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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<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>The compound 1-benzyl-1H-1,2,3,4-tetrazol-5-amine is a tetrazole derivative that has been shown to inhibit the growth of gram negative bacteria. It inhibits bacterial growth by inhibiting the production of DnaA protein in the cytoplasm through coordination with a zinc ion. The compound has also been shown to be active against Gram positive bacteria and fungi, but not against yeast. The compound has also been shown to have minimal inhibitory concentrations against human fibroblast cells and science.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl oxazole-2-carboxylate is a cyclic, chiral, methyl ester. It is a congener of the drug Valine and has been shown to have antitumor potential. The methyl oxazole-2-carboxylate is an amide with a cyclic peptide backbone and is synthesized from valine by way of an enzymatic reaction that converts the amino acid into a chiral, cyclic amide. This compound has demonstrated anticancer properties in vitro and in vivo. Methyl oxazole-2-carboxylate also has antiangiogenic activity which may be due to its ability to inhibit protein synthesis in tumor cells.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3,4-Dimethoxyphenyl)prop-2-en-1-ol is a phenolic compound that has been shown to have inhibitory properties in the human liver and hamster V79 cells. It also inhibits the growth of bacteria such as typhimurium and rat liver microsomes. 1-(3,4-dimethoxyphenyl)prop-2-en-1-ol shows reactive properties with sodium carbonate, which is used in the activation of esters. This compound is found in plants belonging to the family Rutaceae and it may be synthesized from 3,4-dimethoxybenzaldehyde by an enzymatic reaction involving alcohol dehydrogenase or cytochrome P450.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Procaine is a local anesthetic that is used to reduce the pain of needle insertion. It also has a bactericidal effect on staphylococcus and epidermidis, and is commonly used as a disinfectant for surgical instruments. Procaine can be detoxified by acetylation with phenoxyacetic acid to produce 4-(phenoxymethyl)benzoic acid, which has an increased spectrum of activity against bacteria. 4-(Phenoxymethyl)benzoic acid is active against methicillin-resistant Staphylococcus aureus (MRSA) and other drug-resistant strains of bacteria. The antibiotic binds to bacterial DNA gyrase, preventing the synthesis of proteins necessary for cell division. This causes bacterial cells to die by inhibiting protein synthesis and cell division.</p>

<p>(1-Phenylcyclopropyl)methanol is an aromatic ketone that can be used in the synthesis of oxazaborolidines. It has been proven to be a good substrate for asymmetric syntheses, which are often used for the development of enantioselective reactions. The mechanism of this reaction is not yet fully understood, but it is thought that the C-O bond in (1-phenylcyclopropyl)methanol reacts with acetophenone to form an intermediate diketone. This intermediate then reacts with an electrophile such as sodium methoxide or methyl iodide to produce the desired product.</p>

<p>Versatile small molecule scaffold</p>

<p>6-Chloro-1-methyluracil is a nucleophilic acylating agent that reacts with primary amines to form N,N'-acylureas. It also reacts with chloride to form chlorinated derivatives. 6-Chloro-1-methyluracil has been shown to react with hydrogen peroxide in an acid solution to produce cyclen and aldehydes. The reaction scheme is shown below:</p>

<p>Versatile small molecule scaffold</p>

<p>2-Pyrrol-1-ylbenzaldehyde is a molecule that is transformed to give the corresponding chloride and ketone. The transformation of 2-pyrrol-1-ylbenzaldehyde to the corresponding chloride and ketone is achieved by reaction with diethyl etherate, followed by treatment with acidified hydrochloric acid. This experiment was conducted in order to produce the cyclised compound intramolecularly by sequential halogenation. The synthesis of heterocycles can be achieved through olefination or pyridine ring formation.</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-Aminothiazolo[5,4-b]pyridine is an isothiocyanate that has potent antiproliferative and anticancer effects. It causes the inhibition of tumor growth by inhibiting the activity of enzymes such as DNA polymerase or topoisomerase II. 2-Aminothiazolo[5,4-b]pyridine also inhibits the proliferation of cancer cells and induces apoptosis. The anticancer effects are due to its ability to inhibit tumor cell growth and induce apoptosis in cancer 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>Sodium 5-Formyl-2-furansulfonate is a water soluble amine that is used as an additive in the production of pharmaceuticals, agricultural chemicals, and coatings. It is an anticoagulant that has been shown to prevent blood clotting by inhibiting platelet activation. Sodium 5-Formyl-2-furansulfonate can be used as a coating on medical devices and implants to prevent clotting. One of its most promising applications is in the development of new drug delivery systems for drugs with low solubility or poor bioavailability. This chemical may also play a role in the prevention of atherosclerosis by modifying fibrinogen and dopamine, which are important for regulating blood pressure.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-3-methoxy-1,2-thiazole is a carboxylic acid. It is a cyanating agent and can be used to form carboxamides. The dealkylation of 4-bromo-3-methoxy-1,2-thiazole gives methyl 4-(4′-bromophenyl)butanoate. Halogenation of the carbonyl group leads to the formation of 4-(4′-chlorophenyl)butanoic acid. 4-(4′-Bromophenyl)butanoic acid can be converted into an isothiazole by reacting with potassium hydroxide in methanol.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl bicyclo[2.2.2]octane-1-carboxylate is a chelate ring that has been shown to enhance the absorption of drugs into the skin and other tissues. It is a cationic surfactant with the ability to form hydrogen bonds in intermolecular and intramolecular configurations. Ethyl bicyclo[2.2.2]octane-1-carboxylate has been used as a catalyst in the synthesis of palladium complexes, as well as an absorption enhancer for hydrophobic compounds such as pesticides, herbicides, and fungicides. The coordination geometry of ethyl bicyclo[2.2.2]octane-1-carboxylate allows it to form hydrogen bonds with nitrogen atoms in proteins and other molecules, which enhances its absorption properties when applied topically on human skin or other tissues.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Benzofuran-5-ylmethanol is an aromatic ether that finds applications in various industries such as research chemicals, medicines, and catalysts. It is used as a building block for the synthesis of compounds like oxalyl glycine, aldehyde dimers, and trifluoroacetic acid. Benzofuran-5-ylmethanol also exhibits antiviral properties and has been studied for its potential in inhibiting viral replication. Additionally, it is a precursor for the synthesis of phenylethylamine derivatives and polyunsaturated fatty acids. With its diverse range of applications, Benzofuran-5-ylmethanol serves as a valuable compound in the field of organic chemistry and industrial processes.</p>

<p>5-hydroxy-4-methoxy-2-nitrobenzoic acid is a synthetic antioxidant that is synthesised from α-tocopherol. It has been shown to be an effective scavenger of hydroxyl radicals and reactive oxygen species, which are involved in the oxidative degradation of biomolecules. 5-Hydroxy-4-methoxy-2-nitrobenzoic acid can be used as an antioxidant in food and cosmetics. This compound also reacts with linoleic acid, forming a phenolic product, which has antioxidant activity.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-1,2,3-benzothiadiazole is an electron donor and ligand that is used as a reagent in organic synthesis. It reacts with an electron acceptor to form a covalent bond. 4-Bromo-1,2,3-benzothiadiazole has been detected by mass spectroscopy and can be used as a molecular weight marker. It is insoluble in water at room temperature and has low solubility in most organic solvents. 4-Bromo-1,2,3-benzothiadiazole is the monomer for the polymerization of poly(4-bromophenylsulfonate) (PBPPS), which is used to produce polymers with different properties. 4-Bromo-1,2,3-benzothiadiazole also reacts with benzene to form 2-(4'-brom</p>