Building Blocks

<p>3-Methylisonicotinamide is an immune-related drug that belongs to the class of heterocyclic compounds. It is an innovative therapeutic agent for inflammatory diseases and cancer. 3-Methylisonicotinamide has been shown to inhibit the production of inflammatory cytokines, chemokines, and prostaglandins. This compound also blocks the production of reactive oxygen species by inhibiting the activation of NADPH oxidase in neutrophils and macrophages. The inhibition of reactive oxygen species prevents cytotoxicity and cell death in vitro. 3-Methylisonicotinamide binds to nuclear receptor subtypes (e.g., PPARγ) that are involved in inflammation, cancer, and neuropathic pain with high affinity. These receptors are located on the surface of cells where they regulate cellular functions such as proliferation, differentiation, and apoptosis.</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>(1S)-1-(3-Aminophenyl)ethan-1-ol is a colorless liquid with an odor that has been used as a precursor for the synthesis of epoxy resins. It is hydrolyzed by strong acids to give formic acid and cyclohexanol. (1S)-1-(3-Aminophenyl)ethan-1-ol reacts with formic acid in the presence of a weak acid catalyst to produce 1,2,3-trioxane. This reaction can be used to synthesize epoxy resins from (1S)-1-(3-aminophenyl)ethan-1-ol and formic acid. The reaction rates are dependent on the concentration of the reactants and catalysts, as well as the temperature and pressure conditions. The kinetic constants for this reaction have been determined using hydrochloric acid as a catalyst at different temperatures and pressures. The reaction rate increases with increased hydrochloric acid</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>3-Cyclopentylbenzaldehyde is an acceptor and a chiral compound. It is an alkylating agent that can form covalent bonds with the oxygen atom of an aromatic ring, as well as with the hydroxyl group of a phenol or alcohol. 3-Cyclopentylbenzaldehyde binds to human serum albumin and has high potency in inhibiting cholesterol ester transfer and cholesteryl ester transfer. 3-Cyclopentylbenzaldehyde has been shown to be effective in screening for new drugs for the treatment of Alzheimer's disease and Parkinson's disease.</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>2,2,2-Trifluoroethyl N-cyclohexylcarbamate is a research tool that has been shown to inhibit ion channels. It can be used for the study of protein interactions and receptor activation. This product is also a ligand and acts as an agonist of peptides. 2,2,2-Trifluoroethyl N-cyclohexylcarbamate has CAS number 201487-98-1.</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>4-Chloroquinoline-3-carbaldehyde is a monosubstituted aromatic compound. It has been studied in biological systems, where it has shown to have antioxidant and anti-inflammatory effects. 4-Chloroquinoline-3-carbaldehyde can be synthesized by the oxidation of 4-chloroquinoline with an oxidant such as hydrogen peroxide or potassium permanganate. The synthetic methods for this compound include the Wittig reaction and the naphthalene dihalogenation reaction, although these reactions are not typically used due to their hazardous nature. This chemical's fluorescence properties make it useful in fluorometric assays.</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>N-Benzyl-2-methyl-4-nitroaniline is a molecule that belongs to the group of organic compounds. It has a phase transition temperature of -3 degrees Celsius and can be found in the crystal system of orthorhombic. The molecular weight of this compound is 194.16 g/mol, its diameter is 2.03 nm, and it has an activation energy of 3.56 eV. N-Benzyl-2-methyl-4-nitroaniline has a dipole moment and hydrogen bonding capabilities, which are due to the presence of polarizability and viscosity. It also has spontaneous emission properties and optical properties that depend on wavelength.</p>

<p>4,5-Dichloro-2-methoxybenzoic acid is a nonsubstituted benzoic acid. It is used as a chemical intermediate in the synthesis of dibenzofurans and catechols. 4,5-Dichloro-2-methoxybenzoic acid has been analyzed for its ability to inhibit the growth of bacteria, including Salmonella and Listeria. The strain of bacteria is unknown. 4,5-Dichloro-2-methoxybenzoic acid can be found in chlorinated and dichlorinated water sources, as well as in congeners such as 2,4,6,-trichlorophenol.</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>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>