Building Blocks

<p>Ethyl 5-chloropentanoate belongs to the class of compounds called test compounds. It was synthesized for the purpose of studying the biological properties of histone lysine residues. The compound has shown a number of biological effects, including activation energy and quantum theory, at low concentrations in women. This chemical is a chloride ion donor and contains an ethyl group and a carbonyl group. It has been shown to be an effective activator of pentene isomers that are present in tissues in order to form reactive intermediates that can initiate reactions with other molecules, such as lysine residues on proteins.</p>

<p>2-(Propan-2-yl)butanedioic acid is a depsipeptide with microbial activity. It inhibits bacterial growth by binding to the beta-subunit of ATP synthase in the microbial cell membrane, which prevents the synthesis of ATP and other metabolites required for cell division. 2-(Propan-2-yl)butanedioic acid has been shown to inhibit Salmonella typhimurium and Staphylococcus aureus in vitro and in vivo. The mechanism by which this drug inhibits bacterial growth is not yet fully understood, but it may be due to its ability to bind to fatty acids or hydrocarbons that are found on the surface of microorganisms.</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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>3-Chloropropyltrimethylsilane is a diphenyl ether that inhibits the cross-linking of proteins and enzymes in infectious diseases. It has been shown to be an effective catalyst for oxidation reactions, such as the conversion of metal carbonyls to unsaturated alkyls. 3-Chloropropyltrimethylsilane has also been shown to inhibit cavities in glycol ethers and corrosion in hydrochloric acid solutions. This chemical has fluorescence properties. The structural formula is CHClSi(CH)CHCl, and it is a colorless liquid with a boiling point of -71°C.</p>

<p>(Trimethylsilyl)acetic acid is an organosilicon compound that has a hydroxyl group and three methyl groups. It is a metastable substance with a boiling point of about 130 degrees Celsius. (Trimethylsilyl)acetic acid can be synthesized by reacting bromoacetic acid with methyllithium or trimethylsilyl chloride. This compound has been shown to have kinetic properties such as molecular ions, kinetic energy, and inorganic acids. It also has functional groups that are able to interact with detergent compositions.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Methoxy-1,4-naphthoquinone is a natural compound that has low potency and significant cytotoxicity. It inhibits the polymerase chain reaction (PCR) by inhibiting DNA synthesis in the bacteria. This compound also exhibits antiinflammatory activity which may be due to its ability to inhibit prostaglandin synthesis. 2-Methoxy-1,4-naphthoquinone has been shown to exhibit minimal toxicity in mice and humans. It is structurally similar to p-hydroxybenzoic acid, a common ingredient found in food and cosmetics. 2-Methoxy-1,4-naphthoquinone has been used for the treatment of infectious diseases such as oral pathogens and bacterial infections caused by Helicobacter pylori or c. glabrata.</p>

<p>Versatile small molecule scaffold</p>

<p>2-[(4-Methylphenyl)amino]acetohydrazide is a crystalline solid that belongs to the group of hydrazides. It has an asymmetric, planar, two-dimensional crystal structure with dihedral angles of 1.2° and 2.6°. The compound contains a benzene ring and two hydrogen bonds.</p>

<p>Chloromethyl Methyl Sulfone is a nucleophilic acceptor for aldehydes and pyridinium compounds. It can be synthesized by the reaction of methyl sulfoxide and hydrochloric acid in the presence of triazole and hydroxide ion. Chloromethyl Methyl Sulfone is a crystalline solid that can be used to study the interaction of kinesin with methyl sulfones. This compound has been shown to have an inhibitory effect on cellular activity, which may be due to its ability to react with chloride ions, forming chloromethyl methyl sulfonium chloride.</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>

Versatile small molecule scaffold

<p>3,4-Diaminobenzenesulphonamide is a chemical compound that is used as an intermediate in organic synthesis and non-apoptotic cell death. 3,4-Diaminobenzenesulphonamide reacts with iron chloride to form ferroptosis, an environmental pollutant. It can also be used for the treatment of various cancers. 3,4-Diaminobenzenesulphonamide binds to the iron in the cell and causes cell death by forming reactive oxygen species that induce ferroptosis. 3,4-Diaminobenzenesulphonamide is also a non-apoptotic cell death agent that inhibits mitochondrial membrane potential and leads to cellular necrosis.</p>

<p>Thianthrene 5-oxide is a molecule that has been synthesized by the reaction of hydrochloric acid and thioxanthone. The molecule contains five rings which are connected with intramolecular hydrogen bonds, forming a pseudoequatorial structure. Thianthrene 5-oxide contains two functional groups, the sulfinyl group and the hydroxyl group. These functional groups are nucleophilic and can react with electrophiles to form transfer reactions.</p>

<p>Trans-2-phenyl-1-cyclohexanol is a hydroxylated cyclohexanol. It is used as a reagent in organic synthesis for the dehydration of alcohols and the acetylation of acyclic carboxylic acids. Trans-2-phenyl-1-cyclohexanol can be prepared from cyclopentene oxide and chloride by the following sequence: trans,trans,trans-2,4'-dichlorobenzophenone → trans,trans,trans-2,4'-dichlorocyclopentene → trans,trans,trans-2-(chloromethyl)cyclohexane → trans,trans,trans-2-(chloromethyl)cyclohexanol. This compound has been investigated as a model system in kinetic studies of transfer reactions such as hydrogen transfer reactions.</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>2,2-dimethylhexan-1-ol is a chemical compound that contains two methyl groups. It has been identified in the atmosphere and in the chromatographic fraction of recycled oils. It is also found in the isopropyl fraction as a result of incomplete alkylation. 2,2-Dimethylhexan-1-ol is used industrially to prepare covalent adducts with tosylates, which are used as reagents for chemical ionization (CI) spectrometry and electron capture detection (ECD). The kinetic energy of 2,2-dimethylhexan-1-ol molecules was measured by atomization velocity and linear regression analysis.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>N-Ethylmethanesulfonamide is an aliphatic compound with a chemical structure containing a benzene ring and an amide group. It has analgesic properties and can be used in pharmaceutical preparations to treat pain. N-Ethylmethanesulfonamide is structurally similar to methadone, but it is not as potent. The drug binds to the opioid receptors in the brain and spinal cord, acting as a bifunctional agonist-antagonist. This binding leads to an increase in neurotransmitter release, which inhibits pain signal transmission.<br>N-Ethylmethanesulfonamide was first synthesized by chemists at Eli Lilly and Company in 1947. The synthesis was based on research performed by scientists at the Mayo Clinic, who were trying to create medicines for animal use that had analgesic effects similar to morphine but were less addictive than morphine itself.</p>

<p>2-Chloro-6-(trifluoromethyl)benzoic acid is a plant growth regulator that inhibits the ethylene synthesis. It is used to stimulate plant growth, particularly in fruit trees and vines. 2-Chloro-6-(trifluoromethyl)benzoic acid binds to an enzyme called ACC synthase that is responsible for converting acetate into ethylene. This binding prevents the formation of ACC, resulting in lower levels of ethylene production.</p>

<p>2-Methyl-3-phenyl-3,4-dihydroquinazolin-4-one is a synthetic compound that has been isolated from natural sources. It is an acetonitrile derivative of the quinazolinones, which are found in plants such as Acacia species and Moringa oleifera. 2-Methyl-3-phenyl-3,4-dihydroquinazolin-4-one has been synthesized using acetylation and ring opening methods. The synthesis of this compound can be achieved by reacting aldehydes with amines or alkylating an amine with carbon source. The reaction mechanism is initiated by the formation of an imine intermediate followed by the addition of a nucleophile to form a second intermediate that undergoes dehydration to produce the desired product. Aluminium powder is used for drying the crude product and removing water.</p>

<p>1-(Prop-1-en-2-yl)-4-(propan-2-yl)benzene is a trinitrate that is used in the polymerization of propylene. It has been shown to stabilize copolymers and bimodal polymers, as well as being able to react with different monomers. 1-(Prop-1-en-2-yl)-4-(propan-2-yl)benzene can be prepared by cationic polymerization of phenylpropionic acid, which is an enantiomer of 1-(prop-1-en-2-yl)-4-(propane -2,3,-diyldioxy)benzene. This drug also has magnetic resonance spectroscopy properties that allow it to be used as a postulated gel permeation chromatography termination agent.</p>

<p>3-Methoxythioanisole is a transfer catalyst that catalyzes the transfer of hydrogen peroxide from an alkali metal salt to an organic substrate. The reaction proceeds via a monoprotonated intermediate. 3-Methoxythioanisole can be used for the synthesis of esters, amides and nitriles. 3-Methoxythioanisole is also a hydrophilic catalyst and can be used in phase transfer catalysis. This compound is derived from the oxidation of thiophene by hydrogen peroxide, which produces a polyoxometalate as a byproduct. 3-Methoxythioanisole has been shown to be effective in catalyzing reactions between ammonium salts and phosphotungstate, yielding ammonium tungstate or hydroxylammonium tungstate as products.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Aminomethylbenzenesulfonic acid is the most potent fluorescent probe for detecting the presence of proteins in cells. It is used as a model protein to study muscle cell biology and in analytical methods to detect protein residues. 4-Aminomethylbenzenesulfonic acid also has degenerative disease-relevant properties because it is reactive with dithionite and can be used as a synthetic amino acid for proteomic studies.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Cis-cyclobutane-1,3-dicarboxylic acid is a molecule that belongs to the class of cycloalkanes. It is an organic compound with the chemical formula CH2=C(CH3)2COOH. The chemical structure consists of a six-carbon ring in which one carbon atom is bonded to three other carbon atoms and two oxygen atoms. Cis-cyclobutane-1,3-dicarboxylic acid has been used as a starting material for organic synthesis, such as the conversion to malonic acid. This reaction system can be optimized by using techniques such as spectrometry analyses and sustainable methods.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chloro-3-iodoanisole is a tetracyclic organic compound. It is an intermediate in the synthesis of arynes and dienes by dehalogenation of substituted benzenes with organolithium reagents. 4CI has been shown to react with dienophiles, such as 1,2-dichlorobenzene, to give the corresponding ethylenic products. The yield of this reaction is dependent on steric factors, such as the electronic nature of substituents on the benzene ring and their orientation relative to one another.</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>Bromocycloheptane is a c6 alkyl that functions as an uptake inhibitor. It is used in the synthesis of other organic compounds, such as imidazole derivatives. Bromocycloheptane has been shown to inhibit uptake in the brain and consequently reduce infarctions in animal models of Alzheimer's disease. Bromocycloheptane inhibits uptake by blocking the function of the carrier protein, which carries neurotransmitters from synapses to axons and dendrites. Bromocycloheptane binds to magnesium ions, which are necessary for hydrolysis of ATP and therefore for uptake into cells. The magnesium ion is found in many enzymes involved in cellular processes, including those that produce ATP, so bromocycloheptane may interfere with cell function by interfering with these enzymes. This drug also blocks the production of lactam, a precursor molecule to GABA, which can be synthesized by glutamic acid decarboxyl</p>

<p>Versatile small molecule scaffold</p>

<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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<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>