Building Blocks

<p>Versatile small molecule scaffold</p>

<p>3-(Trifluoromethyl)phenylacetone is a chiral iminium-type organocatalyst that is used in asymmetric organic reactions. This compound has been shown to be effective for the synthesis of chiral amines and hydroxyl groups, as well as biotransformations. 3-(Trifluoromethyl)phenylacetone binds to substrates through hydrogen bonding, steric interactions, and electrostatic interactions. It also has a high affinity for hydroxides and isosteres. 3-(Trifluoromethyl)phenylacetone can be used as an alternative to L-proline in certain biotransformations because it binds more tightly to the enzyme than L-proline does.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 7-Bromo-5-methoxyindole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Succinylsulfathiazole is a sulfa drug that has antimicrobial activity. It is a structural analogue of sulfanilamide, which is an antibiotic used to treat infectious diseases. Sulfa drugs are structurally related to the amino acid pantothenic acid and have been shown to have beneficial effects in animal models for bowel disease, autoimmune diseases, and other conditions. Succinylsulfathiazole has been shown to inhibit the growth of Aerobacter aerogenes and other bacteria by binding to their cell wall and interfering with synthesis of DNA. Succinylsulfathiazole has been shown to inhibit the growth of Aerobacter aerogenes and other bacteria by binding to their cell wall and interfering with synthesis of DNA.</p>

<p>Sarcosine methyl ester hydrochloride is a pharmaceutical drug that inhibits the production of inosine monophosphate (IMP) and guanosine monophosphate (GMP). It is thought to work by interfering with the synthesis of nucleotides. Sarcosine methyl ester hydrochloride has been shown to inhibit tumour growth in solid tumours. It also has pharmacokinetic properties that include a low volume of distribution, high protein binding, and low clearance rate.</p>

<p>Styrene-divinylbenzene sulfonated copolymer also called Dowex 50W 8X hydrogen form, strongly acidic resin, is a fine mesh spherical ion exchange resin made from a microporous styrene / divinylbenzene (DVB) co-polymer with a sulfonic acid group. Styrene-divinylbenzene sulfonated copolymers are used in fine chemical and pharmaceutical column separations.</p>

<p>This is a chemical intermediate with the CAS No. 937598-86-2. It is a versatile building block that can be used to synthesize new drugs and pharmaceuticals, as well as other fine chemicals. This compound has been shown to be useful in reactions such as the formation of heterocycles, the synthesis of complex compounds, and the preparation of research chemicals. The high quality of this chemical makes it suitable for use in many different types of reactions.</p>

<p>9-Ethylguanine is a protonated guanine derivative that has significant cytotoxicity. It is an analog of the natural nucleobase guanosine and is structurally similar to the group P2 purine base, hypoxanthine. 9-Ethylguanine specifically binds with nitrogen atoms in DNA, forming hydrogen bonds with adjacent bases. The compound has low potency and therefore must be administered at high doses for it to be effective. 9-Ethylguanine has been shown to have anticancer activity against cervical cancer cells in cell cultures, but no biological studies have been conducted on other cancer types.</p>

<p>Component in some dental cements</p>

<p>3-Ethoxy-1,2,4-dithiazolidine-5-one (3ED) is a small molecule that has been shown to have potent antitumor activity against multiple tumor types. It is a selective inhibitor of epidermal growth factor receptor (EGFR) that can be used in combination with chemotherapy or radiation therapy. 3ED has also been shown to inhibit the growth of bladder cancer cells and cervical cancer cells by affecting the EGFR pathway. In addition, 3ED inhibits the proliferation of human urothelial carcinoma cells through its inhibition of the EGFR pathway and can be used as an adjuvant treatment for patients with nonmetastatic bladder cancer and patients with locally advanced or metastatic urothelial carcinoma. 3ED also inhibits creatine kinase, which is an enzyme important in maintaining the health of the detrusor muscle in the urinary bladder and could potentially be used to treat overactive bladder disease.</p>

<p>5-Ethylthio-1H-tetrazole is an angiogenic inhibitor. It has been shown to inhibit the TLR2 and TLR4 pathways by binding to toll-like receptor-inhibitory proteins, which results in the inhibition of the intracellular signaling cascade. This compound also inhibits the expression of inflammatory cytokines and chemokines that are involved in bowel disease. 5-Ethylthio-1H-tetrazole has been shown to be a potent activator of PPARγ, which is a nuclear receptor that regulates the expression of genes important for lipid metabolism and cell proliferation. 5-Ethylthio-1H-tetrazole has also been shown to have antiinflammatory activity through inhibition of cyclooxygenase 2 (COX2) enzyme activity.</p>

<p>2-Ethylpyridine is a chemical compound that can be derived from sodium succinate, 2-ethylpyridine, and trifluoroacetic acid. It has been shown to have biological properties such as the inhibition of mitochondrial membrane potential, which is the driving force for ATP synthesis in mitochondria. This drug also inhibits the production of hydrogen peroxide and nitric oxide by reacting with hydrochloric acid or nitrogen atoms. 2-Ethylpyridine can be used as a solid catalyst for reactions involving hydrogen bond formation or intermolecular hydrogen bond formation. 2-Ethylpyridine reacts with protocatechuic acid to form an intramolecular hydrogen bond and a group p2 type of reaction mechanism.</p>

<p>1,2-Epoxy-5-cyclooctene is a cyclic epoxide that undergoes ring opening with the addition of a nucleophile. This reaction is catalyzed by a bromonium ion, which acts as the electrophile. The product of this reaction is 2-hydroxy-1,2-epoxycyclohexane. 1,2-Epoxy-5-cyclooctene has been used in synthesizing various compounds such as monoepoxides and hydrosilanes. It can also be used to produce compounds that are difficult to access through other methods. 1,2-Epoxy-5-cyclooctene has been studied using x-ray crystallography and conformational analysis.</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl propiolate is a halide that is structurally related to the alkylating agent trifluoroacetic acid. Ethyl propiolate inhibits the activity of several enzymes including phosphofructokinase and pyruvate kinase, which are important for energy metabolism in cells. It also has been shown to have beneficial effects on autoimmune diseases such as lupus erythematosus. The mechanism of action of ethyl propiolate is due to its ability to react with activated oxygen and form an intramolecular hydrogen bond with carbon atoms in the substrate molecule. The reaction between ethyl propiolate and diethyl ketomalonate results in the formation of diethyl 2-propiolate, which can then be hydrolyzed by water into acetaldehyde and diethyl ketomalonate.</p>

<p>5-Amino-2-nitrobenzoic acid is a drug that has been shown to inhibit the activity of proteases. It has been used to detect the presence of protease activity in urine samples, as well as to study the inhibition of protease activity by other drugs. 5-Amino-2-nitrobenzoic acid is an inhibitor of chymotrypsin, trypsin, and elastase. This drug has been shown to be effective in inhibiting these enzymes at low concentrations, with a detection sensitivity of approximately 0.1 μM. 5-Amino-2-nitrobenzoic acid inhibits the growth of bacteria by binding to them and preventing protein synthesis. The compound also inhibits the enzyme dihydrolipoamide dehydrogenase in mitochondria, which is required for cellular respiration and energy production.</p>

<p>2-Bromo-5-chloropyridine is a synthetic compound that acts as an inhibitor of tyrosine kinase. It binds to the active site of the enzyme and blocks its activity. This inhibits protein phosphorylation, which is essential for cell signaling. The mechanism of this inhibition is similar to that of piperidine and diethanolamine, which are competitive inhibitors of the enzyme. 2-Bromo-5-chloropyridine also reacts with chloride ion to give bipyridines, which have been shown to inhibit cholesterol ester transfer protein (CETP) by binding covalently to the enzyme's active site. 2-Bromo-5-chloropyridine has been shown to be effective in inhibiting tumor growth in mice when given orally at doses ranging from 10 mg/kg to 30 mg/kg daily.<br>2-Bromo-5-chloropyridine can also be used as a starting material for</p>

<p>Indole-4-carboxylic acid methyl ester is a fine chemical that is used as a building block in the synthesis of complex compounds. It can be used as a reagent, speciality chemical, or intermediate, and it has versatile applications in the synthesis of pharmaceuticals and dyes. Indole-4-carboxylic acid methyl ester has been shown to react with alcohols to form ketones, which are useful scaffolds for organic chemistry. It can also be used as a reaction component for the synthesis of other compounds.</p>

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