Amides

<p>2-Chloro-N-(4-chlorophenyl)acetamide (2CPA) is an antimycobacterial agent that inhibits the growth of Mycobacterium tuberculosis. The antimycobacterial activity of 2CPA has been demonstrated in a dilution method, where it reduced the number of viable cells in cultures of M. tuberculosis and Mycobacterium smegmatis. The antimicrobial activity of 2CPA was confirmed using a fluorescence assay, which showed that this compound is active against M. tuberculosis H37Rv and M. smegmatis at concentrations above 0.1 mM. 2CPA also has a potent bactericidal effect on Staphylococcus aureus with an MIC value of 0.06 mg/mL at 30 minutes and is active against Enterococcus faecalis with an MIC value of 4 mg/mL at 30 minutes.</p>

<p>Please enquire for more information about N-amino-2-(4-bromo-3,5-dimethylphenoxy)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Piperazin-1-ylacetamide hydrochloride is a drug that binds to the protein PCSK9, which transports cholesterol into cells. It blocks the transport of cholesterol and therefore lowers the level of cholesterol in blood. 2-Piperazin-1-ylacetamide hydrochloride is used for the treatment of bowel disease, atrial fibrillation (a type of irregular heartbeat), congestive heart failure, and as an anti-viral agent. This drug has been shown to reduce levels of LDL cholesterol by up to 60%. 2-Piperazin-1-ylacetamide hydrochloride has also been shown to be effective against cancers such as prostate cancer and inflammatory bowel disease.</p>

<p>2-Hydroxysalicylamide is a low-energy, small molecule that has shown to be an effective inhibitor of serine proteases. It binds to the active site of the protease, blocking catalysis and inhibiting the growth of cancer cells. 2-Hydroxysalicylamide has been shown to inhibit the transcriptional regulation of pro-inflammatory genes in a patterning assay and it inhibits tumor growth in a pain model. This drug also suppresses the expression of suppressor genes and can be used as an analgesic without causing side effects.<br>2-Hydroxysalicylamide is also a polarizer for tissues, meaning that it preferentially accumulates in tissues with high water content such as breast tissue. This property has been shown to be useful for imaging cancerous tumors.</p>

<p>L-Histidine beta-naphthylamide is an allosteric activator of the imidazole group of histidine. It has been shown to regulate sequences and functional groups in subtilisin. L-Histidine beta-naphthylamide binds to the benzyl ester and regulatory allosteric site on the enzyme, which is located between the active site and the substrate binding site. The binding of this molecule stabilizes a transition state intermediate that would otherwise be too reactive to form products.</p>

<p>N-(2-Fluorophenyl)-N-[4-(4-methyl-1,3-thiazol-2-yl)-1-(2-thiophen-3-ylethyl)piperidin-4-yl]propanamide is a drug that is used for the treatment of cancer. This drug is hydrophobic and has a molecular weight of 455. It has been shown to be effective in treating cancer cells by binding to the cell membrane and inhibiting the proliferation of these cells. N-(2-Fluorophenyl)-N-[4-(4-methyl-1,3-thiazol-2-yl)-1-(2-thiophen-3-ylethyl)piperidin]-4-- yl]propanamide also inhibits tumor growth by reducing extracellular matrix production and inducing apoptosis in cancer cells. This drug has a fluorescent property and can be detected with an optical microscope at a</p>

<p>1H-Imidazole-2-carboxamide is a purine derivative that can inhibit the activity of certain molecules. It has been shown to have an inhibitory effect on the metabolism of fatty acids and metabolism disorders, as well as the physiological effects of insulin resistance. The molecule also inhibits uptake and cross-linking in cells, which may be useful in treating cancer or other metabolic disorders.</p>

<p>N-Methyl-N-trimethylsilylacetamide is a bifunctional amide that can react with an electrophile, such as hexane, to form an N-methylated product. The amide group of the molecule can also be deprotonated by a strong base to form an enolate, which can then react with a nucleophile. The NMR spectra of this compound show that it has a multinuclear structure and contains two tautomers. It is used in analytical chemistry for sample preparation, chromatographic science for reaction intermediates, and chemical study for its reactivity.</p>

<p>Please enquire for more information about (2,6-dioxo-4-phenylcyclohexyl)-N-(3-(trifluoromethyl)phenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3-Dichlorobenzamide is a herbicide with a stable structure. It has been shown to be effective against the weed species Agropyron repens and other grasses that grow in wetland conditions. 2,3-Dichlorobenzamide inhibits the growth of these plants by causing chlorosis, which is characterized by yellowing of leaves. 2,3-Dichlorobenzamide is toxic to aquatic organisms and can cause pollution in water systems. The molecular electrostatic potential of 2,3-Dichlorobenzamide has been studied using computer models and the parameters have been used to predict its toxicity to various tissues such as nerves or liver cells.</p>

<p>(+/-)-tert-Butylsulphonamide is a synthetic molecule that is a functional group with two aryl halides. It has been shown to inhibit the mitochondrial protein synthesis by preventing the nitrosylation of tyrosine residues in proteins. This inhibition prevents the production of growth factors and other bioactive molecules, leading to an increase in the cell's sensitivity to genotoxic agents. (+/-)-tert-Butylsulphonamide has also been shown to inhibit viral replication and infectivity by targeting viral RNA polymerase, which is responsible for viral transcription. The chloride anion present in (+/-)-tert-butylsulphonamide may have an inhibitory effect on viruses with a low pH environment, such as naphthalene or carbonic acid; however, it does not affect viruses with a neutral pH.END&gt;</p>

<p>L-Lysine amide dihydrochloride is a crystalline compound that is used for the treatment of tumours. It has been shown to bind to the enzyme iridoid synthase, which is involved in the formation of imines and aldehydes. L-Lysine amide dihydrochloride also inhibits the production of staining compounds, such as fluorine and heterocycles. The compound may also be used cosmetically as an anti-aging agent because it can inhibit the production of collagenase and elastase, which cause degradation of collagen.</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>This compound is a recyclable, multicomponent, element analysis, element, diversity and catalyzed reaction that yields high purity products with high yields. The catalyst is reusable and the NMR data are reproducible.</p>

<p>Chemically a chlorinated salicylanilide, niclosamide is clinically used as an anthelmintic agent. The action of niclosamide has been proven to proceed by inhibiting the STAT3 signaling pathway. Recently, niclosamide, has been considered as an antiproliferative agent in cancer treatment, e.g. melanoma and colorectal cancer. In 2021, niclosamide has been tested for the treatment of COVID-19 patients.</p>

<p>Piperazinophenylacetic acid benzylamide hydrochloride is a versatile building block that can be used in the synthesis of complex compounds for research and development. It is a reagent for the preparation of speciality chemicals and also a useful intermediate for the synthesis of reaction components. Piperazinophenylacetic acid benzylamide hydrochloride is a high quality, commercially available chemical that can be used as a scaffold for the preparation of new chemical compounds.</p>

<p>(E)-N-(3-Methylaminopropyl)-2-thiopheneacrylamide is a high quality chemical that can be used as an intermediate in the synthesis of complex compounds. It is also a useful scaffold and building block for the synthesis of speciality chemicals with versatile reactions.</p>

<p>2-Chloro-N-(3,5-dichlorophenyl)acetamide is a stabilized, crystalline compound. It has a planar structure with an amide bond and hydrogen bonds. The 2-chloro group is bonded to the nitrogen atom of the acetamide group. The 3,5-dichlorophenyl group is bonded to the carbon atom of the acetamide group. The chlorine atoms are in a planar configuration with adjacent chlorine atoms forming a skeletal arrangement. This chemical is used as an intermediate for other compounds.</p>

<p>Please enquire for more information about 2-Chloro-N-(2-chloro-5-nitrophenyl)propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Thioctamide is a drug that belongs to the class of drugs called sulfonylureas. It is an anti-diabetic drug that has been used for the treatment of insulin-resistant type II diabetes. Thioctamide binds to mitochondrial dehydrogenases and lipoamidases, inhibiting mitochondrial functions and energy metabolism. This leads to a decrease in cellular ATP levels, which can be measured by electrochemical impedance spectroscopy (EIS). The effects of thioctamide on cells can also be determined by examining the response of cells to different concentrations of thioctamide using a cell viability assay. This drug has been shown to inhibit the growth of HL60 cells, with IC50 values ranging from 2.6 µM to 6.4 µM depending on concentration. Thioctamide inhibits the expression of toll-like receptor 4 (TLR4) and integrin receptor β1 in HL60 cells, which may be due to its ability to act</p>

<p>Please enquire for more information about 2-((4-Methylphenyl)sulfonyl)-N-(((2-thienylcarbonylamino)thioxomethyl)amino)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Dechloroethyl cyclophosphamide is a metabolic inhibitor that is used in the treatment of cancer. It is classified as an alkylating agent and inhibits ribonucleotide reductase, which prevents the production of DNA, RNA, and protein. The chemical ionization technique has been used to measure the concentration of this compound in human liver and urine samples. N-Dechloroethyl cyclophosphamide can be analyzed using chromatography or mass spectrometry methods.</p>

<p>3,4-Dichlorobenzamide is a synthetic opioid analgesic that binds to the μ-opioid receptor. It has a side-effect profile that is similar to other opioids, with an addiction risk and potential for abuse. 3,4-Dichlorobenzamide has been used in the synthesis of new drugs, such as phenazepam (a benzodiazepine) and etizolam (a thienodiazepine). This drug is chiral and can be synthesized in two stereoisomeric forms: 3-(+)-chloro-N-(2-chlorophenyl)benzamide and 3-(−)-chloro-N-(2-chlorophenyl)benzamide. The former form is marketed under the trade name Analgin, while the latter form is marketed under the trade name Etilex. The (+) form of this drug has a higher affinity for μ receptors than the (−) form.</p>

<p>Tropicamide is a cholinergic agent that is used as a short-term mydriatic, or eye dilator, for diagnostic purposes. It belongs to the group of nonsteroidal anti-inflammatory drugs and has been shown to have a stable complex with benzalkonium chloride. Tropicamide has been shown to affect the signal pathways in cells, leading to an increase in IL-2 receptor expression. This drug also affects locomotor activity and has been studied as a potential treatment for murine sarcoma virus. Tropicamide is administered intravenously and can cause side effects such as blurred vision, nausea, vomiting and convulsions. Tropicamide may be given together with phenylephrine in order to reduce these side effects.</p>

<p>2-Chloro-N-(4-chlorophenyl)propanamide is an acetanilide that is used as a research chemical in the preparation of other compounds. It also has been used to synthesize chloroacetanilides and chloroanilides. 2-Chloro-N-(4-chlorophenyl)propanamide can be prepared by reacting 4-chloroaniline with acetic anhydride and potassium chloride in a basic solution. The reaction will take place at room temperature, but will produce a greater yield when heated to 40°C for 1 hour. This compound can be used as a starting material for the synthesis of other compounds, such as chlorinated analogues of acetaminophen (paracetamol).</p>

<p>Please enquire for more information about Furan-2-carboximidamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>2-Chloro-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)acetamide (CPA) is a chemical compound that belongs to the class of phenyl pyrazoles. It has a thermal stability and is soluble in organic solvents. CPA crystallizes in the monoclinic system with the space group P21/c, with the following unit cell parameters: a = 8.943(4) Å, b = 7.878(3) Å, c = 17.834(6) Å, α = 90°, β = 112° and γ = 90°. In this crystal structure, there are two molecules of chloride per molecule of CPA. The crystal x ray diffraction pattern showed that this compound forms dimers in solution at room temperature and can be dissolved</p>

<p>N-[6-Chloro-5-(2-methoxyphenoxy)-(2,2-bipyrimidine)4-4-yl]-(1,1-dimethylethyl)-benzenesulfonamide is a reagent that can be used as a reaction component in the synthesis of complex compounds. It has high quality and is a versatile building block for the synthesis of speciality chemicals. N-[6-Chloro-5-(2-methoxyphenoxy)-(2,2-bipyrimidine)4-4-yl]-(1,1-dimethylethyl)-benzenesulfonamide is also a useful intermediate in the synthesis of fine chemicals.</p>

<p>N-(3,5-Dichloro-4-Pyridinyl)-2-[1-(4-Fluorobenzyl)-5-Hydroxy-1H-Indol-3-Yl]-2-Oxoacetamide is a prodrug that is metabolized to the active form in vivo. It inhibits the activity of cyclic nucleotide phosphodiesterase (PDE), an enzyme that catalyzes the conversion of cAMP to AMP and PDE, which catalyzes the conversion of cGMP to GMP. This drug has been shown to have a potent inhibitory effect on inflammatory cytokines such as IL-6 and TNFα. N-(3,5-Dichloro-4-pyridinyl)-2-[1-(4 fluorobenzyl)-5 hydroxy 1H indol 3 yl]-2 oxoacetamide has been shown to be effective for treatment of inflammatory diseases such as bronch</p>

<p>Please enquire for more information about L-Histidine amide dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-Alaninamide is a protonated amino acid that reacts with the bacterial cell membrane and causes it to rupture. L-Alaninamide is synthesized by hydrolysis of the ester bond between butyric acid and serine protease in the presence of immobilized d-alanine. The reaction is carried out at a pH of 5.5, and the release of pressor is observed. This reaction takes place in an aqueous solution containing fatty acids as solvents. The type strain of this amino acid is E. coli.</p>

<p>Tolbutamide is a drug that is used to treat diabetes mellitus type 2. It is an inhibitor of the enzyme glucokinase and thus blocks the phosphorylation of glucose, which prevents its utilization by cells. This results in a decrease of blood glucose levels, which can be useful in the treatment of diabetes mellitus type 2. Tolbutamide has shown potent apoptosis-inducing effects on human breast cancer cells and endothelial cells. These effects are thought to be due to inhibition of protein kinase C (PKC) activity by tolbutamide. Additionally, this drug inhibits insulin secretion from pancreatic beta cells and induces cytochrome P450 enzymes, which may lead to increased metabolism of other drugs.</p>

<p>Please enquire for more information about 13,4-diaza-5-(tert-butyl)-2-hydroxy-7-oxotricyclo[6.4.0.0&lt;2,6&gt;]dodeca-1(8),4,9,11-tetraene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about L-Leucine b-naphthylamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Amino-4-methylbenzamide is an interchemical that can be utilized to synthesize naphthol. 3-Amino-4-methylbenzamide is an amide that has been shown to have a molecular modeling structure of a conformation. The interaction of 3-amino-4-methylbenzamide with the P38 kinase enzyme has been shown to inhibit the activity of this enzyme, which may lead to its use as a drug for the treatment of inflammation.</p>

<p>2-Amino-5-chlorobenzenesulfonamide is a synthetic chemical that is used in the manufacture of amides and diazoxide. It is also found naturally in humans as a metabolite of the amino acid histidine. 2-Amino-5-chlorobenzenesulfonamide has been shown to be a potent receptor for the modulation of acetylcholine release by binding to muscarinic receptors, including M1 and M2 subtypes, and inhibiting the enzyme hydrolysis of acetylcholine. This chemical has been shown to be chemically stable at pH 5 or higher, and it has been found to be resistant to hydrolysis by enzymes such as esterases, glucuronidases, glutathione reductase, and cytochrome P450. 2-Amino-5-chlorobenzenesulfonamide is also an enantiomer that can bind to collagen in the human</p>

<p>2-Methoxy-5-(2-oxopropyl)benzenesulfonamide is a metal catalyst that can be used in the synthesis of tamsulosin hydrochloride, an alpha blocker that is used to treat benign prostatic hyperplasia. It catalyzes the reaction between 2-methoxybenzenesulfonyl chloride and 3-amino-1,2,4-triazole. The industrial importance of this compound is due to its ability to be used as a catalyst for various chemical reactions.</p>

<p>Please enquire for more information about 2-(4,5-dichloroimidazolyl)-N-(2-indol-3-ylethyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(4-Methoxyphenyl)propionamide is a compound that belongs to the group of benzene amides. It is synthesized by reacting an excess of 3-bromopropionaldehyde with an amine in the presence of sodium hydroxide. This reaction produces a mixture of products, which are separated by chromatography. The yields for this reaction are approximately 90%. 3-(4-Methoxyphenyl)propionamide has been used as a biomolecular building block, and its traceless nature makes it useful in organic synthesis.<br>3-(4-Methoxyphenyl)propionamide can be used to synthesize alkanesulfonamides and spirolactams, which are important intermediates in chemical synthesis. 3-(4-Methoxyphenyl)propionamide also reacts with phenanthridone to produce chloride derivatives and with arenes to produce linkers.</p>

<p>Glycine amide acetate is a product that contains an imine group. It has been shown to have staining properties when applied to human keratin and is used in the cosmetic industry as a depigmenting agent. Glycine amide acetate has been shown to be effective in the treatment of depression, although it is not yet approved for this use. The molecule also contains an iridoid compound, which may be responsible for its effects on mood.</p>

<p>Polyamide is a synthetic polymer that contains amide bonds. It is characterized by high water vapor permeability, low water solubility, and good chemical stability. Polyamide has been shown to have growth factor-β1 activity in vitro and in vivo for the treatment of tubulointerstitial injury. Polyamide is also used as a template for the synthesis of DNA. It has been shown to have antioxidant properties and inhibit prostate cancer cells. The polyamide chain can be analyzed using monoclonal antibodies and structural analysis methods such as nuclear magnetic resonance spectroscopy, infrared spectroscopy, x-ray diffraction, or electron microscopy.</p>

<p>N-[1-[2-(4-Ethyl-5-Oxotetrazol-1-Yl)Ethyl]-4-Phenylpiperidin-4-Yl]-N-(2-Fluorophenyl)Propanamide is a drug that is used clinically for the treatment of depression. It is an analog of amitriptyline, an antidepressant and a tricyclic compound. N-[1-[2-(4-Ethyl-5-Oxotetrazol-1-Yl)Ethyl]-4-Phenylpiperidin-4-Yl]-N-(2-Fluorophenyl)Propanamide has been shown to increase the concentration of plasma drug levels by increasing transporter gene expression in muscle tissue. This drug also has clinical pharmacology and thermal expansion properties.</p>

<p>1H-Imidazole-4,5-dicarboxamide is a detergent composition that contains antimicrobial agents. It has been shown to inhibit the growth of resistant mutants in vitro and is active against a broad spectrum of bacteria. Hydrogen bonding interactions between 1H-imidazole-4,5-dicarboxamide and the amide group on the cell membrane surface are thought to be responsible for its activity. This compound also inhibits nuclear DNA synthesis by binding to the enzyme topoisomerase II, which is necessary for DNA replication. The molecular weight of 1H-imidazole-4,5-dicarboxamide makes it useful as an analytical reagent in gas chromatography.</p>

<p>Please enquire for more information about (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)-N-(5-methylisoxazol-3-yl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Phenoxyacetamide is an acylating agent that reacts with a hydroxyl group by substitution to form an ester or amide. It is used in clinical studies to combat insulin resistance and metabolic disorders, such as cancer, inflammatory bowel disease, and diabetes. 2-Phenoxyacetamide has been shown to be effective against a number of bacterial species, including Pseudomonas aeruginosa and Cryptococcus neoformans. The drug also inhibits the production of monoamine neurotransmitters in the brain and has been shown to have anti-inflammatory properties.</p>

<p>Homoveratramide is a synthetic drug that is used as an antibacterial agent. It has a broad spectrum of activity against bacteria, fungi, and protozoa. Homoveratramide has been shown to be effective against both Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa, and Klebsiella pneumoniae. Homoveratramide inhibits the synthesis of DNA by binding to the enzyme ribonucleotide reductase. This produces a bacteriostatic effect on the cell by halting DNA replication and transcription.</p>

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

<p>Please enquire for more information about Pigment YellOw 5;2-[(2-NitrOphenyl)azO]-3-OxO-N-phenylbutanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-5-nitrobenzene sulfonamide (2CNS) is a glycol ether that has been shown to inhibit the activity of carbonic anhydrase. It has been shown to be a competitive inhibitor of the enzyme, and can be used as a lead compound for developing new drugs. 2CNS has been shown to inhibit an anhydrase that is found in bacteria, such as Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus aureus. This inhibition causes increased levels of hydrogen ions in the bacterial environment, which leads to the acidification of their surroundings. 2CNS also inhibits chloride ion uptake in these bacteria.<br>2CNS's pharmacophore includes two aromatic hydrocarbon rings with at least one hydrogen bond acceptor group on each ring. This pharmacophore is responsible for its inhibition of carbonic anhydrase and chloride ion binding site.</p>

<p>N-(5-Cyano-2-chlorophenyl)acetamide is a high quality, reagent, and versatile building block. It is a fine chemical that can be used as a building block for the synthesis of other compounds. N-(5-Cyano-2-chlorophenyl)acetamide is also a speciality chemical that can be used in research or as a reaction component. It has been found to be useful as an intermediate in the synthesis of complex compounds.<br>END&gt;</p>

<p>Cyanamide is a nitrogen-containing organic compound that is used as a plant nutrient. It has been shown to increase the activity of enzymes in methyl ethyl x-ray crystal structures and locomotor activity in mice. Cyanamide is also used as an herbicide and chemical pesticide, with calcium as its main target. The cyanamide molecule binds to the calcium ion and undergoes a reaction mechanism that results in the release of ammonia gas, which is toxic to plants. In addition, cyanamide can cause kidney damage in humans due to its ability to inhibit protein synthesis.</p>

<p>4-N-Octyloxybenzamide is a fine chemical that can be used as a building block in organic synthesis, or as a reagent in research. It is available at high quality and has been shown to be versatile. The compound can also be used as an intermediate in the synthesis of other compounds and is useful for the production of pharmaceuticals, pesticides, and herbicides. 4-N-Octyloxybenzamide has CAS number 203243-94-1.</p>

<p>3,5-Dihydroxybenzamide is an amide derivative that has anticancer activity. This compound inhibits the growth of C. glabrata by inhibiting protein synthesis in the mitochondria and DNA replication in the nucleus. 3,5-Dihydroxybenzamide also inhibits the growth of cancer cells by binding to a molecule that is involved in cancer cell proliferation. The inhibitor molecule binds to a specific site on the molecule, preventing it from forming new cancer cells. The mechanism of action for this compound is not known, but may be due to its ability to bind with chloride ions or its ability to form supramolecular chemistry with other molecules.</p>

<p>4-Chloro-3,5-dinitrobenzamide is a bifunctional molecule that contains a chlorine atom. It has been found to react with dipolar solutes as well as vicinal dioxan arylation. The nucleophilic amide group is also labile and can be hydrolyzed by strong acids or bases. The electron lone pair of the chlorine atom in 4-chloro-3,5-dinitrobenzamide can be used for electrophilic substitution reactions with aromatic rings or amines. This molecule has been found to undergo an arylation reaction with imidazole in the presence of dioxan solvent at room temperature.</p>

<p>Please enquire for more information about LY2112688 trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>1-Benzyl-1,4-dihydronicotinamide is a drug that has been shown to have potential in treating metabolic disorders by restoring the balance of nitrogen atoms. It has been shown to be effective in inhibiting the production of nitric oxide and other reactive oxygen species (ROS) which are involved in the pathogenesis of inflammation, septic shock and HIV infection. 1-Benzyl-1,4-dihydronicotinamide also inhibits light emission from cells. This effect is due to its ability to reduce the concentration of NADH and ATP, which are necessary for the light emitting reaction. The drug's mechanism of action is not well understood but it may be related to its ability to block dimethyl fumarate (DMF), an inhibitor of monoclonal antibody production. The physiological function of this drug is not yet well understood but it may be related to its ability to inhibit the proliferation of human immunodeficiency virus (HIV).</p>

<p>2-Amino-4-methylthiophene-3-carboxamide is a small molecule that is a potent inhibitor of the JAK2 kinase. This enzyme is associated with human fibrosis and has been shown to be involved in the development of liver fibrosis in rats. 2-Amino-4-methylthiophene-3-carboxamide inhibits the production of cytokines such as IL1α, IL6, and TNFα. It also blocks the activation of transcription factors such as NFκB, which are involved in inflammation. The compound has been shown to be orally active and has demonstrated efficacy in animal studies. Analogues have also been synthesized for this compound that show similar activity.</p>

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

<p>N-Isopropylacrylamide is a biocompatible polymer that is used in the preparation of polymers. It is a solid phase microextraction material that is used in sample preparation and purification. N-Isopropylacrylamide has a phase transition temperature of -5°C and can be polymerized to form a polymer. This polymerization process can be done with or without catalysts, which are required for the formation of many other types of polymers. N-Isopropylacrylamide has been shown to have good affinity for human serum and wastewater treatment effluent samples, as well as for chitosan polymer surfaces. The kinetic data show that this polymer possesses high capacity for trifluoroacetic acid (TFA) reactivity, which makes it suitable for use in reaction solutions.</p>

<p>3-(Bromomethyl)benzamide is a versatile building block that can be used in the synthesis of a variety of complex compounds. It is also useful as a research chemical and as a reagent. 3-(Bromomethyl)benzamide can be used to produce useful intermediates and reaction components. This compound has been shown to be useful as scaffolds for synthetic organic chemistry.</p>

<p>5-Amino-1,3,4-thiadiazole-2-sulfonamide is a chemical compound that inhibits the growth of skin cancer cells. It has inhibitory properties against choroidal neovascularization induced by dorzolamide hydrochloride and other pharmacological agents. 5-Amino-1,3,4-thiadiazole-2-sulfonamide has also been shown to have antiangiogenic activity in vitro and in vivo assays. 5ATTS inhibits the growth of bacteria and fungi by inhibiting fatty acid synthesis. The drug also has been shown to be effective in treating diabetic neuropathy and fluorescein angiography associated with itchy eyes.</p>

<p>2-(3,4-Dimethoxyphenyl)-N-hydroxyacetamide is a versatile building block that can be used in the production of a wide range of research chemicals. It is also useful as a reagent or speciality chemical for the preparation of pharmaceuticals, agrochemicals and other industrial chemicals. 2-(3,4-Dimethoxyphenyl)-N-hydroxyacetamide is an intermediate that can be used to synthesize complex compounds such as benzodiazepines. This compound has been shown to have high quality and can be used as a reaction component in organic synthesis.<br>2-(3,4-Dimethoxyphenyl)-N-hydroxyacetamide has CAS number 33793-80-5 and its molecular weight is 237.27 g/mol.</p>

<p>Please enquire for more information about 2-indol-3-yl-2-oxo-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>6-Hydroxy-N,2-dimethylbenzofuran-3-carboxamide is a fine chemical which is used as a building block in the synthesis of complex compounds. It can be used as a reactant in various reactions, such as Friedel-Crafts reactions and cycloadditions. This compound has been shown to be a useful intermediate for the synthesis of various heterocyclic compounds and scaffolds for drug development. 6-Hydroxy-N,2-dimethylbenzofuran-3-carboxamide has CAS number 638217-08-0 and is readily available in high quality.</p>

<p>Alkylating agent; anti-cancer agent</p>

<p>N-Methylbis(trifluoroacetamide) is a molecule that is used in the preparation of an analytical method. This molecule reacts with human serum and urine to produce a reaction solution. The matrix effect can be seen in metabolic disorders, such as the case of creatine kinase which is not affected by the derivatization. N-Methylbis(trifluoroacetamide) is also used to prepare samples for solid phase microextraction with basic structures that are amines.</p>

<p>1-Methyl-1,4-dihydronicotinamide (1MDNA) is a flavine adenine dinucleotide analog that has been shown to be a potent inhibitor of the enzyme catalase. 1MDNA binds to the active site of the enzyme and prevents hydrogen peroxide from being converted into water and oxygen. This inhibition slows down or stops the reaction, which leads to reduced production of reactive oxygen species. 1MDNA inhibits other enzymes in a similar manner, including transferases and kinases. The kinetic properties of 1MDNA have been studied by performing kinetic studies on model systems at different temperatures. X-ray crystal structures have also been obtained for 1MDNA bound to catalase and ferredoxin.</p>

<p>4-Amino-2,5-diethoxyphenyl)benzamide is a small molecule that inhibits the enzyme activity of polymerase chain reaction (PCR), DNA topoisomerase I, and DNA gyrase. It has been shown to inhibit the growth of human leukemia cells in culture. 4-Amino-2,5-diethoxyphenyl)benzamide also inhibits rat liver microsomes and can be used for the treatment of neurodegenerative diseases.</p>

<p>N-[4-[1-(2-Fluorobenzyl)-3-butyl-2,6-dixo-2,3,6,7-tetrahydro-1H-purin-8-ylmethyl]phenyl]acetamide is a fine chemical with a diverse range of potential applications. It can be used as a versatile building block in the synthesis of complex compounds and is useful as a reaction component or reagent. Its CAS number is 628279-07-2.</p>

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

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

<p>Quinfamide is a polyunsaturated compound that contains a cevimeline hydrochloride molecule. It is used to treat bowel disease, usually in combination with other drugs. Quinfamide has been shown to have specific treatment effects on the symptoms of inflammatory bowel disease (IBD) when given at doses of 400-800 mg per day for up to 12 weeks. This drug can also be used as an analog for 5-membered heteroaryl compounds, such as benzalkonium chloride, which are also used to treat bowel disease. Quinfamide has been shown to have anti-inflammatory properties and may work by inhibiting fatty acid synthesis or by reducing the number of neutrophils in the gut.</p>

<p>5-Iodosalicylamide is a chemical building block. 5-Iodosalicylamide can be reacted with appropriately functionalised aromatic compounds to afford the corresponding anilides, which have been shown to exhibit anti-fungal and bactericidal properties.</p>

<p>2-Amino-4-chlorobenzamide is a chemical compound that has been shown to be an effective oxidant in biological systems. It is an oxidative condensation product of 4-chloro-2-nitrobenzoic acid and ammonium chloride, which is formed by the reaction of these two compounds at room temperature. The nature of the functional group on 2-amino-4-chlorobenzamide allows it to be used as a transition state analogue for the study of reactions involving amines and nitrates. This compound can also be used in experiments with isatins, due to its ability to react with ammonia hydroxide to form 2-amino-4,6 dichlorobenzamide.</p>

<p>Sulphanilamide is an antimicrobial agent that inhibits the growth of bacteria by binding to their enzymes and blocking protein synthesis. In addition, sulphanilamide has been shown to inhibit the production of sulfanilamide, a potent inhibitor of tetracycline. Sulphanilamide is soluble in water and alcohol but not in organic solvents. The solubility of sulphanilamide can be increased by adding sodium salts or pH adjustment. Sulphanilamide is also used for wastewater treatment as it has inhibitory properties against sulfate-reducing bacteria. X-ray crystal structures have revealed that sulphanilamide binds to the active site of bacterial beta-lactamases through hydrogen bonds with both the NH group and the COOH group on its sulfur atom, resulting in inhibition of these enzymes. Sulphanilamide also interferes with bacterial DNA replication by inhibiting dna gyrase and topoisomerase IV. Sulphanilamide also</p>

<p>N-(Phenylsulfonyl)palmitamide is a versatile building block that can be used to create complex compounds for research. CAS No. is 527-87-2 and it is a reagent and speciality chemical with high quality. It is also useful as a reaction component in the synthesis of other compounds, or as a scaffold for the synthesis of new derivatives.</p>

<p>N-Propyl-N-(2,3-dihydroxypropyl)perfluoro-n-octylsulfonamide is a fine chemical that can be used as a reagent and speciality chemical. It is a versatile building block that can react with other compounds to produce new products. The compound is a complex compound that has been shown to have high quality in the laboratory.</p>

<p>Please enquire for more information about LL-37 amide trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-methylbenzamide (2AMB) is a potent inhibitor of the enzyme dihydropyrimidine dehydrogenase and is used in cancer research for its ability to inhibit tumor cell line growth. 2AMB has been shown to inhibit the synthesis of DNA, RNA, and protein in various human cell lines. The mechanism of this inhibition is not well understood, but it may be due to its ability to inhibit the activity of synthetases involved in nucleotide biosynthesis or by inhibiting the reaction system that converts hydration into ATP.</p>

<p>This compound is a benzamide derivative that is oxidized by nature. It has been shown to undergo ring-opening in the presence of reducing agents, such as sodium borohydride, and yields 2-amino-4-chlorobenzaldehyde. This reaction system uses an efficient catalyst such as manganese dioxide to help speed up the rate of this reaction. The product of this reaction is then converted into a variety of isatins depending on the conditions used.</p>

<p>3-Cyanobenzamide is an organic compound with the formula CHC(N)NH. It is a white crystalline solid that can be obtained by reacting benzamide with cyanoacetylene. There are three possible isomers of 3-cyanobenzamide: 3-cyano-1-(substituted phenyl)benzamide, 3-cyano-2-(substituted phenyl)benzamide, and 3-cyano-3-(substituted phenyl)benzamide. The optimal reaction conditions for the synthesis of 3-cyanobenzamide are in the presence of hydrogen bonding, such as n-hexane, amide, and phase equilibrium. Studies have determined that 3-cyanobenzamide has the potential to cause cancer or liver toxicity in humans. In addition, this chemical has been shown to be an effective inhibitor of alpha glucosidase enzymes in vitro and in vivo.</p>

<p>4-Methyl-3-nitrobenzamide is a nitrile that can be synthesized by the reaction of potassium hydroxide and 3-nitrobenzamide. It has been shown to react with dichloroethane to form 4-methyl-3-nitrobenzoic acid. The optimum temperature for this reaction is 120°C, which leads to a high yield of 4-methyl-3-nitrobenzamide. This product is also available in an isotopic form at high purity.</p>

<p>The drug 4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (BZP) is a histamine H2 receptor antagonist. It binds to the histamine H2 receptor in the stomach and duodenum, thereby blocking stomach acid production. BZP has been shown to be effective for treating symptoms of constipation or diarrhoea caused by inflammatory bowel disease or abdominal surgery. BZP also reduces the risk of relapse after surgery but does not affect long term efficacy. This drug is not available in the United States and has significant interactions with other drugs and symptoms including constipation, bowel disease, long term efficacy, and analytical method.</p>