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1-Benzyl-3-hydroxy-1H-indazole is a hydrophilic matrix that can be used to deliver drugs. The hydrophilicity of the matrix allows it to dissolve in water and form a paste when mixed with water. The drug or drug formulation is dispersed within the paste and delivered to the site of action by the matrix. 1-Benzyl-3-hydroxy-1H-indazole has shown inhibition of inflammation, which may be due to its ability to inhibit prostaglandin synthesis. 1BHI can also be used for electroreduction reactions, such as reduction of metal ions, at temperatures ranging from -10°C to +20°C.

Bis(2,2'-bipyridine)-4'-methyl-4-carboxybipyridine-ruthenium N-succinimidyl ester-bis(hexafluorophosphate) is a molecule that inhibits the activity of matrix metalloproteinases. It binds to the active site of the enzyme and blocks its activity. This drug has been shown to be effective in inhibiting the activity of MMPs in cells, but not in tissue culture because it does not cross cell membranes. Bis(2,2'-bipyridine)-4'-methyl-4-carboxybipyridine-ruthenium N-succinimidyl ester-bis(hexafluorophosphate) has also been shown to have a low detection limit and can detect low levels of matrix metalloproteinase activity in cells.

6-Fluoroindole is an aromatic organic compound that has been shown to have anti-inflammatory and antioxidant properties in vitro and in vivo. 6-Fluoroindole is a 5-methoxyindole and can be synthesized from the amino acid tryptophan, which is a precursor of serotonin. 6-Fluoroindole has also been shown to be active against plant pathogens, human protein, and human pathogens. It can produce hemolytic activity at high concentrations and its chemical stability was tested by incubating it with various acids such as hydrochloric acid or acetic acid. 6-Fluoroindole showed no reaction with either of these acids. The vibrational spectra of 6-fluoroindole was measured using dipolar coupling constants and found to have a dipole moment of 0.01 D for the molecule.

Benzo[c]phenanthrene is a polycyclic aromatic hydrocarbon that has been shown to have carcinogenic properties in rats. It is also a potential mutagen and can cause DNA damage by forming intramolecular hydrogen bonds with guanine residues in DNA duplexes. These adducts are detected in tumor cells of rats treated with benzo[c]phenanthrene, as well as in human liver cells and mouse liver tumor cells. Benzo[c]phenanthrene can be activated by cytochrome P450 enzymes to form reactive metabolites, which bind covalently to DNA, proteins, and other cellular macromolecules. Benzo[c]phenanthrene has been shown to cause cancer in mice when given orally or injected into the peritoneal cavity. This chemical has also been found to cause liver cell necrosis in rats, at doses of 25 mg/kg body weight.

(1S,4S)-1,7,7-Trimethyl-3-(Trifluoroacetyl)Bicyclo[2.2.1]Heptan-2-One is a white solid with a melting point of -76.8°C and a boiling point of 265°C at 10 mm Hg. It has the following functional groups: particle, luminescent, lanthanide, stabilizer, ligand, voltammetry, thermally stable and has nmr spectra that show light emission and coordination chemistry. This compound is a sulfoxide but can also be considered to be a phosphine or an amine depending on its structural features. The compound's nature is dependent on the temperature and pressure as well as the solvent it is being dissolved in.>>END>>

Thiamine sulfate inner salt is a hyaluronic acid that is used in skin cancer treatment. It has been shown to have antimicrobial properties, which may be due to its ability to disrupt the cell membrane. Thiamine sulfate inner salt has also been shown to increase the germination rate of damaged seeds and can be used as a stabilizer for carrageenan. This compound is an acidic substance with a pH of 2-3. It is soluble in water and hydrochloric acid and reacts with magnesium salts, ethylene diamine, diamine tetraacetic acid, and antimicrobial peptides.

8-Hydroxyquinoline-2-carboxylic acid is a 3-hydroxyanthranilic acid derivative that is often used as a biomarker of urine. The 8OHQA can be synthesized from 3-hydroxyanthranilic acid by the action of xanthine oxidase and hydrogen peroxide, and it has been shown to be an inhibitor of protein synthesis. This inhibition may be due to its ability to form hydrogen bonds with the hydroxyl group on the ribose side chain and its ability to coordinate with metals. 8OHQA has been shown to have anti-inflammatory effects in bladder cancer cells, which may be due to its ability to inhibit prostaglandin synthesis.

2-Azaspiro[3.3]heptane HCI is a fine chemical that has many uses in research, manufacturing, and other industries. It is a versatile building block that can be used as an intermediate or reaction component for the synthesis of organic compounds. 2-Azaspiro[3.3]heptane HCI is also a speciality chemical because it has many applications in the pharmaceutical and agrochemical industries. This compound can be used as a reagent for the determination of carboxylic acids, alcohols, and amines by paper chromatography and high performance liquid chromatography (HPLC). 2-Azaspiro[3.3]heptane HCI is also useful in the synthesis of peptides and other complex compounds, such as diazepam.

2-Methyl-6-quinolinecarboxylic acid is a molecule with an affinity for aromatic rings. It has been shown through experiment that this molecule has a stable structure and can be transferred from one ring to another. 2-Methyl-6-quinolinecarboxylic acid has also been shown to have an affinity for aromatic rings in the range of 8.1 × 10 to 8.3 × 10 M−1, with an experimental affinity value of 1.2 × 10 M−1. This compound is known to interact with other molecules in a molecular docking process and can be optimized using parameters such as hydrogen bonding and van der Waals interactions.END> END>

7-Methylindole is a biochemical substance that is synthesized in the body. It is produced in the liver, and it can be found in the brain, heart, and kidney. 7-Methylindole has been shown to have cancer-fighting properties. 7-Methylindole binds to DNA by methylating nucleic acid bases, which causes a change in the genetic code. This leads to tumor cells being more sensitive to treatment with other substances that inhibit DNA synthesis or repair, such as anthranilate and 5-methoxyindole.

Byakangelicol is a naturally occurring furanocoumarin, which is a type of organic compound found predominantly in the roots of certain plants, such as Angelica dahurica. This compound is synthesized through the plant's secondary metabolic pathways, primarily as a defense mechanism against herbivores and pathogens. Byakangelicol exerts its biological effects primarily through the inhibition of various enzymatic pathways, such as cytochrome P450s and monoamine oxidase, which are key in processes like drug metabolism and neurotransmitter regulation.

Indole-7-carboxylic acid is a tetrahydropyridine that can be prepared by formylation of indole-7-carboxylic acid with formaldehyde and hydroxylamine. It is also the reaction product of dimethoxybenzene and cyanoindole in the presence of a base. Indole-7-carboxylic acid has been used in the synthesis of several drugs, including metronidazole and nitrofurantoin.

6-Methylpurine is a product of the nucleotide metabolism in E. coli, which is a model organism for protein synthesis. 6-Methylpurine inhibits protein synthesis and exerts significant cytotoxicity. It has been shown to inhibit the enzyme activities of DNA polymerase alpha, DNA ligase, and RNA polymerase, as well as other enzymes involved in nitrogen metabolism. 6-Methylpurine has been shown to be an analog of adenine and has a similar reaction mechanism. The uptake of 6-methyl purine by cells is mediated by hydrogen bonds with amino acid residues on the cell membrane surface. This molecule also forms glycosidic bonds with ribose sugar groups on cellular surfaces. 6-Methylpurine plays an important role in energy metabolism through its incorporation into glucose and glycogen molecules.

5,5'-Diamino-2,2'-bipyridine is an acidic metalloporphyrin that has been shown to react with epoxides to form nucleophilic adducts. This compound can be used as a ligand for lanthanide ions and reacts with aminopyridine to form bromoethane. 5,5'-Diamino-2,2'-bipyridine has been shown to have carcinogenic properties and may induce bromoethane mutagenicity in the liver. This compound is also mutagenic when added to propylene carbonate. 5,5'-Diamino-2,2'-bipyridine is luminescent in air or water when exposed to UV light.

3-Indolemethanol is a chemical compound that is used for chemiluminescent reaction. It can be used as an experimental model for studying the effects of 3-indolemethanol on murine hepatoma and human osteosarcoma cells in vitro. This compound has been shown to have oral hypoglycemic activity and to inhibit cancer cell growth. 3-Indolemethanol has also been shown to modulate signal pathways, such as the MAPK pathway, which may lead to pro-apoptotic protein activation or inhibition of physiological effects.

Epoxybergamottin is a furanocoumarin derivative, which is a natural bioactive compound. It is primarily sourced from citrus fruits, particularly grapefruit. The primary mode of action of epoxybergamottin is the inhibition of cytochrome P450 enzymes, specifically CYP3A4. This enzyme is a major player in the metabolism of many pharmaceuticals, and its inhibition can lead to increased bioavailability and prolonged effects of drugs metabolized by this pathway.

7-Hydroxyindole is a biochemical that is produced by wild-type strains of Escherichia coli. It has been shown to inhibit the action of an efflux pump, which is a protein that pumps drugs and other foreign substances out of the cell. The alkoxy radical reacts with 7-hydroxyindole to form a hydroperoxide intermediate. This intermediate then reacts with molecular oxygen to form hydrogen peroxide, which may be responsible for the antimicrobial activity of 7-hydoxyindole. Studies have shown that this compound can also inhibit multidrug efflux pumps in Pseudomonas aeruginosa cells, which may lead to an increase in antibiotic uptake.

4-Bromoindole is a model compound that serves as a building block for the synthesis of pharmaceutically important compounds. 4-Bromoindole has been shown to have high catalytic rates for the oxidative coupling of zirconium oxide. This compound can also be used in asymmetric synthesis because it is able to form both R and S enantiomers in moderate yield. The reaction mechanism is thought to involve a nucleophilic attack by bromide on the carbonyl group, followed by elimination of hydrogen bromide from this intermediate. 4-Bromoindole can be synthesized in three ways: (1) via an oxidative coupling reaction with ZrOCl2 and H2O2; (2) via an oxidative coupling reaction with ZrOCl2 and HBr; or (3) by reacting 4-bromoaniline with CuSO4 and Mn(NO3)2.

3-Quinuclidinol is an alkaloid that is found in the bark of Erythroxylum coca, a plant that has been used for centuries to combat hunger and altitude sickness. It is also found in the leaves of various plants such as khat, betel nut and tea leaves. 3-Quinuclidinol is a nicotinic acetylcholine receptor agonist, which means it stimulates the receptors in the brain that are responsible for transmitting messages from one nerve cell to another. 3-Quinuclidinol also activates certain types of protein kinase enzymes, which play a role in regulating metabolism.

Fluorescent dye used in diagnostic culture media

5-Methylindole-3-carboxaldehyde (5MI) is a β-unsaturated aldehydes that is used as an analyte in assays for the detection of α,β-unsaturated aldehydes. It has been shown to be effective in degranulation of cells and induces cellular degranulation. 5MI has also been shown to be an analog of other β-unsaturated aldehydes and acts competitively with these compounds.

4-Oxo-1,4-dihydroquinoline-3-carboxylic acid is a synthetic compound that belongs to the class of quinoline derivatives. It has been shown to inhibit HIV infection in vitro by binding to the receptor CD4 on the surface of T cells. 4-Oxo-1,4-dihydroquinoline-3-carboxylic acid has also been shown to be cytotoxic against cancer cells and other human cell lines. Powders of 4-oxo-1,4-dihydroquinoline 3 carboxylic acid have been synthesized by reacting ethyl esters with diphenyl ether in the presence of radiation or ndimethylformamide. This compound was also used as a molecular model for designing new drugs.

2-Aminoacridone is a fluorescent dye.  The applications of 2-Aminoacridone are extensive in biochemical and analytical research. It is commonly employed in glycoprotein and glycoconjugate studies, leveraging its high sensitivity and specificity in detecting saccharide structures. Researchers utilize this dye in various assays, including high-performance liquid chromatography (HPLC) and electrophoresis, to analyze carbohydrate content and structure. Its role is critical in advancing our understanding of carbohydrate-related biological processes, such as cell signaling and disease pathogenesis, facilitating developments in both diagnostics and therapeutic strategies.

Bathophenanthroline is a fluorescent probe that is used to detect the change in mitochondrial membrane potential. It is also able to measure the concentration of an element in a solution and can be used as a fluorescence probe for electron transfer reactions. Bathophenanthroline has been shown to have high sensitivity, which is attributed to its ability to form hydrogen bonding interactions with other molecules. Bathophenanthroline is an efficient adsorption agent, which can be used in the Langmuir adsorption isotherm technique. This chemical has been used as a fluorescence probe for chronic viral hepatitis and detection of methanol in plasma mass spectrometry.

5-Iodoindole is an organic compound that is used as a nematicide. It has been shown to have cytostatic effects on the growth of human pathogens, juveniles, and model systems. 5-Iodoindole inhibits the production of reactive amines and pyridine in vivo. It also inhibits glutamine metabolism by competitive inhibition at the glutamate dehydrogenase enzyme. 5-Iodoindole also has hemolytic activity and is able to induce transcriptomic changes in P. aeruginosa cells.

4,4'-Dipyridyl is a cyclic peptide with a basic structure. It has been found to have inhibitory effects against the growth of bacteria in human serum and group P2. The x-ray crystal structures reveal that it has strong intermolecular hydrogen bonding interactions. Experimental solubility data and coordination models show that 4,4'-dipyridyl is soluble in anhydrous sodium. Structural analysis and kinetic energy calculations indicate that the inhibitor binding site is located on the hydroxyl groups of the backbone of the molecule. This ligand also binds to metal ions such as copper or zinc.

Applications 3-Bromoquinoline (cas# 5332-24-1) is a compound useful in organic synthesis.

Applications [S-(R*,R*)]-2-[2-tert-Butyloxycarbonylamino-1-oxopropyl]-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic Acid Phenylmethyl Ester (cas# 92829-12-4) is a compound useful in organic synthesis.

Applications 6-Chloro-4-(2-cyclopropylethynyl)-3,4-dihydro-3-(phenylsulfonyl)-4-(trifluoromethyl)-2(1H)-quinolinone is an intermediate in the synthesis of novel quinolinones as HIV-1 reverse transcriptase inhibitors.
References Patel, M., et al.: Bioorg. Med. Chem. Lett., 11, 1943 (2001);

Applications 6-Chloro-3-(phenylsulfonyl)-4-(trifluoromethyl)-2(1H)-quinolinone is an intermediate in the synthesis of novel quinolinones as HIV-1 reverse transcriptase inhibitors.
References Patel, M., et al.: Bioorg. Med. Chem. Lett., 11, 1943 (2001);

Applications Indole derivative

Applications 2-(Cyanomethyl)-1H-indole-1-carboxylic Acid tert-Butyl Ester-13C,15N is an isotope labelled intermediate in the synthesis of endothelial lipase inhibitors.

Applications 7-(4-(4-Chlorobutoxy)butoxy)-3,4-dihydroquinolin-2(1H)-one is an internmediate in the synthesis of Aripiprazole (A771000) related compounds, a selective dopamine D2-receptor antagonist with dopamine autoreceptor agonist activity.
References Nagasaka, Y., et al.: Biopharma. Drug. Dispo., 33, 304 (2012); Chen, X., et al.: J. Med. Chem., 55, 7141 (2012);

Applications 1,1,2-Trimethyl-1H-benzo[e]indole-d6 is a labelled analogue of 1,1,2-Trimethyl-1H-benzo[e]indole (T896032). It is a useful research chemical.

Applications 1-Benzyl-5-bromoindole

Applications A labelled intermediate of Irbesartan (I751000).
References Gillis, J., et al.: Drugs, 54, 885 (1997), Chando, T., et al.: Drug Metab. Disps., 26, 408 (1998), Hines, J., et al.: Eur. J. Pharmacol., 384, 81 (1999)

Applications Methyl 1-(Cyclohexylmethyl)-1H-indazole-3-carboxylate is an intermediate in the synthesis of MDMB-CHMINACA (M203515), a synthetic cannabinoid with potential neurochemical effects at the CB1 receptor.
References Banister, S. ET AL.: ACS Chem. Neurosci., 7, 1241 (2016);

Applications (1S)-3,4-Dihydro-1-phenyl-2(1H)-isoquinolinecarboxylic Acid 2,5-Dioxo-1-pyrrolidinyl Ester is an intermediate in the synthesis of ((R)-1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)((S)-1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)methanone (P309025). ((R)-1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)((S)-1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)methanone is a possible impurity of solifenacin (S676700) which is a muscarinic M3 receptor antagoinst. Solifenacin is used in treatment of urinary incontinence.
References Ikeda K., et al.: Arch. Pharmacol., 366, 97, (2002); Chapple, C.R., et al.: Br. J. Urol., 93, 303 (2004); Ohtake, A., et al.: Eur. J. Pharmacol., 492, 243 (2004); Brunton, S., et al.: Curr. Med. Res. Opin., 21, 71 (2005); Habb, F., et al.: Eur. Urol. 47, 376 (2005); Payne, C.K., et al.: Drugs, 66, 175 (2006)

Applications 3-acetylindole (cas# 703-80-0) is a useful research chemical.

Applications A reagent used in the preparation of biologically active Azaindoles.
References Minakata, S., et al.: J. Agric. Food Chem., 45, 2345 (1997),

Applications 4-Hydroxy-3-quinolinemethanol Benzyl Ether is a reactant used in the preparation of propanol and propylamine quinoline derivatives used as glucocorticoid ligands.

Applications 2-Chloro-5-nitroquinoline is used in the synthesis of potent, orally active corticotropin-releasing factor-1 receptor antagonists.
References Takeda, K., et al.: BIoorg. Med. Chem., 20, 6559 (2012); Verheij, M.H.P., et al.: J. Med. Chem., 55, 8603 (2012); Takeda, K., et al.: Bioorg. Med. Chem. Lett., 22, 5372 (2012);

Applications 6-Chloro-3-(cyclopropylethynyl)-4-(trifluoromethyl)quinolin-2(1H)-one is an intermediate in the synthesis of novel quinolinones as HIV-1 reverse transcriptase inhibitors.
References Patel, M., et al.: Bioorg. Med. Chem. Lett., 11, 1943 (2001);

Applications 3-Amino-4-bromo-5-phenylpyrazole (cas# 2845-78-5) is a compound useful in organic synthesis.

Stability Store in freezer at -20°C
Applications 5-Amino-6-(methylamino)quinoline (cas# 14204-98-9) is a compound useful in organic synthesis.

Applications Quinoline derivative used in the preparation of compounds with anticonvulsant activity as well as compounds with potent antibacterial activity against gram-positive pathogens.
References Guo, L. et al.: Eur. J. Med. Chem., 44, 954 (2009); Jarvest, R.L. et al.: J. Med. Chem., 45, 1959 (2002);

Applications 5-Hydrazino-2(1H)-quinolinone Hydrochloride is an intermediate used in the synthesis of sodium-hydrogen exchanger type 1 inhibitor (NHE-1).

Applications 5-Nitroisoquinoline (cas# 607-32-9) is a compound useful in organic synthesis.

Applications 2-[(Diethylamino)methyl]indole Methiodide is an intermediate in the preparation of carcinogenic indole derivatives.
References Eenkhoom, J.A., et al.: CND. J. Chem., 51, 792 (1973);