Amidi

N,O-Bis(trimethylsilyl) acetamide is a protein that is used as a reagent for the detection of integrin receptors. It can be used to identify human immunoglobulin and human serum proteins. This compound has been shown to be pluripotent in cells, which means that it can differentiate into any type of cell. N,O-Bis(trimethylsilyl) acetamide has been shown to have surfactant properties and can be used as an alternative in toxicity studies. This compound has been shown to be toxic to bowel disease cells when tested with a dose of 3mg/mL. The disulfide bond within this molecule may be important for its biological activity. Synchronous fluorescence spectroscopy and plasma mass spectrometry are two methods that have been used to study the structure of this molecule. Electrochemical impedance spectroscopy is another method that has been used in the structural analysis of this molecule.

2-Methoxybenzamide is an amide with a p-hydroxybenzoic acid moiety. It has been shown to be an effective inhibitor of the enzyme histone deacetylase, which is involved in the regulation of gene expression. 2-Methoxybenzamide also has antiinflammatory activity and has minimal toxicity. This drug is used as a research tool for studying the immune system and its effects on hyperproliferative diseases such as cancer and autoimmune diseases. 2-Methoxybenzamide can also be used to treat metabolic disorders and physiological effects. The drug binds to intracellular targets through intermolecular hydrogen bonds that are mainly found in protein structures, including cytochrome P450s, protein kinases, DNA polymerases, transcription factors, and proteases.

4-Chloro-3-nitrophenylacetamide is a chemical compound that can be used as a reagent, useful scaffold for research, and a high quality research chemical. CAS No. 5540-60-3, this versatile building block is useful for the synthesis of complex compounds and fine chemicals.

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.

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.

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.

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.

Solid phase peptide anchor; tool for the Fmoc solid phase synthesis of peptide amides.
100-200 mesh. 1% DVB, substitution range 0.3-0.6 meq/g

Nipecotamide is a water-soluble drug that inhibits the activity of α1-acid glycoprotein, which is a blood protein that regulates the concentration of hydrogen ions in the body. It has been shown to inhibit the growth of amyloid protein and decrease camp levels in erythrocytes. Nipecotamide is used as an inhibitor for infectious diseases, such as leprosy, tuberculosis, and malaria. The chemical structure of nipecotamide contains nitrogen atoms and an amide bond with carbonyl oxygens. It is also an inhibitor binding to hydrochloric acid and hydrogen bonds with amide groups.

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

N-[(4-Amino-2-methylpyrimidin-5-yl)methyl]formamide (NAMPT) is a triazolo compound that inhibits the ATP binding cassette transporter and blocks the uptake of uridine and pyrimidine compounds. It also inhibits inorganic pyrophosphatase, which is an enzyme that catalyzes the hydrolysis of pyrophosphate to inorganic phosphate. NAMPT has been shown to be a substrate for hypochlorous acid production in neutrophils, suggesting it may play a role in the regulation of oxidative stress. Chemical biology studies have demonstrated that NAMPT plays a physiological function as an intermediate in vitamin B1 biosynthesis.

Agonist of D2 dopamine receptors

Modulator of CFTR channel in cystic fibrosis models

Clofenamide is a drug that is used to treat insulin resistance. It is an at1 receptor antagonist that blocks the action of histamine, which stimulates the release of insulin from the pancreas. Clofenamide has been shown to reduce systolic blood pressure in patients with autoimmune diseases and cardiac hypertrophy. It is also used for treating infectious diseases, such as pneumonia and tuberculosis. Clofenamide reduces inflammation by inhibiting inflammatory enzymes, such as butyric acid. This drug has been found to have anticancer activity in cell-based studies by inhibiting cellular proliferation and inducing apoptosis in cancer cells.

2-Cyanobenzamide is a corrosion inhibitor that is used in the electrochemical industry to protect metals from corrosion. It has been shown to be suitable for use as a corrosion inhibitor in salt water and other corrosive environments. 2-Cyanobenzamide has been shown to have light sensitive properties, which is why it should not be exposed to direct light or stored in dark containers. It also inhibits enzymes that are involved in the production of reactive oxygen species (ROS) such as superoxide anion and hydrogen peroxide. The reaction of 2-cyanobenzamide with aluminium, sodium sulfide, and polymeric matrices has also been studied extensively.
2-Cyanobenzamide can be synthesized by reacting benzoyl chloride with ammonia and cyanogen bromide. This reaction produces a mixture of mono-, di-, tri-, and tetramers of 2-cyanobenzamide. These products can then be separated using analytical methods such as

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.

N-[3-(3-Dimethylamino-1-oxo-2-propenyl)phenyl]-N-ethylacetamide is a high quality, complex compound that is useful as a reagent, intermediate, and building block. The CAS number for this product is 96605-66-2. This product has shown to have use in the synthesis of fine chemicals and research chemicals. It is a versatile building block that can be used as a reaction component.

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.

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.

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.

2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide is an anticancer agent that inhibits the synthesis of proteins required for cell division. It has been shown to have anticancer activity and efficacy in vitro studies against human cancer cells, such as HCT116. This compound also induces apoptosis in infected cells by binding to viral particles and inducing the release of chloride ions. 2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide has been found to be effective against influenza virus and particle production by inhibiting neuraminidase activity.

2,5-Dimethoxybenzamide is a potent inhibitor of the enzyme DECATENASE. This enzyme plays an important role in the biosynthesis of the aromatic amino acids phenylalanine and tyrosine. 2,5-Dimethoxybenzamide has been shown to have anticancer activity in vitro and in vivo. Remoxipride is a synthetic drug that competitively inhibits the action of benzodiazepines on GABA receptors by binding to them with high affinity. It was developed as an antipsychotic agent but was never marketed for this indication due to its adverse effects on motor coordination. Remoxipride has also been shown to have estrogenic activity, which may be due to its ability to bind with high affinity and inhibit the enzyme aromatase, which converts testosterone into estradiol.

4-Cyanobenzamide is a naphthalene derivative that is both reactive and intramolecular. It has been shown to react with the amino group of peptides, forming a ruthenium complex. The functional groups are acceptors and donors that can be used in assays for the detection of anions or cations. 4-Cyanobenzamide reacts with water to release hydrogen gas, which can be used to measure its hydration ability. This compound has been synthesized using solid-phase synthesis and it has amide bonds that vibrate at a specific frequency.

Prothionamide is a drug that belongs to the group of drugs called sulfonamides. It is used to treat bowel disease by inhibiting the growth of bacteria and fungi. Prothionamide inhibits bacterial growth by binding to bacterial DNA and preventing it from synthesizing new proteins. This drug also has a matrix effect, which means that it binds to the inside of the bacterial cell wall and prevents the production of new cells, leading to cell death. Prothionamide has been shown to be effective against tuberculosis in mice, although there are few data on its use in humans. The most common side effects associated with prothionamide are nausea and vomiting.

2,4,6-Trimethoxybenzamide is a triggered compound that reacts with lithium to form an efficient regiospecific lithium 2,4,6-trimethoxybenzamide complex. This reaction occurs at low temperatures and has been shown to be more efficient than other methods for the synthesis of acridones. The reaction has not been shown to be reversible and requires the use of a strong base such as lithium.

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.
2-Veratramide inhibits NOS by competitively binding to the heme moiety at the active site of the enzyme, thereby blocking access to substrate arginine.

Indapamide is an antihypertensive drug that inhibits the activity of the enzyme carbonic anhydrase, which is involved in the conversion of carbon dioxide to bicarbonate. It is used to treat high blood pressure and congestive heart failure. Indapamide has been shown to be effective in reducing oxidative injury to red blood cells and preventing cardiovascular events such as stroke and heart attack. Indapamide also has a long-term efficacy with no withdrawal symptoms or rebound hypertension when it is discontinued.

N-Allyl-N-Ethylheptadecafluorooctanesulphonamide is a chemical substance that belongs to the group of sulfonates. It is an oily liquid with a boiling point of about 160°C, and is soluble in water. N-Allyl-N-Ethylheptadecafluorooctanesulphonamide has been used as a component of mixtures, such as cleaning agents and cosmetics. The chemical properties of this substance are not well studied due to its limited use.

N-Benzyl Hexadecanamide is a long-chain amide that is used in analytical chemistry as a sample preparation agent and to extract fatty acids from biological samples. It has been shown to have neuroprotective properties by reducing the uptake of glutamate and preventing neuronal cell death. N-Benzyl Hexadecanamide has also been found to prevent tumor growth and induce apoptosis in human cancer cells, which may be due to its ability to inhibit creatine kinase activity. This compound has also been shown to have anti-inflammatory effects, which are mediated through the inhibition of the activation of nuclear factor kappa B (NF-κB).

a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide is a hydrogen bond donor. It has been shown to have cytotoxicity in vitro, with parameters that can be used for accurate prediction of descriptors. These descriptors are informative and insightful, which can be used for regression analyses and linear regression methods. The pharmacokinetic properties of a-[2-(Diisopropylamino)ethyl]-a-phenyl-2-pyridineacetamide have been studied in humans and have shown linearity between dose and plasma concentration.

(E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide is a reagent and research chemical that can be used as a building block in the synthesis of other compounds. It is also a versatile building block in organic chemistry. (E)-N-(2-Chloro-6-methylphenyl)-3-ethoxyacrylamide has been shown to be an effective intermediate for the synthesis of various complex compounds, such as pharmaceuticals and pesticides. This compound is also a useful scaffold for the synthesis of other fine chemicals.

2N-Boc-2',2''-triaminotriethylamine-bis(chloroacetamide) is a fine chemical and reagent for the synthesis of pharmaceuticals. It is also a useful building block for the synthesis of complex compounds. This product can be used as a reaction component in organic chemistry, or it can be used as a reagent in research or development laboratories.

L-Pyroglutamic acid-beta-naphthylamide is a cell nucleus pressor that has been shown to stimulate locomotor activity in rats. It is a highly selective agonist at the 5-HT2 receptor, which is involved in the regulation of energy metabolism and feeding behaviour. L-Pyroglutamic acid-beta-naphthylamide also stimulates cholinergic and serotonergic systems. This drug also inhibits bacterial growth by binding to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity. L-Pyroglutamic acid-beta-naphthylamide is an antimicrobial agent that can be used to treat infections caused by bacteria resistant to erythromycin. The antimicrobial effect of this drug is due to its ability to bind to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity.

N-(5-Bromoacetamidylpentyl) acrylamide is employed in the synthesis of substrates used for nucleotide sequence determination, covalently linked to polymer coatings such as poly(N-(5-azidoacetamidylpentyl)acrylamide-co-acrylamide) (PAZAM). Polynucleotide-binding substrates find application as molecular arrays and flow cells.

Triethylenephosphoramide (TEP) is a model system for studying the reaction mechanism of the enzyme phosphotriesterase. TEP has been used in reactions with water vapor, which causes the release of hydrogen chloride. The reaction solution is analyzed by mass spectrometry to determine the reaction products. TEP has also been shown to inhibit nitrite ion-dependent enzymes such as nitrate reductase and aminopeptidase N. TEP reacts with fluorescence probes that have been modified with response elements to detect the binding of these probes to DNA and RNA. This helps researchers identify the location of TEP in proteins and nucleic acids.