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

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.
PB-22 is an analog of JWH-073 and has been shown to have a stronger effect on locomotor activity than JWH

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

4-[(Methylsulfanyl)methyl]benzoic acid is a chiral compound with a sulfur atom. It can be prepared by the reaction between methylsulfonyl chloride and benzoyl chloride in chloroform or by the reaction of methoxysulfur trifluoride with benzoic acid. 4-[(Methylsulfanyl)methyl]benzoic acid can also be synthesized by the reaction of sulfone and carboxylic acid derivatives, such as benzyl or cyano. 4-[(Methylsulfanyl)methyl]benzoic acid is used as a fungicide, insecticide, and herbicide. The substituents on this molecule are able to form bonds with other molecules to create an array of different structures. The most common substitution is for methoxy, which has a hydroxy group attached to it. This substitution is found in many different types of molecules including some drugs, hormones, vitamins,

2-Chloro-N-(2-cyanoethyl)acetamide is a potent and selective inhibitor of the protein kinase C (PKC). The PKC protein kinases are enzymes that regulate the activity of cells in response to stimuli. 2-Chloro-N-(2-cyanoethyl)acetamide has been shown to be effective against some viruses and tumor cells, but not against bacteria. It inhibits the growth of some cancer cells and has been shown to inhibit the replication of animal viruses such as influenza virus. This drug is also used for treatment of abdominal infections, hepatitis, pancreatitis, mesenteric adenitis, and animals with cancer. 2-Chloro-N-(2-cyanoethyl)acetamide can act as a noncompetitive inhibitor by binding to a site on the enzyme that is different from ATP binding site.

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.

Versatile small molecule scaffold

3-(4-Nitrophenoxy)propionic acid is a promiscuous compound that can be used to synthesize other compounds. It reacts with hydrochloric acid, nitro groups, and phosphorus pentoxide to produce nitro compounds. 3-(4-Nitrophenoxy)propionic acid reacts with benzoylamine in the presence of a cocatalyst to form alkoxycarbonyl products. The cocatalyst is typically a metal such as zinc or magnesium. 3-(4-Nitrophenoxy)propionic acid is also used as an agrochemical for controlling influenza virus and Influenzae bacteria.
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2,5-Dioxopyrrolidin-1-yl formate is a solubilized ATP analog that has been clinically developed for the treatment of cancer. This drug binds to cell membranes and causes alkylation of the acidic phospholipids in the membrane, leading to increased permeability of the membrane and release of intracellular components. 2,5-Dioxopyrrolidin-1-yl formate also interacts with lysosomes and increases their acidity, which may lead to an increase in lysosomal enzyme activity. This drug has been shown to inhibit tumor growth in a mouse model by binding to erythrocytes while it was being simultaneously administered intravenously. The chemical structures of this drug are closely related to those of phaseolus, which is known for its anticancer effects.

N,N-Dimethylcyclohexanecarboxamide is an acid salt of besylate that is used as a drug for the treatment of hyperglycemia. It has been shown to have a rapid onset and short duration of action. The chemical name for N,N-Dimethylcyclohexanecarboxamide is 1-[2-(2-methoxyethoxy)ethyl]-4-methyl-1,4-dihydropyridine 2,4-dicarboxylic acid methyl ester. This compound inhibits insulin release from the pancreas and stimulates glucagon release from the alpha cells in the pancreas. These effects lead to an increase in blood glucose levels.

Versatile small molecule scaffold

1-(4-Chlorophenyl)-1H-imidazole-2(3H)-thione is a crystalline solid that belongs to the class of imidazoles. It has been synthesized by reacting 1,2-dibromoethane with sodium methoxide in methanol. The compound was found to have a melting point of about 183°C and a molecular weight of 212.06 g/mol. This compound has been shown to interact with methanol, methoxide, and ethoxy groups. Crystallization occurs when the substance is heated to about 183°C in vacuum and then cooled slowly.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

1-(2-Methylphenyl)propan-2-amine is a fatty acid ester that is used as an excipient in pharmaceutical dosage forms. It is used to increase the viscosity of drug solutions and suspensions, and to provide a protective coating for tablets. 1-(2-Methylphenyl)propan-2-amine is insoluble in water, but soluble in organic solvents such as alcohols and acetone. It can be prepared by reacting a primary amine with a fatty acid chloride or anhydride. The compound has been shown to have high affinity for 5HT2A receptors in vitro, which may account for its psychoactive effects.

Versatile small molecule scaffold

The peptide is a research tool that can be used to activate certain antibodies and ion channels. It has also been shown to inhibit protein interactions. The peptide is soluble in DMSO, ethanol, and acetonitrile. It has a molecular weight of 438.4 g/mol and an empirical formula of C14H20N2O3S. The CAS number for the peptide is 436091-57-5. The chemical name of the peptide is ({2-[(5-methylisoxazol-3-yl)amino]-2-oxoethyl}thio)acetic acid.

Versatile small molecule scaffold

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

2-(Trifluoromethyl)azetidine is a synthetic compound that has been used in the synthesis of other compounds. It is an ionic, organometallic reagent that can be used as a catalyst for a variety of reactions. The trifluoromethyl group on 2-(trifluoromethyl)azetidine is electrophilic and nucleophilic and can catalyze reactions involving heterocycles, connect, or electron-deficient alkynes.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

6-Chloro-9-(propan-2-yl)-9H-purine is an intermediate in the synthesis of nucleoside analogues. It is obtained by the catalyzed reaction of acetonitrile and purines, which undergoes regioisomerization to form a mixture of 6-chloro-9-(propyl)- and 6-chloro-9-(butyl)purine. This intermediate can be used for the alkynylation of amino acids or peptides with alkynes. The selective formation of one regioisomer can be achieved by using a chiral catalyst or by reacting with an optically active reagent such as (+)-camphor sulfonic acid.

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%.

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

Please enquire for more information about 4,5-Dihydro-1H-imidazol-2-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

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.