Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Semapimod is an orally bioavailable small molecule drug candidate with anti-inflammatory and neuroprotective properties. Semapimod inhibits the activation of macrophages, which are a type of white blood cells that play a key role in inflammation. This drug also inhibits the production of proinflammatory cytokines, such as IL-1β and TNF-α. Semapimod has been shown to prevent the development of encephalomyelitis, which is a disease that causes inflammation in the brain and spinal cord, by preventing demyelination (the loss or damage of the myelin sheath) in mice. It has also been shown to be effective at treating patients with multiple sclerosis who have not responded to other treatments.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

1-Methyl-2-oxoimidazolidine-4-carboxylic acid is a metabolite of imidazolines. It is a chemical substance that is produced during the metabolism of many substances, including drugs and environmental contaminants. 1-Methyl-2-oxoimidazolidine-4-carboxylic acid exposure has been associated with an increased risk for neurodegenerative disease, such as Parkinson's disease. 1MICA can be measured in urine using liquid chromatography tandem mass spectrometry or gas chromatography methods.

Versatile small molecule scaffold

Versatile small molecule scaffold

3-(Hydroxymethyl)benzene-1,2-diol is an organic compound. The product is a colorless solid that has a molecular weight of 144.17 g/mol. 3-(Hydroxymethyl)benzene-1,2-diol reacts with metal surfaces and can be used in the synthesis of amides and amido groups. This product is reactive and acidic at high temperatures, but will not react with alcohols or amines. 3-(Hydroxymethyl)benzene-1,2-diol is also a reaction product from the synthesis of dopamine.

3,5-Dinitrobenzaldehyde is an experimental herbicide that has been shown to be effective in the control of weeds. 3,5-Dinitrobenzaldehyde is a protonated electrophilic species that reacts with a variety of electron-rich aromatic compounds by nucleophilic attack at the ortho position. The reaction with benzene, for example, yields phenyl trifluoride and benzenesulfonic acid. This molecule also reacts with chloride to form chlorobenzene and dinitrobenzene. 3,5-Dinitrobenzaldehyde has kinetic properties that are dependent on frequency and layeredness as well as kinetic and dihedral angles. It is also a catalytic reagent that undergoes rapid reaction at room temperature.

2-Phenyl-2,3-dihydropyridazin-3-one is a natural product that has been found in the human liver. It is also an organic solvent that is used in pest control to kill insects and spiders. 2-Phenyl-2,3-dihydropyridazin-3-one is a model system for studying cancer, as it has been shown to induce tumor formation in animals. It is also active against cervical cancer cells at low concentrations and induces apoptosis at high concentrations. This compound can be used as a potential therapeutic agent for the treatment of cancer in humans.

Versatile small molecule scaffold

N-benzylsulfamide is a synthetic cannabinoid derivative that is activated by hydrochloric acid in the stomach. It is an agonist of the cannabinoid receptor, which is found in the brain and nervous system. N-benzylsulfamide has been shown to produce muscle relaxation by increasing potassium efflux from muscle cells and decreasing calcium influx, leading to decreased contractions. N-benzylsulfamide has also been shown to have anti-inflammatory effects. It inhibits prostaglandin synthesis by inhibiting cyclooxygenase activity, thus reducing inflammation. The molecule also binds to benzodiazepine receptors and can be used as a treatment for seizures or convulsions.

4-Hydrazinothieno[2,3-d]pyrimidine is an anti-cancer drug that is activated by xylene. It is used in the treatment of bowel disease and cancer. 4-Hydrazinothieno[2,3-d]pyrimidine has been shown to have antibacterial properties against Gram-positive bacteria and may be effective as a topical agent for skin infections. This drug also has platelet activating properties, which are mediated through the p2y12 receptor. This receptor is involved in inflammatory bowel disease, as well as other tissues such as the brain and heart. 4-Hydrazinothieno[2,3-d]pyrimidine may be useful in treating cancer because it inhibits the production of TNF-α (tumour necrosis factor alpha) which leads to tumor growth inhibition.

(-)-Menthone is a plant metabolite that is found in peppermint and other mint oils. It can be synthesized by the action of caffeic acid esterase on menthol, which is also present in peppermint oil. (-)-Menthone has been shown to inhibit the enzyme activities of human pathogens such as Salmonella typhimurium, Escherichia coli, and Shigella sonnei. (-)-Menthone also has genotoxic activity and has been shown to cause chromosome breaks in human lymphocytes. The reaction mechanism of (-)-menthone involves an intramolecular hydrogen transfer from one carbon atom to another. X-ray diffraction data from (-)-menthone crystals show a phase transition temperature of approximately -5°C for the molecule.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Please enquire for more information about D-Myo-inositol 1-monophosphate dipotassium including the price, delivery time and more detailed product information at the technical inquiry form on this page

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

(6R)-6-(Hydroxymethyl)piperidin-2-one is an organic compound that is used as a chiral auxiliary in the asymmetric synthesis of enantiomerically pure compounds. It can be used to produce racemic mixtures of molecules with high enantiomeric excess, which are then separated by chromatography or crystallization. The (6R)-6-(hydroxymethyl)piperidin-2-one is obtained from the reaction between ethyl acetate and 2-aminoethanol. It has been shown to be trackable and its enantiomers can be identified by NMR spectroscopy.

Versatile small molecule scaffold

Versatile small molecule scaffold

1-Iodo-4-methoxy-2-methylbenzene (1IMMB) is an iodide which has been used as a precursor in the synthesis of carbonyl groups. This compound has also been shown to have high yields and mechanistic. The carbonyl group is located at the 1,3 positions and the methoxy group is located at the 2 position. This compound reacts with acetonitrile to form a naphthalene derivative. 1IMMB also reacts with an alcohol to form a cyclic ether with regiospecificity. It can also be used as a catalyst in the synthesis of unsymmetrical compounds that contain both carbonyl groups and alcohols.

Versatile small molecule scaffold

1-Cyclohexylpropyl carbamate is a diagnostic agent that can be used to measure inflammatory bowel disease. It is an analog of 1-cyclohexyl-2,2,2-trifluoroethyl carbamate. The compound is insoluble in water and must be reconstituted with a diluent prior to use. The particle size of the reconstituted compound can be adjusted by varying the concentration of the diluent. 1-Cyclohexylpropyl carbamate binds to herpes simplex virus type 2 (HSV-2) with high affinity and has been shown to inhibit HSV-2 replication in cell culture. Iontophoresis is a technique for delivering ionic molecules into tissue by means of an electric field. This technique has been shown to increase the concentration of 1-cyclohexylpropyl carbamate within cells infected with HSV-2.

Methyl 2,2-dimethyl-3-oxopropanoate is an enantioselective propionate with an asymmetric synthesis. The enantiomers of methyl 2,2-dimethyl-3-oxopropanoate are separated by the use of a chiral auxiliary. The enantioselective synthesis of propionates is achieved by crotylboration, a reaction that uses boron and crotyl alcohol as substrates. Methyl 2,2-dimethyl-3-oxopropanoate is an example of a polyketide synthesized via the polyketide pathway. This compound is used in the synthesis of halipeptin, which is an antibiotic that inhibits bacterial growth by inhibiting protein synthesis and cell division.

1-(4-Chlorophenyl)propan-1-ol is a ligand that binds to the active site of enzymes, such as chiral alcohol dehydrogenase and amino alcohol dehydrogenase. It was used to catalyze the synthesis of optically pure products in enantioselective reactions. 1-(4-Chlorophenyl)propan-1-ol has been shown to be an excellent precatalyst for asymmetric catalysis. It also reacts with amino alcohols to form optically pure products in an experiment involving the use of chiral azetidine.

2-(4-Methoxybenzyloxy)ethanol is a reversible and efficient catalyst for the dehydration of adenine. It is used in chemical synthesis to make 2,4-dibromoacetic acid. This compound has also been shown to be an effective dehydratase for clostridium.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

N-[4-Chloro-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide is a white crystalline solid that belongs to the class of chains. This compound has hydrogen bonds and pivaloyl groups. It is also torsion and has a benzene ring. N-[4-Chloro-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide is used in the synthesis of pharmaceuticals.

1-(2-Bromoethyl)naphthalene is a heterocyclic compound with two bromine atoms attached to the same carbon atom. It has two stereoisomers, one of which can be synthesized from phenacyl and the other from diketone. It is used in organic synthesis as a reactive intermediate for the alkylation of various substrates. The rate of reactivity is dependent on the electron donating ability of the substrate, with electron-donating groups resulting in faster reaction rates. This product has been shown to undergo enthalpic transfer reactions at room temperature, and chemoselective alkylation reactions at elevated temperatures.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold