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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

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>

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>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Aureusimine A is a natural product that has been identified as a potential biomarker for Staphylococcus aureus. This molecule is produced by the bacterial species Aureobasidium pullulans and has been shown to have antibacterial, antifungal, and antiparasitic properties. The molecule also inhibits protease activity in Staphylococcus strains and prevents the growth of bacteria. It is also a potential therapeutic agent for the treatment of staphylococcal infections.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

1-Methylisoquinolin-5-amine is a drug that is used to treat cancer. It inhibits the growth of cancer cells by binding to DNA and altering the gene expression in the cell. 1-Methylisoquinolin-5-amine binds to and acetylates two residues on the deoxyribose of DNA, thereby inhibiting DNA synthesis. The inhibitory potency of 1-methylisoquinolin-5-amine has been shown in clinical trials using L1210 murine leukemia cells. This drug also decomposes into carboxaldehyde, which is excreted through the urinary system. 1-Methylisoquinolin-5-amine has been shown to have an inhibitory effect on homogenates of human l1210 cells incubated with radioactivity.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

2-(2-Naphthyl)-2-propanol is a reactive chemical that is orally administered, and interacts with tissues to produce extents. The molecule has been shown to be magnetic resonance spectroscopic (MRS) detectable. 2-(2-Naphthyl)-2-propanol reacts with chloride ions and produces 2-chloro-1-naphthol and 2-(2-naphthyl)ethanol, which can be used as biomarkers for its presence in the body. This chemical also reacts with isopropyl groups to form epoxides or peroxides, depending on the extent of reaction. Irradiation of this compound by UV light yields hydroxypyridinium salts. 2-(2-Naphthyl)-2-propanol may interact with metal ions such as iron, copper, or zinc.

<p>8-Methoxychroman-4-one is a natural product that inhibits the activity of dopamine beta-hydroxylase, an enzyme that converts dopamine to norepinephrine. It also has inhibitory effects on dopaminergic neurons in vivo and has been shown to be effective in reversing streptozotocin-induced diabetes in rats. 8-Methoxychroman-4-one may also have potential as a prophylactic agent for diabetic nephropathy. The extract of the rhizomes has been shown to contain both 8-methoxychroman-4-one and oxime, aminoguanidine, which is an inhibitor of nitric oxide synthase.</p>

<p>Versatile small molecule scaffold</p>

<p>7-Chlorobenzo[d]thiazol-2-amine is a synthetic intermediate used in the production of dyes, pigments, and pharmaceuticals. It is prepared by the reaction of 2-aminobenzothiazole with nitrous acid and 7-chloroacetophenone. 7-Chlorobenzo[d]thiazol-2-amine can be cleaved at the 2 position to produce 2,4,5-trichlorobenzothiazole. The infrared absorption spectrum of 7-chlorobenzo[d]thiazol-2-amine has been recorded in the solid phase at room temperature and shows three bands between 1710 cm−1 and 1700 cm−1.</p>

<p>7-Bromo-1,3-benzothiazol-2-amine is a heterocyclic compound with the chemical formula CHBrN. It is synthesized by reacting 2-aminobenzothiazole with aniline in the presence of acid. The product has been shown to have traceless reactions and can be used for solid phase synthesis. 7-Bromo-1,3-benzothiazol-2-amine has been shown to undergo cleavage under acidic conditions, which is useful for the synthesis of other heterocyclic compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>2,2-Dimethyl-1,2,3,4-tetrahydroquinoline is a molecule with the chemical formula C8H10N. It is a white crystalline solid that has a pyridine ring and a tetrahydroquinoline ring. 2,2-Dimethyl-1,2,3,4-tetrahydroquinoline has been shown to interact with nitrogen atoms in its environment. This process can lead to the formation of an N-oxide or carbonyl groups at the nitrogen atom. The molecule has also been shown to react with methyl groups and form stoichiometric amounts of n-oxides or carbonyl groups. 2,2-Dimethyl-1,2,3,4-tetrahydroquinoline can be used as a desorption agent for gas chromatography (GC).</p>

<p>1-Bromo-5-methylnaphthalene is a chemical compound that belongs to the group of organic compounds. It can be synthesized by deoxygenation of 1,2-dibromonaphthalene with lithium diisopropylamide and diisopropylamide in an alkaline medium. The reaction yields high yields of 1-bromo-5-methylnaphthalene. The synthesis can also be achieved by the regioisomeric lithium–diels–alder reaction.</p>

<p>N-(4-Propoxyphenyl)acetamide is a crystalline solid that has the chemical formula C8H11NO2. This compound belongs to the group of hydrogen bond coplanar molecules. It has a molecular weight of 153.19 and a melting point of 209 degrees Celsius. Its crystal structure is monoclinic with chains that are parallel to each other and have an angle of 90 degrees, with four propoxyphenyl groups at one end and one acetamide group at the other end.</p>

<p>Versatile small molecule scaffold</p>

<p>3-(2-Methoxyphenoxy)propanoic acid is a nonracemic compound that is an enantiomer of phenoxyacetic acid. 3-(2-Methoxyphenoxy)propanoic acid has been shown to inhibit the growth of bacteria by inhibiting protein synthesis. It also inhibits the production of proteins essential for cell division and causes bacterial cells to undergo apoptosis, which leads to cell death. 3-(2-Methoxyphenoxy)propanoic acid is active against both Gram-positive and Gram-negative bacteria, but is not active against Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Azidoquinoline is a molecule with the molecular formula CHN. It is classified as an oxadiazoloquinine and has a range of chemical properties that make it suitable for use in medicine, including its ability to form halides and nitro groups. 5-Azidoquinoline can also be used to synthesize other molecules, such as chloroacetone, by nucleophilic substitution reactions. The electronegativity of the 5-azido group makes it an excellent nucleophile, which allows for kinetic reactions. This molecule has six different heterocycles and can be substituted with halogens or other azides.</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>3-(4-Methoxyphenyl)propionaldehyde is an enantioselective compound that can be synthesized in four steps from trichloroacetimidate and d-proline. This compound has been shown to be efficient for the olefination of aldehydes with allylic alcohols. The reaction is catalyzed by Cu(OAc)2, which is used as a catalyst to promote the reaction between the aldehyde and the allylic alcohol, leading to the formation of acetic acid esters.</p>

<p>1-(Propan-2-yl)imidazolidine-2-thione is a thione that has been shown to be a degradable molecule. It has been used in devices such as hydrogen bonding interactions, sublimable, targetable, and dispersive. The properties of 1-(Propan-2-yl)imidazolidine-2-thione make it an ideal candidate for diagnostic or therapeutic applications of iontophoresis and coordination chemistry.</p>

2-(Trimethylacetyl)thiophene is a thiophene derivative that is used as a precursor to other organic compounds. It reacts with carbon tetrachloride in the presence of light to yield 2-chloro-1,3-dithiole-4,5-dithiol and 2-trimethylacetylthiophene. The kinetics of this reaction has been studied using magnetic resonance spectroscopy. The abundances of the two products have been measured by gas chromatography/mass spectrometry (GC/MS). The dihedral angles for the reactant and product molecules have also been determined by NMR spectroscopy. This compound's conformational studies have revealed dipole moment values and frequencies that are different than those found in other thiophenes.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 4-oxo-5-phenylpentanoate (ETP) is a synthetic chemical that can be used as a test compound for cancer research. ETP has been shown to inhibit the growth of human breast cancer cells in vitro and in vivo. It has also been shown to have an inhibitory effect on the growth of liver cancer cells. ETP inhibits the production of endogenous retinoids, which are naturally occurring compounds derived from vitamin A, by binding to lysine residues on histones. This prevents the transcription and replication of DNA, thereby preventing cell division. The terminal half-life of this compound is approximately 1 hour in humans.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>