Acides aminés (AA)

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2-Amino-5-methyl-4-phenylthiazole is an organic compound that is a reactive intermediate. It can be used in treatments such as second order rate constants, stabilization, and kinetic. This chemical has a dimethylamine group, which is an amine with two methyl groups attached to it. 2-Amino-5-methyl-4-phenylthiazole has chloride and thiazolone groups, which are both heterocyclic rings of carbon atoms with nitrogen and sulfur atoms attached to them. The phenyl isothiocyanate group is also a heterocyclic ring of carbon atoms with sulfur attached to it. 2-Amino-5-methyl-4-phenylthiazole has the constant of K = 1.2 x 10 M^sup -1
s^{sup -1} at 25 degrees Celsius. It reacts with acetonitrile and ethylpyridine

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Please enquire for more information about 2-amino-7-methyl-4-(2-naphthyl)-5-oxo-4,6,7,8-tetrahydro2H-chromene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 4-((4-methoxyphenyl)amino)-3,5-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-Oxo-4-(4-(3-phenylprop-2-enyl)piperazinyl)but-2-enoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Amino-3-bromo-5-methylpyridine is an imidazopyrazine that interacts with the magnetic field and can be used as a ligand. It has been synthesized from pyrazole derivatives and has been shown to have antimicrobial activity against Cryptococcus neoformans. 2-Amino-3-bromo-5-methylpyridine has also been shown to inhibit the growth of bacterial cells by binding to the nicotinamide adenine dinucleotide phosphate (NADP) cofactor in bacterial cells, thereby preventing ATP production. This drug is structurally related to fluoroquinolones, which are known for their antibacterial activity. 2-Amino-3-bromo-5-methylpyridine is an amido compound that ionizes in acidic environments and transfers electrons via resonance transfer. Its FTIR spectra show strong absorption bands at 3595 cm−1

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4-oxo-5-phenyl-2,5-thiazolidinylidene)methane-1,1-dicarbonitrile is a molecule that has been shown to stabilize the phenyl ring in some experimental conditions. The intramolecular dihedral parameters of 4-oxo-5-phenyl-2,5-thiazolidinylidene)methane are not experimentally determined but can be calculated by molecular docking. Molecular docking is a technique that predicts the binding of one molecule to another by simulating the docking process. Docking simulations can be used for understanding the structure and dynamics of molecules.

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H-Glu(His-OH)-OH is a protein, which can be found in the plasma samples of patients with fatty acid metabolism disorders. It is one of the most selective markers for identifying these disorders and has been extensively used for profiling and genomic analyses. H-Glu(His-OH)-OH is also present in rat cerebral cortex and it has been shown to be statistically significantly elevated in cerebral cortex samples from patients with Alzheimer's disease. This protein has been observed to have an acidic property and can be used as a biomimetic marker. Regression analysis has shown that H-Glu(His-OH)-OH levels are correlated with the severity of neuronal damage. This protein may serve as a biomarker for different diseases, including Parkinson's disease, Huntington's disease, or amyotrophic lateral sclerosis (ALS).

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3-Amino-2-phenylindenone is a lactam molecule with a five-membered ring and a carbonyl group. The compound's acetylation, protonation, and skeleton are important to its structure. 3-Amino-2-phenylindenone is an aromatic compound that has two deuterium atoms. It has the chemical formula C9H6N2O2, which consists of one chloride atom and two nitro groups. 3-Amino-2-phenylindenone has three deuterium atoms that can be seen in its proton resonances at 1.5 ppm on the IR spectrum. The compound's proton resonances are at 2.8 ppm on the IR spectrum. The compound's chloroformate can be seen in its IR spectrum at 1780 cm^(-1). This molecule has no nonequivalence in its bonds because it does not have any double or

Please enquire for more information about 1-phenyl-3-methylthiosemicarbazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications (3S)-3-Methyl-methylester Heptanoic Acid is used as a reagent in the synthesis of stereoisomers of 5,9-dimethylheptadecane, the major sex pheromone component secreted by female moths of the mountain-ash bentwing (Leucoptera scitella).
References Taguri, T., et al.: Tetrahedron Asymmetry, 23, 852 (2012)

Applications N,N-[Iminobis(trimethylene)]bis-D-gluconamide (cas# 86303-20-0) is a compound useful in organic synthesis.

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N-Methyl-L-proline is a choline analog that is used to prepare cell culture media and as a nutrient for microorganisms. It has been shown to have an inhibitory effect on the growth of the bacteria Pseudomonas aeruginosa and Salmonella enterica. N-Methyl-L-proline has also been shown to be taken up by the bacteria and to decrease their bioavailability in low salinity environments.

N-Methyl-5H-dibenzo[a,d]cycloheptene-5-propylamine hydrochloride (NMBPD) is a drug with anti-inflammatory properties that belongs to the class of tricyclic antidepressants. It has been shown to have synergistic effects with synthetic matrix in vitro. This drug also has receptor activity and can be used to treat infectious diseases such as HIV and tuberculosis. NMBPD is excreted in the urine, which can lead to kidney fibrosis. The drug is metabolized by α1-acid glycoprotein, which may be related to its potential adverse effects on the liver and kidneys. The analytical method for quantification of NMBPD includes gas chromatography with mass spectrometry detection (GC/MS).

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Z-NH-PEG2-CH2CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG2-CH2CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

4-Methoxybenzene-1,3-diamine sulfate (4MBD) is a chemical substance that inhibits the activity of cytochrome P450 enzymes. It has been shown to inhibit the activity of rat liver microsomal p-450 enzymes, and is used in studies on the effects of chemicals on protein synthesis. When 4MBD is administered to rats at dietary concentrations, it causes an increase in thyroid hormone levels and a decrease in renal function. The enzyme inhibition caused by 4MBD may be due to its ability to acylate amines, which are located near the active site of the enzyme. Linear regression analysis showed that there was a strong correlation between dietary concentrations and the inhibition of protein synthesis caused by 4MBD.

4-Phenylbenzoyl chloride is a primary amino compound that has been studied extensively in the context of biological studies and as an electroluminescent device. It is also used to study the effects of alkylation on biological systems. 4-Phenylbenzoyl chloride has been shown to be cytotoxic against monocytic cell lines, with a mechanism of action that involves its ability to react with DNA, forming adducts that interfere with DNA replication. In addition, it also reacts with amines in human tissue samples, which may lead to carcinogenic effects. This compound is also effective against protozoan parasites and Leishmania species, although not thiosemicarbazide.

7-Methylquinoline is an organic compound that can be used to synthesize antimalarial drugs. It is a quinoline derivative with a methyl group at the 7th position. The structure of 7-methylquinoline contains a nitrogen atom and hydrogen atoms, which are bonded to fluorine, chlorine, and bromine atoms. This molecule has been shown to be stable in the presence of Friedel-Crafts catalysts and chloride ions. The reaction mechanism for 7-methylquinoline is intramolecular hydrogen transfer from the chloroform molecule to the quinoline ring system. The formation rate for this compound is slow because it requires two steps: nucleophilic substitution and electrophilic addition reactions.

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Z-D-Lys(Boc)-OH is a synthetic peptidomimetic that has been shown to selectively kill cancer cells. Z-D-Lys(Boc)-OH binds to the lysine residue on the target cell surface, which is not present in normal cells. This binding inhibits serine protease activity and disrupts the synthesis of peptides, which are essential for cellular function. The electron microscopic images show that this compound causes an enhancement of biological function in human pathogenic chlamydia.

DL-4-Hydroxyphenylglycine is an active analogue of the natural amino acid L-glycine, which is a precursor in the biosynthesis of sulfamides. DL-4-Hydroxyphenylglycine has been shown to be active as an anti-infective agent against many bacteria and fungi that are resistant to other sulfa drugs. It is synthesized by reacting sodium carbonate and ammonia with the amide of 4-hydroxybenzeneacetic acid. The cyclic peptide is then hydrolyzed to form free DL-4-hydroxyphenylglycine. This drug has also been shown to have a strong inhibitory effect on fatty acid metabolism in liver cells, which may be due to its ability to bind to fatty acids and reduce their uptake by cells.

L-Tyrosine hydrochloride is a pharmaceutical preparation that has been used clinically in the treatment of infectious diseases, cancer, and autoimmune diseases. Tyrosine is an amino acid with a hydroxyl group on its side chain. Tyrosine can be synthesized from phenylalanine by hydroxylation of the phenolic group and decarboxylation of the carboxylic acid group. It is also a precursor to catecholamines and other important biological molecules. L-Tyrosine hydrochloride is used as an intermediate in the production of monoclonal antibodies for use in cancer research. In addition, it has been shown to be an effective inhibitor of virus replication when combined with ester hydrochloride, which prevents the release of progeny virus particles from infected cells.

Ac-Arg-pNA·HCl is a substrate that is activated by hydrogen fluoride to form a nitro group. This compound can be used in the synthesis of nitrobenzene and other aromatic compounds. Ac-Arg-pNA·HCl also has enzymic activity, which is catalyzed by an enzyme called benzyloxycarbonyl (Boc).

(±)-3-Methyl-2-oxovaleric acid is a fatty acid that is found in the mitochondria of liver cells and other tissues. It is an intermediate in the citric acid cycle and can be converted into acetyl-CoA, which is used for energy production. (±)-3-Methyl-2-oxovaleric acid has been shown to cause necrotic cell death when it binds to the mitochondrial membrane potential and causes a loss of ATP production. This results in a lack of energy for the cell, leading to cell death. (±)-3-Methyl-2-oxovaleric acid has also been shown to inhibit protein synthesis by decreasing uptake and increasing creatine kinase activity. This inhibition leads to decreased body formation and tissue culture growth in vitro. In vivo, (±)-3-Methyl-2-oxovaleric acid causes primary sclerosing cholangitis, a disease characterized by inflammation of bile ducts that

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7-Chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine is a metabolically stable benzodiazepine that binds to the benzodiazepine receptor. It has been shown to have a higher affinity for this receptor than alprazolam and other related compounds. 7-Chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine has been used as an active ingredient in a number of pesticide products that are used against termites and ants. This compound has also been found to be an effective insecticide against mosquitoes. 7C2HDBZ has been shown to be stable in the environment and is not readily degraded by hydrolysis or pyrolysis.

L-phenylglycinol is a chiral compound that is synthesized by the reaction of phenylglycinol with hydroxide solution in the presence of an asymmetric synthesis catalyst. It is used as a precursor to chiral amides and aziridines, which are important for addressing the need for enantiopure compounds. The reaction mechanism involves nucleophilic substitution at the amino function, which can be catalyzed by copper complexes in solution. This reaction can also be monitored using liquid chromatography methods.

Dexamethasone 21-(3-phenylpropionate) is a corticosteroid that is used for the treatment of a variety of inflammatory skin conditions. Dexamethasone 21-(3-phenylpropionate) has been shown to be effective in the treatment of cutaneous lesions in mice and rabbits. This drug also has an anti-inflammatory effect, which may be due to its ability to inhibit cytokine production. Dexamethasone 21-(3-phenylpropionate) is not metabolized by liver enzymes and has a long half life, making it more predictable than prednisolone. This medication should not be used during pregnancy or if you are trying to become pregnant, as it may cause abortion or premature birth. It should also not be used by women who are breastfeeding, as it can pass through breast milk and affect the baby.

L-glutamic acid is a nonessential amino acid that is used as a food additive. L-glutamic acid is found in the form of sodium salt, called monosodium glutamate (MSG), and is used to enhance the flavor of foods. L-glutamic acid has been shown to be essential for the growth of certain bacteria, such as corynebacteria. The l-glutamic acid gene can be found in corynebacteria and corynebacterium glutamicum. It has been shown that l-glutamic acid can be synthesized by these organisms under conditions of low magnesium concentration, high pH, and high temperature.

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Z-NH-PEG5-CH2CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG5-CH2CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

1-Phenyl-1H-pyrazole-4-carbaldehyde is an antibacterial agent that has been shown to have bactericidal activity against bacteria. It inhibits the growth of bacteria by binding to the pyrazole ring in the bacterial cell wall and blocking the formation of a hydrogen bond. 1-Phenyl-1H-pyrazole-4-carbaldehyde has been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) and Ciprofloxacin resistant Pseudomonas aeruginosa isolates, but not against Mycobacterium tuberculosis or Mycobacterium avium complex.

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3-Phenyl-1-propanol is an organic compound that belongs to the class of trifluoroacetic acids. It has a molecular weight of 134.24 and a molecular formula of C8H12O2F3. 3-Phenyl-1-propanol is a reactive compound that reacts with germinating seeds, causing them to stop growing. The reaction products are fatty acid esters, which may be responsible for the inhibition of seed germination. 3-Phenyl-1-propanol can be prepared by reacting phenylacetaldehyde with trifluoroacetic acid in the presence of potassium hydroxide at high temperature and pressure. This method also produces 4-vinylbenzyl alcohol as a side product, which is used in the production of polymers and plastics.

Cis-4-Methylcyclohexylamine is a cyclic amine that is found in the form of its decarboxylated derivative, 4-methylcyclohexanamine, which is used as an inhibitor for various enzymes. The methyl group on the cyclohexane ring is responsible for the compound's activity. Magnetic resonance spectroscopy has shown that cis-4-Methylcyclohexylamine binds to the active site of carbonyl reductase and inhibits its enzymatic activity, thereby blocking a step in the citric acid cycle. Cis-4-Methylcyclohexylamine has also been shown to have anti-inflammatory effects by inhibiting protein kinase C (PKC) and NFkB activation.

H-Cys(Me)-OH is an organosulfur compound that contains a sulfhydryl group. It is used as a model system for the study of the p2 group of compounds in nitrogen chemistry and enzyme activity. H-Cys(Me)-OH has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. The compound also exhibits carcinogenic potential, as it induces mitochondrial membrane depolarization and kidney bean necrosis in rats when administered at high doses.

Phthaloyl-L-alanine is a molecule with a hydrochloric acid group and a carbonyl group. It has been shown to have the ability to bind to peptidyl molecules and immobilize them, leading to an inhibition of the reaction mechanism. This process can be induced by enzymatic inactivation or by hydrogen bonding with chloride. The cisplatin-induced apoptosis of cancer cells has been demonstrated using patch-clamp technique on human erythrocytes. Caspases are proteins that are activated during apoptosis and have been found to interact with Phthaloyl-L-alanine in vitro. Molecular modeling studies suggest that Phthaloyl-L-alanine may inhibit caspases by binding to the enzyme's active site.

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2-Methylbenzenesulfonamide is a chemical compound that has been shown to induce apoptosis in bladder cancer cells. It is an acid conjugate of the drug 2-methylbenzene-1,4-sulfonamide and it can be used for the treatment of bladder cancer. The compound binds to the apoptosis protein and inhibits its function, leading to cell death. The cytotoxic effects of 2-methylbenzenesulfonamide have been shown in short term toxicity studies in rats. In long term animal studies, this compound showed no adverse effects on the liver or kidneys, but did show some indication of reproductive toxicity. 2-Methylbenzenesulfonamide is not mutagenic and does not affect male fertility when given orally at doses up to 2000 mg/kg body weight for 90 days. 2-Methylbenzenesulfonamide binds to receptors on the surface of cancerous cells and induces apoptosis by inhib

3,4-Dehydro-DL-proline is a monoclonal antibody that is known for its ability to bind to the amino acid proline. It has been shown to be effective in the treatment of resistant mutants in plant science, tissue culture, and biological studies. 3,4-Dehydro-DL-proline binds to collagen, amide and proline analogs and hydrogen bonds with them. 3,4-Dehydro-DL-proline also has conformational properties that are important for its function as an anti-inflammatory agent.

1-Phenylcyclohexanol (1-PC) is an organic compound that is used as a reagent in the synthesis of other compounds. It is a colorless liquid with a pleasant odor. 1-PC has been shown to have synergic effects when reacted with various types of oxidizing agents, such as magnesium and boron trichloride. The reaction products are cyclohexanol, dehydration, and modifiers. When 1-PC reacts with phenylcyclohexene, it forms the antigen hemiketal.

Ile-Ile-OH is a zwitterion that is the product of an enzyme serine protease. It has been shown to exhibit serine protease activity against corynebacterium, and it can be used for the production of active enzymes such as corynebacterium glutamicum. Ile-Ile-OH is synthesized from serine and hydrochloric acid in a reaction catalyzed by the enzyme serine protease. The rate of this reaction depends on pH and temperature, which causes the conversion of ile-ile to ile-ole at higher temperatures. Ile-Ile-OH exhibits conformational properties that are similar to those found in natural amino acids, which may be due to its zwitterionic nature. This compound also has protonation properties that have been shown to be important for uptake assays in L6 cells.

3-Methyl-1-pentyn-3-ol is a chemical that has been shown to have interactive effects on the metabolism of urea nitrogen and low light. 3-Methyl-1-pentyn-3-ol has been shown to produce a depressant effect in animals, which may be due to its ability to inhibit the production of acetylcholine by blocking the enzyme cholinesterase. This chemical has also been shown to react with hydroxyl groups, producing a pharmacological agent. The reaction mechanism for 3-methyl pentynol is via hydrolysis by hydrochloric acid or pentobarbital sodium.

3-O-Methyl carbidopa is a metabolite of L-3,4-dihydroxyphenylalanine that is used as a drug in the treatment of Parkinson's disease. 3-O-Methyl carbidopa is a racemic mixture of two stereoisomers that have different chemical properties. The (+) form is more active and has been shown to be more potent than the (-) form. Analysis of this compound by magnetic resonance spectroscopy (NMR) at different magnetic fields showed that it has six distinct resonances: three from the protonated molecule and three from the deprotonated molecule. The proton nmr spectrum showed peaks at 2.02 ppm (D1), 2.81 ppm (D2), 3.84 ppm (D3), 4.07 ppm (D4), 4.28 ppm (D5), and 4.53 ppm (D6). These peaks correspond to resonances for protons

2-Methyl pentanoic acid is a coordination complex that is synthesized by the condensation of propionyl chloride and 2-methylpentanoyl chloride. It has been shown to have anticancer activity against human cervical cancer cells, inhibiting the growth of cells in culture. The mechanism of action may be due to its ability to inhibit the production of mitochondrial proteins, leading to cell death. 2-Methyl pentanoic acid also has a strong affinity for fatty acids and can be used as an inhibitor of fatty acid synthase, which is an enzyme that catalyzes the synthesis of long chain fatty acids in mitochondria. 2-Methyl pentanoic acid can also be used as a treatment for seizures caused by divalproex sodium and isovaleric acid. It inhibits the production of 3-hydroxyisovaleric acid, which is responsible for these seizures, through competitive inhibition with valine at the 3 position on the enzyme's active site.

D-(+)-2-Chlorophenylglycine is a synthetic, chiral aldehyde that serves as an industrial solvent. It is used to produce other organic compounds and has been shown to cause environmental pollution. D-(+)-2-Chlorophenylglycine is also used in the synthesis of thiourea and organocatalysts. This compound is synthesized from quinidine and enantiomeric (D or L) thionyl chloride, which are both manufactured on an industrial scale. The stereoselective process for D-(+)-2-chlorophenylglycine involves the use of a chiral catalyst.

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Isovaleryl-Phe-Nle-Sta-Ala-Sta-OH (IVAS) is a small molecule that has been shown to be an angiotensin system inhibitor. IVAS blocks the binding site of the angiotensin receptor and prevents the activation of this system. This effect is dose dependent and can be used to treat high blood pressure in humans. IVAS is a long-acting drug and has been shown to be effective in primates as well as humans. The drug is rapidly absorbed from the gastrointestinal tract and eliminated by metabolism, mainly through hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. IVAS also specifically binds to markers expressed at high levels in Mycobacterium tuberculosis strains (e.g., ESX-1 secretion system protein) and inhibits cell growth in culture.

(1S,2S)-(+)-2-Amino-1-phenyl-1,3-propanediol is a synthetic compound that has been synthesized and studied as an amide. It has a hydroxy group on the skeleton of the molecule. The enantiomer of this compound is (1R,2R)-(-)-2-amino-1-phenyl-1,3-propanediol. This compound contains two chiral centers and four stereoisomers. These stereoisomers are not mirror images of each other. (1S,2S)-(+)-2-Amino-1-phenyl-1,3-propanediol has been shown to be effective against cryptococcus neoformans in cell culture experiments.

Z-NH-PEG3-CH2CH2COOH is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Z-NH-PEG3-CH2CH2COOH is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.

(S)-3',5'-Bis(trifluoromethyl)-1-phenethanol is a choline derivative that is used in the treatment of liver cancer. It has been shown to increase the permeability of cell membranes and to suppress the growth of tumor cells by inhibiting protein synthesis. (S)-3',5'-Bis(trifluoromethyl)-1-phenethanol can be used as a surfactant and a hydrophobic solvent for optimization of reaction parameters. This chemical also has been shown to be active against Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis, but not against Gram-negative bacteria such as Escherichia coli or Pseudomonas aeruginosa. The mechanism of this effect is mediated by chloride ions that act as bioreductive agents on cellular membranes, leading to increased permeability and cell death.

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