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

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

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

Trans-4-Cyclohexyl-L-proline is an enolate that is used as a pharmaceutical intermediate. It has been shown to be effective in the synthesis of fosinopril sodium, a drug used for the treatment of hypertension and heart failure. Trans-4-Cyclohexyl-L-proline also has shown potential use as an antimicrobial agent. It can act as a nucleophilic agent, reacting with chloride ions to form an alkylating agent. The chlorinated product can undergo hydrolysis by hydrochloric acid to yield c1-4 alkyl chloride and hydrogen chloride.

Versatile small molecule scaffold

2-Chloro-1-(1H-indol-5-yl)ethanone is an aminated product that can be synthesized by the reaction of nitromethane and aluminium chloride. This product is a side-chain condensation product of indoline and chloroacetyl chloride. The product yields are about 68%.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

5-(Benzyloxy)pentanal is a quinoline derivative that inhibits the enzyme reverse transcriptase, which is an extracellular enzyme that synthesizes DNA from RNA. It also inhibits nucleotide synthesis and interacts with other enzymes such as DNA polymerase. 5-(Benzyloxy)pentanal has been shown to inhibit tumor growth by inhibiting the production of cancer-related proteins. The compound was synthesized in a stereoselective manner by reacting piperidine with allyl bromide followed by oxidation to form the corresponding aldehyde. This method was used to produce an enantiomerically pure compound, which exhibits inhibitory activity against HIV-1 integrase.

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

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Chroman-2-ylmethanamine is an indole alkaloid that has been shown to have high affinity for the 5-HT1A receptor. It also has neuroprotective properties and prevents apoptotic cell death in a dose-dependent manner. This drug has also been shown to reduce extracellular glutamate levels in brain tissue and inhibit dopamine release. Chroman-2-ylmethanamine is an agonist at the 5-HT1A receptor, which causes it to inhibit extracellular acidification by hydrochloric acid. It also inhibits glutamate release by binding to the AMPA receptor, which leads to its anti-ischemic effects.

2-Cinnamoylthiophene is a synthetic compound that has been shown to have an apoptotic effect on cancer cells in culture. It is produced by the reaction of 2-aminothiophenol with acetic anhydride and cinnamic acid. The molecular structure of 2-cinnamoylthiophene has been determined using nuclear magnetic resonance (NMR) spectroscopy and quantum chemical calculations. This molecule is oxidized by hydrogen peroxide to generate reactive intermediates, which then react with DNA bases to form DNA adducts. These adducts are detected by the tetrazolium dye MTT, which is used as a cell viability assay. 2-Cinnamoylthiophene also contains functional groups that can be used for further study.

3-Chloro-5-methylbenzene-1,2-diol is an organic compound that is used as a substrate in assays to measure the activity of enzymes that oxidize it. This compound has been shown to be mineralized by a number of bacterial strains, and its formation rate has been shown to be dependent on the presence of oxygen. 3-Chloro-5-methylbenzene-1,2-diol can also be dechlorinated by a number of bacterial strains and its gene product (3CMB) has been identified in Bacillus subtilis. Magnetic resonance analysis revealed that 3CMB is produced from 3CMB by a dehydrogenase enzyme in the active site. The enzyme is homologous to the dehydrogenases found in Escherichia coli and Pseudomonas aeruginosa.

Versatile small molecule scaffold

2-Chloro-3-nitroaniline is a trifluoroacetic acid derivative that has been synthesized from anilines. This chemical is used in the synthesis of quinoline derivatives and other synthetic intermediates. It can be used as a ligand to form metal complexes with metals such as copper, lead, or zinc. 2-Chloro-3-nitroaniline is also used as a chromatographic chiral stationary phase or to generate solutes with specific functional groups for use in chemical interactions.

Versatile small molecule scaffold

Versatile small molecule scaffold

Ethyl trimethylacetate is a solvent that is used in analytical chemistry. It has been shown to be a strong inhibitor of nerve cells, which may be due to its ability to form hydrogen bonds with the cell membrane or carbonyl groups that disrupt the cell membrane. Ethyl trimethylacetate also inhibits cancer cell growth by inhibiting the production of fatty acids and glycol ethers. The deuterium isotope effect is observed when ethyl trimethylacetate is used as a solvent for chemical structures that contain deuterium atoms.

2-(2,3,4-Trimethoxyphenyl)ethan-1-amine is a drug with anti-diabetic properties that belongs to the class of drugs called aminoguanidine derivatives. It is an optically active compound and has an asymmetric carbon atom. The active enantiomer is 2-(2,3,4-trimethoxyphenyl)ethanamine and the inactive enantiomer is 2-(2,3,4-trimethoxyphenyl)ethylamine. This drug inhibits the activity of aldose reductase which converts glucose into sorbitol. Sorbitol accumulation then leads to diabetic complications such as cataracts and nerve damage. 2-(2,3,4-Trimethoxyphenyl)ethan-1-amine also inhibits platelet aggregation and thrombus formation by inhibiting the release of serotonin from platelets and preventing platelet adhesion to

Versatile small molecule scaffold

Versatile small molecule scaffold

2-Ethyl-p-cresol is an ester compound that is soluble in water. It has a cycloalkyl group and aryl group and a pyrogallol, phloroglucinol, and resorcinol moiety. 2-Ethyl-p-cresol is resistant to heat and acidic conditions. It also has an ester function, which makes it soluble in water.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

1,1-(9H-carbazole-3,6-diyl)diethanone is an aromatic compound with a molecular formula of C12H10N2O that belongs to the class of enol ethers. It can be used as a framework for the synthesis of other compounds. The acylation reaction is catalyzed by a transfer catalyst and carried out in dioxane at room temperature. After filtration and washing with deionized water, it is then dried under vacuum to yield the product. Friedel-Crafts acylation or a metal salt may be used during this process. 1,1-(9H-carbazole-3,6-diyl)diethanone has also been shown to act as a ligand for transition metals such as copper and zinc in certain reactions.

Versatile small molecule scaffold

N-Methyl-4-phenylaniline (NMP) is a fatty acid inhibitor that can be used to treat hepatitis. It is an inhibitor of the enzyme known as N-hydroxy-4-aminobiphenyl amidohydrolase, which is involved in the second step of the synthesis of arachidonic acid, a precursor of prostaglandins. The inhibition of this enzyme reduces the production of prostaglandin E2 and other eicosanoids that are important for inflammation. NMP has also been shown to have potential mechanism for treating primary sclerosing cholangitis (PSC). This drug binds with bile salts in the intestines and prevents their reabsorption back into circulation. This leads to increased bile salt concentrations in the liver, which may help reduce inflammation and fibrosis in PSC.

1-Indanone oxime is a sulfonylating agent that reacts with primary amines to produce sulfonylureas. It is a model system for the study of chemical diversity and isozymes. 1-Indanone oxime has been shown to be an efficient synthetic agent for preparing hydroxyl compounds and oxime derivatives, and can be used to synthesize chlorides, secondary amines, and tertiary amines. The reaction time required for this chemical is shorter than other reagents such as sodium hypochlorite or nitrous acid. The reaction solution can be used in the synthesis of hydrochloric acid, nitric acid, chloroform, and vinyl chloride. 1-Indanone oxime has also been used to produce amino acids such as L-tryptophan or L-tyrosine.

N-Carbamoylmaleimide is a maleimide that reacts with amides to form N-hydroxysuccinimidyl esters. It is used as an alternative to succinimidyl esters for the synthesis of cross-linked polymers. The reaction proceeds via a cyclic intermediate, and is catalyzed by metal ions such as iron. The product is stable at room temperature, but decomposes at elevated temperatures. N-Carbamoylmaleimide can be synthesized by the reaction of methylbenzene with ammonia in the presence of sodium hydroxide, followed by dehydration with sulfuric acid. This compound can also be synthesized using a solid phase synthesis technique, which involves reacting an amine with vinyl ether and dimethylformamide in the presence of a carbonylating agent such as dicyclohexylcarbodiimide (DCC).

1-Chloroisoquinolin-4-ol is a phenylpyrimidine with anti-inflammatory properties. It is used in the treatment of sensitivity and mediated diseases, such as osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. 1-Chloroisoquinolin-4-ol inhibits the enzymatic activity of matrix metalloproteinases (MMPs), which are enzymes that break down collagen and other proteins in the body. The inhibition of MMPs by 1-chloroisoquinolin-4-ol leads to reduced inflammation and pain. This compound is also an effective inhibitor of the activities of chloride channels involved in acid secretion by cells in the stomach lining, thus inhibiting acid production. 1-Chloroisoquinolin-4-ol has been shown to have anticholesterolemic effects on liver cells due to its ability to inhibit cholesterol synthesis through inhibition of HMG CoA

Versatile small molecule scaffold

1-Phenylpentane-2,4-dione is a molecule that absorbs light. It has been shown to be an efficient absorber of solar radiation and has the potential to be used in photovoltaic devices. 1-Phenylpentane-2,4-dione can be used as an electron donor in polymer solar cells because it is able to act as both a chelate and a light absorber. 1-Phenylpentane-2,4-dione can also be used in acetone peroxide based solar cells because it is able to absorb light efficiently. In addition, 1-phenylpentane-2,4-dione may have use as an optical element for positioning systems such as telescopes or cameras.

N1-Cyclohexylpropane-1,3-diamine is a potent compound that has been shown to inhibit cholesterol synthesis and mitochondrial membrane potential. This drug also has anti-cancer effects and can be used for the treatment of cancers in which nuclear DNA is affected by light emission. N1-Cyclohexylpropane-1,3-diamine has been shown to have physiological activities such as cell growth inhibition, matrix effect, and intracellular hydrogen release. The drug binds to the enzyme activity site with a coordination geometry that is similar to other inhibitors of cholesterol synthesis. N1-Cyclohexylpropane-1,3-diamine was crystallized from methanol at room temperature and its molecular structure was determined by X-ray diffraction techniques.

Versatile small molecule scaffold

Versatile small molecule scaffold

1-(Isocyanomethyl)-2-methoxybenzene is a reactive compound that can be used to make other chemicals. It is a member of the homodinuclear class of compounds, which means that it has only one type of atom in each molecule. This compound can be used to make polymers and plastics, as well as other chemicals. The reactivity of this compound is due to its ability to bind metal ions, such as copper and zinc, which are important for many chemical reactions. 1-(Isocyanomethyl)-2-methoxybenzene has been shown to react with x-rays in the diffraction technique.

Versatile small molecule scaffold