Compuestos policíclicos

<p>cis-Khellactone is a naturally occurring organic compound, which is a type of coumarin derivative sourced predominantly from the roots of Peucedanum and Angelica species, plants native to various regions. These botanical sources are known for yielding secondary metabolites with diverse biological properties.</p>

<p>Please enquire for more information about 8-[(2-Hydroxyethyl)(methyl)amino]-1,3,9-trimethyl-3,9-dihydro-1H-purine-2,6-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Aminoquinoline-2-one is a nonsteroidal anti-inflammatory drug that has tuberculostatic activity. It binds to the nitrogen atoms of the enzyme dihydropteroate synthase, which is involved in the synthesis of folic acid and DNA. This leads to an increase in reactive oxygen species and inflammation, which causes disease activity. 4-Aminoquinoline-2-one has been shown to be synergistic with monoclonal antibodies when used as a treatment for inflammatory diseases. In order for 4-aminoquinoline-2-one to be taken up by cells, it must bind to cellular uptake proteins through hydrogen bonds or disulfide bonds.</p>

<p>1,2-Dihydrobenzene (1,2-DH) is a molecule that has the chemical formula C6H6. It is a colorless liquid with boiling point of 147°C and melting point of -11°C. 1,2-DH has been shown to form hydrogen bonds with water molecules. This compound is also insoluble in water, which may be due to its dehydrating properties. When catalyzed by an acid or base, 1,2-DH undergoes dehydration reactions. Acidic or basic conditions are required for this reaction to occur and the resulting product can be determined by x-ray diffraction studies. 1,2-DH has been shown to form coordination complexes with metal ions such as copper (Cu) and zinc (Zn). These complexes have been shown to have ligand binding properties that lead to supramolecular structures. Intermolecular hydrogen bonding interactions between 1,2-DH molecules have also been observed during</p>

<p>Imidazole is a highly polar aromatic compound with two annular nitrogen atoms. Imidazole is widely used in the affinity purification of proteins with polyhistidine tags (His-Tag). In the protein purification process, imidazole is used for the elution of His-Tag-fused recombinant proteins from a metal-immobilised resins. In the elution buffers, imidazole is typically used in the 50 – 500 mM concentration range (Bornhorst and Falke, 2000).</p>

<p>3-(2-Aminoethyl)-N-methyl-1H-indole-5-methanesulfonamide (AMIS) is an intermediate in the preparation of medicaments. It is a stable process and can be used as an intermediate for other compounds. AMIS is prepared by reacting methanesulfonic acid with methanol and ammonium carbonate, which produces methanesulfonamide, succinic acid and ammonium hydroxide. The reaction liquid is then heated to produce a crystalline solid. The crystals are then recrystallized to yield AMIS as a white solid.</p>

<p>Please enquire for more information about 2,2,4-Trimethyl-1,2-dihydroquinolin-6-yl phenylacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2,3,4,5-Tetrahydro-5-methyl-1H-pyrido[4,3-b]indol-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Methyl 3-formyl-4,6-dimethoxy-1-methyl-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Iodo-1-tritylimidazole is an organic molecule that has a chemical stability comparable to that of a nucleophile. It is a molecule with a heterocycle and accepts electrons from carbinol compounds, halides, and other functional groups. 4-Iodo-1-tritylimidazole can be synthesized by the palladium-catalyzed coupling reaction between organometallic reagents and histidine. This compound has been shown to have properties that are similar to those of biomimetic molecules, such as cross-coupling.</p>

<p>Neobyakangelicol is a phytochemical compound, which is a natural product derived from various plant species. Its source is predominantly the roots of certain medicinal plants that are known for their array of bioactive constituents. The mode of action of Neobyakangelicol primarily involves interacting with specific biochemical pathways, potentially including modulation of enzyme activity or receptor binding, which could result in diverse pharmacological effects.</p>

<p>Please enquire for more information about 1-(2-Methoxyethyl)-1H-indole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trans-decahydroquinoline is a chiral compound that can be synthesized by an asymmetric synthesis. It is an amide with a carbonyl group and a dialkylamino group. Trans-decahydroquinoline can be used to synthesize different compounds, such as enantiopure drugs, pharmaceuticals, and agrochemicals. The synthesis of trans-decahydroquinoline can be accomplished through the aldol cyclization or the addition of an acid to the carbonyl group. The magnetic resonance spectroscopy (NMR) and molecular modeling techniques have been used to study its structure and properties.</p>

<p>Please enquire for more information about 7-Azaspiro[4.5]decane including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Umbelliprenin is a naturally occurring prenylated coumarin, which is primarily isolated from plants in the Apiaceae family. These plants are rich sources of various biologically active compounds. The mode of action of umbelliprenin is attributed to its ability to modulate multiple cellular pathways, including apoptosis and cell cycle arrest. This modulation is largely due to its interaction with reactive oxygen species and various signaling molecules within the cell.</p>

<p>5-Methoxyquinoline (5MQ) is a chemical compound that belongs to the quinoline derivatives. It has shown anticancer activity in tumor models through a proton-transfer mechanism. 5MQ reacts with an acidic proton, such as the hydronium ion, to produce a reactive intermediate that can react with DNA and other cellular macromolecules. The drug also has been shown to inhibit the growth of bacteria by inhibiting protein synthesis. This inhibition is due to its ability to transfer protons from one molecule to another, which alters the charge distribution on that molecule and prevents it from reacting with other molecules.</p>

<p>Please enquire for more information about 6-Chloro-1-methyl-1H-indole-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Bromo-3-chloro-1H-indazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromoindazole is an antibacterial agent that binds to the protonated form of the staphylococcal enzyme methicillin-resistant penicillinase (MRP) and prevents the enzyme from participating in the synthesis of cell wall precursors. The molecular modeling studies of 4-bromoindazole have shown that it can bind to pyogenes, a bacterium that causes streptococcal pharyngitis, by hydrogen bonding between its amide group and pyogenes' carboxylic acid group. 4-Bromoindazole also has anticancer activity against cancer cells with v600e mutation. It has been shown that 4-bromoindazole inhibits cancer cell proliferation by binding to the oxacillin site on DNA gyrase and topoisomerase IV, leading to DNA damage and apoptosis.</p>

<p>1,1'-Bicyclo[1,1,1]pentane-1,3-dicarboxylic acid monomethyl ester is a chemical compound used in research and as a building block for complex compounds. It is a high quality and versatile compound that has a wide range of uses in the production of fine chemicals. This compound is an intermediate for the synthesis of 1,4-benzodioxan. CAS No. 83249-10-9</p>