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<p>3-Bromoquinoline is a brominated quinoline derivative that can be synthesized by cross-coupling reactions. The compound's chemical structure is similar to the 3-azidoquinoline, which was studied in quantum theory and molecular modeling. The 3-bromoquinoline molecule has been shown to exist in two different coordination geometries: octahedral and trigonal bipyramidal. In the octahedral geometry, the 3-bromoquinoline molecule is bound to three bromine atoms and one nitrogen atom, with an intramolecular hydrogen bond between the nitrogen atom and the quinoline ring system. The trigonal bipyramidal geometry also features an intramolecular hydrogen bond between the nitrogen atom and quinoline ring system, as well as a halogen bonding interaction with one of the three bromine atoms.</p>

<p>Cichoriin is a coumarin glycoside, which is a type of phytochemical compound found in certain plants. It is primarily sourced from plants of the Asteraceae family, particularly chicory (Cichorium intybus). The compound exhibits its biochemical effects by interacting with various cellular pathways, including acting as an antioxidant and displaying potential anti-inflammatory and antimicrobial properties.</p>

<p>Please enquire for more information about Calipteryxin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(α-Acetonylbenzyl)-4-hydroxycoumarin sodium is an anticoagulant compound, which is a synthetic derivative of coumarin. It is primarily sourced via chemical synthesis in laboratory settings. Its mode of action involves inhibiting the synthesis of vitamin K-dependent clotting factors, specifically factors II, VII, IX, and X. This inhibition impairs blood coagulation, leading to uncontrolled bleeding.</p>

<p>Please enquire for more information about (1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Azaspiro[4.4]nonane hydrochloride is a versatile building block that is also used in research, as a reagent, and as a speciality chemical. It has been shown to be an excellent building block for complex compounds, with wide applications in the pharmaceutical industry. 1-Azaspiro[4.4]nonane hydrochloride has a CAS No. of 1417567-64-6 and can be found under the trade name Azapropynalene Hydrochloride (AP). It is soluble in water, alcohols, ethers and acetone but insoluble in most other solvents. 1-Azaspiro[4.4]nonane hydrochloride has been shown to have high quality and stability when stored under appropriate conditions; it is also resistant to degradation by light or air.</p>

<p>1,4-Diazabicyclo[2.2.2]octane is an organic compound that belongs to the group of coordination compounds and has antimicrobial activity. It is a colorless solid with a melting point of -117°C and a boiling point of 245°C. The molecular geometry is planar, which means that all bonds are linear. The compound can be found in water vapor or as colloidal gold sols in reaction with water vapor. It can also be obtained by reacting triethylenediamine with hydrochloric acid at 100°C under vacuum conditions. 1,4-Diazabicyclo[2.2.2]octane has been shown to have antibiotic properties and is able to inhibit the growth of bacteria through coordination geometry and phase transition temperature effects on the bacterial cell membrane.</p>

<p>N10-Methyl pteroic acid is a novel immunosuppressant that inhibits T-cell proliferation and promotes regression of inflammatory bowel disease. It has been shown to be effective in treating cancer patients, with the terminal half-life being approximately 20 hours. N10-Methyl pteroic acid is a potent inhibitor of human acute lymphoblastic leukemia cells. It can also be used as an immunosuppressant for organ transplantation, with desorption from gels using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI TOF MS) and bioanalytical methods such as high performance liquid chromatography (HPLC).</p>

<p>Please enquire for more information about 4,4'-Dithio-2,2'-bipyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Xanthoxyletin is a coumarin, which is a type of natural organic compound commonly found in plants, particularly in the Rutaceae family. It is sourced from various plant species, including Zanthoxylum, known for their ethnobotanical uses. Xanthoxyletin functions primarily through its biochemical activity, including the inhibition of certain enzymes and modulation of cellular pathways that influence its pharmacological effects.</p>

<p>Please enquire for more information about tert-Butyl 4-hydroxy-1-oxa-9-azaspiro[5.5]undecane-9-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>3,4-Dihydro-7-(4-chlorobutoxy)-2(1H)-Quinolinone is a crystalline organic base. It is used as an intermediate in the synthesis of piperazine derivatives. 3,4-Dihydro-7-(4-chlorobutoxy)-2(1H)-Quinolinone can be used to acetylate phenols and amines. This compound also has been shown to be useful in the industrial production of carbostyril and other pharmaceuticals. 3,4-Dihydro-7-(4-chlorobutoxy)-2(1H)-Quinolinone is also a high yield coupling agent for the production of heterocyclic compounds such as 1,5,6,8-tetrahydropyrimidines and benzimidazoles.</p>

<p>3-Azabicyclo[3,3,0]octane HCl is an inorganic base that is used as a catalyst for organic reactions. It is often used to convert ester hydrochlorides into chiral esters. 3-Azabicyclo[3,3,0]octane HCl has been shown to be a suitable reducing agent for the reduction of various substances. The reaction proceeds via an intramolecular process and can be used with various parameters. 3-Azabicyclo[3,3,0]octane HCl is crystalline and has a melting point of 179 degrees Celsius. It also has optical activity due to its chirality.</p>

<p>Please enquire for more information about 1-Benzyl-3-[3-(diethylamino)propoxy]-1H-indazole 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 4-Aminobicyclo[2.2.2]octane-1-carboxylic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Indole-7-methanol is a flavin cofactor that catalyses the formylation of indole-7-carboxylic acid. Indole-7-methanol can be synthesized by the conversion of indole-7-carboxaldehyde with formaldehyde and ammonium acetate. The macrocyclic, isomeric, and formylated forms of indole-7-methanol have been shown to have utilisation activity in the synthesis of various compounds. These reactions are catalyzed by flavins such as FAD or FMN. Mutant, unsymmetrical derivatives of indole-7-methanol are also known to undergo these types of reactions. The most common derivative is indirubin, which has been shown to inhibit DNA polymerase III and IV in vitro.</p>

<p>Please enquire for more information about 2-(2-Aminoethyl)-3',6'-bis(diethylaMino)spiro[isoindoline-1,9'-xanthen]-3-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Hydroxy-7-methoxyquinoline is an anti-malarial drug that belongs to the class of trimethyl, trifluoromethyl group. It is a cyclic compound and its synthesis starts with cyclization of the methyl derivative, which forms a ring. This product is used in clinical practice as an inhibitor of malarial protozoa and has been shown to have mechanistic effects on the cytochrome bc1 complex containing red blood cells. 4-Hydroxy-7-methoxyquinoline also inhibits the growth of bacteria by binding to the enzyme methionine synthase, which is involved in the biosynthesis of methionine from homocysteine. The product also has an inhibitory effect on DNA synthesis and protein synthesis.</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>N-Acetylimidazole is a drug that belongs to the class of glycol esters. It is an inhibitor of the enzyme acetylcholinesterase and has been used in the treatment of autoimmune diseases, such as myasthenia gravis. N-Acetylimidazole can inhibit the activity of other enzymes, such as p-nitrophenyl phosphate oxidase, which may be responsible for its anti-inflammatory properties. This drug has been shown to inhibit microbial growth in vitro by inhibiting the synthesis of choline and acetylcholine in the body. N-Acetylimidazole also inhibits bacterial growth by acting as a substrate molecule for bacterial enzymes that catalyze transfer reactions, including phosphotransferases and hydrolases.</p>

<p>Pangelin is a novel biochemical agent, which is meticulously derived from a unique microbial source with advanced bioconversion techniques. This product functions primarily through a targeted enzymatic mechanism that modulates specific biochemical pathways, ensuring high specificity and efficacy in its action. The enzymatic process engages with targeted substrates to yield predictable and controlled outcomes, making it a potentially valuable tool in biochemical research and applications.</p>

<p>Please enquire for more information about Methyl 4-(benzyloxy)-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>Please enquire for more information about 6-Benzyloxy-5-methoxyindole-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Timapiprant is an amide that acts as a selective inhibitor of the prostanoid receptor CRTH2, which is involved in regulating the inflammatory response. Timapiprant inhibits skin eosinophilia, which is associated with inflammatory skin diseases such as atopic dermatitis and psoriasis. It has been shown to be safe in clinical trials and has a good safety profile. The drug's mechanism of action may be due to its ability to inhibit the production of IL-4 and IL-13 by Th2 cells and its ability to inhibit lung function. Timapiprant has shown efficacy in treating allergic rhinitis, asthma, chronic obstructive pulmonary disease, erythema multiforme, pyoderma gangrenosum, and other types of inflammatory skin diseases.</p>

<p>Please enquire for more information about Methyl 6-Bromo-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>2,4-Dioxo-9-(phenylmethyl)-3,9-diazaspiro[5.5]undecane-1,5-dicarbonitrile is an aliphatic compound that is used in the synthesis of formaldehyde and amines. It has been shown to react with formaldehyde to produce a mixture of aliphatic amines. This reaction can be used for the production of commercial products such as dyes and pharmaceuticals.</p>

<p>7,8-Dihydroxy-4-methylcoumarin is a bioactive compound, specifically a derivative of coumarin. This compound is naturally derived from plant sources, where it acts as a metabolite in various biochemical pathways. Its chemical structure is characterized by the presence of two hydroxyl groups at the 7 and 8 positions, along with a methyl group at the 4 position of the coumarin core, contributing to its unique pharmacological profile.</p>

<p>5-Amino-8-hydroxyquinoline dihydrochloride (5-AQDH) is an anticancer drug that inhibits the activity of survivin, a protein that is overexpressed in cancer cells. It has been shown to be effective in vivo against melanoma tumor growth. 5-AQDH binds to the unpaired cysteine residues of the survivin molecule and inhibits its function by binding to the active site, blocking access to ATP and preventing DNA synthesis. The efficacy of 5-AQDH has been confirmed in vitro by studying the effect on cell viability and DNA synthesis, as well as by measuring plasma mass spectrometry data from melanoma patients. This drug is currently being investigated for its potential use as an anticancer agent.</p>

<p>Poly(1,2-dihydro-2,2,4-trimethylquinoline) is a high molecular weight polymeric quinoline. It is an intramolecular hydrogen bond donor. The nitrogen atoms in the polymers are bound to hydrogen and form a ring with two amino groups. Poly(1,2-dihydro-2,2,4-trimethylquinoline) has been shown to be resistant to many chemical agents such as hydrogen fluoride and glycoside derivatives. It also has a carcinogenic potential and can induce liver lesions. The carcinogenesis studies of poly(1,2-dihydro-2,2,4-trimethylquinoline) have shown that it may cause cancer in animals via diazonium salt and methyl ethyl hydrochloric acid</p>

<p>Please enquire for more information about 1-Allyl-3,7-dimethyl-8-phenylxanthine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-1H-imidazo[4,5-c]pyridine (4CI) is a nucleoside analog that inhibits the replication of RNA and DNA. It has significant inhibitory activity against herpes simplex virus type 1 and human immunodeficiency virus type 1 (HIV-1). 4CI inhibits the synthesis of adenosine, an important component in the synthesis of RNA and DNA. This drug also has antiviral properties against influenza A and B viruses. 4CI's effect on plasma cholesterol levels is thought to be due to inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase.</p>

<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>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>Murrangetin is a flavonoid compound, which is a natural phytochemical sourced from the peels of various citrus fruits. Its mode of action primarily involves the modulation of inflammatory pathways, potentially through the inhibition of specific enzymes like cyclooxygenases and lipoxygenases. This flavonoid is also known for its antioxidative properties, which contribute to its ability to scavenge free radicals, thereby reducing oxidative stress in biological systems.</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 Heratomol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methyl-1H-imidazole-5-carboxylic acid is a molecule that belongs to the class of antibiotics. It has been shown to be an effective inhibitor of lipases and other enzymes, which is due to its carboxylate group. The immobilization of this molecule has been studied by X-ray crystallography. The oxygen atoms in the molecule are covalently immobilized on a silica surface via a linker chain, which prevents the loss of these atoms. Dichroism spectroscopy was used to study the effects of different solvents on this molecule's ability to rotate light. 2-Methyl-1H-imidazole-5-carboxylic acid was also successfully immobilized using an enzyme called lipase, with residue carboxylate groups positioned at the bottom of the binding cavity.</p>

<p>Indole-3-acetyl-L-glutamic acid is an endogenous substance that is found in plants. It is the conjugated form of indole-3-acetaldehyde and L-glutamic acid. Indole-3-acetylglutamic acid has shown to have antioxidant potential and can be used to regulate plant growth, as well as protect against environmental stresses. Indole-3-acetylglutamic acid also has a role in regulating the production of other hormones, such as ethylene and auxin, which are involved in plant growth regulation.</p>

<p>8-Hydroxyquinoline copper(II) salt is a metal chelate that can be used as an analytical reagent. It is prepared by the reaction of ethylene diamine with 8-hydroxyquinoline and copper(II) chloride. The product has been found to emit light when irradiated with UV light. This product is also used as a substrate for methyl transferase, which is an enzyme involved in the metabolism of drugs. 8-Hydroxyquinoline copper(II) salt has been shown to inhibit the activity of P-glycoprotein (Pgp), which is a drug transporter protein found in mammalian cells that functions to pump xenobiotics from the inside of cells out into the bloodstream. When Pgp is inhibited, it causes cellular accumulation of certain drugs, such as cyclosporin A and tacrolimus.</p>

<p>Trans-Khellactone is a naturally occurring lactone derivative, which is isolated from plants of the Apiaceae family. This compound exhibits a variety of biological functions due to its unique chemical structure, which includes a dihydropyran ring. Trans-Khellactone's mode of action involves interacting with various cellular pathways, potentially modulating enzyme activity, receptor binding, and influencing signal transduction processes.</p>

<p>8-Bromo-2-methylquinoline is a naphthalene derivative that has an oxidant function. It can be used as a solvent for chlorobenzene and as a catalyst for the production of bipyridines and piperazine. 8-Bromo-2-methylquinoline is also used as a ligand in the preparation of metal complexes. This compound reacts with methyl groups, chlorine, and halides to form methyl quinolines and dichloromethanes. 8-Bromo-2-methylquinoline may react with fatty acids to form polyunsaturated acid esters or with polyunsaturated fatty acids to form polyethers.</p>

<p>(2R)-1-[2-[(3-Hydroxytricyclo[3.3.1.1(3,7)]dec-1-yl)amino]acetyl]-2-pyrrolidinecarbonitrile is a drug that belongs to the class of DPP-IV inhibitors and is used for the treatment of type 2 diabetes mellitus. It has been shown to be effective in reducing postprandial blood glucose levels in patients with type 2 diabetes mellitus. The mechanism of action of this drug is not fully understood, but it may have an effect on insulin release from pancreatic beta cells and/or inhibition of gastric emptying or intestinal absorption of glucose. This drug has been shown to reduce tubulointerstitial injury in diabetic rats and can be used as a combination therapy for type 2 diabetes mellitus. There are no known clinically relevant interactions between (2R)-1-[2-[(3-Hydroxytricyclo</p>

<p>4-Amino-3-bromoisoquinoline is an isocyanide that reacts with nucleophilic heteroatoms such as the amino group. It also reacts with bromine to form a bromopyridine. The nitrile group of 4-amino-3-bromoisoquinoline can be reduced with sodium borohydride to produce 4-aminoquinoline. This compound has shown potential for use in chemotherapy and treating bacterial infections.</p>

<p>Pranferol is a phytochemical compound, which is derived from natural plant sources. It possesses unique immunomodulatory properties, affecting cellular pathways that regulate immune responses. The bioactive components in Pranferol interact with specific receptors on immune cells, modulating signaling cascades and gene expression to enhance or suppress specific immune functions depending on the physiological context.</p>

<p>Graveolone is a bioactive compound that functions as a plant defense enhancer, which is derived from certain plant species known for their antimicrobial properties. Its mode of action involves the activation of multiple signaling pathways that bolster the plant's innate immune response. By enhancing the synthesis of defensive proteins and secondary metabolites, Graveolone effectively fortifies plants against pathogenic challenges and abiotic stresses.</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>

<p>3-Chloro-1H-indole-2-carbaldehyde is a bifunctional reagent that can be used to form amides. It reacts with primary and secondary amines, as well as dialkyl and methylene amines, to produce the corresponding chloro-, phenylhydrazine-, or nitrosoaminoureas. This reaction is intramolecular and yields the desired product in high yield. The reactant can also be used as a chloride source. 3-Chloro-1H-indole-2-carbaldehyde is manufactured by reacting phenylhydrazine with chloroacetic acid in an organic solvent at room temperature (25°C).</p>

<p>Please enquire for more information about Ethyl 7-Methoxy-1H-Indazole-3-Carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Isobergapten is a naturally occurring furanocoumarin, which is primarily derived from plants in the Apiaceae family, such as celery and parsley. The compound is structurally characterized by its fused furan and coumarin rings. It exerts its effects through its ability to interact with cellular enzymes and DNA, often influencing photodynamic processes. This interaction can result in modifications to DNA replication and transcription, making it a compound of interest in photochemotherapy and photobiology.</p>