Carboxylic Acids

<p>(S)-BoroLeu-(+)-pinanediol-trifluoroacetate is a useful scaffold, building block, and intermediate for the synthesis of complex compounds. It is a high quality reagent that can be used in research chemicals and speciality chemicals. (S)-BoroLeu-(+)-pinanediol-trifluoroacetate is a versatile building block because it can be used as a reaction component in the synthesis of fine chemicals and as an intermediate in the synthesis of other reagents. CAS No. 477254-69-6</p>

<p>Suberic acid is a sodium salt that is soluble in water. It has been shown to have biochemical properties, such as x-ray crystal structures and biocompatible polymer. Suberic acid has been shown to be effective against a number of human tumor cell lines and can inhibit the growth of hl-60 cells in vitro. Suberic acid is also found to have anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. The hydroxyl groups on the aromatic ring allow it to form hydrogen bonding interactions with other molecules. Suberic acid also has the ability to form complexes with vancomycin hydrochloride, providing an alternative drug for treating infectious diseases caused by methicillin-resistant Staphylococcus aureus (MRSA).</p>

<p>2,6-Dichloropyrimidine-4-carboxylic acid is a pyrimidine that can be used as a starting material for the synthesis of other compounds. It is an intermediate in the manufacture of anilines and pyrimidines. 2,6-Dichloropyrimidine-4-carboxylic acid is also used in the production of dyes and agrochemicals.</p>

<p>6-Hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid, also called Trolox, is a water-soluble analogue of vitamin E and an antioxidant used in biological or biochemical applications to reduce oxidative stress or damage. It is commonly used as a standard or positive control in antioxidant assays.</p>

<p>[(1-Methyl-1H-indol-5-yl)methyl]amine acetate is a versatile building block that can be used in the preparation of a wide range of chemicals. This compound has been shown to react with a variety of reagents, such as phenyliodine diacetate and chloroacetic acid to give various products. [(1-Methyl-1H-indol-5-yl)methyl]amine acetate also reacts with potassium hydroxide (KOH) to produce indole. It is an important intermediate in the synthesis of other chemical compounds and has been reported in more than 200 scientific publications. The chemical formula for [(1-Methyl-1H-indol-5-yl)methyl]amine acetate is C13H14N2O4.</p>

<p>4-Methoxy-3-nitrobenzoic acid is a hydroxybenzoic acid, and belongs to the group of heterocyclic compounds. It is a preactivated hydroxybenzoate that can be used in the synthesis of griseoluteic acid with chloride as an electron donor. Griseoluteic acid has inhibitory activities on isolated yield. This compound also has potent antitumor activity, which may be due to its ability to inhibit DNA synthesis and protein synthesis by binding to DNA polymerase and ribosomes respectively. Preparative high performance liquid chromatography (HPLC) using this compound is possible with marine microorganisms as the stationary phase. The x-ray absorption spectrum shows that 4-methoxy-3-nitrobenzoic acid has potential for use as a contrast agent for x-rays in imaging tissues.</p>

<p>Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid 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. Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid 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.</p>

<p>4-Methoxybenzoic acid sodium is an amide that has been used as a preservative and antimicrobial agent in food products. It is also a second-order rate constant with a Ca2+ concentration of 0.1 mM for staphylococcus. The fatty acids of 4-methoxybenzoic acid sodium are hydrophobic and inhibit the growth of microorganisms by disrupting the cell membrane, which leads to leakage of cellular content. This compound also inhibits the activity of fatty acyl coenzyme A reductase and has been shown to have a microbicidal effect on gram-positive bacteria, such as Staphylococcus aureus. 4-Methoxybenzoic acid sodium has also been shown to be effective against Candida albicans, Streptococcus pyogenes, and Bacillus subtilis when combined with an antimicrobial peptide or cationic surfactant.</p>

<p>Please enquire for more information about (Des-Gly10,D-Trp6,D-Leu7,Pro-NHEt 9)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Laxative</p>

<p>Please enquire for more information about Methyl 3-aminothieno[2,3-β]pyridine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Ala-Phe-Lys-AMC trifluoroacetate salt is a chemical compound that can be used as an intermediate in the synthesis of peptides, peptidomimetics, and other organic compounds. This reagent is a high quality, versatile building block that can be used in the synthesis of complex compounds. H-Ala-Phe-Lys-AMC trifluoroacetate salt is a fine chemical that has been assigned CAS No. 120928-02-1. It is a useful scaffold for the synthesis of novel compounds with potential pharmaceutical value.</p>

<p>2-Hydroxy-4-aminobutanoic acid is a synthetic compound that has been shown to be a potent antibacterial agent. It is active against both Gram-positive and Gram-negative bacteria, including Pseudomonas aeruginosa, Enterococcus faecalis, Staphylococcus aureus, and Escherichia coli. 2-Hydroxy-4-aminobutanoic acid is also an indole alkaloid that can be produced from the amino acid tryptophan by the enzyme pyridoxal phosphate. This prebiotic is found in tissues of many animals and humans. 2-Hydroxy-4-aminobutanoic acid has been shown to have antiinflammatory properties in human serum.</p>

<p>4,5-Difluoro-2-methylbenzoic acid is a versatile building block that can be used in research and industrial settings. It is a high quality chemical with a CAS number of 183237-86-7. 4,5-Difluoro-2-methylbenzoic acid can be used as a building block for the synthesis of complex compounds. This chemical is also useful as an intermediate or scaffold for organic reactions.</p>

<p>Please enquire for more information about 3-((2-Fluorophenyl)piperazinylcarbamoyl)prop-2-enoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-6-fluorobenzoic acid is a carboxylate that has been used in the treatment of prostate cancer cells. It is activated by nucleophilic attack to form a reactive intermediate, which then reacts with the fluorine or chlorine substituents on DNA bases. This reaction leads to the replacement of the fluorine or chlorine with bromine, resulting in the formation of a quinazolinone. The substituted nucleotide is then recognized by enzymes, leading to cell death.<br>2-Bromo-6-fluorobenzoic acid has also been shown to be active against other cancer cells, such as lung and breast cancer cells.</p>

<p>2-(2,4-Difluorophenoxy)-2-methylpropanoic acid is a versatile building block that can be used in research and development of complex compounds. It has CAS No. 667413-00-5 and is classified as a fine chemical. 2-(2,4-Difluorophenoxy)-2-methylpropanoic acid can be used in the synthesis of useful scaffolds and reaction components. It is also a reagent for use in the synthesis of speciality chemicals. This compound has high quality and is an important intermediate for the production of other compounds.</p>

<p>3,5-Dibromophenylboronic acid is a boronic acid with the chemical formula B(OH)Br. The boron atom in this molecule has a unique electron configuration that allows it to form strong bonds with other atoms and molecules. This reactive compound can be used as a ligand in cross-coupling reactions or to modify an organic molecule by coupling it to another molecule. 3,5-Dibromophenylboronic acid is typically used as a precursor for the synthesis of nanomaterials and can be synthesized from monomers at temperatures ranging from -78°C to 80°C.</p>

<p>4,6-Dichloroindole-2-carboxylic acid (DCI) is a potential drug candidate for the treatment of neurological disorders. DCI binds to glutamate receptors, which are involved in many neurological diseases. It has been shown to inhibit glutamate dehydrogenase and thus block the production of glutamate from glucose. DCI also prevents neuronal death caused by excessive levels of glutamate and inhibits the activation of N-methyl-D-aspartate (NMDA) receptors. This drug is currently being investigated as a therapy for inflammatory diseases such as multiple sclerosis and Alzheimer's disease. One study has shown that DCI may be useful for treating cerebellar granule cells in a model system. It has been found to inhibit glycogen synthase kinase 3, which is an enzyme involved in signaling pathways that regulate cell growth and survival.</p>

<p>2-Fluoro-6-methoxybenzoic acid is a monocarboxylic acid that is synthesized from 2,6-dichlorobenzoic acid by a mediated, synthetic sequence. This compound can be used as a substrate for kinetic analyses of the transport of carboxylic acids across cellular membranes. The uptake of 2-fluoro-6-methoxybenzoic acid is expressed in the apical surface membrane of Caco2 cells. Kinetic studies indicate that this compound reacts rapidly with butyllithium to form an enamine intermediate. The enamine intermediate then reacts with either water or methanol to produce a final product, depending on the reaction time.</p>

<p>4-Hydroxyphthalic acid is a hydroxybenzoic acid. It is a reaction product of pyrite and protocatechuic acid. It has been shown to bind to the receptor site in phagocytic cells, which may be due to its ability to form an adduct with the hydroxyl group on the cell membrane. 4-Hydroxyphthalic acid also has antimicrobial properties that inhibit bacterial growth by destroying the cell wall and inhibiting protein synthesis. This compound also has pharmacokinetic properties that make it suitable for drug delivery applications. 4-Hydroxyphthalic acid is metabolized by hydrolysis and oxidation, with most of it being excreted unchanged in urine or bile. The reaction products are converted back into protocatechuic acid, which can be recycled again through other reactions to create more 4-hydroxyphthalic acid.</p>

<p>3-Bromo-4-fluorocinnamic acid is a useful intermediate that reacts with amines to form 3-bromo-4-fluoroaniline, which is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.</p>

<p>10-Formyl folic acid is a type of folic acid that is found in the human serum. It can be detected by liquid chromatography-mass spectrometry (LC-MS/MS). 10-Formyl folic acid has been studied for its potential to be used as an early indicator of leukemia, and can also be used to study the effects of matrix effects on chromatographic methods. 10-Formyl folic acid is often used in product research because it has high detection and can be used to detect streptococcus faecalis.</p>

<p>Fmoc-12-amino-4,7,10-trioxadodecanoic acid 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. Fmoc-12-amino-4,7,10-trioxadodecanoic acid 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.</p>

<p>Isonipecotic acid is a potent antagonist that binds to the response element of the platelet cyclic adenosine monophosphate (cAMP) receptor. This receptor is a regulatory protein that controls the activity of cAMP in cells, including platelets. Isonipecotic acid can be used to treat coronary heart diseases and autoimmune diseases by regulating blood clotting, as well as for treatment of insect resistance and autoimmune diseases. It has been shown to have pharmacokinetic properties that are similar to those of other coumarin derivatives.</p>

<p>Methyl 2-(chlorosulfonyl)acetate is a chemical compound that has been shown to reduce the number of ovarian cells in mice. It has also been shown to have anti-inflammatory properties, as it inhibits the production of prostaglandin, which is a hormone that causes inflammation. Methyl 2-(chlorosulfonyl)acetate also has the ability to induce cell apoptosis and is being studied for its potential use as an anti-cancer agent. This chemical compound binds to chloride ions and ammonium nitrate ions and forms a carbanion. The carbanion can then react with hydrogen bonds with other molecules, forming new compounds. X-ray diffraction studies have revealed that methyl 2-(chlorosulfonyl)acetate binds to cancer cells through hydrogen bonds and kills the cells by causing them to undergo apoptosis, or programmed cell death.</p>

<p>Intermediate in the synthesis of nintedanib</p>

<p>3-(4-Fluorobenzoyl)-6-Methoxy-2-Methyl-1H-Indole-1-Acetic Acid is a prodrug that is metabolized to 6-fluoro-3,4 dioxo tamoxifen in the liver. It has been shown to have anticholinergic, cytosolic calcium and c1-4 alkyl properties. 3-(4-Fluorobenzoyl)-6-Methoxy-2-Methylindole Acetic Acid also has a basic group, cyclopentane ring, and pyridine ring.</p>

<p>2,3-Dimethylbenzoic acid is a reagent that is used as a molecular ion in mass spectrometry. It is volatile and can be used to identify carboxylic acids that are aliphatic or oxygenated. 2,3-Dimethylbenzoic acid can also be used to identify methyl groups and the conjugate acid of an ester.</p>

<p>3-Bromo-4-hydroxyphenylacetic acid is an organic compound that belongs to the class of bromophenols. It can be found in urine samples, and is used as a biomarker for the evaluation of eosinophil peroxidase activity. 3-Bromo-4-hydroxyphenylacetic acid is metabolized through a number of metabolic pathways, including oxidation by hypobromous acid or catalysis by dehalogenase enzymes. This metabolite may also be involved in the pathogenesis of allergic reactions.</p>

<p>2-Boc-6-Chloro-3,4-dihydro-1H-isoquinoline-1-carboxylic acid is a useful scaffold for the production of various chemical compounds. It is a versatile building block that can be used as an intermediate in various chemical reactions or as a speciality chemical. 2-Boc-6-Chloro-3,4-dihydro-1H-isoquinoline-1 carboxylic acid has been shown to be a high quality and reliable reagent for use in research and development.</p>

<p>3,4-Difluoro-2-methoxybenzoic acid is a chemical compound that can be used as a reaction component or reagent. It is also a useful scaffold for organic synthesis of complex compounds and can be used as a building block to produce fine chemicals. 3,4-Difluoro-2-methoxybenzoic acid has the CAS number 875664-52-1 and is listed under the chemical name 3,4-difluoro-2-methoxybenzoic acid.</p>

<p>Di-O-benzoyl L-tartaric acid is a chiral compound that is used in the synthesis of enantiopure compounds. It is a racemic mixture of two diastereoisomers, which means it has an asymmetric carbon atom. The two diastereoisomers can be separated using high performance liquid chromatography (HPLC). Di-O-benzoyl L-tartaric acid is used to produce β-amino acids from α-amino acids, and also as a chiral auxiliary for organic synthesis. Di-O-benzoyl L-tartaric acid can also be obtained by hydrolysis of malonic acid with hydrochloric acid or sodium hydroxide.</p>

<p>2,6-Pyridinedicarboxylic acid is a chemical compound that is mainly used as an antimicrobial agent. It binds to DNA by hydrogen bonding interactions and alters the polymerase chain reaction (PCR) process. This leads to inhibition of DNA synthesis and cell death. 2,6-Pyridinedicarboxylic acid has been shown to have synergistic effects when combined with sodium salts. It also inhibits transfer reactions in bacteria, which may be due to its ability to bind to picolinic acid. The structural analysis of 2,6-pyridinedicarboxylic acid showed that it contains a pyridine ring fused with two carboxyl groups. 2,6-Pyridinedicarboxylic acid reacts with picolinic acid in the presence of sodium salts and undergoes a series of reactions leading to the formation of picolinamide, which may explain its inhibitory properties.</p>

<p>3,4-Dichlorophenylacetic acid is a chemical compound that can be found in plants and animals. 3,4-Dichlorophenylacetic acid has been shown to inhibit the activity of receptors that are involved in the regulation of blood pressure. It also binds to lysine residues on proteins, which may be part of its inhibitory effect. 3,4-Dichlorophenylacetic acid is a selective ligand for the alpha2A adrenergic receptor. This chemical has a molecular weight of 122.09 g/mol and a chlorine atom in its structure.</p>

<p>1-Adamantylmalonic acid is a hydrolytic impurity of the drug adamantine, which belongs to the class of anti-inflammatory drugs. It has been shown that 1-Adamantylmalonic acid can be produced by hydrolysis when piperidine is added to a reaction solution containing malonic acid and an alicyclic compound with a constant structure. The responsiveness of 1-Adamantylmalonic acid to light has been determined in several experiments. It has been shown that this impurity is stable, but it is more sensitive to light than adamantine. Optical properties have also been studied and it was found that 1-Adamantylmalonic acid absorbs in the ultraviolet region and fluoresces at wavelengths between 300 and 320 nm.</p>

<p>3-Methoxy-4-t-Butyl-Benzoic acid is a building block that can be used in the synthesis of a variety of organic compounds. This chemical has been used as a reagent, as well as in research and development. It is also used to synthesize complex compounds and may be used as a versatile building block or intermediate for reactions.</p>

<p>Bazedoxifene acetate is a selective estrogen receptor modulator (SERM) that prevents bone loss and reduces the risk of breast cancer in postmenopausal women. Bazedoxifene acetate has been shown to be safe and effective for the treatment of endometriosis, as it inhibits the growth of uterine tissue outside the uterus. Bazedoxifene acetate also acts on estrogen receptors in breast tissue and may be used to prevent breast cancer.</p>

<p>5-Methoxysalicylic acid sodium (MSAS) is a drug that is used to treat intestinal ulcers. It is also used to reduce the viscosity of blood and as an adjuvant in the treatment of rheumatoid arthritis. The bioavailability of MSAS is increased when it is administered with cefmetazole, which enhances the absorption of this drug in the small intestine. MSAS has a hypoglycemic effect and can be used to treat high blood sugar levels. This drug binds to muscle cells and prevents their contraction, which can lead to relief from muscle pain or spasms. MSAS may also have a pharmacological effect on ligation, which occurs when tissue is cut off from its blood supply.</p>

<p>6-Bromo-1H-indole-3-carboxylic acid is a natural product that is isolated from the marine sponge Smenospongia purpurea. It was first reported in 1979 and has been used for the synthesis of other compounds. 6-Bromoindole, a precursor to 6-bromo-1H-indole-3-carboxylic acid, is biosynthesized from methyl ester and NMR spectra indicate that it has a dihedral angle of 173°. This compound has been shown to have antibacterial activity against staphylococcus.</p>

<p>5-Methyl-2-thiophenecarboxylic acid is an organic compound with the molecular formula CH3COOH. It has a carboxyl group at one end and a methyl group at the other, hence its name. 5-Methyl-2-thiophenecarboxylic acid is used in the synthesis of esters that are useful as intermediates in the production of pharmaceuticals, pesticides, and other chemicals. The asymmetric synthesis of 5-Methyl-2-thiophenecarboxylic acid was accomplished by reacting it with sodium hydroxide in methanol. The compound is also found to have anticarcinogenic properties. A study conducted on mice showed that 5-Methyl-2-thiophenecarboxylic acid inhibited skin cancer by inducing apoptosis in melanoma cells and inhibiting cell proliferation. 5-Methyl-2-thiophenecarboxylic acid has been shown to</p>

<p>β-Naphthoic acid ethyl ester (BNAE) is a synthetic compound that has been used as an intermediate in the synthesis of organic compounds. It is also used to prepare hydroxamic acids, which are active methylene compounds. BNAE reacts with nucleophiles and is susceptible to nucleophilic attack. The reaction mechanism for this type of compound involves a cavity with a constant volume, which increases the reactivity of the molecule. This type of reaction can be explained using the functional theory and the use of organic solvents. BNAE is stable when exposed to carbon tetrachloride and hydroxamic acids, but not when exposed to diethyl succinate or chemical agents such as sodium nitrite.</p>

<p>2-Fluoro-4-methylbenzoic acid ethyl ester is a versatile building block that is used in the synthesis of complex compounds with a wide variety of biological and chemical properties. This compound has been used as a reagent for research, as well as in the production of pharmaceuticals and other speciality chemicals. It has also been found to be useful in the synthesis of compounds with high quality. 2-Fluoro-4-methylbenzoic acid ethyl ester can be used as an intermediate in reactions, or as a scaffold for further synthesis. The CAS number for this compound is 500579-61-3.</p>

<p>2-Chloronicotinic acid is a chemical compound that belongs to the group of phosphorus compounds. It is a colorless liquid that is soluble in water and has a pungent odor. 2-Chloronicotinic acid can be found in wastewater treatment, as it binds strongly to phosphorus compounds. It also participates in the Suzuki coupling reaction with various organometallic catalysts, such as palladium and nickel, to produce amides and n-oxides. 2-Chloronicotinic acid inhibits the growth of Pseudomonas aeruginosa and other bacteria by binding to the bacterial ribosome and inhibiting protein synthesis. 2-Chloronicotinic acid has been shown to inhibit prostaglandin synthesis, which may be due to its ability to bind nonsteroidal anti-inflammatory drugs (NSAIDs) by hydrogen bonding at their active site.</p>

<p>Fmoc-NH-PEG10-propionic acid 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. Fmoc-NH-PEG10-propionic acid 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.</p>

<p>4-Ethoxycinnamic acid is a phenolic compound that is found in many plants and fruits. It has been shown to have bioactivities such as anti-inflammatory, anti-allergic, and anticancer activities. 4-Ethoxycinnamic acid has been shown to inhibit tyrosinase activity by interacting with the enzyme's active site. This inhibition reduces the production of melanin, which may be due to its ability to inhibit dopamine oxidation or the conversion of dopachrome into dopaquinone. 4-Ethoxycinnamic acid also inhibits prolyl hydroxylase activity, which can lead to increased collagen synthesis and reduced inflammation.</p>

<p>Benzyl (4-hydroxyphenyl)acetate is a prodrug that is converted to its active form, phenylephrine, in the cytosol. It has been shown to inhibit carbenes and enhance the contractions of muscle cells. Benzyl (4-hydroxyphenyl)acetate has been shown to be effective in reducing blood pressure and normalized blood glucose levels in diabetic mice. The drug has also been shown to have a dose-dependent effect on nerve cells.</p>

<p>R-(-)-Arundic acid is a chiral compound, which is a derivative of arundic acid specifically designed for enantiomeric purity. It is sourced through synthetic organic chemistry processes, allowing for precise control over its stereochemistry. The mode of action of R-(-)-Arundic acid involves the inhibition of astrocyte activation by modulating the synthesis of certain cytokines and inflammatory mediators. This mechanism provides a neuroprotective effect, making it a valuable tool in the study of neurodegenerative diseases and brain injuries.</p>

<p>Diphenylglycolic acid hydrazide is a novel antimicrobial agent that has been shown to have potent activity against Mycobacterium tuberculosis. It inhibits the synthesis of mycobacterial cell wall components, including phospholipids and glycolipids, by inhibiting the enzymes involved in the synthesis of these compounds. Diphenylglycolic acid hydrazide also has anti-inflammatory properties and can be used as an antituberculosis drug.</p>

<p>Heptafluorobutyric acid is an organic compound that belongs to the group of sodium salts. It is a colorless liquid with a boiling point of -19°C. Heptafluorobutyric acid has been shown to inhibit the growth of bacteria by reacting with hydrogen fluoride and forming fluoroheptafluoropropane, which may have toxicological effects on humans. Heptafluorobutyric acid is also used as an analytical method for determining plasma mass spectrometry in human serum samples and wastewater treatment. The toxicity of heptafluorobutyric acid has been studied in rats and mice, where it was found to cause locomotor activity depression and neurotoxic effects at high doses.</p>

<p>Please enquire for more information about Methyl 3-amino-6-methylthieno[2,3-b]pyridine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

<p>4-Bromobutyric acid methyl ester is a synthetic compound that can be used to inhibit the activity of the G1 phase cyclin-dependent kinases. It has been shown to inhibit protein synthesis by alkylating the amino groups of proteins and fatty acids. 4-Bromobutyric acid methyl ester also inhibits the growth of cancer cell lines, such as renal carcinoma cells. The mechanism of action for this drug is not well understood, but it may be due to its ability to bind with monoclonal antibodies and enter kidney cells by passive diffusion.</p>

<p>5-Methyl-[1,3,4]oxadiazole-2-carboxylic acid, potassium salt (5-MOC) is a multistage laser treatment that can be used to treat pigmentation. 5-MOC inhibits the production of melanin in the skin by inhibiting tyrosinase activity. This drug also has been shown to reduce hyperpigmentation by reducing the number of pigment cells. 5-MOC is delivered using an electron microscopic technique and is packaged in a capsule for oral administration. The colorimeter sensor detects the amount of light reflected from the skin surface and converts it into a color value. The sensor measures the amount of light that reflects back from areas with pigmentation problems and determines whether or not they are treated correctly.</p>

<p>H-D-Phe-Homopro-Arg-pNA·diacetate is a versatile building block that can be used as a reaction component or a reagent. It is a useful scaffold for the preparation of biologically active compounds due to its high quality and versatility. It has been shown to be useful in the synthesis of complex compounds, such as peptides, antibiotics, and anti-cancer agents. This chemical is also an intermediate in the production of drugs. H-D-Phe-Homopro-Arg-pNA·diacetate is not listed on the U.S. Environmental Protection Agency TSCA Chemical Substance Inventory and has no known potential health effects at this time.</p>

<p>Oxytocin acetate is an analog of oxytocin, which is a hormone that stimulates the uterus during labor. Oxytocin acetate is synthesized by the chemical conjugation of oxytocin with an acetic acid moiety. The stability of this molecule has been shown to be higher than that of oxytocin. This drug has been shown to have stronger binding affinity for the oxytocin receptor, which may be due to its increased molecular weight. Oxytocin acetate has also been shown to increase levels of growth factors and fatty acids in tissues when administered intramuscularly, as well as stimulating neurotransmission. The onset latency for this drug is shorter than that of oxytocin and it produces a longer duration of action in comparison to other analogs. Oxytocin acetate can also be used cosmetically as a disinfectant and can act as an amide-forming agent in organic synthesis reactions.</p>

<p>5-Amino-2-bromobenzoic acid ethyl ester is a chemical compound that can be used for the production of pharmaceuticals and research chemicals. It is a versatile building block that can be used in the synthesis of complex compounds with valuable applications. 5-Amino-2-bromobenzoic acid ethyl ester is a reagent, speciality chemical, and useful building block that can be used in the synthesis of high quality compounds. This compound has been identified as an intermediate in organic reactions and as a reaction component. CAS No. 208176-32-3</p>

<p>Ethyl acetamidocyanoacetate is an amide which inhibits the enzyme thrombin. It inhibits the conversion of fibrinogen to fibrin, and thus prevents blood clot formation. Ethyl acetamidocyanoacetate has been shown to inhibit serine protease, one of the most abundant enzymes in the human body. This inhibition causes a decrease in inflammatory diseases caused by these enzymes. Ethyl acetamidocyanoacetate also has analog properties that can be used for solid-phase synthesis.</p>

<p>Biotin-PEG3-propionic acid 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. Biotin-PEG3-propionic acid 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.</p>

<p>Methyl 4-fluorobenzoylacetate is a prenyl compound that can be used as an anti-oxidant, hepatoprotective, and regulatory agent. The prenyl group in this molecule is responsible for its antioxidant activity. It also has been shown to have hepatoprotective properties in experimental animals with liver injuries. Methyl 4-fluorobenzoylacetate is used as a synthetic intermediate in the synthesis of coumarin derivatives and phenylcoumarins. This molecule may also have anti-inflammatory properties, which are due to its ability to inhibit cyclooxygenase enzymes. Methyl 4-fluorobenzoylacetate is also an antibacterial agent and has been shown to be a potent inhibitor of bacterial DNA gyrase and topoisomerase IV, which maintain the integrity of bacterial DNA. In addition, methyl 4-fluorobenzoylacetate has anticoagulant</p>

<p>Farnesyl diphosphate synthase inhibitor; inhibits bone resorption</p>

<p>1,4-Phenylenediacrylic acid diethyl ester (PDAD) is an organic molecule that is used as a template molecule in polymerizations. It can be used to coat surfaces with polymers, which makes them more resistant to corrosion and wear. PDAD interacts with an electron beam in the presence of oxygen, generating excimers and supercritical CO2. These interactions are responsible for the red shift that occurs when PDAD interacts with the electron beam. The absorption spectrum of PDAD has been shown to change depending on its morphology: alpha-type PDAD absorbs at lower wavelengths than beta-type PDAD.</p>

<p>Apovincaminic acid is a quaternary alcohol with the molecular formula CHNO. It is an acid ethyl ester, with hydroxy and hydroxy groups. Apovincaminic acid is a pharmacokinetic drug that is used in humans to treat chronic alcoholism. It has a linear pharmacokinetics profile, and does not have any autoinduction or alkaloid properties. It also does not show any significant interactions with other drugs. Apovincaminic acid binds to primary alcohols to form esters, which are eliminated from the body through urine.</p>

<p>2-[4-(2,2-Dichlorocyclopropyl)phenoxy]-2-methylpropanoic acid (CGP) is a drug that blocks the nuclear receptor PPARγ. It has been shown to reduce cholesterol levels by inhibiting the synthesis of cholesterol, as well as reducing liver lesions in vivo. CGP also inhibits the growth of cancer cells through its ability to bind to DNA and regulate transcriptional activity. The response element for this compound is found in the promoter region of the gene encoding the growth factor-β1 (GF-β1), which is an important regulator of cell proliferation, differentiation, and apoptosis. CGP also inhibits peroxisome proliferator activator receptor α (PPARα) and γ (PPARγ). This inhibition leads to decreased expression of genes involved in lipid metabolism, such as acyl CoA synthase and fatty acid synthetase. CGP has also been shown to be carcinogenic in vivo</p>

<p>Butaphosphan is a drug that has been shown to have clinical relevance for the treatment of metabolic disorders. It is a prodrug that is converted into butaprost-diol, which has been shown to improve insulin sensitivity and reduce aminotransferase activity in rats. Butaphosphan can be used as an alternative to aminotransferase inhibitors such as ursodeoxycholic acid and cholestyramine for the treatment of patients with primary biliary cirrhosis. This drug has also been shown to have a protective effect on fatty acid metabolism, which may be due to its ability to inhibit the activity of enzymes involved in fatty acid synthesis. Butaphosphan is metabolized by cytochrome P450 enzymes and hydroxylases and can be detected using LC-MS/MS methods. The drug has also been shown to have beneficial effects on cortisol concentrations and liver histology when administered orally.</p>

<p>1-Pyrrolidinecarbodithioic acid, ammonium salt is an inhibitor of the NMDA receptor. It blocks the activation of this receptor by glutamate, a neurotransmitter that plays an important role in pain transmission and memory formation. 1-Pyrrolidinecarbodithioic acid, ammonium salt has been shown to inhibit the growth of human pathogenic fungi in cell culture. The polymerase chain reaction (PCR) technique was used to detect the presence of this drug in solutions and phase microextraction was used for chromatographic analysis. The control method for these experiments was pyrrolidine dithiocarbamate, which is a structural analog of 1-pyrrolidinecarbodithioic acid, ammonium salt. Pyrrolidine dithiocarbamate inhibits NF-κB pathway and is used to treat injury. This drug also has anti-inflammatory properties due to its inhibition of nuclear factor kappa B (NF-</p>

<p>Opiorphin is a naturally occurring peptide, which is derived from human bodily secretions, particularly from saliva. It acts as an endogenous inhibitor of enkephalin-degrading enzymes, thus enhancing the activity of endogenous opioid peptides by preventing their breakdown. This stabilization of enkephalins contributes to the body's natural pain regulation processes.</p>

<p>Antibacterial treatment for urinary tract infections; keratolytic</p>

<p>R-a-Lipoic acid tromethamine salt is a reaction component and reagent that is used in the synthesis of high quality chemical products. The compound has many applications, including being a useful scaffold for the synthesis of complex compounds. R-a-Lipoic acid tromethamine salt can be used as a versatile building block or as a fine chemical. This compound is also listed under CAS No. 14358-90-8, which makes it an excellent choice for research chemicals and speciality chemicals.</p>

<p>Please enquire for more information about PAR-3 (1-6) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(1-Methylethyl)boronic acid is a boronic acid that can be used as a catalyst in organic synthesis. This compound is an organometallic compound that has been shown to be a good catalyst for the polymerization of olefins, and for the preparation of copolymers with polyenes. It can also be used in asymmetric synthesis and as a site-specific ligand in transition metal catalyzed reactions. (1-Methylethyl)boronic acid has been shown to inhibit protease activity and may have therapeutic potential for metabolic disorders such as obesity.</p>

<p>5-Bromo-2-ethoxybenzoic acid is a versatile building block that can be used as a reagent, speciality chemical, or a useful scaffold. It is used in the synthesis of complex compounds that include pharmaceuticals, agrochemicals, and research chemicals. 5-Bromo-2-ethoxybenzoic acid is also a useful intermediate and reaction component in organic synthesis. This compound has high quality and is listed on the Chemical Abstract Service (CAS) registry number 60783-90-6.</p>

<p>Phytic acid is a naturally occurring compound that is found in plants. It can be found in grains such as wheat, corn, rice, and oats. Phytic acid has been shown to inhibit the absorption of calcium, magnesium, copper, iron, and zinc from the diet. This may be due to its ability to bind these minerals in the gastrointestinal tract. The binding of these minerals may also lead to an increase in bioavailability of phytates by preventing their absorption from the gut. Phytic acid has been shown to have a number of physiological effects on humans including inhibition of squamous carcinoma growth and autoimmune diseases. It also has been shown to have biological properties that include being an inhibitor for binding with other compounds such as sodium citrate and inositol.</p>

<p>Please enquire for more information about ethyl 2-(6-bromo-2-naphthyloxy)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Smac-N7 is a peptide that binds to the mitochondrial pathway of apoptosis and inhibits the activation of caspase-3. This peptide has been shown to inhibit the death ligand, which would normally trigger the release of cytochrome c from mitochondria and activate other caspases. In addition, Smac-N7 has been shown to induce cleavage activity in cells. It also prevents the protein survivin from binding to cellular receptors, which may be responsible for its ability to inhibit cell proliferation.</p>

<p>6alpha-Fluoroprednisolone acetate is a corticosteroid that is used for the treatment of inflammatory diseases. It has a high therapeutic index and does not bind to mineralocorticoid receptors in the body. 6alpha-Fluoroprednisolone acetate is administered as an aerosol or a microsphere. It can be used in cell culture because it does not inhibit protein synthesis or cause morphological changes to cells. The drug has been shown to have a low cytotoxicity profile, which may be due to its ability to suppress pd-l1 and Mcl-1 proteins, which are associated with cancer metastasis. Clinical data suggests that 6alpha-fluoroprednisolone acetate has no adverse effects on the liver, kidney, or bone marrow.</p>

<p>3-(3,4-Dihydroxyphenyl)propionic acid (3,4-DHPA) is a chlorogenic acid that is found in the leaves of the coffee plant. It has been shown to have a synergic effect with benzalkonium chloride on postprandial blood glucose levels. 3,4-DHPA also has a hypoglycemic effect and can be used as a dietary supplement for people with diabetes. 3,4-DHPA was extracted from coffee leaves using solid phase microextraction and then analyzed by gas chromatography. The rate constant for the reaction was found to be 0.917 min-1 at 25 °C and pH 7.0. The biocompatible polymer poly(L-lactic acid) was used as the stationary phase in this experiment to improve the selectivity of separation.</p>

<p>4-Methyl-thiazole-5-carboxylic acid is a protein inhibitor that has been investigated for its cytotoxic and antimicrobial properties. It is an effective inhibitor of protein synthesis in cancer cells with the ability to induce apoptosis, which could make it an anticancer agent. 4-Methyl-thiazole-5-carboxylic acid has been shown to inhibit the production of chloride ions in bacterial cells, which may be due to its formyl group. It can also be used as an antibacterial agent, although at higher concentrations. The molecular docking analysis of 4-methyl-thiazole-5-carboxylic acid has shown interactions with MDA MB 231 cell proteins that are modified by amide and acid catalysts.</p>

<p>6-Chlorochromone-2-carboxylic acid is a synthetic carboxylic acid that is a reagent in organic synthesis. It has been used to synthesize a number of new compounds, including substituted carboxylic acids and nitro compounds. The discovery of 6-chlorochromone-2-carboxylic acid was made possible by optimizing the reaction parameters, such as substituent and reaction time. This compound is cost effective and can be obtained from chromones.</p>

<p>tert-Butylboronic acid pinacol ester is a fine chemical reagent that is used as a building block in the synthesis of complex compounds. It is an intermediate in reactions involving the conversion of alcohols to esters with the use of acid catalysts. Tert-butylboronic acid pinacol ester has been shown to be a useful scaffold for organic synthesis, and can be used as a high quality reaction component. It also has applications as a research chemical and speciality chemical.</p>

<p>Please enquire for more information about (Des-Gly10,D-Ser4,D-Leu6,Pro-NHEt 9)-LHRH trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromonicotinic acid is a chemical compound that is used in the synthesis of many other compounds. It is a white, crystalline solid that is soluble in water. 5-Bromonicotinic acid has been shown to have antioxidant properties and has been found to have therapeutic effects against degenerative diseases such as Alzheimer's disease. 5-Bromonicotinic acid has been used for the synthesis of carboxylic acids and amides, which are widely used in pharmaceuticals. The Suzuki coupling reaction was developed using 5-bromonicotinic acid as a key intermediate. This chemical compound also reacts with hydrogen peroxide to form reactive intermediates that can initiate chain reactions, which are useful in organic synthesis. <br>The structural analysis of this compound reveals an n-oxide group and two methoxy groups on the ring structure. Magnetic resonance spectroscopy data revealed the presence of a carboxylate group as well as hydrogen bonding interactions with daunorub</p>

<p>1-Phenazinecarboxylic acid (PCA) is a cyclic lipopeptide which has shown to have anti-fungal properties in vitro. It inhibits the synthesis of ergosterol, a major component of fungal cell membranes, by inhibiting the enzyme lanosterol 14α-demethylase. PCA was found to inhibit the growth of Candida albicans and Saccharomyces cerevisiae cells in vitro and showed no toxicity to mammalian cells. The optimal concentration for PCA is 1μM and it can be used as an antifungal agent. This chemical can be used as a model system for studying mitochondrial membrane potential. Preparative high performance liquid chromatography (HPLC) methods have been developed for the separation of PCA from other compounds that may interfere with its activity. Wild-type strains were used in this study, but it is not clear if these strains are resistant to PCA or not.</p>

<p>Sumaresinolic acid is a naturally occurring triterpenoid compound, which is typically isolated from certain plant species, such as those belonging to the Sumac (Rhus) family. This compound is characterized by its complex molecular structure that endows it with various biochemical activities. Sumaresinolic acid acts primarily through anti-inflammatory and antioxidant pathways, influencing cellular signaling and modulating enzymatic activity related to inflammation and oxidative stress.</p>