Carboxylic Acids

<p>Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester is a fatty acid analog that has antimicrobial properties. It is used in the treatment of bone cancer, and can be used to diagnose and treat other diseases such as glomerular filtration rate, receptor binding, and malonic acid. Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester binds to receptors on cells, which leads to an increase in the amount of monoamine neurotransmitters released by the cells.</p>

<p>Please enquire for more information about Ethyl 3-(difluoromethyl)-1H-pyrazole-5-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Aminoguanidine is a selective inhibitor of the enzyme succinic dehydrogenase, which catalyzes the conversion of succinic acid to fumarate. Aminoguanidine is used in the treatment of diabetic complications and other conditions that result from high levels of blood glucose in order to lower the levels of blood sugar. The drug is administered orally or intravenously as aminoguanidine hydrochloride, which is converted to aminoguanidine in the body. Aminoguanidine can also be synthesized by reacting succinic anhydride with guanidine hydrochloride in a regioselective reaction. This synthesis yields quantitatively aminoguanidine, with little or no formation of guanidine. The product can be purified by washing with alkali and recrystallizing it from water. X-ray diffraction studies have shown that aminoguanidine hydrochloride exists as zwitterions in solution at physiological pH values.</p>

<p>Please enquire for more information about Diphenylsulfone-3,3'-disulfonic Acid Disodium Salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2,5-Bis(2,2,2-trifluoroethoxy)benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(Chloromethyl)benzoic acid (CMBA) is a reactive chemical that can be used as an oxidant or a carbanion. CMBA is activated by sulfinyl, alicyclic, and sulfoxides, which are organic compounds with one or more sulfur atoms. These reactions may be either alkylation or condensation reactions. The activated CMBA can then react with chlorine to form chlorinated products. This reaction can be catalyzed by low energy sources, such as light or heat.</p>

<p>Please enquire for more information about Ac-Lys(Ac)-D-Ala-D-lactic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (1-Isopropyl-1H-indol-3-yl)acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-{[1-(tert-Butoxycarbonyl)azetidin-3-yl]oxy}benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tyrosinase protein:<br>Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV) is a human tyrosinase-derived (369-377) peptide by posttranslational conversion of the sequence YMNGTMSQV. Tyrosinase is an oxidase membrane-bound protein. Tyrosinase play a key role in the melanin synthesis pathway. Tyrosinase is presented on the surface of HLA-A*02:01 melanomas and also expressed in melanocytes. Tyrosinase has been still suggested to be a tumor antigen and might be implicated in improvement of immunotherapeutic strategies such as for efficient anticancer vaccine development.<br>Applications of Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV):<br>Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV) is used to stimulate specific cytotoxic T lymphocytes (CTL) in PBMCs and then to analyze CTL response especially the cytokine production by ELISPOT assay. Peptide Tyrosinase (Asp371) – HLA-A*0201 (YMDGTMSQV) is also involved in experimental therapies of metastatic melanoma by allogeneic hematopoietic stem cell transplantation. In fact, cytotoxic T cells were generated from peripherical blood mononuclear cells (PBMCs) of HLA-A*02:01 healthy donors after being stimulated by injection of Asp371 antigen (2). This strategy raises issues which concern the graft versus tumor (GvT) effect and graft versus host disease (GvHD).</p>

<p>Please enquire for more information about tert-Butyl azetidine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dehydrotumulosic acid is a natural product that has been shown to inhibit the activity of P-glycoprotein (P-gp) in vitro. It also inhibits tumor growth and metastasis by inducing apoptosis in HL60 cells, as well as inhibiting the proliferation of human leukemia cells. Dehydrotumulosic acid is not toxic to normal cells because it does not induce apoptosis in these cells. The effect on tumor cell proliferation was found with an acetate extract of dehydrotumulosic acid and matrix effects were observed by use of poria, which may lead to a more accurate analytical method. Pharmacokinetic studies have been done with dehydrotumulosic acid, but no toxicity or adverse effects have been reported for this drug. This compound is being investigated for its potential use in cancer therapy and treatment.</p>

<p>Please enquire for more information about 6-Deschloro-4-chloro cyproterone acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethyl 4-chloroacetoacetate is a chiral organic compound that is synthesized by the asymmetric synthesis of ethyl chloroacetate. This reaction is performed in an organic solution, using sodium salts as the solvent. The expression plasmid and logarithmic growth phase are needed for the enzyme catalysis and stereoselective reactions. The reaction solution is recombined with hydrochloric acid and chiral compound to produce high yields of ethyl 4-chloroacetoacetate.</p>

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<p>N-Hexylboronic acid is an organometallic compound that has been used as a model system to study the catalytic mechanism of the Suzuki coupling reaction. It has also been shown to be a substrate film for use in the suzuki coupling reaction when combined with Raney nickel, which can be used to synthesize organic compounds. N-Hexylboronic acid has been shown to inhibit the activity of pancreatic lipase, but not cholesterol esterase or cholesterol ester hydrolase. The skeleton of this molecule is made up of six carbon atoms and one boron atom. Hydrogen chloride and aliphatic hydrocarbons are inhibitors of N-hexylboronic acid.</p>

<p>2-Methylnicotinic acid methyl ester is a synthetic chemical compound that belongs to the isomer family. It has been used in the synthesis of cocaine and isomers, as well as in the modification of drugs. 2-Methylnicotinic acid methyl ester can be synthesised from 2-methylpyridine and formaldehyde via the method of methylmagnesium iodide. 2-Methylnicotinic acid methyl ester has been shown to be a potent inhibitor of human platelet aggregation, which may be due to its structural similarity to nicotine.</p>

<p>Ethyl (2,3,4,5-tetrafluorobenzoyl)acetate is a new oxazine derivative that inhibits bacterial growth by binding to the DNA gyrase and topoisomerase IV. It also exhibits antibacterial activity against Gram-positive bacteria such as methicillin-resistant Staphylococcus aureus (MRSA). This compound is an analog of the quinolone antibacterials. The most efficient example of this class of compounds is ofloxacin.</p>

<p>Please enquire for more information about 4-(4-Bromophenoxy)butanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Ketobutyric acid is a chemical compound that is an intermediate in the metabolism of amino acids. It can be synthesized from malic acid and glutamic acid by asymmetric synthesis. 2-Ketobutyric acid inhibits the production of ATP, leading to metabolic inhibition. Sprague-Dawley rats were used to prove this theory. 2-Ketobutyric acid has also been shown to inhibit insulin resistance and cell culture. Hydrogen bonds between 2-ketobutyric acid and the enzyme glutamate dehydrogenase are thought to be responsible for this effect on glucose uptake and conversion into energy.</p>