Amino Acids (AA)

2-Methylmercaptobenzothiazole is a biologically active compound that is generated by the reaction between 2-methylbenzothiazole and hydrochloric acid. It has been shown to activate in vitro assays, such as hydroxylation of logistic regression. In vivo, this compound has been shown to inhibit pancreatic enzyme activity and n-dimethyl formamide, which affects the proliferation of K562 cells. The biological function of 2-methylmercaptobenzothiazole is not well understood.

Applications N-PHENYL-4-METHOXYBENZYLAMINE (cas# 3526-43-0) is a useful research chemical.

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2,3,5-Tribromo-4-methylthiophene is a vitamin B2 analog that has been shown to have uptake and affinity properties. It is not only active against mycobacteria but also against other bacteria such as lactococci. The development of 2,3,5-Tribromo-4-methylthiophene has been enhanced by the use of diphosphate as a transport molecule and pyrrole as an analog to increase its hydrophobicity. This compound has been shown to be scalable in synthesis and could be used as an antibiotic or vitamin B2 substitute.

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Applications 2-Acrylamide-2-methylpropanesulfonic Acid is used in preparation of PAMPS/PHEMA/PEDOT Hydrogel Polyelectrolyte for activated carbon electrode. References Zhang, X., et al.: Faming Zhuanli Shenqing, (2020);

Please enquire for more information about C-(5-Phenyl-isoxazol-3-yl)-methylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Dimethyl-(2-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-ethyl)-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

1,2-Dimyristoyl-rac-glycerol (1,2-DMG) is a monomolecular fatty acid that has been found to inhibit the replication of herpes simplex virus. It binds to the surface glycoprotein and inhibits the release of diacylglycerol from the lipid membrane. 1,2-DMG also inhibits the activity of acyl chain enzymes, which are necessary for the synthesis of fatty acids in trypanosomes. This inhibition prevents the growth and proliferation of lung fibroblasts and may be beneficial in treating cancer. The ionisation mass spectrum shows that 1,2-DMG has a molecular weight of 270 Da. The binding affinity between 1,2-DMG and water is 9 x 10 M at room temperature.

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1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine is a growth factor that has been shown to bind to histone proteins and human pathogens. It has physiological effects on prostate cancer cells and fatty acid metabolism. 1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine is also antibacterial agent that has potent activity against bacterial cell walls. This drug inhibits the enzyme Clavatadine, leading to the inhibition of protein synthesis in bacteria. The spacing of nitrogen atoms in this molecule is responsible for its potent inhibition of kinase activity. 1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine is localized in the cellular cytoplasm and nucleus.

Dimethyl (2E,2'E)-3,3'-(1,4-phenylene)bisacrylate is a monomer that can be polymerized by chain growth. It is a colorless liquid with a boiling point of 65°C. Dimethyl (2E,2'E)-3,3'-(1,4-phenylene)bisacrylate is reactive and polymerizes readily in the presence of radiation or heat to form polymers. Dimethyl (2E,2'E)-3,3'-(1,4-phenylene)bisacrylate has been used to produce polymers with high molecular weights and it undergoes crystallization at -40°C. The infrared spectrum of dimethyl (2E,2'E)-3,3'-(1,4-phenylene)bisacrylate is characterized by two bands at 1705 cm-1 and 1670 cm-1.

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N-Methyldiethylamine is a proton donor in the reaction. The pKa of the conjugate acid is 4.5 and the pH range where the protonation equilibrium lies is from 5 to 8. N-Methyldiethylamine has been shown to inhibit replication by binding to ATP channels on the surface of the HIV virus, which prevents the release of viral particles from infected cells. This inhibition can be reversed by increasing pH levels. N-Methyldiethylamine also inhibits radiation induced DNA damage in human lymphocytes and can be used as a protective agent for radiation exposure.

Please enquire for more information about 2-(2-Ethoxyphenyl)-6-methylquinoline-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Methyl-1H-1,2,3-benzotriazole is a corrosion inhibitor that is used in the treatment of wastewater. It has been shown to have synergic effects with other corrosion inhibitors such as benzotriazole, glycol ethers, and sodium citrate. 4-Methyl-1H-1,2,3-benzotriazole also inhibits organic matter degradation by acting as an inhibitor. This compound has been shown to adsorb on Langmuir monolayers at low concentrations and can be used as an analytical method for copper ions. The adsorption of 4-methylbenzotriazole onto metal hydroxides was found to be dependent on pH and the presence of other ions in solution.

Please enquire for more information about 3-(4'-Pyridyl)-D-alanine including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Phenyl-3-hydroxypropylamine is a synthetic compound that has been shown to inhibit the activity of enzymes such as nucleophilic, metal cations, and high detection. The enzyme inhibition is due to its ability to act as an inhibitor by binding to the active site of the enzyme. 3-Phenyl-3-hydroxypropylamine has been found in a number of biological systems including viruses, bacteria, and human cells. It has also been shown to be effective against immunodeficiencies such as HIV and cancerous cells by inhibiting viral replication through competitive inhibition with viral reverse transcriptase. 3-Phenyl-3-hydroxypropylamine inhibits protein synthesis by acting as an inhibitor on RNA polymerase II. This drug also binds water molecules and can form hydrogen bonds with other compounds. 3-Phenyl-3-hydroxypropylamine is used in the treatment of some cancers such as leukemia

Please enquire for more information about 3-Methylthio-1,2,4-triazino[5,6-b]indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Methyl-1,3-thiazole-5-carboxylic acid is a byproduct of the manufacture of thioesters. It is also a byproduct of the photolysis of thiazole-5-carboxylate esters and thioamides. The chemical can be synthesized by the reaction of trifluoroacetic acid with sulfur or x-ray irradiation. 2-Methyl-1,3-thiazole-5-carboxylic acid reacts with acetonitrile to form an x-ray crystal structure in which it is bound to a thioamide. Fluoroacetic acid can be used as a solvent for this compound.

Prednisolone is a steroid hormone that has been used for the treatment of inflammatory bowel disease. It has been shown to be effective in the treatment of bowel diseases and is also used as a replacement therapy for adrenal insufficiency. Prednisolone has an excellent safety profile and does not cause insulin resistance or weight gain, unlike some other steroids. It can be used to treat inflammatory diseases such as rheumatoid arthritis and psoriasis. The anti-inflammatory properties of prednisolone are due to its ability to bind to the mineralocorticoid receptor, which prevents the binding of cortisol. This blocks the conversion of cholesterol into pregnenolone, which is required for the production of glucocorticoids and mineralocorticoids. 16a-Methyl-9,11-dehydro prednisolone (16D) is a metabolite that can be found in blood plasma after oral administration of prednisolone. 16D binds

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1-Oleoyl-sn-glycerol is a component of the phosphatidylcholine class of lipids. It is a fatty acid that contains one oleic acid molecule and one glycerol molecule in ester linkage. 1-Oleoyl-sn-glycerol is a ligand for toll-like receptor 4 (TLR4), which has been shown to play an important role in the innate immune response. TLR4 binds to 1-oleoyl-sn-glycerol, activating nuclear factor erythroid 2 p45 related factor 2 (Nrf2) and increasing mitochondrial biogenesis through the transcriptional regulation of genes encoding proteins involved in mitochondrial function, such as ATP synthase subunit beta, NADH dehydrogenase subunit 3, and cytochrome c oxidase subunit II. As a result, 1-oleoyl-sn glycerol has been found to have antioxidant properties.

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O-tert-Butyl-D-serine is a serine derivative that can be used as a diagnostic marker for Borrelia infections. O-tert-Butyl-D-serine is an intermediate in the synthesis of polypeptides, and it can be found in human cells, where it has been shown to have a variety of biological functions. O-tert-Butyl-D-serine is also involved in the development of autoimmune diseases and symptoms. This chemical compound inhibits the growth of bacteria such as Borrelia, which are known to cause Lyme disease. Serological tests for O-tert-Butyl D-serine are available for diagnosis.

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1-Methyl-2-naphthalenylboronic acid is a boronate ester of an indole. It reacts with potassium t-butoxide to form a potassium salt, which undergoes a Suzuki reaction with phenyl boronic acid to produce the corresponding indole. The 1-methyl group on the naphthalene moiety is removed by hydrolysis in acidic conditions to produce the desired product.

3-Methyl-benzoylhydrazide is a chemical compound that has been shown to have antibacterial effects against Gram-positive bacteria. It has been found to inhibit the growth of chickpea, acrylonitrile, and subtilis at acidic pH levels. 3-Methyl-benzoylhydrazide inhibits bacterial growth by reacting with the enzyme protein imine (NAD+), which is required for oxidative metabolism in bacteria. This reaction results in the formation of an iminium ion, which is highly reactive and can lead to the destruction of DNA, RNA, and proteins. 3-Methyl-benzoylhydrazide also reacts with staphylococcus by inhibiting its growth at alkaline pH levels. This compound also has nutritional benefits because it contains amino acids such as cysteine and methionine.

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D-3,5-Dibromotyrosine is a chemical compound that has been shown to have neuroprotective and anti-epileptic properties. It has been found to be effective in animal models of epilepsy and depression. D-3,5-Dibromotyrosine also has the potential to inhibit the activation of glutamate receptors. The mechanism of action is through receptor binding and activation by glutamate. This may lead to a decrease in excitotoxicity, which is the overstimulation of neurons that can lead to cell death.

Applications 6-FLUORO-DL-TRYPTOPHAN (cas# 7730-20-3) is a useful research chemical.

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Please enquire for more information about Fmoc-O-tert-butyl-L-threonine 4-alkoxybenzyl alcohol resin including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Z-Phe-Ala-OH is a synthetic amino acid with the chemical formula of C10H13NO3. This compound is a racemic mixture of L-Z-Phe and D-Z-Phe. Z-Phe-Ala-OH has been shown to inhibit protein synthesis by acting as an enzyme inhibitor, which leads to neuronal death. It also has reactive properties that can lead to cell death, which may be due to its ability to react with methyl ketones. Z-Phe-Ala-OH's acidic nature makes it a toxic compound for cells and can cause apoptotic effects. The reactive properties of this compound make it a potential candidate for use in cancer therapy and other treatments that target glutamate receptors and their signaling pathways, such as excitotoxic or glutamate antagonists.

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Fmoc-Asn(Trt)-Wang resin is a supramolecular biomaterial that is used as a coating for biomedical devices. It has been shown to be effective in the prevention of radiation-induced injuries in animal models. Fmoc-Asn(Trt)-Wang resin has also been shown to promote collagen production, which may be due to its ability to bind hyaluronic acid and stabilize it. This material can also be used as a scaffold for tissue regeneration and repair. Fmoc-Asn(Trt)-Wang resin displays a molecular profile similar to the extracellular matrix, which allows it to mimic the properties of natural tissues. Finally, this material has been shown to inhibit tyrosinase activity, an enzyme that plays an important role in skin pigmentation.

Fmoc-O-phospho-L-serine is a phosphoric acid derivative that is used in the solid-phase synthesis of peptides. It reacts with amino acids on the resin to form phosphopeptides. The addition of an acid, such as trifluoroacetic acid, removes the methoxy protecting group and releases the peptide from the resin. This product also has been shown to be a result of a reaction between phosphoric acid and monobenzyl ester.

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Fmoc-NH-PEG3-CH2COOH is an natriuretic agent that has been synthesized to inhibit tumor growth. It binds to the response elements for natriuretic peptides in the nucleus and prevents the binding of transcription factors. Fmoc-NH-PEG3-CH2COOH also inhibits inflammatory diseases, such as amines, by inhibiting the production of prostaglandin E2 (PGE2). This drug has been shown to be effective in treating cancer and atrial fibrillation. Fmoc-NH-PEG3-CH2COOH has also been shown to have a positive effect on immune reactions, such as tetronic acid and benzylidene acetal. This drug has also been shown to prevent cancer therapy side effects.

3-Phenylpropanimidamide hydrochloride is an inhibitor that binds to cation channels and blocks the transport of cations across the cellular membrane. It has been shown to inhibit chronic prostatitis, bowel disease, and inflammatory bowel disease in animal models, with no adverse effects on infant growth or development. 3-Phenylpropanimidamide hydrochloride also inhibits protein synthesis at the ribosome level by blocking bacterial macrophages and human macrophages from activating Tlr4. This drug has been shown to be nonselective and non-selective for different types of cation channels.

Applications (E)-4-methoxy-2,3,6-trimethyl-5-(3,7,11,15-tetramethylhexadec-2-en-1-yl)phenol is a useful chemical reagent.

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