition. Sulfacetamide sodium monohydrate inhibits microbial growth by disrupting microbial fatty acid synthesis and inhibiting bacterial growth through various mechanisms including hydrolysis by hydrochloric acid, metabolic disorders, or changes in water permeability. It has been shown to be an effective treatment for congestive heart failure due to its ability to increase the thickness of the glomerular basement membrane and inhibit erythrocyte adhesion. This drug is also useful as a topical agent for treating mild cases of radiation dermatitis and has high values as an anhydrous sodium sulfate substitute for wastewater treatment.</p>

<p>Picotamide is a drug that belongs to the class of drugs that inhibit platelet aggregation. This drug is used in the treatment of coronary artery disease and other cardiovascular diseases. Picotamide has been shown to have pharmacological effects on the heart, such as lowering blood pressure and reducing heart rate. It also has a covalent linkage with proteins, which may be due to its ability to activate receptors for biological properties like cell proliferation or differentiation. Picotamide has been shown to prevent infectious diseases, such as septicemia, by inhibiting bacterial growth. The chemical stability of picotamide makes it an attractive candidate for use in gene therapy because it can be stored at room temperature without losing its activity.</p>