Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Octahydroindolizin-7-one is a heterocyclic compound that has been isolated from the fungus Ganoderma lucidum and the bacterium Streptomyces griseus. It has an enamine structure, which can be converted to an amine by reduction with lithium aluminum hydride. Octahydroindolizin-7-one has been shown to inhibit bacterial growth through the inhibition of protein synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Methyl-3,4-dihydroisoquinoline is a chemical compound that is used in the synthesis of 1-methyl-3,4-dihydroisoquinoline N-oxide. 1,2-Dihydroisoquinolines are amine derivatives that are important for their physiological properties. The asymmetric synthesis of 1,2-dihydroisoquinolines is important for the development of new drugs and pharmaceuticals. This reaction scheme includes two steps: the first step involves the condensation of an imine with a catecholamine to form an imine; the second step involves cyclization of this imine to form a 1,2 dihydroisoquinoline. The use of additives such as sodium methoxide or dimethylsulfate can increase selectivity and yield by stabilizing one enantiomer over another. The products from this reaction are methylated with methyl iodide in the presence of potassium</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,2,3,3-Tetramethylcyclopropyl)methanol is a reagent that is used in the synthesis of insecticides and in the preparation of other organic compounds. It is prepared by reacting phosphorus with chlorinating agents such as thionyl chloride or phosphoryl chloride. This chemical can also be synthesized from halogenated alkanes by catalytic chlorination. 2,2,3,3-Tetramethylcyclopropyl)methanol has been employed as a Grignard reagent and Wittig reaction catalyst.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-3-methyl-3,4-dihydropyrimidin-4-one is a compound that belongs to the group of imines. It can exist as two isomers: an enamine and a ketimine. The enamine of 2-amino-3,4-dihydropyrimidin-4-one has been found to be a transition state analogue for ammonolysis reactions. The ketimine form of this compound has been shown to have tautomeric properties that are analogous to those of acetaldehyde. Chemists use spectroscopy to study the magnetic properties, dichroism, and spectra of the compound in order to learn more about its structure and reactivity.</p>

<p>Quinoxaline-1,4-diium-1,4-bis(olate) is a genotoxic agent that has been shown to cause DNA damage and mutations. In vitro assays have shown that this substance is reactive with human serum in a photochemical reaction, which generates malonic acid and oxidative DNA. It also inhibits bacterial growth by binding to the bacterial 16S ribosomal RNA molecule, thereby inhibiting protein synthesis. This substance has been shown to be active against solid tumours in vivo. The structure of quinoxaline-1,4-diium-1,4-bis(olate) contains a chlorine atom at position 1 and 4 of the aromatic ring system. This chlorine atom can be displaced by an n-oxide group or reduced to form a quinone methide species. These reactions are thought to be responsible for the biological properties of this compound.</p>

<p>2,6-Dimethyl-4-nitrophenol is a chemical with the potential to inhibit anions. It has been shown to be active against some medicines and has been used as a reagent in chemical ionization. 2,6-Dimethyl-4-nitrophenol has been found in phosphoric acid solutions that were used to treat blood pressure problems. It also inhibits the production of human estrogen receptors by binding to them and preventing their activation. This inhibition can lead to changes in cellular function that are associated with cancer.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Racemic 2-bromocyclohexanol is a cyclopentyl compound that has been shown to have experimental and theoretical studies of conformational changes in the hydroxyl group cavity. Racemic 2-bromocyclohexanol has axial stereochemistry and its bromohydrins are alicyclic isomers with different conformations. The population of each conformer depends on the isotopic effects, which can be experimentally determined using molecular simulations.</p>

<p>4-Methoxy-2,6-dimethylphenol is a phenolic compound that has been studied using magnetic resonance spectroscopy and other techniques. The compound can be found in a variety of plants, such as the leaves of the tea plant Camellia sinensis. It is used in some natural products for its antioxidant and antimicrobial properties. 4-Methoxy-2,6-dimethylphenol has been shown to have an effect on cell proliferation by inhibiting mitochondrial respiration and electron transport. This may lead to cancer prevention.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Hydroxynaphthalene-1-carboxylic acid is a natural product that inhibits the growth of bacteria. It was first isolated from Streptomyces lividans, an actinobacterium, and was shown to be effective against gram positive and gram negative bacteria. 5-Hydroxynaphthalene-1-carboxylic acid has been used to study the molecular structure of benzene derivatives, including biphenyls, which are responsible for the degradation of polychlorinated biphenyls (PCBs). The skeleton structures found in 5-hydroxynaphthalene-1-carboxylic acid were determined to be monosubstituted by substituent effects. This natural product also has antiinflammatory properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclohexanesulfonamide is a synthetic high-potency sweetener that has been shown to have the same sweetness as sucrose in water. Cyclohexanesulfonamide can be used as a functional sweetener in foods and beverages. The compound has been shown to inhibit inflammation, which may be due to its ability to bind to the receptor for inflammatory mediators. Cyclohexanesulfonamide has also been shown to have antidepressant properties and may be useful for treating depression, hyperproliferative diseases, and other conditions involving inflammation.</p>

<p>(2S)-2-(Dimethylamino)-4-methylpentanoic acid is a synthetic, stable isotope-labeled, fluorescent probe that is used in proteomics and analytical chemistry. The (2S)-2-(Dimethylamino)-4-methylpentanoic acid reacts with the amine groups of proteins and can be detected using UV-vis absorbance spectroscopy. This probe has been shown to be effective in the detection of cancer cells by measuring the concentration of protein markers such as triazine. This probe is metabolized by the body into 2-(dimethylamino)octanoic acid, which can be detected in urine samples.</p>

<p>Versatile small molecule scaffold</p>

<p>5-(Benzyloxy)-1-methyl-1H-indole is a potent inhibitor of human prostate enzyme. It also has inhibitory activity against other nonsteroidal human enzymes, including the potent inhibitory activity against human benzoyl peroxide reductase. 5-(Benzyloxy)-1-methyl-1H-indole inhibits steroid biosynthesis in the human prostate gland, inhibiting the conversion of cholesterol to testosterone. This compound may be used as an alternative to finasteride for treating benign prostatic hyperplasia, due to its low toxicity and lack of side effects.</p>

<p>4-Phenyl-1,2-oxazole is a catalytic anion with a systematic name of 4-phenyl-1,2-dihydro-2H-1,2-oxazole. It belongs to the class of isoxazoles and has been shown to be used as antithrombotic agents in the process of coagulation. It has also been shown that this compound can be used for the synthesis of heterocycles. The kinetic reaction rate is dependent on the concentration of proton and carboxylic acid anions. This reaction is catalysed by metal ions such as copper and nickel. 4-Phenyl-1,2-oxazole has been synthesized from phenylacetic acid through a laborious process involving chlorination and oxidation reactions.</p>

<p>2,6-Di-tert-butylbenzene-1,4-diol is a phenoxy radical that can be used to study the kinetics of polymeric biomaterials. It has been used in manometric and kinetic studies of polymerization reactions. 2,6-Di-tert-butylbenzene-1,4-diol is an organic compound with a molecular weight of 170.2 g/mol and a chemical formula of C12H24O2. The compound is soluble in ethanol, ether and chloroform. Spectrophotometry has shown that 2,6-Di-tert-butylbenzene-1,4-diol absorbs light with wavelengths between 200 nm and 400 nm.</p>

<p>N-Hydroxy-N-methylbenzamide is an organic compound that contains a radical chain of alkyl substituents. It can react with amines to form N-hydroxy-N-methylbenzamide, which has been shown to inhibit the growth of bacteria. This amide can be synthesized by reacting benzoyl chloride with methanamine and hydroxylamine. The synthesis method is catalyzed by nitric acid, which also forms a ligand complex with the benzoate moiety. The ligand complex is chiral, and therefore the product can exist in two different forms: one containing an R configuration and the other containing an S configuration.</p>

<p>6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one is a biomolecular compound that belongs to the class of aminophenols. It is synthesized by the oxidative coupling of deoxyvasicinone with sodium hypochlorite and irradiation. The reaction time for this reaction is 10 minutes at room temperature. 6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one has been shown to have antimicrobial activity against bacteria and fungi in vitro. Its structure is similar to mackinazolinone and synthetic analogues such as 2-(4'-aminophenyl)thiazole. 6H,7H,8H,9H,11H-Pyrido[2,1-b]quinazolin-11-one also reacts with dien</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 1-naphthoate is an organic molecule that has been shown to inhibit the glycogen synthase kinase-3 (GSK-3), which is a protein involved in the progression of cancer. Methyl 1-naphthoate also inhibits other proteins, such as the mcl-1 protein, which is involved in cell death. This compound has been shown to have anti-inflammatory properties and may be used to treat inflammatory bowel disease or fatty acid oxidation disorders. Methyl 1-naphthoate can be synthesized in a solid catalyst and has been used as an optical sensor for carbonyl groups.</p>

<p>(S)-Benzyl 2-amino-4-methylpentanoate hydrochloride is a diastereomer of (R)-benzyl 2-amino-4-methylpentanoate hydrochloride. This compound is a ketoxime with the same reactivity as benzoyl peroxide, but it has been shown to be more efficient than benzoyl peroxide in catalytic oxidation reactions. It is also an antibiotic that inhibits the growth of bacteria by binding to DNA and RNA polymerases.</p>

<p>Methyl 9-Octadecenoate is a fatty acid that belongs to the group of natural compounds. It has been identified as an antidiabetic compound and has shown anti-inflammatory properties. Methyl 9-Octadecenoate has been studied for its use in light-induced dry weight loss and process optimization. This chemical is also a reaction product of acetate extract, which can be used as biodiesel or for other purposes. The methyl ester of this fatty acid is methyl eicosanoate.</p>

<p>Versatile small molecule scaffold</p>

<p>1,2,3-Tris(2-cyanoethoxy)propane is a contaminant that has low detection limits and can be detected on-line. It has been shown to interact with oxygenated solutes in the chromatographic method used to analyze silicone. 1,2,3-Tris(2-cyanoethoxy)propane has also been shown to be an injectable solute that can desorb from silicone during the chromatographic analysis. This contaminant is not expressed by S. pneumoniae or S. pyogenes, but is expressed by E. coli and Streptococcus sp.</p>

<p>1,3-Dihydro-2-benzothiophene is a hydroxylated thiophene that binds to the benzothiazole receptor. It has been shown to inhibit the growth of cancer cells in vitro. 1,3-Dihydro-2-benzothiophene also has anti-inflammatory properties and is used to treat chronic bronchitis and inflammatory diseases such as Crohn's disease and ulcerative colitis. This drug may have some side effects, such as allergic reactions and low bioavailability. It can be toxic if taken by an infant or pregnant woman.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-5-ethylbenzoic acid (2A5EB) is a chalcone that has been shown to have antimicrobial and antitumor properties. 2A5EB inhibits the synthesis of proteins by binding to the ribosomal RNA, which prevents the production of proteins vital for cell division. 2A5EB also inhibits protein synthesis by binding to the ribosomal RNA in mammalian cells. 2A5EB has been shown to have anticancer activity against human cancer cell lines and has also been used as a lead compound in drug discovery programs.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-2-ethylbenzoic acid is a naturally occurring amino acid. It is a vasopressin analog that has been shown to lower blood pressure in vivo. 4-Amino-2-ethylbenzoic acid binds to the receptor for arginine vasotocin, which is the natural ligand for this receptor and activates the receptor. It also has a high lipophilicity and extracellular Ca2+ binding capacity. 4-Amino-2-ethylbenzoic acid may act as an estrogen antagonist by competing with estradiol for binding to estrogen receptors on cells.</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-Nonylquinolin-4-ol is a molecule that binds to the human receptor and has a trajectory. It has been shown to be a potent antimicrobial agent against bacteria, fungi, and viruses. The lysing of cells in vitro is an indication of the cytotoxicity of 2-nonylquinolin-4-ol. This molecule is also known for its ability to inhibit HIV infection by binding to CD4 receptors. This compound has an n-oxide group, which is formed from the reaction of oxygen with a hydroxyl group on the C2 position of the quinoline ring. 2-Nonylquinolin-4-ol can be found in chemical structures such as polymers and dyes.</p>

<p>N-Tert-butylbenzenesulfonamide is a sulfonamide that reacts with an azide to form a five-membered ring. This reaction is known as the aziridination reaction. N-Tert-butylbenzenesulfonamide is insoluble in water and has a molecular weight of 200 g/mol. It is used in polymerase chain reactions, which are experiments where the enzyme DNA polymerase replicates the DNA molecule by adding nucleotides to each end of the strand. N-Tert-butylbenzenesulfonamide has been shown to inhibit RNA polymerase activity and cellular growth in vitro. This agent also inhibits protein synthesis by interfering with the binding of tRNA molecules to ribosomes, preventing amino acids from being incorporated into proteins.</p>

<p>2-(4-methylphenyl)-1,2-benzisothiazol-3(2H)-one (BMS) is a chemical compound that has been shown to have inhibitory properties against infectious diseases. BMS is an analog of ethylene diamine and selenium compounds, which are known for their inhibitory effects against bowel disease. It has been found to be effective against subcutaneous tumors in mice. In addition, it has been shown to have a beneficial effect on inflammatory bowel disease in mouse models and skin cancer in rats.<br>BMS also inhibits the proliferation of granulosa cells and K562 cells by inhibiting cell signaling pathways.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-6-nitro-1,3-benzothiazole is a synthetic compound that is used in optical chemistry. It functions as a coupling agent and has been shown to be efficient in its use. 2-Bromo-6-nitro-1,3-benzothiazole also has magnetic properties, which can be useful for synthesizing polymers. This compound is an organic compound that belongs to the family of heterocycles and has redox properties, electrochemical properties, and structural properties. The synthesis of 2-bromo-6 nitrobenzothiazole involves the following steps:</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Propylbenzenamine is an attractant for tsetse flies. 3-Propylbenzenamine has been shown to be a potent carbonate catalyst and can also be used as a carbamate pesticide.</p>

<p>Methyl 5-bromo-3-methylfuran-2-carboxylate (MBM) is a metabolite that is synthesised from the sesquiterpenoid, furan. MBM is an efficient sponge for atmospheric bromine and has been shown to be an intermediate in the biosynthesis of acyclic compounds.</p>

<p>Heptanoyl chloride is an organic chemical compound that belongs to the group of acyl halides. It is a colorless gas that has a strong, unpleasant smell. Heptanoyl chloride reacts with hydrochloric acid and trifluoroacetic acid to form heptanoic acid and trifluoroacetone. The nucleophilic attack on the carbonyl carbon leads to formation of the corresponding alkyl halide. The reaction of heptanoyl chloride with nitro leads to formation of the corresponding nitroalkane. Heptanoyl chloride can be used in detergent compositions as a fatty acid or galacturonic acid substitute. It is also used in pharmaceutical preparations for the treatment of inflammatory diseases such as arthritis, asthma, and psoriasis.</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 2-nitropropionate is an organic compound that is a monosubstituted nitroalkane. It is a colorless liquid with a characteristic odor. This compound has been used in the production of polyacrylamide, polyacrylic acid, and polyacrylonitrile resins. It is also used as a chemical intermediate in the production of quaternary ammonium salts or alkylating agents. Ethyl 2-nitropropionate is activated by chloride and reacts with amines to form nitrosamines. The nitro group on this compound can undergo nucleophilic attack by alcohols to form nitrate esters (e.g., ethyl 2-nitropentanoate).</p>

<p>Versatile small molecule scaffold</p>

<p>2,2,2-Trichloro-N'-hydroxyethanimidamide (TCEH) is a potent antibacterial agent that has been used in analytical chemistry as a reagent for the determination of anilines. It inhibits bacterial growth by binding to DNA and RNA. The profile of TCEH was determined by ultrasonication and found to be active against most Gram-positive bacteria, but inactive against Gram-negative bacteria. In addition, this drug was shown to be effective against oxadiazole-resistant strains of bacteria. The mechanism of TCEH is based on the reaction with an acyl halide to generate a reactive intermediate which attacks the nucleophilic center of the DNA molecule. This results in strand breakage and subsequent inhibition of bacterial growth. TCEH can be used as a substitute for other more toxic compounds such as mercury or arsenic compounds that are often used in chemical synthesis reactions.</p>

<p>2-Oxobicyclo[2.2.1]heptane-1-carboxylic acid is an organic compound that belongs to the group of carboxylic acids. It can be synthesized by dehydration of formic acid with ethyl bromoacetate, followed by hydrolysis of the resulting 2-formylbicyclo[2.2.1]heptane-1-carboxylic acid with base. The compound can also be obtained by catalytic demercuration of oxymercuration products of tetrahydrofuran, and has been shown to have analogous reactions as methyl formate and acetone.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>7-Methyloxepan-2-one is a synthetic chemical that is produced by the reaction of an amine with acetyl chloride. It is also biotransformed by bacteria, such as Clostridium, to produce 7-methyloxepan-2-ol. This compound is used as a polymerization initiator and has been shown to be useful in the synthesis of polymers with desirable properties. 7-Methyloxepan-2-one can be used in the production of ethylene gas for use in the petrochemical industry and as a chemical intermediate for other products.</p>

<p>1-Hydroxy-3-methylanthraquinone is a quinone compound that has been shown to have binding constants for the fungal filamentous fungus, Vulgare L. (strain pachybasin), and bacterial strains. This chemical has also been shown to have biological properties such as antimicrobial activity against Acetobacter aceti, inhibition of growth of the human pathogen Streptococcus pyogenes, and induction of locomotor activity in mice. 1-Hydroxy-3-methylanthraquinone binds to fatty acids in the cell membrane and alters the permeability of this membrane. 1HMR spectroscopy data suggests that this compound is regiospecific with respect to its two hydroxyl groups.</p>

<p>3-Methyl-2-hexanone is a chemical that belongs to the group of carbonyl compounds. It has been shown to be an attractant for the triatomine bug and reduviidae, which are insects that transmit Chagas disease. 3-Methyl-2-hexanone is also used as a pesticide and in polymerized form as a microcapsule for the treatment of urinalysis samples. The structure of 3-methyl-2-hexanone consists of a linear response with four carbon atoms. The compound contains two carbonyl groups, which are common in organic acids, and can be broken down by bond cleavage. 3-Methyl-2-hexanone has been detected in human urine at concentrations ranging from 0.04 to 8.9 µg/L, depending on age and sex.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N,N-Dimethyl-5-nitropyridin-2-amine is a molecule with high polarizability. It is used in the production of optoelectronics and functional theory. The kinetic constants are determined by protonation and deprotonation reactions. The thermodynamic constants are determined by protonation and deprotonation reactions, as well as by the dipole moment of the compound. Preparative methods include intramolecular hydrogen transfer reaction or reductive amination. The impurities present in this molecule are aminopyridine and proton.</p>

<p>Versatile small molecule scaffold</p>

<p>7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one is a disubstituted coumarin nucleus and a potent anti-HIV agent. It has been synthesised as a lead compound to inhibit HIV reverse transcriptase by binding to its active site, which is the enzyme responsible for DNA synthesis. The probe exhibits dose dependent inhibition of HIV replication, with an IC50 of 0.5 μM. This compound also inhibits cysteine proteases, such as cathepsin B, and reverses the effects of certain chemotherapeutic agents on cancer cells. 7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one is fluorescent in solution and this property can be used for detection purposes.</p>

<p>N-Methylcaprolactam is a white, crystalline compound with a melting point of 28.5°C. It is soluble in water and insoluble in organic solvents. N-Methylcaprolactam has a molecular weight of 152.2 g/mol and its chemical formula is C8H14N2O2. The divalent hydrocarbon has an aromatic hydrocarbon ring with two protonated nitrogen atoms bonded to this ring, which are responsible for the molecule's polarizability. N-Methylcaprolactam has been shown to activate rat liver microsomes, which may be due to its ability to bind to the enzyme adenylate cyclase and inhibit protein synthesis. This drug also causes a decrease in the level of water vapor and chloride ions in the environment and can be found as an environmental pollutant from metal hydroxides or water molecules reacting with aliphatic hydrocarbons such as methane or ethane. Struct</p>

<p>4-(1H-benzo[d]imidazol-2-yl)-N,N-dimethylaniline is a molecule with the chemical formula C8H6N2. It has an optimised vibrational profile that can be used to identify it. The functional theory of molecular orbitals predicts that 4-(1H-benzo[d]imidazol-2-yl)-N,N-dimethylaniline will have a molecular electrostatic potential (MEP) of -0.13 kcal/mol and a shift of 0.04 cm(-1). The MEP and shift are calculated by using a single crystal x-ray diffraction experiment. This molecule has conformational parameters that can be calculated by using optimised atomic orbital parameters, which will give the conformational probability for each conformation as well as the total energy for each conformation. The conformations are then plotted on a graph in order to find the most probable con</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-Butylacrylamide is a monomer that is used in the production of polymers. It is a colorless, oily liquid that is soluble in organic solvents but not water. N-Butylacrylamide has been shown to inhibit microbial growth by binding to phosphonates and organic solvents, which are found on the surface of bacteria. These interactions lead to cell death by preventing the uptake of nutrients and causing leakage of cellular contents. The phase transition temperature for N-butyl acrylamide is below room temperature, making it an ideal candidate for use as an anti-infective agent.</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>6-[2-(4-Methoxyphenyl)-1H-1,3-benzodiazol-6-yl]-5-methyl-2,3,4,5-tetrahydropyridazin-3-one hydrochloride (6MP) is a potent inhibitor of Cox-2 with IC50 values in the low nM range. 6MP has been shown to inhibit xanthine oxidase activity and to protect against oxidative stress in rat heart cells. 6MP also inhibits cell factor activity in human carcinoma cell lines and is able to induce apoptosis in these cells. 6MP has been shown to be an effective inhibitor of dpp IV activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(2-Aminopropyl)-N,N,3-trimethylaniline (4APTMA) is a drug that has been shown to be a 5-HT receptor antagonist. It binds to the 5HT1A receptor and inhibits its activity. 4APTMA can be used for the treatment of metabolic disorders such as obesity and bowel disease. The drug has also been shown to have inhibitory properties in animal models of inflammatory bowel disease, which may be due to its ability to block the uptake of serotonin into the brain.<br>br&gt;br&gt;<br>4APTMA is metabolized by CYP2D6 and CYP3A4 enzymes. It has also been shown that 4APTMA has an irreversible inhibition effect on dopamine uptake in a model system. This means that it prevents use of dopamine by binding to the transporter protein responsible for this action.</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>