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>3-Ethyl-2-propyl-1H-indole is an indole that can be used as a synthetic intermediate. It can also be used in nucleophilic substitution reactions to produce functionalized indoles. 3-Ethyl-2-propyl-1H-indole is nontoxic and does not react with most functional groups. This chemical is a good nucleophile and reacts regioselectively with electron deficient or neutral substrates to generate substituted indoles.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Bis(furan-2-yl)methanone is a furyl compound that is activated by trifluoromethanesulfonic acid. It has been shown to be an effective dose for the treatment of bacterial infections that are resistant to erythromycin and other antibiotics. Bis(furan-2-yl)methanone is used in veterinary medicine to treat infections caused by bacteria such as Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, and Streptococcus agalactiae. This drug has been shown to be active against Gram-positive bacteria, including Bacillus cereus, Clostridium perfringens, Clostridium tetani, Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus pneumoniae.</p>

<p>3-Methylenebicyclo[3.3.1]nonan-7-one is a chiral molecule that has been synthesized as a racemic mixture of two enantiomers. This compound is an amine with a hydroxy group and an isopropyl side chain. It has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit cyclooxygenase and lipoxygenase activity. 3-Methylenebicyclo[3.3.1]nonan-7-one also has antiviral properties, which are due to its inhibition of protein synthesis in viruses by blocking the activity of ribonucleotide reductase, an enzyme required for nucleic acid synthesis. The reaction mechanism involves the formation of a covalent bond between the amantadine and the active site of ribonucleotide reductase through either radical or hydrogen atom transfer mechanisms.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-2,3,6-trimethylphenol (4ATMP) is a halogenated phenol that has been used as a developer in the production of silver halide photographic emulsions. It interacts with hydrogen chloride to form a gaseous product and can be used as an indicator for the presence of chlorine gas. 4ATMP is also known to react with formaldehyde and acetaldehyde to produce formic acid and acetic acid respectively. 4ATMP is most commonly prepared by reacting phenol with diethylaminopropyl chloride in the presence of hydrogen chloride gas.</p>

<p>2-Phenoxyethyl)amine hydrochloride is a chlorinated, industrial, synthetic chemical used as a reaction solvent. It can be derived from cyclohexylamine and ethanolamine by reacting with phenol. The reaction product is then hydrolyzed to produce 2-phenoxyethyl)amine hydrochloride.</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>5-bromo-1,7-naphthyridine is a heterocyclic compound that can be derived from pyrrole by the introduction of an electron deficiency. This molecule has been shown to react with nucleophiles such as water and amide in order to yield unsaturated products. The molecule also has electron-donating groups on it, which can be used to optimize yields. 5-bromo-1,7-naphthyridine is often used as a reagent in organic synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>1,5-Naphthyridin-2-ylamine is a monocyclic heterocycle that is derived from the amination of 1,5-naphthyridine. It has been used in the preparation of amides and carbocycles. The reaction also produces nitro compounds. The naphthyridinone reacts with a variety of alkyl groups to produce either alkenyl or alkynyl groups. This reaction can be carried out on an industrial scale by using Grignard reagents. The reaction proceeds via a tautomerization mechanism to produce the desired products. It has been shown that this chemical is toxic to cells and can produce DNA damage.</p>

<p>A 1,6-Naphthyridin-2-amine is a chemical compound that can be synthesized in various yields by extracting it from coal tar. It has been used in the past to make n-substituted derivatives for use in combinatorial and screening studies. A 1,6-Naphthyridin-2-amine can be synthesized using a microwave irradiation technique that uses malononitrile as its starting material. The microwave irradiation technique is operational at low temperatures and can be tracked with a radiotracer. Microwave irradiation of malononitrile produces an intermediate that reacts with ammonia to produce the desired 1,6-naphthyridinone product. This product can then be converted into the desired 1,6-naphthyridin-2 amine via hydrogenation or nitration.</p>

<p>2-[2-(2,4-Dichlorophenyl)-1,3-thiazol-4-yl]acetic acid is a small molecule inhibitor that belongs to the class of peptides. It inhibits protein interactions by binding to peptide receptors on the surface of cells. This inhibitor is used as a research tool for studying the function of receptor molecules. 2-[2-(2,4-Dichlorophenyl)-1,3-thiazol-4-yl]acetic acid has been shown to activate ligand and receptor interactions in vitro. The purity of this product is high and it can be used as a research tool in life science and ion channels.</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-Oxocyclohexanecarbonitrile (3OHC) is a novel chemical compound with analgesic properties. 3OHC has been shown to be effective in reducing the inflammation of the human body. The mechanism of action has not yet been elucidated, but it may be due to its ability to inhibit prostaglandin synthesis and reduce the oxidative stress by forming reactive oxygen species. 3OHC is also an active antinociceptive agent that can be used in combination with other drugs to treat inflammatory diseases. 3OHC is able to reduce the pain caused by inflammatory diseases by reducing the production of prostaglandins, which are a group of chemicals that are responsible for causing pain and inflammation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(Z-Amino)-1-butanol is a synthetic chemokine that has been shown to be an effective vaccine adjuvant. It is believed that this drug works by enhancing the immune response to the vaccine and increasing the production of cytokines. 4-(Z-Amino)-1-butanol has been shown to be effective in treating damaged cells, such as those caused by cancer cells or viruses. This drug also prevents replication of HIV and other virus infections, which may be due to its ability to inhibit viral DNA polymerase. 4-(Z-Amino)-1-butanol binds with high affinity to the chemokine receptor CXCR3, which is expressed on activated T cells and macrophages. The binding induces chemotaxis, activation, and differentiation of T cells into effector 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,4-Dibromo-2-(chloromethyl)benzene is a synthetic compound that has been used as an anti-hepatitis C virus (HCV) agent. It is effective against HCV genotype 1 and 2, but not 3. It has been shown to be active in inhibiting the replication of HCV RNA by binding to the viral enzyme RNA polymerase. This drug has also been found to inhibit the growth of Mycobacterium tuberculosis and is being investigated for use in treating tuberculosis. The drug is prepared by reacting bromobenzene with sodium hydroxide and chloromethyl chloride in aqueous solution at 0°C. Dibromoethane reacts with paraformaldehyde and cuprous cyanide to form 1,4-dibromo-2-(chloromethyl)benzene, which can then be treated with hydrochloric acid to form the desired product.</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>

<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>1-Amino-4-methoxynaphthalen HCl is an alkaloid that is synthesised from 1-Amino-4-(N,N-dimethylamino)naphthalene. It is a tetracyclic compound and it has been shown to be effective in the treatment of hypertension and other cardiovascular diseases.</p>

<p>Versatile small molecule scaffold</p>