Amidas

Beta-naphthamide is an inhibitor binding to the dinucleotide phosphate (DNP) in bacterial cells. This binding prevents the enzyme from carrying out its normal function, which is the production of ATP, and it also inhibits various other enzymes. Beta-naphthamide inhibits the growth of Gram-positive bacteria by inhibiting their cell wall assembly and also has a bactericidal effect on Gram-negative bacteria. Beta-naphthamide has been shown to be active against multidrug efflux pump proteins that are present in Gram-negative bacteria, such as Escherichia coli. DNP is a receptor for dopamine and beta-naphthamide inhibits dopamine receptors in mammalian cells, which may lead to Parkinson's disease. Beta-naphthamide has been shown to inhibit the polymerase chain reaction (PCR) mechanism by binding to DNA polymerase. Beta-naphthamide binds to receptors on trigeminal nerve endings, which leads to paralysis of

4-Iodo-N-(4-methoxyphenyl)-N-methylbenzamide is a useful scaffold that can be used in the synthesis of complex compounds. It is also a versatile building block and has been found to be useful as an intermediate and building block. 4-Iodo-N-(4-methoxyphenyl)-N-methylbenzamide is a fine chemical with CAS No. 320734-40-5. This reagent is high quality, research chemicals, and can be used in the synthesis of speciality chemicals.

<p>2-Chloro-N-(hydroxymethyl)acetamide (2CHAA) is an inhibitor that has been shown to be effective against a number of infectious diseases. 2CHAA inhibits the growth of bacteria by inhibiting the synthesis of proteins from RNA. This drug is also active against viruses, including herpes simplex virus and human immunodeficiency virus type 1, as well as fungi, such as Aspergillus niger. 2CHAA has no genotoxic effects in humans, but it does have carcinogenic potential and can cause allergic reactions. It also reacts with strong acids to form toxic compounds.</p>

<p>N-(2-Chlorophenyl)benzamide is a phenanthridone that reacts with chlorides in the presence of anilines to form singlet carbonyls. The photocyclization of these carbonyls yields an electron-deficient product that can be converted to a reactive electrophile by the addition of chlorine. This electrophilic species reacts with electron-rich aromatic compounds, such as phenols and benzene, to produce substitution products. The reaction rate for this process is dependent on the isotope effect, which is the change in reactivity due to changes in the mass number of atoms. The use of deuterium chloride instead of hydrogen chloride provides a kinetic isotope effect, which enhances the reaction rate.</p>

2-Iodo-N-phenylbenzamide is a palladium compound that inhibits bacterial growth by binding to DNA and preventing transcription. The drug binds to the DNA as a monomer, but also forms polymeric matrixes with other drugs. 2-Iodo-N-phenylbenzamide has been shown to have genotoxic effects on subtilis and methicillin resistant Staphylococcus aureus (MRSA) in vitro, which may be due to its ability to form crosslinks between adjacent strands of DNA. 2-Iodo-N-phenylbenzamide has been shown to be an effective anti-bacterial agent against MRSA, methicillin resistant coagulase negative staphylococci and erythromycin resistant strains of Streptococcus pyogenes.

Gly-pro-4-methoxy-beta-naphthylamide is a synthetic substrate that is used to measure the activity of human plasma phosphatases. Gly-pro-4-methoxy-beta-naphthylamide is synthesized in an organic solvent and then reacted with diazonium salt to form a glycosylated aminophosphonic acid. The product is purified by chromatography and identified by mass spectrometry. Gly-pro-4-methoxy beta naphthylamide has been shown to inhibit the growth of cancer cells in vitro, as well as having antiinflammatory properties. This drug also has been shown to be effective in treating patients with severe hyperbilirubinemia who are undergoing hematopoietic stem cell transplantation.

<p>N-[3-(Diethylaminomethyl)-4-hydroxyphenyl]acetamide is a molecule that has been shown to have acetylcholine esterase (AChE) inhibitory activity. It binds to the active site of AChE, preventing it from breaking down acetylcholine, leading to the accumulation of this neurotransmitter. The inhibition of AChE by N-[3-(Diethylaminomethyl)-4-hydroxyphenyl]acetamide prevents muscle contraction and leads to paralysis and death by asphyxiation. This drug has been used in the treatment of sarin gas poisoning. The molecular structure of N-[3-(Diethylaminomethyl)-4-hydroxyphenyl]acetamide is similar to that of pyridinium chlorides, which are used for synthesizing nerve agents such as sarin and soman. This drug also has a proton</p>

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

5-Amino-N-(3-amino-2,2-dimethyl-3-oxopropyl)-4-hydroxy-2-isopropyl-7-[4-methoxy-3-(3-methoxypropoxy)benzyl]-8-methylnonanamide fumar ate is a drug that inhibits the activity of angiotensin II, which is a hormone produced by the body. It is used as monotherapy for treatment of hypertension. 5AMINO has been shown to be effective in lowering blood pressure when administered alone and has been shown to be well tolerated. For this drug, the most frequently reported adverse reactions are nausea and dizziness. This drug should not be taken with other antihypertensive drugs or nonsteroidal antiinflammatory drugs such as ibuprofen (Motrin®). In addition, patients with diabetes should monitor their blood sugar levels carefully while taking this medication.

<p>4-Chloro-3-pyridinesulfonamide is an antibacterial sulfonamide that inhibits the enzyme carbonic anhydrase. It has been shown to inhibit the growth of cancer cells in vitro and in vivo. The anticancer effect may be due to its ability to block the growth of cancer cells by interfering with DNA synthesis and inducing apoptosis, which causes cell death. 4-Chloro-3-pyridinesulfonamide also inhibits tuberculosis and tuberculostatic activity may be due to its inhibition of mycobacterium tuberculosis ribosomes. 4-Chloro-3-pyridinesulfonamide binds to the active site of bacterial anhydrase as well as human carbonic anhydrase II, blocking the conversion of CO2 into bicarbonate ions, which leads to a decrease in pH. This drug also binds to DNA and RNA, inhibiting DNA synthesis and RNA synthesis respectively, leading to cell</p>

N-Methyl-N-(1-naphthyl)-1-chlorobenzamide is a versatile and useful chemical that can be used in the preparation of many different compounds. It is a reaction component and reagent, as well as a useful scaffold for the synthesis of many different compounds. It has high quality and is used in research chemicals. N-Methyl-N-(1-naphthyl)-1-chlorobenzamide has CAS No. 74881-60-0 and is a speciality chemical. It can also be used as a versatile building block or intermediates for the synthesis of more complex compounds.

N-(4-Cyano-2-chlorophenyl)acetamide is a versatile building block that is used in the synthesis of complex compounds. N-(4-Cyano-2-chlorophenyl)acetamide has been shown to be a useful intermediate in the synthesis of important compounds such as 4-aminoantipyrine, 4,5-dichloroanthranilic acid and 2,6-dichloropurine. This chemical has also been found to be an effective reagent for the preparation of other chemicals.

<p>Alpha-naphthamide is a high-resistance antimicrobial agent that belongs to the group of benzalkonium chloride. It is used in disinfectant products and has been shown to be effective against invertebrates such as mosquitoes and leeches. Alpha-naphthamide binds to the dinucleotide phosphate and inhibits enzyme activities by acting as an alkylsulfonyl and cytosolic Ca2+ inhibitor, leading to cell death. Alpha-naphthamide has also been shown to inhibit multidrug efflux pump activity in bacterial cells, which may be due to its structural similarity with c1-c6.</p>

2-Iodo-N-methyl-N-phenylbenzamide is a cyclised molecule that has been synthesized by intramolecular arylation and reductive cyclisation. 2-Iodo-N-methyl-N-phenylbenzamide can be used as an industrial catalyst for the production of phenols, benzaldehydes, and indoles. The catalytic activity of 2-Iodo-N-methyl-N-phenylbenzamide is high, with yields of up to 99%. This molecule is recyclable because it can be easily regenerated from the crude product. It also has high catalytic activity due to its cyclic structure.

<p>Sulfamide is a pharmacological agent that inhibits the growth of bacteria. Sulfamide has been shown to be reactive with hydrogen fluoride, which may result in the formation of sulfamoyl chloride. This reactive form of sulfamide may react with other compounds and cause unwanted side-effects. <br>Sulfamides are used for the treatment of infectious diseases such as pneumonia and urinary tract infections, as well as for the treatment of other conditions like congestive heart failure and rheumatoid arthritis. They work by inhibiting enzymes necessary for bacterial growth, including target enzymes such as dihydropteroate synthase, which is involved in folate synthesis. Sulfamides also have inhibitory properties on human osteosarcoma cell proliferation.</p>

2-Amino-2-cyanoacetamide is a chemical compound that has been shown to be reactive in the human liver and animal models. It is a purine derivative with a diatomic molecule, which has been shown to inhibit cancer cells in animals. 2-Amino-2-cyanoacetamide has been shown to inhibit the replication of pestivirus, an RNA virus that causes encephalitis and other diseases in humans. The nitrogen atoms on this molecule are responsible for its transport properties, including uptake by the gut and its ability to cross the blood brain barrier. 2-Amino-2-cyanoacetamide also inhibits the activity of amide hydrolase, which is an enzyme responsible for hydrolyzing peptides into amino acids. This process leads to a decrease in protein synthesis, which can lead to cell death.

N-alpha-[2,4-Dinitro-5-fluorophenyl]-D-alanine amide is a potential drug for the treatment of cancer. It has been shown to be effective in inhibiting the proliferation of human prostate carcinoma cells in culture. This compound is a potential anticancer drug that binds to DNA and inhibits topoisomerase II, which is an enzyme involved in DNA replication. The mechanism of action of this drug was studied using methods such as optimization, isomers, plates, trifluoroacetic acid, tautomers, amino acid analysis and nanomolar concentrations. N-alpha-[2,4-Dinitro-5-fluorophenyl]-D-alanine amide has also been shown to inhibit cyanobacteria growth.

N-Methyl-N-(1-naphthyl)-2-bromobenzamide is a high quality reagent that is used as a complex compound. It has CAS No. 74881-58-6 and it can be used as a useful intermediate, fine chemical or speciality chemical. N-Methyl-N-(1-naphthyl)-2-bromobenzamide is also a versatile building block that is used in reactions to synthesize other compounds.

Methyl 2-naphthylbenzoate is a high quality reagent that is used as a complex compound, useful intermediate and speciality chemical. It is also a useful building block for the synthesis of other compounds. The CAS number 74881-61-1 identifies Methyl 2-naphthylbenzoate as a fine chemical with an interesting scaffold. This chemical is suitable for research purposes and versatile in its use as a reaction component.

3,5-Diacetoxybenzamide technical is a solvent that can be used in organic synthesis. It is soluble in hydrochloric acid and has a boiling point of 210 degrees Celsius. 3,5-Diacetoxybenzamide technical is soluble in water and has an LD50 (lethal dose) of over 5 g/kg when administered orally to pigs. 3,5-Diacetoxybenzamide technical is also used as a reagent for the preparation of peracetates and esters of aromatic ketones. This product can be used as a reaction medium for lipase or porcine pancreatic lipase. It is also used in the manufacture of pharmaceuticals, fragrances, dyes, herbicides and pesticides.

<p>1-Z-N'-Hydroxypropanimidamide is a novel anion that has been shown to inhibit the proliferation of human cancer cells. It binds to the cholinergic receptor subtype and inhibits the uptake of acetylcholine, which leads to a reduction in the production of nitric oxide. 1-Z-N'-Hydoxypropanimidamide also inhibits the growth of Mycobacterium tuberculosis and possesses antimycobacterial activity. This compound is a ligand that binds bidentate to both DNA and RNA molecules and inhibits chemokine signaling.</p>

2-Iodo-N-(4-methoxyphenyl)-N-methylbenzamide is a versatile building block that can be used in research and as a reagent. It is a high quality chemical and useful as a building block or intermediate for the synthesis of more complex compounds. This chemical is also a useful scaffold for the synthesis of more complex molecules.

<p>3,5-Dimethoxycinnamide is a compound that has been shown to inhibit the C1-4 alkoxy and C1-4 alkyl esterase activity of the enzyme secretase. This enzyme is involved in the production of amyloid beta peptides and is thought to be an important contributor to Alzheimer's Disease. 3,5-Dimethoxycinnamide also inhibits the aspartyl protease activity of aspartyl proteases, which are enzymes that may play a role in Alzheimer's disease. 3,5-Dimethoxycinnamide binds to the hydrophobic region of these enzymes and prevents them from binding to their substrates. The affinity of this compound for these enzymes precludes its ability to bind with other proteins in the brain, thereby reducing its potential toxicity. 3,5-Dimethoxycinnamide can be labeled with halogeno groups or other chemical moieties for profiling purposes.</p>

<p>Diacetone acrylamide is a chemical compound that has the molecular formula C3H6O2N2. It is a colorless liquid with a low boiling point and an unpleasant odor. Diacetone acrylamide has been used as an intermediate in the production of polyvinyl acetate. It can also be used as an additive to rubber, plastics, and other materials. The thermal expansion coefficient of diacetone acrylamide is similar to that of polyvinyl chloride and polystyrene, making it a useful material for constructing models of those substances.</p>

Gamma-L-glutamyl-b-naphthylamide is a high quality, reagent, complex compound that is used as an intermediate in the production of fine chemicals such as speciality chemicals and research chemicals. Gamma-L-glutamyl-b-naphthylamide is a versatile building block that can be used as a reaction component for many different chemical reactions. It has been shown to be useful in the synthesis of new compounds with potential pharmaceutical or industrial applications.

<p>Erucamide is a fatty acid amide that is a natural compound and part of the biochemical composition of microbial organisms. Erucamide has been shown to have antimicrobial activity against Gram-positive bacteria but not against Gram-negative bacteria. The mechanism by which erucamide kills bacteria is unknown, but it may be due to its hemolytic activity or its ability to inhibit protein synthesis. Erucamide is resistant to hydrolysis by trifluoroacetic acid and glycol ester, which makes it difficult for microbes to metabolize it.</p>

Boc-L-leucine N,O-dimethylhydroxamide is a chemical compound with CAS number 87694-50-6. It is a white crystalline solid and has a molecular weight of 144.17 g. This product is soluble in water and ethanol, but insoluble in ether. Boc-L-leucine N,O-dimethylhydroxamide can be used as a reaction component or reagent for organic synthesis, including research chemicals and speciality chemicals. It can also be used as an intermediate for the production of complex compounds and fine chemicals.

Ropivacaine is a local anaesthetic of the amino ester group that is used to provide relief from pain caused by surgery or other medical procedures. It is a potent inhibitor of the enzyme activity of cholinesterases, which are enzymes responsible for the degradation of acetylcholine. Ropivacaine also inhibits the activity of cardiac Na+/K+ ATPase and Na+-Ca2+ exchanger, thereby reducing the excitability and contractility of heart muscle. This drug has shown pharmacokinetic properties in maternal blood that are similar to those observed in plasma, indicating that it can cross the placenta. Ropivacaine has been shown to have bactericidal effects against bacterial strains such as Escherichia coli and Staphylococcus aureus. In addition, ropivacaine has been shown to inhibit colorectal adenocarcinoma cells in vitro and in vivo. Levobupivacaine

L-Isoleucine amide hydrochloride is a high quality reagent that is useful as an intermediate, fine chemical or speciality chemical. It can be used to synthesize compounds with a wide range of properties and uses. L-Isoleucine amide hydrochloride can be used in research for the development of new drugs or other chemicals. The versatility of this reagent makes it a useful building block for reactions involving amino acids, peptides, nucleosides, and carbohydrates.

4-(tert-Butyl)benzenesulfonamide is a pyrimidine derivative that has an affinity for metal ions and can be used as a catalyst. It is insoluble in water but soluble in acetonitrile and other organic solvents. This compound is a strong oxidant when it reacts with ethylene, styrene, or propyl gallate. 4-(tert-Butyl)benzenesulfonamide has been shown to be highly reactive with the oxygen in air, leading to the formation of 4-dimethylaminobenzoic acid, formyl group, and phosphorus oxychloride.

<p>Adamantyl-2-chloroacetamide is an analog of adamantyl acetamide and has been shown to be a potent inhibitor of Mycobacterium tuberculosis. Adamantyl-2-chloroacetamide inhibits the growth of Mycobacterium tuberculosis by inhibiting the synthesis of DNA, RNA, and protein. This compound also shows selectivity for Mycobacterium tuberculosis over other bacteria such as Escherichia coli. Adamantyl-2-chloroacetamide may have a role in the treatment of tuberculosis because it can inhibit the synthesis of DNA, RNA, and protein in Mycobacterium tuberculosis while leaving these functions intact in other bacteria.</p>

<p>2,2-Dimethylthiopropionamide is an organic compound with the chemical formula C4H7NOS. It is a nucleophilic, unsymmetrical, n-benzyltrifluoroacetamide that is soluble in chloroform and reacts with nucleophiles to give products of desulfurization. 2,2-Dimethylthiopropionamide has been shown to react with electron-deficient amines such as azetidine and elucidate their structures. The reaction of 2,2-Dimethylthiopropionamide with chloroformate gives a dipole product and can be analysed by infrared spectroscopy.</p>

<p>3-(Aminomethyl)-N,N-dimethylbenzamide (DMBA) is a compound that can be used as a chemical marker for the identification of bacteria. It has been tested on an automated DNA sequencer and found to be effective in identifying different strains of bacteria. DMBA is applied to plates containing bacterial colonies and then contacted with a device containing the sequence analyzer. The analyzer measures the amount of DMBA that binds to the bacterial colony and generates a profile of the colony's DNA. This information can then be used to identify the bacterial colony type.</p>

Beta-casomorphin (1-4) amide (bovine) acetate salt is a peptide hormone. It is an opioid and has been shown to bind to the kappa-opioid and δ receptors. Beta-casomorphin (1-4) amide (bovine) acetate salt has also been shown to have biological properties. Beta-casomorphin (1-4) amide (bovine) acetate salt is structurally similar to morphiceptin and analogs of this drug have been synthesized that are more potent than beta-casomorphin (1-4) amide (bovine) acetate salt. These analogs have not yet been tested in vitro or in vivo, but it is believed that they will be more potent than beta-casomorphin (1-4) amide (bovine) acetate salt because of their structural similarity.

4-Butoxyphenyl)acetamide is a synthetically produced chemoattractant that is used in vitro to study the migration of cells. It is soluble in non-polar solvents and can be expressed from many organisms, including bacteria and plants. 4-Butoxyphenyl)acetamide has been shown to induce cell movement by binding to the G protein coupled receptor that stimulates the release of calcium ions from intracellular stores. This molecule also has photophysical properties, which have been studied in rat liver microsomes and hydrochloric acid, hydroxamic acids, and spermatozoa. 4-Butoxyphenyl)acetamide can be absorbed from the intestine into plasma, where it binds to odorant receptors on sensory neurons in the nose. These receptors are also found in plant physiology, where they are responsible for detecting chemicals that attract pollinators such as bees or insects.

<p>3-Hydroxy-N,N-dimethylpropanamide is a versatile chemical compound. The compound has been used as an intermediate in research and industrial processes, including the synthesis of various pharmaceuticals. 3-Hydroxy-N,N-dimethylpropanamide is also a reagent and building block for many other compounds. It has been shown to have high quality properties that make it useful for research purposes.</p>

<p>Deacetamide linezolid azide is a molecule that binds to the regulatory domain of TNF-α, inhibiting its activation. This drug has been shown to have anticancer activity against cells that produce TNF-α. Deacetamide linezolid azide has been shown to be effective in the treatment of pancreatitis and neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, and Huntington's disease. Deacetamide linezolid azide is also used in the diagnosis of cancer by identifying the presence of tumour necrosis factor-α (TNF-α) induced hallmarks in cancer cells.</p>

<p>2-Iodo-N-methyl-N-p-tolylbenzamide is a fine chemical that has the CAS No. 1387529-49-8 and is a versatile building block with a wide range of applications, including research chemicals, reaction components and speciality chemicals. 2-Iodo-N-methyl-N-p-tolylbenzamide is soluble in organic solvents such as ethers, chloroform and benzene, while insoluble in water. It has been shown to be a useful intermediate for the synthesis of complex compounds and can be used as a reagent to prepare other compounds. 2Iodo-Nmethyl--Np--tolylbenzamide has been shown to have high quality and is an excellent building block for synthesizing pharmaceuticals.</p>

N-Benzyltrifluoroacetamide is an amide that inhibits the activity of the enzyme fatty acid synthase, which catalyzes the synthesis of fatty acids. It has been shown to be effective against a number of cancers and has been used in the treatment of patients infected with HIV. N-Benzyltrifluoroacetamide is active against a range of cancer cell lines, including breast, pancreatic, ovarian, prostate, and colorectal carcinomas. Its mechanism of action is not known but may involve inhibition of protein synthesis or induction of apoptosis.

<p>2-Amino-4,5-dimethoxybenzamide is an anticancer agent that inhibits the epidermal growth factor receptor tyrosine kinase. It binds to the linker region of the epidermal growth factor receptor and prevents autophosphorylation. 2-Amino-4,5-dimethoxybenzamide has shown in vitro cytotoxic activity against testicular cancer cells and acute lymphoblastic leukemia cells. 2-Amino-4,5-dimethoxybenzamide is a synthetic compound that has been shown to have bioisosteric properties with other growth factors such as epidermal growth factor.</p>

2-Bromo-N-(4-methoxyphenyl)-N-methylbenzamide is a fine chemical that is used in the synthesis of other chemicals. It is also a reagent and a speciality chemical, which can be used as a reaction component or as an intermediate in the synthesis of other compounds. 2-Bromo-N-(4-methoxyphenyl)-N-methylbenzamide can be used to make a wide variety of compounds, including polymers and pharmaceuticals. This compound has been shown to be useful for the synthesis of polycarbonates, polyurethanes, polyesters, polyamides, and polystyrenes.

<p>1-Methyl-nicotinamide iodide is a drug that has been used in clinical trials for the treatment of type 2 diabetes mellitus. It is thought to work by increasing the sensitivity of cells to insulin, which may be related to its ability to bind to protein amide groups and form hydrogen bonds with the amino acid side chains. The compound also has been shown to increase the activity of the enzyme glycogen synthase in rats. 1-Methyl-nicotinamide iodide is soluble in water and human serum, and shows low solubility in ethanol. It has not been studied in humans, but animal studies have shown that it can be absorbed orally and metabolized into hippuric acid, which is excreted as a metabolic product through urine. Animal studies also showed that 1-methyl-nicotinamide iodide inhibits glucose production by pancreatic beta cells, which may lead to an increased insulin response after eating.</p>

<p>(1E)-N',2-Dihydroxyethanimidamide (DHEEA) is a versatile building block in organic synthesis. It is an important intermediate in the synthesis of various drugs, such as metoprolol, amlodipine, and clomiphene. DHEEA is also used as a reagent in organic chemistry for the preparation of other compounds and as a research chemical. The compound has CAS No. 73728-45-7 and can be purchased from chemical suppliers or synthesized by reacting formaldehyde with ethanolamine.</p>

2-(Indenylamino)acetamide, hydrochloride salt is a potential drug that is an uptake inhibitor. It prevents the uptake of dopamine in the brain and has been shown to be neuroprotective in animal research. It also has potential to treat diabetic neuropathy, inflammatory diseases, and pain. The kinetic properties of this drug were studied using rat striatal cells. 2-(Indenylamino)acetamide, hydrochloride salt inhibits the transport of dopamine into these cells by blocking the movement of dopamine from outside the cell to inside the cell. This drug could potentially be used for treatment of Parkinson's disease or other conditions involving dopaminergic dysfunction.

L-Valinamide hydrochloride is an amide with a reactive group. It binds to the CB2 receptor and the CB1 receptor, which are found in the brain and immune system. L-Valinamide hydrochloride has been shown to have anti-inflammatory effects in animal models of inflammatory diseases, such as rheumatoid arthritis. L-Valinamide hydrochloride has also been shown to be a synthetic cannabinoid that inhibits pain transmission by binding to the same receptors as delta-9 tetrahydrocannabinol (THC), one of the active components of cannabis.