Building Blocks

Versatile small molecule scaffold

Methyl 3-methanesulfonamidobenzoate is an organic compound that is used as a reagent in organic synthesis. It has the chemical formula CH3O2C(CH2)2SO2CH=NOH. Methyl 3-methanesulfonamidobenzoate is a methyl ester of benzoic acid, which is also known as methyl benzoate. This compound has been shown to react with DNA, forming adducts with guanine and cytosine bases.

Versatile small molecule scaffold

Versatile small molecule scaffold

Trifloxacin is a broad-spectrum antibacterial drug that belongs to the class of formyloxy compounds and the cephalosporin family. It has been shown to be active against both Gram-positive and Gram-negative bacteria, with activity against strains resistant to penicillin, ampicillin, erythromycin, and chloramphenicol. Trifloxacin binds to the bacterial ribosome by displacement of a pyridyl group in the ribosomal RNA, inhibiting protein synthesis. This binding inhibits cell growth by preventing the production of proteins that are vital for cell division.
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Trifloxacin has also been found to inhibit DNA gyrase and topoisomerase IV in vitro. Trifloxacin's mechanism of action is similar to that of other quinolones such as norfloxacin and ciprofloxacin.

3,4-Dihydro-2H-1-benzopyran-7-ol is a monomer that is used to synthesize medicines. It has the formula CH3COCH=CH(OH)CH3 and belongs to the group of flavonoids. 3,4-Dihydro-2H-1-benzopyran-7-ol has acidic properties, which are due to its isoflavones. It can be used as an acid catalyst in organic synthesis reactions and is a reaction product of chloropropane. 3,4-Dihydro-2H-1-benzopyran-7-ol also has high yield and can act as a bioisostere for other compounds such as chromene.

Versatile small molecule scaffold

2-(Methylsulfonyl)-1H-benzo[d]imidazole (MSBI) is a relatively new class of catalysts that can be used to promote the oxidation of alcohols. The catalytic system consists of copper, iodides, and MSBI. The first step in the catalytic cycle is the formation of a complex between MSBI and copper. This complex reacts with an alcohol to give a more reactive species, which then oxidizes iodide to iodine. The iodide is reduced back to iodide by hydrogen peroxide generated from the reaction with water. The spectrum of MSBI shows peaks at 1706 cm-1 and 1684 cm-1 due to its methyl groups, while the peak at 1202 cm-1 corresponds to the stretching vibration in the imidazole ring. Experimental results show that MSBI has a low density and high theoretical activity.

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

The Opn4 antagonist is a chemical that blocks the activity of the protein melanopsin, which is involved in regulating circadian rhythms. It has been shown to inhibit melatonin synthesis and muscle fiber contraction when applied intravitreally. These effects may be mediated by membrane channels that are activated by chloride ions. The effect of the Opn4 antagonist on photoreceptor cells is not yet known.

1-(2-Methylprop-2-en-1-yl)piperidin-4-amine is an inhibitor that blocks the activity of ion channels. It is a competitive antagonist at the NMDA receptor and has been shown to inhibit the binding of glutamate, which is a neurotransmitter involved in synaptic transmission. 1-(2-Methylprop-2-en-1-yl)piperidin-4-amine also inhibits β 2 -adrenergic receptors and has been shown to be a potent activator of G protein coupled receptors. This chemical may also be used as a research tool for studying the effects of ligands on cell biology, peptides, pharmacology, or life science. It has high purity and CAS No. 1082454-34-9.

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

3-Bromo-2-methyl-furan is a substituted quinoline. It is a synthetic reagent that can be used for the synthesis of bromofuran derivatives. The methyl group on the 3rd carbon atom in 3-bromo-2-methyl-furan is a substituent that can be exchanged with other substituents, such as alkylation, to produce a variety of products.
3-Bromo-2-methyl furan has been shown to be able to extract metal ions from their complexes and form stable complexes. This property makes it an ideal reagent for metalation reactions.

3-Hydroxy-5-methylpyridine (3HMP) is a chemical substance that has been classified as an amine. It is a product of the metabolism of purines, which are nitrogenous bases found in DNA and RNA. 3HMP is produced by aerogenic bacteria (such as Enterobacter), and can be used to estimate the number of these bacteria present in water samples. 3HMP has been shown to have antiviral properties against influenza virus, and can be used as a biomarker for the presence of other viruses in animals. 3HMP also has mineralization properties, which have been studied extensively, particularly with regards to pancreatic disease.

Versatile small molecule scaffold

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%.

1-Hydroxycyclopentane-1-carbonitrile is a monomer that is hydrolyzed to form benzoin and cyanohydrins. It can be used in the production of scifinder as a monomer or dimerizer.

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4,5-Dihydroxy-2,3-pentanedione is a carbonyl compound that is the product of the oxidation of ascorbic acid. It is used in wastewater treatment and has antimicrobial properties against infectious diseases. This compound has been shown to inhibit protein synthesis by binding to the ribosome and preventing the formation of peptide bonds between amino acids. 4,5-Dihydroxy-2,3-pentanedione has also been shown to bind to plasma proteins, which may be due to its acyl chain structure. 4,5-Dihydroxy-2,3-pentanedione can be synthesized in a catalytic mechanism that involves dehydroascorbic acid and molecular oxygen.

Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.