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>

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>L-Alaninol is a chemical compound that is used as a building block in organic synthesis.</p>

<p>Benzo[d][1,2,3]thiadiazole is a benzothiadiazole with a redox potential of -0.25 V that is stable in the absence of oxygen and light. It can be used to synthesize chemical pesticides by reacting with hydrochloric acid. The reaction mechanism of benzo[d][1,2,3]thiadiazole has been determined using nuclear magnetic resonance spectroscopy and quantum chemical calculations. This compound reacts with hydrogen bond acceptors on the enzyme active site to form covalent bonds. It also interacts with the enzyme's steric environment by forming hydrogen bonds and van der Waals forces. Benzo[d][1,2,3]thiadiazole also emits light when it reacts with nitric oxide in solution.</p>

<p>Imidazo[4,5-b]pyrazine is a chemical compound that binds to calcium ions and has been used in the treatment of metabolic disorders. The symptoms of imidazopyrazine include fatigue, weight loss, fever, chills, and muscle aches. Imidazopyrazine is also used for the treatment of autoimmune diseases such as rheumatoid arthritis. In vitro assays have shown that it activates macrophages and lymphocytes and may be useful in the treatment of skin lesions caused by an infection. Imidazopyrazine has been found to have pharmacokinetic properties with a half-life of 3 hours when administered orally. This drug has also been shown to have biological activity against rat liver microsomes.</p>

<p>[1,3]Thiazolo[4,5-b]pyridine is a heterocyclic compound that is structurally similar to pyridine. It has been shown to act as an acceptor for hydrogen bonds and can be used in the synthesis of other compounds. [1,3]Thiazolo[4,5-b]pyridine has been shown to inhibit the growth of Staphylococcus aureus and amine-producing strains of bacteria such as Pseudomonas aeruginosa, Escherichia coli, and Klebsiella pneumoniae. This compound also acts as a nucleophile in pharmacophores that contain amines.</p>

<p>Rac-(1S,5R)-6-azabicyclo[3.2.1]octane hydrochloride is a natural product that belongs to the group of lactams. It has been found in marine sponges and cyanobacteria. Rac-(1S,5R)-6-azabicyclo[3.2.1]octane hydrochloride has been shown to be an inhibitor of phosphoranes and epoxides, which are enzymes that catalyze the formation of phosphoranes, epoxides, and other reactive oxygen species. Rac-(1S,5R)-6-azabicyclo[3.2.1]octane hydrochloride inhibits these enzymes by binding to their active sites with high specificity and affinity, leading to the inhibition of their enzymatic activity and subsequent reduction of reactive oxygen species levels in cells.</p>

<p>3-Oxa-7-azabicyclo[3.3.1]nonane is a linker that contains a hydroxyl group, heterocycle, intramolecular hydrogen, and fluorine. It has been shown to be an effective inhibitor of the HIV protease enzyme in vitro, although it is not active against other enzymes such as the human serum albumin or cytochrome P450. 3-Oxa-7-azabicyclo[3.3.1]nonane binds to the active site of the HIV protease by forming hydrogen bonds with amino acids near the active site and by stabilizing the conformation of its piperidine ring. This drug also has an axial orientation with respect to its fluoroquinolone plane and benzyl group that makes it stereoisomeric with 2 possible configurations: cis or trans.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Azacycloundecane is a cycloalkane that is used as a solvent. The use of this compound in vivo models has been demonstrated to be useful in the study of drug uptake and distribution, as well as having clinical applications. Azacycloundecane is often used in detergent compositions due to its ability to solubilize fatty acids and inhibit their oxidation. This chemical has also been shown to have low energy, which makes it a suitable candidate for use in osmosis experiments. Azacycloundecane does not react with hydrogen chloride or carbonyl groups. It can be found naturally in fatty acids, amines, benzofuran derivatives, and aliphatic hydrocarbons.</p>

<p>1-Methyl-6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxamide is a fatty acid ester with antihistaminic effects. It is used in pharmaceutical preparations as an antitussive and an excipient in diagnostic tests. It has been shown to be effective against acute or chronic inflammation of the respiratory tract, including bronchitis and asthma. 1-Methyl-6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxamide has also been shown to inhibit prostaglandin synthesis by acting on the enzyme cyclooxygenase.</p>