Building Blocks

<p>Acrylaldehyde is a reactive compound that can bind to the enzyme tyrosinase, inhibiting its activity. 3-(4-Chlorophenyl)acrylaldehyde (3-CA) is a small molecule that has shown an inhibitory effect on the proliferation of leukemia cells in vitro and in vivo. It also has broad-spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). Tyrosine kinases are enzymes that catalyze the transfer of phosphate groups from ATP to tyrosine residues in proteins, leading to cellular signaling and cell division. 3-(4-Chlorophenyl)acrylaldehyde binds to tyrosine kinases and inhibits their function, which may be responsible for its cytotoxic effects.</p>

<p>Ammonium 2,2'-(cyclobutane-1,1-diyl)diacetate (ACDA) is a salt of ACDA and ammonium. It is an analogue of barbiturates that has been used in medicine to relieve neuralgia and sciatica. ACDA is injected intravenously or intramuscularly as the ammonium salt. The toxic effects of ACDA are similar to those of other barbiturates. These are due to its depressant effect on the central nervous system and include narcosis, respiratory depression, and death from respiratory arrest.</p>

<p>1-Phenyl-1H-pyrazol-4-ol is an organic compound that is a white crystalline solid with a strong odor. It is used in the manufacture of pyrazoles and as a reagent for the synthesis of other compounds. 1-Phenyl-1H-pyrazol-4-ol can be used to synthesize pyrazoles, which are important in the production of several pharmaceuticals.</p>

<p>Glycinamide ribonucleotide (GAR) is a glycinamide that is used as an inhibitor of formyltransferase. It forms a reversible covalent bond with the active site cysteine residue of the enzyme, thereby inhibiting its activity. GAR has been shown to inhibit both eukaryotic and prokaryotic formyltransferases, and also inhibits the related enzyme ribonucleotide reductase. This compound may have potential for use in treating cancer due to its ability to inhibit tumor growth by interfering with DNA synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>Hexylbenzene is a colorless liquid that is soluble in alcohol, ether, and benzene. Hexylbenzene has been shown to undergo a suzuki coupling reaction with aniline and phenylboronic acid. The yield of chloride was site specific, as the reaction occurred more readily at the ortho-positions than the para-positions. Hexylbenzene has been used as a model system for studying transfer reactions in proteins. In this system, hexylbenzene reacts with peroxidase to form hydrogen peroxide, which then reacts with p-nitroaniline to produce p-aminophenol and nitrite ions. The detection sensitivity of light emission from hexylbenzene was significantly higher than that of other compounds such as tetracycline or ampicillin.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>6-Methoxyquinaldine is a fluorescent chemical that is used to study the structural changes of proteins. 6-Methoxyquinaldine is oxidized by various reagents, such as anilines and sulphates, to produce fluorescent products. The fluorescence intensity of the product can be quantified using fluorimetric analysis or microscopy techniques. The fluorescent products can be visualized using UV irradiation (365 nm) or by fluorescence microscopy. 6-Methoxyquinaldine can also be used in calibrating imaging techniques, such as confocal laser scanning microscopy.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Benzyl(1-phenylpropan-2-yl)amine is a piperidine derivative that acts as an inhibitor of cytochrome P450 enzymes. It binds to the CYP2D6 enzyme and has been shown to have an inhibitory effect on the activity of this enzyme in rat liver microsomes. The binding constants for benzyl(1-phenylpropan-2-yl)amine with the CYP2D6 enzyme were determined by competitive inhibition studies and it was found that this compound has a high binding affinity with the CYP2D6 enzyme. Studies also demonstrated that benzyl(1-phenylpropan-2-yl)amine inhibits the activity of CYP3A4 and CYP3A5 enzymes. This drug may be useful in treating some individuals who are taking drugs metabolized by these two enzymes, but will not be effective in people who are not taking any drugs metabolized by these two enzymes.</p>

(2S)-3-Carbamoyl-2-[5-(dimethylamino)naphthalene-1-sulfonamido]propanoic acid is a fluorescent probe that binds to human serum albumin. It has been used as an inhibitor of the enzyme α1-acid glycoprotein, which is involved in the degradation of fatty acids and glycopeptides. The binding constants have been determined by fluorescence titration and are site specific. (2S)-3-Carbamoyl-2-[5-(dimethylamino)naphthalene-1-sulfonamido]propanoic acid is a molecule that can be used for metal chelation, which has been demonstrated by its ability to inhibit the activity of enzymes such as α1-acid glycoprotein. This compound also has a role in endogenous substances such as fatty acids and tryptophan fluorescence.

N-Cyano-N'-(2-methylbutan-2-yl)guanidine is an antihypertensive drug that inhibits the activity of enzymes involved in the synthesis of fatty acids. It has been shown to be effective against cardiac hypertrophy, as it reduces the activity of phospholipase A2, which is required for the formation of arachidonic acid, a precursor to prostaglandins and thromboxanes. This drug also has a depressant effect on fatty acid metabolism and decreases the production of fatty alcohols by inhibiting their synthesis. N-Cyano-N'-(2-methylbutan-2-yl)guanidine is used as a pharmaceutical dosage for treatment of hypertension and depressive disorders.

<p>Octan-4-amine is a metastable cation that has been used as a label for deuterium in various studies. The labeling of octan-4-amine with deuterium has been shown to produce stable, nonradioactive isotopes for use in various studies. It has also been shown to be an effective radical cations and cleavage agent. As a result, it can be used to generate molecular ions and isomers from larger molecules. Octan-4-amine is also capable of isomerizing other compounds and generating radical cations when heated. This chemical may be used as a precursor to create other compounds through the process of isomerization, such as the production of isomers by the addition of hydrogen atoms or removal of hydrogens from their molecular structure.</p>

<p>1,6-Dimethyl (2E,4E)-hexa-2,4-dienedioate is a hydrocarbon that can be synthesized from ethylene. The compound is a building block for polyunsaturated compounds and can be used as a feedstock in the production of monomers or polymers. It has been shown to have radiation catalysis properties and is sustainable with low environmental impact. 1,6-Dimethyl (2E,4E)-hexa-2,4-dienedioate has been shown to produce high yields and is not toxic to humans or animals. This product also has applications in the production of cosmetics and pharmaceuticals.</p>

<p>Nonanamide is a glycol ester with an amide group. It has been shown to be effective against infectious diseases, such as HIV and hepatitis B. It has a pyrazole ring that interacts with the amide group, forming hydrogen bonds. Nonanamide has also been shown to inhibit the production of inflammatory cytokines in mice with autoimmune disease, which may be due to its ability to inhibit water vapor. The molecular weight of nonanamide is 134.2 g/mol and it has a melting point of -54°C. Nonanamide is soluble in water and glycol ethers but insoluble in alcohols and oils.</p>

<p>Di-n-octylamine is a reactive chemical that is chemically stable in the presence of nitrogen. It is used in chemical biology as a transport agent for amines and other organic compounds. Di-n-octylamine has been shown to have optimum solubility in glycol ethers, magnesium salts, and trifluoroacetic acid. This compound reacts with fatty acids to form hydroxyl groups and can be used as an extractant for glycol ethers. The mechanism of this reaction involves intramolecular hydrogen transfer from the hydroxyl group on the fatty acid to the n-octyl amine molecule.</p>

<p>2-Hydroxybenzenethiol is an analytical reagent that reacts with oxygen to form a fluorescent complex. It is used for the detection of infectious diseases, such as tuberculosis and other bacterial infections. 2-Hydroxybenzenethiol is also used in analytical chemistry as a reaction solution to study the oxidation of organic compounds. The compound has been shown to react with nitrogen atoms in certain groups, such as p2, by forming chelate ligands. This compound can be prepared by reacting hydrochloric acid with molybdenum (Mo), which has been electrochemically coated with a hydroxyl group on one side and a hydroxy group on the other. The Mo acts as a model system for studying intramolecular hydrogen bonding between two hydroxy groups that are separated by one carbon atom.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2,3-Dimethylcyclohex-2-en-1-one is a phenylhydrazine derivative that can be converted into aporphine alkaloids. It is also an isomer of cyclohexenones and epoxides. This compound has substituents at the 2 and 3 positions which are either methyl or hydrogen, respectively. The carbonyl group in 2,3-Dimethylcyclohex-2-en-1-one is a ketone or aldehyde, depending on the substitution pattern. The oxygen function in this molecule is an ether or ester. 2,3-Dimethylcyclohex-2-en-1-one has properties that are similar to those of diketones and spirolactones because it contains both carbonyl and oxygen functions. It can be classified as an aporphine alkaloid because it has two rings fused together with one nitrogen atom between them</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-1-methylpyrimidin-2(1H)-one is a chemical compound that belongs to the group of pyrimidine compounds. It has been shown to be an inhibitor of viral life, with its activity against HIV being most well studied. The tautomers of 4-amino-1-methylpyrimidin-2(1H)-one are protonated and stable, meaning that they do not undergo any chemical change in the body. 4-Amino-1-methylpyrimidin-2(1H)-one is also able to form stable complexes with nitrogen atoms. The xray crystal structure for this compound shows that it coordinates with group P2, which contains two nitrogen atoms and one oxygen atom. The interaction between these three atoms is called a dinucleotide phosphate. This group binds to DNA by hydrogen bonds, forming intramolecular hydrogen bonds. The groups on the other side of the molecule bind</p>

<p>Cyclohexanecarboxamide is a carboxamide that has been shown to inhibit the growth of bacteria. It binds to the bacterial receptor and inhibits the activity of the enzyme carboxide, which is involved in the synthesis of monoamine neurotransmitters. Cyclohexanecarboxamide has also been shown to inhibit axonal growth in mammalian cells, which may be due to its ability to block potassium channels on nerve cells. Cyclohexanecarboxamide has been shown to have antimicrobial properties against a range of organisms including those resistant mutants.</p>

Versatile small molecule scaffold

Cyclopentylpropan-2-one (1CPA) is an aliphatic hydrocarbon that has been shown to act as a light-sensitive molecule. It is used as a polymerization initiator and is also found in the human body as a metabolic intermediate. 1CPA is found in the form of a diacylglycerol and can be converted into an allyl carbonate, which reacts with methoxy groups to form an allyl ether. 1CPA has also been shown to have structural similarities with pyrimidine compounds and formyl groups. The 1CPA molecule contains a carbonyl group, which is the reactive functional group that allows for this chemical to react with other compounds.

<p>3,5-Dimethyl-2-cyclohexen-1-one is a β-unsaturated ketone that has been synthesized using an efficient method. It has been shown to have anti-inflammatory properties and is used for the treatment of pulmonary fibrosis in humans. The compound also binds to polyene compounds and supramolecular substrates. 3,5-Dimethyl-2-cyclohexen-1-one reacts with chloride ions to form a β unsaturated ketone chloride that can undergo alkylation with an electron donor such as acetonitrile. This reaction is catalyzed by microsomal cytochrome P450 enzymes and requires a reaction time of about two hours to complete.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Methylcyclohexane-1-carboxamide is a sclerotiorin, which are natural substances that have been shown to have inhibitory effects against fungi. It has been shown to be effective against Sclerotinia sclerotiorum and Gaseous Botrytis cinerea. The inhibition of sclerotiorin 1-methylcyclohexane-1-carboxamide is due to its ability to inhibit the synthesis of ergosterol, which is an important component of the fungal cell membrane. This drug has also been shown to have inhibitory effects on carbon bond formation in natural substances such as ginseng root or solid form.</p>

<p>Versatile small molecule scaffold</p>

<p>3,3-Dimethylglutarimide is a molecule that has been shown to inhibit the enzyme butyrylcholinesterase in a stepwise manner. This inhibition prevents the breakdown of acetylcholine, which leads to increased levels of this neurotransmitter and an improvement in cognition. 3,3-Dimethylglutarimide also has protonation properties that allow it to form complexes with metal ions such as zinc and copper. These complexes are formed by the interaction of functional groups on the molecules with protons on the metal ions.</p>

Versatile small molecule scaffold

<p>4-Chloro-2,6-dimethylphenol is a reactive molecule that is found in the environment and can be produced by the human body. It is an antimicrobial agent that reversibly binds to nucleophilic sites on peroxidases and other enzymes, thereby blocking their activity. 4-Chloro-2,6-dimethylphenol inhibits enzymatic reactions in bacteria by reacting with the hydroxyl group of enzymes such as catalase and glutathione reductase. This agent has been shown to have an effect on human pathogens such as Staphylococcus aureus and Escherichia coli.</p>

<p>2-Phenyl-1-propanol is a molecule with a hydroxyl group at the 2 position and a phenyl group at the 1 position. It is used as a film-forming polymer in coatings, adhesives, and elastomers. It is also used as an ingredient in glycol ethers, fatty acids, and enolate anions. 2-Phenyl-1-propanol has been shown to be synthesized by oxidative dehydrogenation of benzaldehyde and acetophenone. This reaction mechanism has been shown using chromatographic methods on two different solvents: one polar (water) and one nonpolar (tetrahydrofuran). The reaction proceeds with the formation of an enolate anion intermediate that reacts with water to form the alcohol product. The hydration process can be catalyzed by either sodium or potassium salts. The phase transition temperature for this compound is between -30°C and 60°</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chloro-2,5-dimethylphenol is a phenolic compound that is used as an intermediate in the synthesis of other organic compounds. It has low ph and can form adducts with methanol at high ph. 4-Chloro-2,5-dimethylphenol can be reacted with hydrogen chloride to produce the corresponding chloride or with a coupling agent to produce the corresponding imine. 4-Chloro-2,5-dimethylphenol can also be used as an elimination agent.</p>

<p>1,4-Diiodo-2,5-dimethylbenzene is an iodide that can be used in the industrialization of iodine. It can be prepared from bicyclopropylidene and nitrosobenzene by coupling with a carbonyl group. The yield of this reaction is high and the product is stable. 1,4-Diiodo-2,5-dimethylbenzene can also be prepared by palladium-catalyzed cross coupling or a Diels–Alder reaction between 2,5-dimethylaniline and 3-(bromomethyl)cyclobutane. This process yields only one regioisomer because there are no other reactive groups on the ring to form a second regioisomeric product.</p>

3,5-Dimethyl-1H-pyrazole-1-carbothioamide (DMPC) is a nitrogen-containing compound that has been shown to have high cytotoxic effects on leukemia cells. DMPC interacts with cisplatin and thiosemicarbazide, both of which are inorganic molecules that have been used as chemotherapeutic drugs for the treatment of cancer. DMPC is an amide with two nitrogen atoms and a conformational vibrational frequency at 4.6 MHz. It is also a ligand for the cytotoxic effect of cisplatin and thiosemicarbazide.

<p>Versatile small molecule scaffold</p>

<p>4-(Aminomethyl)-1,2-benzenediol hydrochloride is a potent inhibitor of monoamine neurotransmitter synthesis. It has been shown to inhibit the polymerase chain reaction (PCR) and is effective in the preparation of samples for PCR analysis. 4-(Aminomethyl)-1,2-benzenediol hydrochloride is chemically stable and has an electrochemical detector that can be used in its detection. This chemical also inhibits the incorporation of thymidine into DNA during DNA synthesis, leading to a decrease in DNA synthesis. The monoclonal antibody technique has been used to detect this compound in human serum and tissue biopsies.</p>

<p>2-Azaspiro[4.4]nonane-1,3-dione is a linker that is used in the synthesis of active derivatives of drugs. It has pharmacological and physicochemical properties that are similar to those of methylene. 2-Azaspiro[4.4]nonane-1,3-dione is used as an analytical standard for rp-hplc analysis and x-ray structural analysis. It can be used to synthesize pentylenetetrazole and imine derivatives for anticonvulsant properties, which have been shown to have properties similar to those of phenytoin.</p>

<p>1-Ethylcyclohexane-1-carboxylic acid is an organic compound that is a monocarboxylic acid. It is a liquid at room temperature and has a boiling point of 110°C. 1-Ethylcyclohexane-1-carboxylic acid can be used as an inhibitor for tissue plasminogen activator, which is a protease that activates plasminogen to break down fibrin. 1-Ethylcyclohexane-1-carboxylic acid inhibits the activity of this enzyme, preventing clot lysis and promoting blood coagulation. 1-Ethylcyclohexane-1-carboxylic acid also has been shown to be cytotoxic to mammalian cells in culture, but not to bacterial cells.</p>

Versatile small molecule scaffold

<p>1H-Pyrrole-2,3-dicarboxylic acid is a naturally occurring organic compound that is an important building block for the synthesis of melanin. It has been shown to inhibit tyrosinase activity and to be cytotoxic at high concentrations. 1H-Pyrrole-2,3-dicarboxylic acid has also been used as a model system for skin cancer and hydrochloric acid has been shown to have a protective effect on the morphology of 1H-pyrrole-2,3-dicarboxylic acid crystals.</p>

<p>5-Chloro-3-methylbenzofuran is a condensation product of 5-chloro-2,4-dinitrobenzene and 3-methylbenzoic acid. It is an antimicrobial agent that belongs to the thiazolidinone class of anticonvulsant drugs. This compound has been shown to have antitubercular activity and has been used in the treatment of Mycobacterium tuberculosis. 5-Chloro-3-methylbenzofuran also has anticonvulsant effects and can be used for the treatment of epilepsy.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2-Phenylpropanamide is an amide that has been shown to have anti-inflammatory activity in a variety of animal models. It is also a metalloprotease inhibitor and suppresses the release of inflammatory cytokines. 2-Phenylpropanamide has shown some efficacy against cancer in human cell lines, and inhibits the production of the enzyme acetylcholinesterase. This drug also binds to adenosine A3 receptors, which are involved in inflammatory processes. 2-Phenylpropanamide has antioxidant properties, as it can scavenge radicals and inhibit hydroxyl radical formation. 2-Phenylpropanamide also has a high affinity for magnesium ions, which may explain its long elimination half-life after oral administration.</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Dihydrobenzo[e][1,3]oxazin-2-one is an organic compound that is used as a catalyst in the synthesis of pharmaceuticals. It reacts with halides and alkali metal to form quaternary ammonium salts. This reaction can be represented by the following scheme:</p>

<p>3-Methyl-1H-indol-6-ol is a metabolite of estrone sulfate, which is produced by the activity of cytochrome P450 enzymes. It has been shown to be an effective inhibitor of chemical reactions in urine samples and primary cells. 3-Methyl-1H-indol-6-ol also has a role in the metabolism of estrogens and may play a part in the development of symptoms such as those seen in human liver disease or testicular cancer. 3-Methylindole can be found as an endogenous metabolite in schizophrenic patients and is known to inhibit constitutive androstane receptor (CAR) activity, which regulates gene expression and cellular growth.</p>

<p>4-Cyclopropylbenzonitrile is an electrophilic compound that reacts with a nucleophile to form a covalent bond. The reactivity of 4-cyclopropylbenzonitrile is activated by the addition of chloride. It can be used as a precursor to yield chloroform and other compounds, such as chloride and oxide. 4-Cyclopropylbenzonitrile can also react with sulfur or nitrosyl to form an electrophilic sulfur or nitrosyl compound.</p>

<p>2-(2-Phenylethyl)oxirane is an organic compound that belongs to the class of epoxides. It is a colorless liquid with a strong odor. It can be used as a chemical treatment for phosphine, epoxides and haloalkyl, and has been shown to have efficient methods for synthesizing polymers. 2-(2-Phenylethyl)oxirane is also an adrenergic receptor agonist that has been shown to produce neurodegenerative diseases in rats.</p>

<p>N-Butylaniline is a reactive chemical that is used as a cross-linking agent, and to prepare quinoline derivatives. It is also used in the preparation of polycarboxylic acids and electrochemical methods. N-Butylaniline can be used for bladder cancer treatments, and has been shown to inhibit viral replication in vitro. This chemical is not toxic to humans at low doses, but it may cause autoimmune diseases such as systemic lupus erythematosus if ingested in high doses.</p>

Ethyl 1-hydroxycyclohexanecarboxylate is an aliphatic, cyclic compound that belongs to the group of superacids. It is a byproduct of the reaction between benzene and ethyl chloroformate. This reaction requires a catalyst, such as potassium tert-butoxide or tetrabutylammonium fluoride. The molecule has a tetrahydrofuran ring with a hydroxy group and can be classified as an aldehyde, which is formed by the removal of two hydrogen atoms from the carbonyl carbon atom. Ethyl 1-hydroxycyclohexanecarboxylate also undergoes a shift in its equilibrium position when it interacts with other compounds, such as elemental analysis or five-membered hydrocarbons.

<p>Versatile small molecule scaffold</p>

<p>4-(Dimethylamino)benzyl Alcohol is a chemical compound with the formula CH3(CH2)3NH2. It is used as an antibiotic drug and has been shown to have an average particle diameter of 80 nanometers, bulk polymerization, hydroxy group, and polymerization initiator. 4-(Dimethylamino)benzyl Alcohol has been shown to be effective against bacteria that are resistant to penicillin, ampicillin, erythromycin, or tetracycline. This chemical compound has FTIR spectra in the range of 400-4000 cm-1 and can be used for the synthesis of polymeric matrices in many applications.</p>

Versatile small molecule scaffold

2,4-Dimethyl-6-oxo-1,6-dihydropyridine-3-carbonitrile is a nitrile that is synthesized by reacting 2,4-dimethylpyridine with formaldehyde. It has a molecular weight of 202.2 g/mol and density of 1.42 g/cm³ at 20 °C. The functional theory predicts the transformation of 2,4-dimethylpyridine to 2,4-dimethyl-6-oxo-1,6-dihydropyridine through the intermediate formation of formaldehyde and nitrile. This reaction can be confirmed by diffraction experiments and the experimental study on the pathway for this transformation. The experiment also revealed that 2,4-dimethylpyridine reacts with formaldehyde to produce formic acid as well as 6 molecules of water. The density functional theory supports the experimental data and predicts that there are two possible pathways for this

<p>2-[2-(Dimethylamino)ethoxy]ethanol (DMAEE) is a chemical that belongs to the group of amines. It is used as a surfactant in the form of ethylene diamine or metal hydroxides and has been shown to have transport properties. DMAEE's protonated form has been shown to adsorb on metal oxides, such as iron oxide, aluminum oxide, and titanium dioxide. This adsorption mechanism may be due to its cationic nature. DMAEE also reacts with nitrous acid in water to form an intermediate which can be oxidized by atmospheric oxygen. The reaction mechanism for this oxidation is not yet well understood.</p>

<p>2,5-Dimethylanisole is a solvent that is used in organic synthesis. It can be used to remove protein targets from the reaction mixture and as a reagent for alkoxyphenols. 2,5-Dimethylanisole has been shown to have high values in luminescence properties. 2,5-Dimethylanisole can also be used as an indicator for hydrogen chloride. 2,5-Dimethylanisole has been found to react with alzheimer 's disease and acetonitrile to form eugenol, an acceptor. The transfer reactions of 2,5-dimethylanisole are not yet fully understood but are thought to involve metal ions and hydrogen chloride or acetonitrile.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>4-(2-Hydroxyethoxy)benzenecarboxylic acid is a polyester that has been shown to have heat resistance, high mechanical properties, and biologic activity. It is prepared by the polymerization of benzoic acid with titanium and a catalyst. This polyester can be used as a structural material for implants or as a polymerization catalyst for polycondensation reactions. 4-(2-Hydroxyethoxy)benzenecarboxylic acid has an aliphatic group with 2 aliphatic groups and an aliphatic substance. It also exhibits catalytic activity in promoting the formation of polyesters from diols and diacids.</p>

<p>2,1,3-Benzothiadiazole-4,5-diamine is a ketone that can be derived from the condensation of styrene with ammonia. The yield of this reaction is low and it requires an excess of styrene. 2,1,3-Benzothiadiazole-4,5-diamine has been found to be environmentally viable as it does not produce any harmful byproducts when heated at high temperatures. This compound has also shown to have promising results in animal studies as a potential treatment for malaria.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Isopropenyl-4-methoxybenzene is a halide that can be used as a catalyst for the hydroxylation of styrene, yielding 1-isopropenyl-3-methoxybenzene. This reaction is catalyzed by acid or base. The hydrogen peroxide present in the reaction mixture oxidizes the methoxy group to an aldehyde, which then reacts with the styrene. In addition, this reagent can be used to methylate chlorides and transfer alkyl groups. The electroreduction of this compound yields c–h bond and peroxide. This reagent can also act as an oxidant in organic synthesis.</p>

Versatile small molecule scaffold

<p>2-Cyclohexylideneacetaldehyde is a carbinol that is synthesized from the reaction of an alkyl group with phosphorus pentoxide and hydroxy group. It is used as a reagent in organic synthesis, specifically for the production of hyaluronic acid. 2-Cyclohexylideneacetaldehyde may be used as an additive in cosmetics and personal care products to provide moisturizing effects. It also has pheromone-like activity, which can be used to attract insects such as mosquitoes and fruit flies.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>4-Thioureidobenzenesulfonamide (4-TBS) is a biochemical that interacts with β-catenin and inhibits the proliferation of cardiac and cancer cells. 4-TBS has been shown to have anticancer activity in vitro, but clinical studies have not yet been conducted. 4-TBS has been shown to inhibit the growth of testicular cancer cells in whole-cell patch-clamp assays. 4-TBS also has an inhibition potential for heart disease, which may be due to its ability to reduce carbonic anhydrase 2 levels.</p>

Methyl 4-(methoxymethyl)benzoate is a monomer that can be used to synthesize bioplastics. It is dehydrating and has a furanic ring, which makes it a good candidate for polymerization. Methyl 4-(methoxymethyl)benzoate can be used as an alternative to ethylene as the monomer in polyethylene terephthalate (PET). PET is a thermoplastic that has been shown to degrade slowly in the environment. The dehydration of methyl 4-(methoxymethyl)benzoate takes place at low temperatures with zirconium, which provides the activation energy needed for this reaction. The dehydration of methyl 4-(methoxymethyl)benzoate also produces 5-hydroxymethylfurfural (HMF), which can be used as a renewable fuel or chemical feedstock. Strategies for synthesizing methyl 4-(methoxymethyl)benzoate

<p>1,9-Decadiyne is a monolayer that has been synthesized from the coupling of two phenylacetylene molecules. This molecule has a molecular weight of 204. The interpunctella and pteleifolia species are the only known natural sources of 1,9-decadiyne. These species were bioassayed for antifungal activity against a number of fungi, including Aspergillus niger and Candida albicans. The optical properties of 1,9-decadiyne have been characterized using UV-visible spectroscopy and found to be similar to those of eugenol. Molecular modeling studies have shown that 1,9-decadiyne copolymerizes with polystyrene in an alternating fashion. Pharmacokinetic properties have been studied in rats and show that it is absorbed through the skin and metabolized by esterases in the liver. Gel permeation chromatography results show that there is a large amount</p>

<p>1-(2-Methylpyridin-3-yl)ethanone is a ketone that can be synthesized using the reaction of methyl sulfone, benzyl sulfone, and sulphone. It has been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis and has been used as a nonsteroidal anti-inflammatory drug (NSAID). 1-(2-Methylpyridin-3-yl)ethanone has also been shown to have analgesic effects in mice. This synthetic compound may be useful in treating inflammation, pain, and fever.</p>

Versatile small molecule scaffold

<p>Ethyl 2-methylnicotinate is a synthetic compound that has been used in the synthesis of other compounds. It is derived from nicotinic acid and ethyl alcohol, and its chemical formula is C9H11NO2. The compound is decarboxylated to give ethoxycarbonyl, which reacts with quinolizine to form an amide. Ethyl 2-Methylnicotinate can be synthesized by reacting hydrochloric acid with an amide, or it can be obtained from the reaction of acetaldehyde and amine. This process produces an n-oxide as a byproduct, which can then be converted into other products.</p>

<p>2,3-dimethylquinoline is a molecule that is used in wastewater treatment. It can be synthesized from 2,3-dimethylaniline and hydrochloric acid. This compound has been shown to have a high affinity for amines and other functional groups, which makes it a good candidate for use in activated sludge systems. The redox potential of this molecule also allows it to oxidize glyoxal and naphthalene. The immobilized form of this compound is used as an adsorbent for the removal of particles from wastewater.</p>

<p>Cyclododecanol is a non-polar solvent that has been used in pharmaceutical preparations. Cyclododecanol is produced by the reaction of cyclododecanone with dodecanedioic acid, fatty acids, and hydrogen fluoride. The hydroxyl group of cyclododecanol reacts with piperazine to form a solid catalyst. This reaction solution can then be separated into two layers using a section: the lower layer contains cyclohexane and the upper layer contains cyclododecanol. Cyclododecanol has a hydrophobic effect due to its lack of polar functional groups.<br>Molecular Weight: 150<br>Boiling Point: <br>Melting Point: -156°C<br>Solubility: Soluble (0.1 g/100 mL) in water<br>Flash Point: <br>Vapor Pressure: <br>Density: 0.988 g/mL at 25°C</p>

Versatile small molecule scaffold

<p>3-Iodo-2-propynol is a microbicidal agent, which belongs to the group of phenyl substituted alkylthio compounds. It is active against acarids and reactive with metal ions and organic solvents. 3-Iodo-2-propynol has been shown to have a high microbicidal activity against microorganisms such as Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. The chemical structure of 3-iodo-2-propynol can be described as a chlorinated derivative of 2-propenal.<br>3-Iodo-2-propynol is an ester hydrochloride with the molecular formula CHClNO that was synthesized in 1885 by A. Wurtz and C. Perkin. The chemical properties of this compound are similar to those of phenylethyl alcohol (PEA).</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>8-Bromonaphthalene-1-carboxylic acid is an organic compound with the chemical formula C6H4BrO2. It is a white solid that is soluble in water, methanol, and ethanol. 8-Bromonaphthalene-1-carboxylic acid can be synthesized by hydrolysis of ethyl esters of naphthalene with alkali or sulphonation. The yields are usually low (25%). The product can also be made via the diazotization of naphthalenes in the presence of sodium azide to form naphthamide, which then reacts with bromine to form 8-bromonaphthalene-1-carboxylic acid. 8-Bromonaphthalene carboxylic acid has been used as a nucleophile in organic synthesis for conjugate addition reactions.</p>

<p>Dimethyl Dodecanedioate is a chemical compound that belongs to the group of glycol esters. It is a solid catalyst for the production of nitrogen-containing organic compounds. Dimethyl Dodecanedioate can be used as a starting material in the synthesis of various chemical structures, such as fatty acids, which are important in the chemical and pharmaceutical industries. This product also has catalytic properties, which make it useful for hydrogenation and oxidation reactions.</p>

<p>3-Methyl-5-phenyl-1,2-thiazole is a heterocycle that is biologically active. It is an intramolecular nucleophilic addition to a carbonyl group. This reaction has been shown to be one of the most efficient methods for the synthesis of 5-substituted isothiazoles, which are bioactive substances with anticancer properties. The strategy of using 3-methyl-5-phenyl-1,2-thiazole as a substrate in cross coupling reactions has been used in cancer chemotherapy.</p>

Versatile small molecule scaffold

<p>2-(Acetyloxy)-5-chlorobenzoic acid is a potent apoptotic agent that is being investigated for its potential use in the treatment of cancer. It has been shown to inhibit tumor growth and increase survival in animal models and has been assessed in human clinical trials. 2-(Acetyloxy)-5-chlorobenzoic acid induces apoptosis by inhibiting DNA synthesis, protein synthesis, or both. It also inhibits the activity of caspases, enzymes that are involved in tumor cell death. This compound may be used to treat Alzheimer's disease because it inhibits tau phosphorylation, which is an important marker for Alzheimer's disease pathology.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold