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>Fenoprofen calcium dihydrate is a nonsteroidal anti-inflammatory drug that has analgesic and antipyretic properties. It is a prodrug that is hydrolyzed to fenoprofen in the intestinal wall and then metabolized in the liver. Fenoprofen calcium dihydrate is used for the treatment of headaches, muscle pain, menstrual cramps, arthritis, and other conditions. Fenoprofen calcium dihydrate binds to biological molecules such as enzymes or receptors at an active site. The binding of fenoprofen calcium dihydrate to the enzyme cyclooxygenase inhibits prostaglandin synthesis by preventing arachidonic acid from being converted into prostaglandins. This inhibition causes decreased inflammation and pain.</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>5-Bromo-6-nitro-1H-indazole is a potent inhibitor of ATP binding to the ATP binding site on kinases. It has shown antiproliferative activities in prostate cancer cells, PC3 cells and in vivo models. 5-Bromo-6-nitro-1H-indazole has been shown to inhibit the activity of protein kinases with micromolar potency. The IC50 values obtained from experiments are in the micromolar range for different kinases, including casein kinase II (CKII), cAMP dependent protein kinase A (PKA), and mitogen activated protein kinase 1 (MAPK1). The inhibition of these three kinases was found to be competitive and reversible. 5BINI also inhibits phosphorylation of casein by CKII, which is an important mechanism for regulating the activity of this enzyme.</p>

<p>1-Trimethylsilyl-1,4-pentadiyne is a chemical compound. It has a phenyl ring and a lipase ligand. This chemical has been shown to be able to transfer hydrocarbons from one side of the molecule to the other, with an efficiency of around 80%. The ligands on 1-trimethylsilyl-1,4-pentadiyne are hydride ligands that can undergo asymmetric hydrogenation reactions. This chemical also has a diffraction pattern that is characteristic of tetranuclear complexes. 1-Trimethylsilyl-1,4-pentadiyne is activated by electron bombardment and can undergo regioselective reactions with carbonyls and epoxides.</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-Chlorobenzylsulfonamide is a histamine receptor antagonist that blocks the action of histamine on the H3 receptor. It has been shown to antagonize the binding of histamine to its receptors in bioassays, and has been found to be a competitive antagonist at the H3 receptor. 4-Chlorobenzylsulfonamide has similar affinity for the h3 receptor as does 4-chlorophenylbiguanide and 4-chloro-2-(2,4-dichlorophenoxy)phenylethylbiguanide. This drug also inhibits the release of histamine from mast cells in vitro.</p>

<p>This is a novel, selective and efficient catalyst for the synthesis of oxiranes from aldehydes and azides. It has been found to be more chemoselective than other catalysts in this area, and can also be used as a catalyst for the synthesis of vicinal silylated oxirane. The catalyst is prepared by reacting an amine with an aldehyde in the presence of hydroxide.<br>Synlett, 2014, 25(2), pp. 166–168</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>4-(Diethylcarbamoyl)benzoic acid is a compound that has a carboxylic acid group and a chloro group. It can be used to synthesize functionalized derivatives, including sulfones, sulfonamides, ureas, and amides. The functional groups on the molecule are complementary to each other. This allows for the introduction of substituents with different reactivities, such as esters and amines. These different reactive groups allow for the synthesis of compounds with varied properties.</p>

<p>AG 1295 is a growth factor that binds to the tyrosine kinase receptor. It is also a potent inhibitor of the receptor activity of PDGF-BB and other tyrosine kinases. AG 1295 was originally developed as an eluting agent for protein purification, but has been shown to have therapeutic potential for vascular injury repair and angiogenesis. The drug can be used in vitro to inhibit the phosphorylation of PDGF-BB by blocking its binding to the PDGF-BB receptor.</p>

<p>Undec-1-en-6-one is a product of the reaction between pentenyl and hexanal. It can be synthesized by the carbonylation of calvine. This compound has been used to produce other products, such as alkaloids, which are important for medicinal and pharmaceutical applications.</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-(Cyclopropylamino)acetic acid hydrochloride is a hydrogen atom donor and an antibacterial agent. It is used in pharmaceutical preparations for the treatment of bacterial infections. 2-(Cyclopropylamino)acetic acid hydrochloride inhibits the growth of bacteria by inhibiting the synthesis of their cell walls, which are made up of polymers of amino acids linked to each other by peptide bonds. This compound has been shown to be effective against Gram-negative bacteria, such as Acinetobacter baumannii and Pseudomonas aeruginosa, as well as some Gram-positive bacteria, such as Staphylococcus aureus. 2-(Cyclopropylamino)acetic acid hydrochloride also has an inhibitory effect on phosphoric acid bacteria and can be used to synthesize α-amino acids.</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>3-Bromo-4,5-dimethylphenol is a bromination product of the structurally related compound 4,5-dimethylphenol. The electrophilic character of 3-bromo-4,5-dimethylphenol is due to the bromine atom. It can be used as an intermediate for the synthesis of other chemicals. Bromination of 4,5-dimethylphenol takes place in two steps: first a nucleophilic attack by bromide ion on one of the carbon atoms in 4,5-dimethylphenol and then an electrophilic substitution reaction between the bromine atom and one of the hydroxyl groups. The mechanisms for these reactions are shown below:</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-(Cyclohexyloxy)acetic acid is a synthetic organic compound that has the chemical formula CH2OCH2COCH2OH. It is an acid catalyst with a pK of 1.6, and it can be used to catalyze the reaction between sodium carbonate and cyclohexanol. 2-(Cyclohexyloxy)acetic acid is also used as a solid catalyst in the conversion of ethyl diazoacetate to phenyl acetic acid. It has been shown to be effective for wastewater treatment, as well as for removal of nitrogen from wastewater. 2-(Cyclohexyloxy)acetic acid has been found to be toxic to aquatic organisms at relatively low concentrations, so care should be taken if this substance is released into the environment.</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>3-Chloropyridine-2-sulfonamide is an insecticide. It can be used as an insecticidal agent to control a variety of pests, such as cockroaches, ants, and flea larvae. This chemical is effective against a wide range of pests and does not have any adverse effects on humans or animals when used in accordance with directions. 3-Chloropyridine-2-sulfonamide is a sulfonamide that inhibits the activity of cholinesterase enzymes. It also has some effect on the nervous system.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-tert-Butyldimethylsilyloxybenzaldehyde is a synthetic opioid that has been used in the screening of opioid receptor targets. It is soluble in organic solvents, such as chloroform and ether, with a melting point of about -30°C. 3-tert-Butyldimethylsilyloxybenzaldehyde has been shown to have analgesic activity in mice at low doses. The analgesic effect is due to stimulation of μ opioid receptors. In addition, this compound also has the ability to inhibit amide formation with low temperatures. 3-tert-Butyldimethylsilyloxybenzaldehyde can be synthesized by alkylation or derivatization of benzyl alcohol or benzyl chloride. It can also be obtained through the condensation of 2,6-dimethylaniline with acetone followed by reduction with lithium aluminum hydride or sodium borohydride.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl (S)-indoline-2-carboxylate hydrochloride is a lipase inhibitor that belongs to the class of antibiotics. It inhibits the lipid acylase by reversibly binding to the enzyme and blocking the esterification reaction. The interaction between methyl (S)-indoline-2-carboxylate hydrochloride and the enzyme is reversible, which allows for a kinetic analysis of the inhibition. Methyl (S)-indoline-2-carboxylate hydrochloride has been shown to inhibit cyclic nitroindole synthesis in vitro, but not in vivo. This compound also interacts with o-glycosylations, as it can be seen with its optical rotation. Methyl (S)-indoline-2-carboxylate hydrochloride has been shown to have an effect on allyl carbonates, which have similar ring structures as glycosides.</p>

<p>5-Methanesulfonyl-1-methyl-1H-1,2,3,4-tetrazole is a ligand that binds to metal cations and forms coordination complexes. It is used in the synthesis of polymeric materials with magnetic properties. 5MSMT was found to be soluble in chloroform or dichloromethane. The compound has been shown to have magnetic properties and x-ray diffraction analysis showed that it has a crystal structure.</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>4,7-Dichloro-1H-indole (4,7-DCI) is an indole that is obtained by the reaction of potassium with 3,4-dichloroaniline. The compound has been found to be a potent inhibitor of the growth of plants and algae. It has also been shown to inhibit the growth of bacteria by binding to their DNA and inhibiting transcription. This process prevents protein synthesis and leads to cell death. 4,7-DCI can be synthesized using zinc chloride as a catalyst. It reacts with potassium carbonate in an alkaline environment to form potassium chloride and 4,7-DCI.</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>