Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 1,1',1''-(1,3,5-Triazinane-1,3,5-triyl)tris(2-bromoethan-1-one) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about DL-Tropic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-(1H-Tetrazol-5-yl)aniline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (R)-1-Propylpiperidin-3-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Polycarbosilane is a cross-linking agent that can be used to modify the surface properties of polymers. It reacts with the hydroxyl groups on the polymer to form carbosilane bonds, which lead to a change in the viscosity and other physical properties of the material. Polycarbosilane is insoluble in water and has an absorption peak at 350 nm. When reacted with argon gas, polycarbosilane reacts with oxygen or nitrogen to produce carbonyls or amines, respectively. Polycarbosilane can react with x-rays or magnetic resonance spectroscopy to produce elemental analysis data for a variety of elements. This chemical also has optical properties that make it useful as an organic solution for optical devices such as lenses and mirrors. Polycarbosilane is stable under most conditions and can be used as an efficient method for environmental pollution control by removing heavy metals from wastewater streams.</p>

<p>Pyrazin-2-ylboronic acid is a white crystalline solid that is soluble in water. It is an efficient and economical selenium source for use in the synthesis of selenides and other selenium compounds. Pyrazin-2-ylboronic acid can be produced by the reaction of aniline with borohydride, or by the reaction of pyrazine with borane. This synthetic process also provides a convenient way to produce diaryl compounds.</p>

<p>Please enquire for more information about N-​Nitroso hydrochlorothiazide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-Nitroso ramipril including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-Me-D-Ala-OMe·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl 3,4-dimethoxybenzoate is an acetate extract that has been shown to inhibit tyrosinase activity. This compound also has a potent inhibitory effect on the production of p-hydroxybenzoic acid. Methyl 3,4-dimethoxybenzoate can be synthesized from protocatechuic acid and methoxy groups. It is a chemical reaction involving three steps: condensation, dehydration, and reduction. Tyrosinase is an enzyme in the melanin biosynthetic pathway that catalyzes the conversion of tyrosine to dopaquinone. Tyrosinase activity can be inhibited by methyl 3,4-dimethoxybenzoate through competitive inhibition or by its ability to reduce the availability of substrate for this enzyme.</p>

<p>α-Ketoglutaric acid (α-KGA) is a natural metabolite of glucose and is an intermediate in the citric acid cycle. α-KGA has been shown to have powerful anti-cancer properties, which may be due to its ability to inhibit glucose uptake and metabolism in tumor cells. α-KGA has also been shown to reduce locomotor activity, which may be due to its ability to induce transcriptional regulation of genes that are involved in glucose regulation. In addition, α-KGA has been shown to regulate fatty acid synthesis by inhibiting acetyl CoA carboxylase, which is an enzyme that catalyzes the production of malonyl CoA.</p>

<p>4-Iodo-1-methylpyrazole is a reductive agent that is used in organic synthesis. It can be used as a reducing agent for the conversion of aldehydes and ketones to alcohols. 4-Iodo-1-methylpyrazole can be crystallized from diethyl etherate and blood. The product yield from this reaction is high, but it requires an oxidant such as trifluoride or plavix to react with the diacetates. 4-Iodo-1-methylpyrazole can also be synthesized by reacting allylsilanes with iodine gas in the presence of a base. This synthesis method produces 4-iodo-1-methylpyrazole in good yield and with little difficulty.</p>

<p>5-Iodo-2-nitrobenzoic acid is a fine chemical that is used as a building block in the synthesis of complex compounds and research chemicals. This compound has been shown to be an effective reagent for the synthesis of many different types of compounds. It can also be used as a reactant or intermediate in organic syntheses, such as those involving cross-coupling reactions. 5-Iodo-2-nitrobenzoic acid is a versatile building block that can be used in both simple and complex chemical reactions.</p>

<p>Please enquire for more information about Imidazolepyruvic acid hydrobromide hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Inosine 5'-monophosphate disodium hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Imidazole methyl carboxylate is a drug that inhibits the activity of dehydrogenases and other enzymes. It has been shown to be an inhibitor of the enzyme catalase in vitro and in vivo, which may be due to its ability to bind bidentately with the active site. 4-Imidazole methyl carboxylate is effective when administered orally, and it has been shown to improve symptoms of neurodegenerative diseases such as Alzheimer's disease. This drug also has a trifunctional chemical structure that contains a macrocyclic ring system with an imidazole group and a carboxylic acid group. The redox potential of this molecule makes it suitable for use as an antioxidant.</p>

<p>Please enquire for more information about 1-Boc-2-methyl (2R,3S)-3-hydroxypyrrolidine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>3-Fluorobenzyl bromide is a fluorinated benzyl derivative that can be used as a fluorescent probe for the study of cellular uptake and metabolism. 3-Fluorobenzyl bromide has been shown to have potent inhibitory activity against the growth of cancer cells in culture. It has also been shown to reduce ischemia reperfusion injury in cardiac tissue. The pharmacokinetic properties of 3-fluorobenzyl bromide have been studied in detail, revealing a rapid uptake into cells and elimination by renal excretion. This compound also inhibits the growth of P. aeruginosa in an animal model, with no effect on other bacterial strains or mammalian cells.</p>

<p>N-Fluorobenzenesulfonimide is an organic compound with the molecular formula CHFNS. It is a fluorinating agent that can be used for the synthesis of organic compounds. N-Fluorobenzenesulfonimide has been shown to have anti-inflammatory properties and has shown promising results in animal studies for the treatment of hepatitis. The mechanism of action is not fully understood, but it may involve the formation of hydrogen bonds between N-fluorobenzenesulfonimide and amino acid residues in proteins, leading to inhibition of protein synthesis.</p>

<p>Please enquire for more information about 2-Furanamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethyl-2-oxazoline is a structural analysis of 2-ethyl-2-oxazoline. It is a biocompatible polymer that has been shown to be cytotoxic to cells in culture. The mechanism for this cytotoxicity is not clear, but it may be due to the significant hydroxyl group present in the molecule. 2-Ethyl-2-oxazoline is also a pharmacological agent and can be used as an adjuvant in vaccines. This polymer has shown no significant antibody response and has water vapor permeability properties.</p>

<p>3,4-Difluoro-1H-Pyrrole is a neutral compound with a molecular weight of 136.17 g/mol. It has the chemical formula C6H3F2N and it can be found in reactions involving the congener and coordination chemistry. 3,4-Difluoro-1H-Pyrrole is an intermediate in organic synthesis that is used as starting material for other organic compounds such as pharmaceuticals and agrochemicals. The redox potential of 3,4-Difluoro-1H-Pyrrole is -0.42 V for the reaction with chloride solution and its basicity is 0.89 mM at 25°C. This molecule has been studied by X-ray crystallography and by titration calorimetry for hydrogen bonding interactions.</p>

<p>2,5-Dimethyl-1,4-benzenediamine is an amine that is used as a reagent in organic synthesis. It is also used to derivatize other molecules and as a precursor to other compounds. 2,5-Dimethyl-1,4-benzenediamine has been shown to be a good nucleophile and can react with electrophiles such as difluoride and the metal ion Ag(I). The reaction rate of 2,5-dimethyl-1,4-benzenediamine can be determined using high performance liquid chromatography or electrospray ionization. This compound can be synthesized from phenylmagnesium bromide and methyl iodide in the presence of aluminium chloride. It is possible to immobilize 2,5-dimethyl-1,4-benzenediamine on mesoporous silica by attaching it to the surface of the porous material with aminop</p>

<p>1,1'-Carbonimidoylbis-1H-imidazole is a ligand that binds to amines and isosteres. It can be activated with electrophilic reagents to form an activated linker. This ligand has been shown to inhibit the growth of xenograft tumor cells in mice by binding to functional groups on the cell surface. This drug also has been shown to bind to the receptor for advanced glycation end products (RAGE) and inhibit its function. 1,1'-Carbonimidoylbis-1H-imidazole has also been evaluated as a cancer therapeutic agent in animal models.</p>

<p>Veterinary drug, ectoparasiticide</p>

<p>2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride is a benzimidazole derivative. It has a chemical stability and can be used for wastewater treatment. It is also a pump inhibitor and can be used for anhydrous sodium magnesium salts. This product is synthesized from the reaction of protonated 2-bromo-4-methoxyphenol with 2,6-dimethylpyridine in the presence of hydrochloric acid. The reaction was carried out in an asymmetric synthesis using a proton transport system. 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride is soluble in water and has a pH of 1 to 3. It has been shown that this product can be used as an antioxidant and as a metal chelation agent.</p>

<p>Cyclobutanethiol is a 1-cyclopentene-1-carboxylic acid, which is a cyclic form of the alkylthio group. It is an organic solvent with a hydroxyl group at one end and an alkyl group at the other end. Cyclobutanethiol can be used as a sealant or as a solvent in organic chemistry. The compound has been shown to inhibit insulin resistance by binding to cb1 receptors on cells, thereby inhibiting the production of glucose. Cyclobutanethiol also absorbs ultraviolet light, so it can be used in photochemistry.</p>

<p>Please enquire for more information about H-beta-Cyclohexyl-Ala-OMe·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>R-(-)-3-Chloro-1,2-propanediol is a chiral epoxide that is used in the synthesis of other chemicals. It has been shown to be active against bacterial strains such as corynebacterium and coryneform bacteria. This chemical can be synthesized from hydrochloric acid and chlorinated propane with an asymmetric synthesis. The R-(-)-3-Chloro-1,2-propanediol can also be synthesized through electrochemical methods using chloride ion as the reducing agent. This compound is soluble in water and shows kinetic activity with carbon sources when used as an antibiotic.</p>

<p>6-Chlorohexanol is a fatty alcohol with a hydroxyl group. It is soluble in water and has a phase transition temperature of -114°C. 6-Chlorohexanol can be synthesized by reacting 2,6-dichlorophenol with hydrochloric acid and sodium hydroxide in the presence of azobenzene. The reaction solution is then heated to about 300°C for 3 hours. 6-Chlorohexanol is used as a model system for studying the photochemical reactions of fatty acids. Hydroxy groups are susceptible to light exposure, which leads to the formation of carbonyl compounds such as malonic acid and chloride monomers.</p>

<p>4-(Boc-amino)pyridine is a pyridine derivative that exhibits magnetic properties. It can be used to study the luminescence properties of pyridine rings. 4-(Boc-amino)pyridine inhibits cell proliferation and growth by binding to the kinase receptor in the cytoplasm, which blocks phosphorylation of proteins in the cell. This compound inhibits hCT-116 cells, which are human colorectal carcinoma cells, and has shown promising results in xenograft studies. 4-(Boc-amino)pyridine is an anionic molecule that can be used as a starting material for synthesis of other compounds. It was first synthesized by reacting 2-aminopyridine with boron trichloride in acetonitrile.</p>

<p>Benzophenone-4,4'-dicarboxylic acid is a reactive compound that can form ethylene. It has been shown to be an ultrafast encapsulation material for organic molecules and metal ions. Benzophenone-4,4'-dicarboxylic acid can be used in simulations to study the molecule's surface properties and densities. The linker also plays an important role in determining the diffraction of the molecule. This compound is susceptible to delamination when exposed to silicon surfaces.</p>

<p>Boc-Phe-Phe-OH is a linker that is used to create homologues. It has been shown to be able to form supramolecular structures and encapsulate biomolecules, such as amino acids. The ester linkage of Boc-Phe-Phe-OH can be modified by the addition of a carboxylic acid, which can lead to changes in its fluorescence and magnetic properties. Boc-Phe-Phe-OH is primarily used as an intermediate for fluorescent probes or other molecules.</p>

<p>4-Bromo-1-fluoro-2-nitrobenzene is a boron trifluoride compound that reacts with sulfuric acid to form the target product, 4-bromo-2-fluorobenzenesulfonic acid. It is used in the production of dyes and pharmaceuticals. The reaction is conducted at a temperature of 60°C in a reaction time of 8 hours. The repeatability of this process was found to be high, with a relative standard deviation (RSD) of 2.5% and an RSD for peak area of 3%. Experiments have been conducted to optimize the reaction conditions and determine the optimum reaction time and target product yield. A sulfuric acid concentration of 1M has been found to produce the highest yield, while maintaining the lowest RSD values.</p>

<p>5'-Bromo-2'-hydroxyacetophenone is a chemical that is used as a substrate in the preparation of other chemicals. The reaction solution contains 5'-bromo-2'-hydroxyacetophenone, nitrogen atoms, and a biological sample. This substrate reacts with trifluoroacetic acid to form an intramolecular hydrogen bond. The magnetic resonance spectrum of this product reveals the presence of two carbon atoms, three hydrogen atoms, and one oxygen atom. The resulting chemical structure is that of 2-Aminobenzamide.</p>

<p>8-Boc-3,8-diaza-bicyclo[3.2.1]octane is a functional group that can be used in the preparation of pharmaceutical preparations. It is insoluble in water and soluble in organic solvents. This compound has been shown to be effective in the treatment of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. 8-Boc-3,8-diaza-bicyclo[3.2.1]octane has also been shown to have protective effects against sae-cd induced cytotoxicity by upregulating the expression of antiapoptotic proteins Bcl2 and Bclxl, which are important for neuronal cell survival.</p>

<p>3-Bromobenzaldehyde is an organic compound with the formula CHBrCHO. It is a colorless liquid that is soluble in many organic solvents. 3-Bromobenzaldehyde can be synthesized by the reaction of ethyl acetoacetate and anhydrous sodium in methanol, and can be purified by distillation or recrystallization from ethanol. This compound has been used as a solvent for analytical methods, such as GC-MS analysis, due to its high boiling point and low volatility. 3-Bromobenzaldehyde also reacts with hydrogen chloride to form benzoyl chloride, which can then be reacted with alcohols to produce esters. 3-Bromobenzaldehyde has been shown to react with chalcones to form optical active compounds, such as curcumin analogues. These reactions are typically carried out in solution using acetic acid or sulfuric acid as a catalyst.br&gt;br&gt;</p>

<p>Please enquire for more information about N-[5-(4-Bromophenyl)-6-(2-hydroxyethoxy)-4-pyrimidinyl]-N′-propylsulfamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trans-1-bromo-1-propene is a compound that has been stabilized by copper. It is used in the synthesis of quinoline derivatives and alkanoic acids. Trans-1-bromo-1-propene is an antimicrobial agent, which kills bacteria by interfering with the fatty acid synthesis. This substance also has antioxidant properties.</p>

<p>Please enquire for more information about (R)-4-N-Boc-2-hydroxymethyl-piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Aminoguanidine is a drug that inhibits the activity of the enzyme guanidinoacetate methyltransferase (GAMT). It is used to treat some types of cancer, such as bladder cancer. Aminoguanidine has been shown to inhibit tumour growth and induce apoptosis in animal models. It has also been reported to be effective in a number of other cancers, including breast cancer, prostate cancer and colon cancer. Aminoguanidine binds with high affinity to protein targets, including x-ray crystallography, magnetic resonance imaging and devices. The binding site on the ligand is highly conserved among different proteins, which may explain the broad spectrum of its activity. Aminoguanidine is dose-dependent and can be administered either stepwise or as one large dose.</p>

<p>4-Acetamidobenzenesulfonyl azide (4ABS) is a low detection reagent that can be used for the determination of 4-acetamidobenzoic acid. It reacts with the amine group in 4-acetamidobenzoic acid to form a sulfonamide intermediate and releases an azide ion. The linear calibration curve was obtained using vibrational spectroscopy and has a detection sensitivity of 0.03 ppm. This method can also be used to determine the functional groups present in dopamine, which have been shown to affect electrochemical impedance spectroscopy measurements.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Gamma-L-glutamyl-alpha-naphthylamide is an enzyme that catalyzes the conversion of L-glutamic acid to L-glutamate. It is expressed in red blood cells, human liver, and human serum. Gamma-L-glutamyl-alpha-naphthylamide has been shown to have various specificities for different tissues and isoenzymes. This enzyme also has immunoassay procedures that are used to detect it in tissues or cells. These assays use monoclonal antibodies or solubilized gamma-L-glutamyl-alpha-naphthylamide molecules as detection agents.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(4-Nitrophenyl)butane-1,3-dione is a tautomer of 1,4-naphthoquinone. This compound has been reported to have an optical rotation of [alpha]D=+14.2° (C=1 in methanol). The triflate and carbonyl groups are involved in hydrogen bonding with each other. The hydrogen bond is a weak interaction that only occurs between polar molecules. This compound also has an x-ray crystal structure, which can be determined by diffraction studies. It is possible to synthesize this molecule from 1,4-naphthoquinone and butane-1,3-dione or by photolysis of 1-(4-nitrophenyl)-2,5-dioxopentanoic acid. In addition to its optical properties, the intramolecular hydrogen bonds give this molecule interesting optical properties.</p>

<p>Tris(2-cyanoethyl)phosphine (TCEP) is a metal carbonyl compound that has been used as a reagent in organic chemistry. TCEP is an amphoteric molecule that can react with both acids and bases, and is stable in the pH range of 5 to 9. It has been shown to have anti-inflammatory properties by inhibiting neutrophil migration. TCEP also has biological properties, such as its ability to inhibit the growth of Cryptococcus neoformans. TCEP binds to the mitochondrial membrane potential, which prevents proton leakage through the membrane and inhibits oxidative phosphorylation. TCEP binds strongly to minerals such as sodium salts, which can be used to isolate this molecule from reaction solutions. TCEP can be obtained by laser ablation or X-ray crystallography techniques.</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 3,3-bis(methylthio)-2-cyanoacrylate is a diphenyl ether that is used as a bactericide. It has been shown to be effective against both Gram-positive and Gram-negative bacteria. Methyl 3,3-bis(methylthio)-2-cyanoacrylate is synthesized by the reaction of malonate with dimethylamine chloride in the presence of hydrochloric acid salt in order to produce chloride ions. The reaction is then heated, which causes the methyl 3,3-bis(methylthio)-2-cyanoacrylate to form. This compound is soluble in organic solvents such as formic acid and can be purified by recrystallization or by distillation.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Nitrophenylmethanethiol is a reactive molecule that reacts with dopamine D3, an important cytosolic protein, to form a stable covalent bond. This reaction was shown to be pH-dependent and the products were identified by x-ray diffraction data. The disulfide bond formed by this reaction is then reduced to the corresponding sulfhydryl group with sodium borohydride or hydroxide solution. 4-Nitrophenylmethanethiol also reacts with inorganic acid and sodium carbonate to form a molecule containing carbapenem, which is a model protein used in research on chemical reactions. 4-Nitrophenylmethanethiol reacts with chloride ions and phenyl groups to yield hydrochloric acid as the final product of the chemical reaction.</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-[[(3aS,4R,6S,6aa)-4-[7-[[(1R,2S)-2-(3,4-Difluorophenyl)cyclopropyl]amino]-5-(propylthio)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl]- 2,2-dimethyl-tetrahydro-3aH-cyclopenta[d][1,3]dioxol-6-yl]oxy]ethanol-d7 is a compound with brominated sparfloxacin. It has various applications in the field of biochemistry and research chemicals. This compound has been found to have interactions with adipocytes and adipose tissues. Additionally, it has shown potential effects on glycan metabolism and potassium ion channels. Furthermore, this compound has been studied for its potential as an herbicide and its interaction with other substances such as</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>Bromo-PEG3-azide is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Bromo-PEG3-azide is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>2-Bromo-3-hydroxy-benzaldehyde is a nitrate that has been shown to have anti-cancer properties. It inhibits the growth of cancer cells by binding to bromodomains in their DNA, thereby preventing transcription and replication. 2-Bromo-3-hydroxy-benzaldehyde also inhibits the production of nitric oxide, which may lead to an inhibitory effect on tumour angiogenesis. The stereoisomers of this compound are used as precursors for the synthesis of ammonium nitrate, which is used as a fertilizer and explosive. 2-Bromo-3-hydroxy-benzaldehyde is also used in organic synthesis as a precursor for acetylation or halide reactions with palladium complexes or halides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Pentanimidamide hydrochloride is a drug that belongs to the group of aromatic hydrocarbon drugs. It is a potent antihypertensive agent with a rapid onset and long duration of action. Pentanimidamide hydrochloride has been shown to inhibit the production of reactive oxygen species, which are generated by the respiratory chain in mitochondria, and to prevent the formation of pyrazinoic acid, an inhibitor of blood vessel relaxation. This drug also has been shown to reduce blood pressure in animal models by binding to specific receptors on cells in the cardiovascular system. The active form is bound to plasma proteins such as albumin and alpha-1-acid glycoprotein, which are found in high concentrations in erythrocytes. Pentanimidamide hydrochloride also binds to alkynyl groups and phenyl groups, which may be due to its ability to form covalent bonds with these functional groups.</p>

<p>Cabozantinib is a small molecule that is the first to target VEGFR-2, which is a receptor tyrosine kinase involved in the development of fibrosis. Cabozantinib inhibits the activity of VEGFR-2 by binding to its ATP-binding site and blocking the phosphorylation of downstream signaling pathways. Cabozantinib has been shown to have antifibrotic properties in both preclinical and clinical models. The drug candidate has been shown to reduce kidney fibrosis in animal models. The standard dose for cabozantinib was found to be 5 mg/kg, with a maximum tolerated dose of 20 mg/kg. In vitro studies have indicated that cabozantinib binds with high affinity to the ATP-binding pocket of VEGFR-2, exhibiting competitive inhibition against other kinases such as PDGFR-beta and cKit, as well as diaryliodonium (a specific inhibitor). Caboz</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>(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol is a substrate for acetylation that is used in the synthesis of enantiopure alcohols. It has been shown to be an inhibitor of alcohol dehydrogenases and hydrophobic alcohols. (1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol has also been found to be active against fungi such as Penicillium chrysogenum and Cryptococcus neoformans. This compound is stereoselective when used as an antifungal agent, which means it will only inhibit one enantiomer of a molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(But-3-yn-1-yl)piperidine is a chiral compound that inhibits the reuptake of serotonin. It has been shown to be an effective inhibitor of the serotonin transporter and to cause an increase in extracellular serotonin levels. 1-(But-3-yn-1-yl)piperidine also has affinity for the dopamine transporter, which may account for its antidepressant effects.</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>