Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Bromo-5-methyl-1H-imidazo[4,5-b]pyridine is a stabilizer that is used to protect polymers from degradation by light or heat. It can also be used to give plastics a yellow color.</p>

<p>Versatile small molecule scaffold</p>

<p>Tetramethyl-1,3-cyclobutanediol is a diacid that can be used as a monomer for the production of polyesters. It has conformational properties that are different from other diols. Tetramethyl-1,3-cyclobutanediol is soluble in hydrochloric acid and reacts with coatings containing dibutyltin oxide to produce residues. This chemical also reacts with copper oxide, resulting in the formation of copper cyclohexanol and dibutyltin oxide. Tetramethyl-1,3-cyclobutanediol is able to react with carboxylic acids to form esters. This compound has been shown to be employed in the synthesis of polycarboxylic acids such as adipic acid and sebacic acid. Tetramethyl-1,3-cyclobutanediol has been used in the production of polyester resins by reacting with ethylene glycol and tere</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloro-4-iodopyridin-2-amine is a chemical compound with the formula CHI. It is a white solid that can be used in evaluating cross-coupling reactions, such as the coupling of an alkyne with a chlorine atom. This chemical has been shown to react well with chlorination reagents and to form substituted cyanides. The nature of the substituent on the chlorine atom determines its regioselectivity and reactivity, making this compound useful for regiocontrolled synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>PB-22 is a synthetic cannabinoid, which can be classified as a CB1 receptor agonist. It is one of the many cannabinoids that have been created in an attempt to circumvent drug laws by creating compounds that are similar to those found in cannabis but have different chemical structures. PB-22 has shown to increase locomotor activity and stimulate the cb1 receptor in mice. Magnetic resonance spectroscopy (MRS) and assays were used to determine the binding affinity of PB-22 for the CB1 receptor. The MRS data showed that PB-22 bound with high affinity to the CB1 receptor and had a lower affinity for CB2 receptors. This suggests that PB-22 may be more potent than other synthetic cannabinoids, such as JWH-018 and CP 55,940, which bind better with CB2 receptors than CB1 receptors.<br>PB-22 is an analog of JWH-073 and has been shown to have a stronger effect on locomotor activity than JWH</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxylate is a heterocyclic compound that is used as a reagent in organic synthesis. It is a polyfunctionalized heterocycle that contains an ethyl ester and an acid ethyl ester moiety. The compound can be prepared by the reaction of thiophene with nitromethane and ethyl iodide followed by hydrolysis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-({5,6-Dimethylthieno[2,3-d]pyrimidin-4-yl}sulfanyl)benzoic acid is a synthetic nonpeptide compound that belongs to the group of ligands. This inhibitor binds to nicotinic acetylcholine receptors and inhibits their activity. 2-({5,6-Dimethylthieno[2,3-d]pyrimidin-4-yl}sulfanyl)benzoic acid has been shown to be a potent activator of these receptors. This compound also inhibits voltage dependent potassium channels and calcium channels.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Bromocyclopent-2-en-1-one is an organic compound that belongs to the group of cycloalkenones. It is a methyl ester with a cyclopentane backbone and a ketone group at the end of the molecule. 3-Bromocyclopent-2-en-1-one is synthesized by a cross-coupling reaction between zinc chloride and 3,4,5,6,7,8,9,10,11 bromodecane. The product can be isolated in crystalline form as well as in yields up to 90%. The product has been shown to act as an analog for prostaglandin E2.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methyl-4-oxo-4-phenylbutanenitrile is a chemical compound that is used in the synthesis of pharmaceuticals. It can be obtained by reacting an organic base with an organic acid. This reaction takes place in a reaction vessel and requires an inorganic base and inorganic reagents. The process also requires ethyl cyanoacetate as the starting material and produces 2-methyl-4-oxo-4-phenylbutanenitrile as the product. The use of this chemical has been linked to environmental pollution, so it should never be released into the environment or come into contact with water.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Pyridinecarboxylic Acid Ethyl Ester is a compound that belongs to the group of pyridinecarboxylic acids. It is a metabolite of nicotinamide, which is converted to 4-pyridinecarboxylic acid ethyl ester by esterases in the intestine. Nicotinamide is an important component of the vitamin B3 and has been shown to be effective for treating autoimmune diseases such as rheumatoid arthritis. 4-Pyridinecarboxylic Acid Ethyl Ester may have similar effects on inflammatory bowel disease and alopecia areata. The reaction mechanism of this compound has not been elucidated, but it has been shown to inhibit amyloid protein production in rat intestines. Hydroxyl groups on the side chain likely play a role in hydrogen bonding interactions with receptors in inflammatory bowel disease and alopecia areata.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Methylbenzo[b]thiophene-2-carboxylic acid (MBTCA) is a heterocyclic compound that is an intermediate in the synthesis of 3-methylthiophene-2-carboxylic acid, a precursor to other drugs. MBTCA is an aerobic, nonpolar compound that has shown antimicrobial activity against some bacteria and fungi. It also has been shown to have practicality as a biomolecular probe for methyl groups in organic solvents. MBTCA can be synthesized by nitration of benzene in the presence of sulfur and sulfoxides. This reaction produces nitrobenzene, which can then be oxidized by potassium permanganate or hydrogen peroxide to produce MBTCA. The most common isomer of MBTCA is 2-(3,5-dimethoxybenzylidene)tetrahydrofuran, with three methyl groups on the</p>

<p>Please enquire for more information about 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-3-oxo-5-isobenzofurancarbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Phenoxyaniline is a nitro compound that can be converted to the corresponding palladium complexes. It is an inhibitor of the acylation reaction, which is a type of chemical reaction in which an organic molecule reacts with an acid. The inhibition of this reaction has been shown to have an effect on heart disease, specifically by lowering cholesterol levels and reducing atherosclerosis. 2-Phenoxyaniline has also been shown to inhibit the activation energy for electron transfer reactions, making it useful as a catalyst in analytical methods. 2-Phenoxyaniline also undergoes vibrational spectroscopy when exposed to liquid chromatography and other analytical methods.</p>

<p>Versatile small molecule scaffold</p>

<p>2,2',4,4'-tetrahydroxybenzophenone is a hydroxylated benzophenone that has immunomodulatory effects. It binds to the receptor in the immune system and can cause an increase in cytokine production. 2,2',4,4'-tetrahydroxybenzophenone is cytotoxic and has significant toxicity in vitro. The molecule has been shown to disrupt mitochondrial membrane potential. This may be due to its ability to form hydrogen bonds with molecules on the mitochondrial membrane. 2,2',4,4'-tetrahydroxybenzophenone also modulates transcriptional regulation of genes involved in cell proliferation and apoptosis. The drug is detectable at low levels by mass spectrometry and is not known to have any toxicological effects.END&gt;&gt;</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Acetylbenzoic acid is a functional molecule that contains an acetyl group. It can form hydrogen bonds with other molecules and has been shown to induce apoptosis in cells. The reaction products of 2-acetylbenzoic acid are malonic acid, acetylsalicylic acid, and 2-benzoylbenzoic acid. These three compounds are made by the addition of hydrogen or hydroxide to the molecule 2-acetylbenzoic acid. The molecule has two functional groups: a carbonyl group and an acetyl group. The chemical structure of this molecule can be seen in the figure below.<br>2-Acetylbenzoic Acid</p>

<p>2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about H-Ser-Ala-Glu-Glu-Tyr-Glu-Tyr-Pro-Ser OH trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Givinostat hydrochloride is a research chemical that has shown potential in various fields. It is a molybdenum-based compound that has been studied for its effects on dopamine release and hydrogen evolution. Givinostat hydrochloride has also been investigated as an osteoclast inhibitor, which may be beneficial in the treatment of bone-related disorders such as osteoporosis. Additionally, it has shown promise as a retinoid and calpain inhibitor, suggesting its potential use in dermatological conditions and neurodegenerative diseases. The compound contains fluorine atoms, making it suitable for imaging studies using fluorine MRI techniques. Givinostat hydrochloride has been tested on MDA-MB-231 cells and has shown inhibitory effects on their growth, indicating its potential as an anticancer agent.</p>