Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Indolizine-7-carboxylic acid is an organic compound that is used in research as a fluorescent probe. It is sensitive to acidic environments and has been shown to be selective for the detection of carboxylic groups. Indolizine-7-carboxylic acid has a chemical structural formula of C6H5N3O2 and a molecular weight of 154.14 g/mol. This compound exhibits fluorescence emission between 585 nm and 605 nm, which can be observed when it is excited at 488 nm. The fluorescent probe can also be used to detect sulfoxide groups, which are present in methanesulfonic acid and dimethyl sulfoxide.</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>Methyl-pseudouridine-5'-triphosphate trisodium is the triphosphate of 1-Methylpseudouridine is a substitute for uridine in modified mRNA. This substitution has shown to increase transfection by reducing immuogenicity. UV max wavelength = 272nm</p>

<p>Applications 1,3,5-Trifluorotrichlorobenzene is a useful reagent.<br></p>

<p>Applications 4-Diazobenzenesulfonic acid (cas# 305-80-6) is a useful research chemical.<br></p>

<p>Please enquire for more information about 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-3-oxo-5-isobenzofurancarbonitrile 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 Depropyl rotigotine 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>Please enquire for more information about Domperidone N-oxide 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-Desmethyl-2-methyl celecoxib 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 4,5-Dihydro-1H-imidazol-2-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Phenyl-1H-pyrazol-4-amine is a white crystalline solid that can be used in organic synthesis. It is soluble in water and acetone, but insoluble in ether and chloroform. The chemical formula for 1-phenyl-1H-pyrazol-4-amine is C6H5N3O. It has a molecular weight of 147.17, an empirical formula of C6H5N3O and a density of 1.47g/mL at 20°C. 1-Phenyl-1H-pyrazol-4-amine reacts with the hydroxyl group on l -glutamic acid to form the corresponding ester, which can be hydrolyzed under alkaline conditions to produce ammonia and benzoic acid. This molecule also contains an anion that can be deprotonated by an alkali metal such as sodium or potassium to form the corresponding salt, which</p>

<p>Please enquire for more information about 6,​7-​Dichloro-​1-​cyclopropyl-​1,​4-​dihydro-​4-​oxo-3-​quinolinecarboxylic acid 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>Bromo-PEG4-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-PEG4-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>Versatile small molecule scaffold</p>

<p>4-Hydroxy-5-methoxy-2-nitrobenzaldehyde (4HMN) is a proton donor that can be used as a crosslinking agent. It is an acidic compound that binds to the substrate, usually via hydrogen bonds. 4HMN has been shown to have good binding affinity for tumour cell lines and can be used as a crosslinking agent in bioconjugation reactions. It is also a reversible chemical reaction, which means it can be hydrolyzed under certain conditions. 4HMN has been shown to be capable of enhancing the rate of enzymatic reactions by acting as a cofactor or coenzyme, such as degradable enzymes and enzymes with low turnover rates. The kinetic process of these reactions are measured by fluorescence techniques and gel permeation chromatography.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Oxohexanoic acid (2-OHBA) is a fatty acid that is synthesized from the amino acids lysine and methionine. It is involved in mitochondrial metabolism and has been found to be necessary for spermatozoa motility. 2-OHBA has been shown to inhibit the activity of glutamate dehydrogenase, an enzyme that catalyzes the conversion of glutamate to α-ketoglutarate, which is required for energy production. This inhibition leads to a decrease in ATP levels, which may cause a variety of symptoms, including fatigue and weight loss. Furthermore, 2-OHBA inhibits protein synthesis by blocking the incorporation of amino acids into proteins. The inhibition of this process can lead to high ammonia levels in the blood and accumulation of other nitrogenous wastes in tissues such as liver or muscle tissue. Analysis of urine samples has shown that 2-OHBA is excreted unchanged in urine.</p>

<p>Versatile small molecule scaffold</p>

<p>5-bromo-6-methoxy-1H-indole is a synthetic, nonsteroidal compound that is structurally related to prednisolone. It has been shown to induce the synthesis of collagen by stimulating fibroblasts in culture. This drug also has anti-inflammatory and modulating effects on s1p receptors, which may be due to its ability to inhibit the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα). 5-bromo-6-methoxy-1H-indole is a potent inhibitor of acid methyl esters, which are involved in inflammation and tissue destruction. 5-bromo-6-methoxy-1H--indole also has an effect on dermal cells, which may be due to its ability to inhibit the production of matrix metalloproteinase enzymes. This drug can also cause atrophy in granuloma cells and prevent the development of inflammatory</p>

<p>Methyl 2-(chloromethyl)nicotinate is an organic compound that belongs to the class of esters. It is a reaction product of methyl 3-hydroxybenzoate and nitrous acid. This compound has antimicrobial activity and can be used to treat bacterial infections. Methyl 2-(chloromethyl)nicotinate has been shown to inhibit the growth of various bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonella typhi, and Salmonella typhimurium. The cyano group in this molecule may be responsible for its antibacterial activity. <br>The efficiency of methyl 2-(chloromethyl)nicotinate varies with different types of bacteria. For example, it was more effective against MRSA than against Escherichia coli or Klebsiella pneumoniae</p>

<p>5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole is an activator that is used in palladium catalyzed reactions to form a phosphine ligand. 5-bromo-3,3-dimethyl-2,3-dihydro-1H-indole is also used as a vasotropic agent and reagent for organic synthesis. It is used to synthesize ethylesters and salts of 5-(5'-bromo)-2,2'-dihydroquinoline carboxylic acid. This compound can be hydrolyzed with alkaline solution to produce the corresponding amine.</p>

<p>Ethyl cyclopropaneacetate is an organic compound that belongs to the class of aminophenyl ethyl esters. It has been shown to inhibit neutrophil migration and angiotensin II-induced vasoconstriction in cerebral arteries, suggesting that it may have a role in the treatment of chronic bronchitis. Ethyl cyclopropaneacetate has also been shown to have antimycotic activity against Candida albicans and Aspergillus niger, as well as cancer-fighting effects. This compound is synthesized by reacting triethyl orthoformate with adenosine under mild conditions. The reaction system is high yielding and can be used for the synthesis of other drugs.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Acetylbenzoic acid is a functional molecule that contains an acetyl group. It can form hydrogen bonds with other molecules and has been shown to induce apoptosis in cells. The reaction products of 2-acetylbenzoic acid are malonic acid, acetylsalicylic acid, and 2-benzoylbenzoic acid. These three compounds are made by the addition of hydrogen or hydroxide to the molecule 2-acetylbenzoic acid. The molecule has two functional groups: a carbonyl group and an acetyl group. The chemical structure of this molecule can be seen in the figure below.<br>2-Acetylbenzoic Acid</p>

<p>1-Adamantane carboxylic acid is a hydrophobic molecule that can form a complex with metal hydroxides. It is used in the process optimization of the synthesis of sodium salts. 1-Adamantane carboxylic acid binds to metals, such as magnesium and calcium, in a coordination geometry that is similar to that observed for water molecules. The complexation of 1-Adamantane carboxylic acid with metal ions results in an acidic environment, which is important for bowel disease. This acid complex also has anti-inflammatory properties. The hydroxyl group on the 1-adamantane carboxylic acid reacts with oxygen to form an alcohol group and this reaction mechanism may be involved in physiological functions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-4-bromopyridine is a potent, selective antagonist of the nicotinic acetylcholine receptor (nAChR) that has been shown to inhibit the proliferation of cancer cells in vitro. 2-Amino-4-bromopyridine binds to the nAChR and stabilizes it by binding to an allosteric site on the receptor. 2-Amino-4-bromopyridine is synthesized from 4,5-dibromobenzene and 2,6-diaminopyridine in two steps with a yield of 47%. The synthesis of 2-amino-4-bromopyridine proceeds via reaction mechanism involving electrophilic substitution at the bromine atom followed by nucleophilic addition at the nitrogen atom.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</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>2-(Boc-aminomethyl)benzoic acid is a versatile building block with a wide range of applications in the field of organic chemistry. It has been shown to be useful as a reagent in the synthesis of complex compounds and fine chemicals, as well as a reaction component for the preparation of pharmaceuticals. 2-(Boc-aminomethyl)benzoic acid can also be used as an intermediate in the synthesis of speciality chemicals such as herbicides, pesticides, and fungicides.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Imidazolidone-4-carboxylic acid is a potent inhibitor of matrix metalloproteinases, which are enzymes that break down proteins in the extracellular matrix. 2-Imidazolidone-4-carboxylic acid inhibits the activity of both serine protease and matrix metalloproteinase, two enzymes involved in the inflammation process. 2-Imidazolidone-4-carboxylic acid has been shown to inhibit the transport of amino acids, leading to decreased protein synthesis and cell growth. It also inhibits cancer cells by disrupting their ability to grow new blood vessels and invade other tissues.</p>

<p>Hexahydro-1H-pyrrolizin-1-amine is a synthetic compound that is used to control endophytic fungi and fungal diseases in plants. The activity of this molecule is due to the acid molecules that are released when it reacts with plant tissue, which prevents the growth of fungi by inhibiting their cell membranes. Hexahydro-1H-pyrrolizin-1-amine also has an antibacterial effect, which may be due to its ability to bind to bacterial 16S ribosomal RNA and inhibit protein synthesis. This product can be used on plants that are infected with endophytic fungi or fungal diseases. It can also be applied as a preventative measure against future infections.<br><br>The following table summarizes the information for each product:<br><br>Product Name <br>Characteristics <br>Description</p>

<p>1,2-Bis(chlorodimethylsilyl)ethane is a reactive chemical that is synthesized from hydroxychloroformates and hydrogen chloride. It reacts with silicon to form chlorosilanes, which are then used in the polymerization of siloxanes. 1,2-Bis(chlorodimethylsilyl)ethane has been shown to be an effective initiator for the polymerization of methyl methacrylate and ethylene glycol dimethacrylate. 1,2-Bis(chlorodimethylsilyl)ethane is also used as a hydroxyl group donor in organic reactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Ethyl-4-methylpyrrole-2,5-dione is a chlorophyll analog. It has been found to be an electron donor in photosystem II of the chlorobium reaction center. The compound was prepared by evaporation of a solution of chlorobenzene and ethyl acetoacetate in carbon tetrachloride with the aid of a vacuum pump. 3-Ethyl-4-methylpyrrole-2,5-dione has also been used as a reagent for the preparation of phycocyanin from Spirulina platensis, which is an important component of blue algae. The compound reacts with phenoxy and furyl groups under acidic conditions to produce carboxylate and calcium carbonate, respectively. Oxidation products are formed in reactions with ethyl group and other organic compounds under alkaline conditions.</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>Versatile small molecule scaffold</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>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>Chloroiodomethane is a chemical that is used as an intermediate in the production of other chemicals. It is a colourless liquid with a strong odour. 3-Bromopropylamine hydrobromide reacts with chloroiodomethane to form 3-bromopropyl bromide, which can be reacted with hydrogen chloride to form the corresponding acid chloride. This reaction product can then be reacted with β-amino acids to form amides or esters. The reaction mechanism of this process involves nucleophilic substitution of chloroiodomethane by the amino group of the β-amino acid to produce an intermediate α,β-unsaturated carbonyl chloride, which undergoes elimination to give the final product. Chloroiodomethane also reacts rapidly with fatty acids and hydroxyl groups in biological systems, leading to inflammatory diseases such as HIV infection.</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>