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Applications Indole-3-acetamide is a compound that is converted to indole-3-acetic acid by indole-3-acetamide hydrolase in auxin biosynthesis in plants.
References Mano, Y., et al.: J. Exp. Bot., 61, 25 (2010)

Applications 4-Chloro-6,7-dimethoxyquinoline, can be used as an intermediate for the synthesis of various pharmaceutical and biologically active compounds. It is used for the preparation of Tivozanib (T447205), and Cabozantinib (C051500), acting as anticancer agents.
References Fu, Y., Zhongguo Xinyao Zazhi, 22, 26 (2013); Liu, M., Adv. Mat. Res., 396, 1490 (2012); Camp, R., et al.: Cancer, 86, 2259 (1999);

Applications Pyridoxamine Dihydrochloride (cas# 524-36-7) is a compound useful in organic synthesis.

Applications 3-Hydroxyindole is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity.
References Rajak, H. et al.: Int. J. Pharm. Sci. Nanotech., 2, 661 (2009); McClay, K. et al.: Appl. Environ. Microbiol., 71, 5476 (2005); Berry, A. et al.: J. Ind. Microbiol. Biotech., 28, 127 (2002)

Applications tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate (cas# 203661-69-2) is a useful research chemical.

Applications Indazolone derivative.

Applications 6-Dimethylaminopurine-9-riboside (cas# 2620-62-4) is a compound useful in organic synthesis.
References Elion, G.B., et al.: JACS, 74, 411-414 (1952), Kelley, J.L., et al.: J. Med. Chem., 32, 1020-1024 (1989)

Applications 2-Butoxyquinoline-4-carboxylic Acid is used in the organic synthesis of o-(β-diethylaminoethyl)cinchoninaldoxime with local anesthetic activity
References Rossi, S., et al.: Farmaco, Edizione Scientifica, 34, 486 (1979)

Applications 1,2,3,4-tetrahydro-1,2-dimethyl-4,8-isoquinolinediol, is a Tetrahydroisoquinoline derivative, that can be used for the synthesis of pharmaceutical drugs, containing tetrahydroisoquinoline skeleton.

Applications Isoquinoline is used in the synthesis of nitrated indenoisoquinolines as a potent topoisomerase I inhibitor.This compound is a contaminant of emerging concern (CECs).
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Morrell, A., et. al.: J. Med. Chem., 49, 7740 (2006)

Applications 1-Ethyl-2,3,3-trimethylindolenium-5-sulfonate (cas# 146368-07-2) is a compound useful in organic synthesis.

Applications 5,7-Diazaspiro[3.4]Octane-6,8-Dione (cas# 89691-88-3) is a useful research chemical.

Applications 2,2':6',2''-Terpyridine (cas# 1148-79-4) is a useful research chemical.

Applications Indoline metabolite
References Lacroix, I., et al.: Nat. Prod. Lett., 7, 15 (1995), Yamada, Y., et al.: Chem. Pharm. Bull., 54, 788 (2006), Whitehead, T., et al.: App. Environ. Microbiol., 74, 1950 (2008),

Applications This compound has estrogenic activity. It exhibits bright blue fluorescence in neutral or acid solution, and greenish-yellow fluorescence in strong alkali solution.
References Wolfbeis, O.S. & K. Schaffner: Photochem. Photobiol., 32, 143(1980), Bickoff et al.: J.Am. Chem Soc. 80, 3969 (1958)

Please enquire for more information about 1-Methylindole-3-acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Phenanthrol is a naturally occurring phenanthrene derivative that is used in the treatment of cervical cancer. It has been shown to be effective in the chemiluminescence method using urine samples, which indicates that it may have an effect on the body's metabolism. 1-Phenanthrol has also been shown to inhibit the production of s-phenylmercapturic acid, which is a metabolite of aromatic amines. This inhibition may be due to its receptor binding properties as it binds to and activates the peroxisome proliferator-activated receptor alpha (PPARα) and PPARγ. 1-Phenanthrol also inhibits angiotensin II type 1 receptors and can cause vasorelaxation by reducing blood pressure.

2,6-Dichloro-3-deazapurine is an isomer of the nucleoside guanosine. It has been shown to inhibit the synthesis of viruses in cell cultures and may be useful in the treatment of leukemia. The synthesis of 2,6-dichloro-3-deazapurine can be achieved through a solid-phase synthesis that uses synthons as starting materials. The molecular modelling studies have shown that this molecule has a potential to bind to adenosine receptor subtypes A2a, A2b, and A3.

2,6-Dichloropurine is a nitrogenous base that inhibits the activity of certain enzymes in the body. It has been shown to inhibit protease activity and nitro reductases, which are enzymes that metabolize nitrosamines. 2,6-Dichloropurine also inhibits the synthesis of epidermal growth factor (EGF) and adenosine A3 receptors in vivo. This drug has potent antitumor activity against various cancer cells and is used for the treatment of HIV infections. 2,6-Dichloropurine can be synthesized from 6-fluoro-3-indoxyl-beta-D-galactopyranoside with an intramolecular hydrogen atom.

Demethylsuberosin is a naturally-occurring compound, specifically a coumarin derivative, which is often extracted from plants. It originates from numerous botanical sources, including the family Rutaceae, where it serves as a secondary metabolite. Its mode of action involves the inhibition of fungal and bacterial growth, achieved by disrupting the integrity of microbial cell walls and interfering with their replication processes.

8-Fluoroquinoline is a quinoline derivative that has been shown to have in vitro anticancer activity against colon adenocarcinoma cells. It is a chiral molecule that can exist as two stereoisomers, (R)-8-fluoroquinoline and (S)-8-fluoroquinoline. These isomers may have different interactions with the tumorigenic cells, but both of them have anticancer activity. 8-Fluoroquinoline also interacts with cytochrome P450 enzymes, enhancing their ability to metabolize carcinogens.

Indole-3-acetyl-l-leucine is a homologous auxin. It is a conjugated acid that is found in plants and has been shown to be involved in postharvest physiology, growth regulation, and plant tissue culture. Indole-3-acetyl-l-leucine has been used as a model system for the study of plant physiology and tissue culture. The physiological function of indole-3-acetyl-l-leucine is not currently known. However, it has been shown to be converted into butyric acid by certain bacteria, which can lead to the formation of conjugates with carboxylic acids.

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.

Biotinyl-6-aminoquinoline is a synthetic chemical that has been shown to inhibit the growth of cancer cells in laboratory mice. It was synthesized to be a substrate for the enzyme quinolinate synthase, which is involved in the synthesis of nicotinic acid. Biotinyl-6-aminoquinoline is an analytical method that has been used in urinary samples from patients with bladder cancer as well as healthy individuals. The sequences of each individual were determined and analyzed using an algorithm that performs logistic regression, which can predict whether or not the patient has bladder cancer.

4,5-Dimethoxyindole is a chemical compound that has been shown to exhibit radical scavenging activity. It is an inhibitor of integrase, which are enzymes involved in the integration of viral DNA into host cell chromosomes. This compound has been synthesized and its optical properties have been studied. The synthesis of 4,5-dimethoxyindole derivatives has also been investigated using molecular modeling. Schrodinger software was used to predict the geometry of these synthesized derivatives. These studies suggest that 4,5-dimethoxyindole may be a potential anti-cancer agent due to its ability to inhibit cancer cell growth and induce apoptosis.

Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid is a pyrimidine analog and an electron transfer agent. It is a potent inhibitor of the enzyme dehydrogenase, which catalyzes the conversion of nicotinamide adenine dinucleotide (NAD) to nicotinamide adenine dinucleotide phosphate (NADP). Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid has been shown to have anti-inflammatory properties and also inhibits the production of b-raf protein. This drug has also been shown to be a potent inhibitor of mitochondrial electron transport in cancer cells. Pyrazolo[1,5-a]pyrimidine-3-carboxylic acid binds to the metal centers in mitochondria, thereby inhibiting oxidative phosphorylation and reducing ATP synthesis. This ultimately leads to cell death by apoptosis.

6-Bromoindole is a synthetic compound that has been shown to have significant anticancer activity in animals. 6-Bromoindole shows cytotoxicity against cervical cancer cells and has been shown to be active against leukemia cells, with the potential for use as a therapeutic agent for both solid tumor cancers and hematological malignancies. The synthesis of 6-bromoindole is based on an asymmetric Friedel-Crafts reaction, which uses hydrochloric acid as a catalyst. This product also shows significant antibacterial activity and has been found to be effective against LPS-stimulated RAW264.7 cells.

Isatin dianilide is an organic compound with the chemical formula C8H6N2O. It is a white solid that is soluble in water, ethanol and acetone. Isatin dianilide can be synthesized by reacting phenylacetic acid with ammonia and formaldehyde. Isatin dianilide has been shown to have efficient oxidation reaction with Baeyer-Villiger oxidation, which makes it suitable for industrial use. Isatin dianilide also has biological activities such as inhibition of aminopeptidase N and aminopeptidase M, which are enzymes involved in protein synthesis. Yields of isatin dianilide are high because it can be produced from the commercially available compounds isatin and amidine.

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.

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.

Columbianadin is a coumarin derivative, which is a natural compound primarily extracted from plants in the Apiaceae family, such as Angelica species. This natural product possesses a unique molecular structure characterized by the presence of a coumarin skeleton, which is responsible for its diverse biological activities.

Hypoxanthine is a nucleoside that is found in human cells. It is synthesized from guanine by the enzyme, xanthine oxidoreductase. Hypoxanthine is also produced from xanthine by adenosine deaminase and converted back to xanthine, which can then be reused for DNA synthesis. Hypoxanthine has been shown to inhibit the growth of photosynthetic bacteria, such as Rhodopseudomonas viridis and Rhodobacter sphaeroides. This inhibition may be due to an equilibrative nucleotide effect on the folate receptor. The x-ray diffraction data collected from the chrysanthemum flower (a source of hypoxanthine) showed that hypoxanthine has a calcium salt structure.

6-Chloro-7-iodo-7-deazapurine is a nucleoside analogue that is synthesized by a cross-coupling reaction between 6-chloro-2,4(1H,3H)-pyrimidinedione and 7-iodo-7-(trifluoromethyl)purine. 6CIDP has been shown to inhibit growth of epidermal cells at concentrations as low as 0.1 µM, with cytostatic effects seen at 10 µM. 6CIDP has also been shown to potently inhibit the replication of the human papilloma virus in vitro and in vivo. 6CIDP is currently being investigated for the treatment of AIDS and other viral infections. The molecular modeling studies on this compound have revealed that it may be a potent inhibitor of the epidermal growth factor receptor (EGFR).

5,12-Dibutylquinacridone is an electron acceptor that is used as a monomer in cationic polymerization. It can be polymerized with acrylates to form polymers that have high fluorescence and photopolymerizable properties. 5,12-Dibutylquinacridone has shown to be reactive with epoxides and diene compounds, which are typically used as monomers in the synthesis of polymers. This chemical has been studied for its use in solar cells and photocurrent generation. The electron spin resonance technique has been used to study the chemical's photophysical properties.

4-Nitroimidazole has a redox potential that is well suited to the reduction of nitro groups. It is an antimicrobial agent that inhibits the growth of microorganisms by inhibiting DNA synthesis. 4-Nitroimidazole can be used for the treatment of infectious diseases such as tuberculosis, leprosy, and brucellosis. In rat liver microsomes, 4-nitroimidazole reacts with NADPH to produce a nitro group and an imidazole ring with a new configuration. The reaction mechanism is based on electron transfer from NADPH to the nitro group in 4-nitroimidazole via a series of reactions that involve cytochrome P450 enzymes. This reaction has kinetic energy and matrix effects that affect its pharmacokinetics and pharmacodynamics.

MAO inhibitor; neuro-protective and cognitive enhancement effects

3,4-Dihydroisoquinolin-1(2H)-one is a potent antagonist of the histamine H1 receptor and has been shown to be safe in animal studies. 3,4-Dihydroisoquinolin-1(2H)-one has also shown efficacy in treating inflammatory diseases, such as asthma and arthritis. This compound was recently tested for its potential to diagnose cancer by targeting the tumor microenvironment. The compound was found to bind to trifluoromethanesulfonic acid (TFMS) with high affinity and selectivity. TFMS is an emerging therapeutic target for cancer therapy because it is highly expressed in the tumor microenvironment and can act as a proton donor for drug delivery systems. 3,4-Dihydroisoquinolin-1(2H)-one has also been observed to have low toxicity profiles in preclinical models, but more research is needed before it can be used clinically.

6-Cyanoindole is a synthetic compound that has been shown to have functional properties. It binds to the receptor of the chemokine, which is a type of protein that regulates inflammatory responses. It also inhibits the activity of coagulation factors, which are proteins involved in blood clotting. 6-Cyanoindole has been shown to inhibit cancer cell growth and induce apoptosis (cell death) in a number of cancer cell lines. The fluorescence properties and lifetimes of 6-cyanoindole have been studied extensively. It has also been used as a monomer in copolymerization reactions and is used as an intermediate in the synthesis of 6-bromoindole.

Indole-3-glyoxylamide is a synthetic compound that was originally developed as a potential anti-cancer drug. It has been shown to inhibit glycogen synthase kinase 3 (GSK-3) and thereby reduce the production of proinflammatory cytokines in bowel disease. Indole-3-glyoxylamide also inhibits inflammatory bowel disease by inhibiting secretory phospholipase A2, which prevents the release of arachidonic acid from phospholipids. This synthesis is required for the production of prostaglandins and leukotrienes, which are involved in the inflammatory process. The compound has been shown to have immunomodulatory effects in chronic bronchitis, with an inhibitory effect on neutrophil chemotaxis, macrophage activity, and cytokine production. Indole-3-glyoxylamide has also been shown to be effective against cancer cells in vitro and in vivo animal models. It is metabolized through

Isosibiricin is a naturally occurring lignan, which is extracted from certain plant sources. This compound is derived from the genus Daphne, traditionally known for its diverse range of biologically active constituents. Its mode of action is primarily through the modulation of key signaling pathways involved in cell proliferation and apoptosis. Isosibiricin exhibits notable inhibitory effects on specific enzymes and receptors implicated in oncogenic processes, making it a subject of interest for cancer research.

5-Ethylindole-2-carboxylic acid is an organic compound that is a decarboxylation product of indole. It can be obtained by catalytic dehydrogenation of ethyl ester or 5-ethylindole-2-carboxylic acid. It has been shown to inhibit the growth of bacteria and fungi, as well as to have anti-inflammatory properties.