Polycyclic Compounds

Nordalbergin, a coumarin isolated from the bark of Dalbergia sissoo, can significantly induce the differentiation of HL-60 cells.

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Applications Quinolin-4(1h)-one (cas# 529-37-3) is a useful research chemical.

Applications Halquinol is an antimicrobial compound belonging to the group of hydroxyl-quinolines indicated for use in poultry and swine. It depresses the activity of the gastro-intestinal tract, causing longer transit time of feed through the intestine, thereby enhancing digestion and absorption of nutrients. It increases weight gain and improve feed conversionprevent and control nonspecific diarrhea or wet dropping in farming animals. References Costa, M. et al.: PLoS One, Vol. 12, (2017);

Natural glycoside

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8-Methoxy-2-methylquinolin-5-amine monohydrochloride is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. 8-Methoxy-2-methylquinolin-5-amine monohydrochloride is an intermediate for the production of research chemicals and pharmaceuticals. It can be used to synthesize speciality chemicals, useful scaffolds, and reagents. It also has a wide range of applications as a reaction component in synthetic organic chemistry. 8-Methoxy-2-methylquinolin-5-amine monohydrochloride has high purity and quality.

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Indole-7-carboxaldehyde is a chemical compound that has significant cytotoxicity. It is also an anti-cancer drug that can be used to treat cancer cells. It inhibits the growth of cancer cells by inhibiting the production of proteins vital for cell division and by inducing apoptosis in cancerous cells. Indole-7-carboxaldehyde has been shown to inhibit the proliferation of MCF-7 breast cancer cells and human leukemia cells. The chemical has been shown to have inhibitory properties against the enzyme called amp-activated protein kinase (AMPK). This inhibition prevents activation of AMPK, which can lead to increased phosphorylation of acetyl CoA carboxylase (ACC) and therefore decreased malonyl CoA levels. This decrease in malonyl CoA will cause a decrease in fatty acid synthesis, leading to cell death.

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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>

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7-Ethyl-1H-indole-2,3-dione is a benzene derivative that can be used as a test compound in bioassays. 7-Ethyl-1H-indole-2,3-dione is structurally related to the natural product isatin and its reactive chlorine atom leads to the formation of new compounds such as 5-chloroisatin. The mechanism of action of this compound has been determined by injecting it into rats and measuring the levels of prostaglandin E2 and furan in their blood plasma.

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.

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Applications 6-Benzylamino-7-deazapurine (cas# 60972-04-5) is a compound useful in organic synthesis. References Tedder, M., et al.: Bioorg. Med. Chem. Lett., 14, 3165 (2004),

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6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (URB602) is a potential antidepressant drug that has been shown to activate the sodium hypochlorite pathway in the brain. URB602 has an excitatory effect and induces nociceptive behaviours in rats. This drug also activates the 2-arachidonoylglycerol (2-AG) system and inhibits periaqueductal grey neurons. These effects may be due to its ability to inhibit lipase activity and diacylglycerol (DAG) synthesis. URB602 also has antinociceptive properties and is scalable for industrial production.

8-Methoxyquinoline-5-carboxylic acid (8MQCA) is an amide that has been shown to have a number of specificities. It is a quinoline derivative and as such, it has been shown to have pharmacological targets such as suzuki, connect, and vanilloid. 8MQCA also has the potential to act as a vanilloid receptor antagonist and PDE4 inhibitor. 8MQCA binds to the pharmacological target site on inflammatory cells and inhibits the production of TNF-α, which is a key mediator in chronic inflammatory diseases.

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3,4-Dihydro-6,7-isoquinolinediol is an inhibitor of tumor cell growth. It has been shown to inhibit tumor cell growth when tested in vitro and in vivo. This compound has been shown to inhibit the proliferation of cancer cells and cause apoptosis by interfering with protein synthesis. 3,4-Dihydro-6,7-isoquinolinediol binds to a specific site on the ribosome, which prevents the addition of amino acids to a growing polypeptide chain. This process leads to inhibition of protein synthesis and ultimately cellular death. The fluorophore that is present on 3,4-dihydro-6,7-isoquinolinediol inhibits tumor cell growth by binding to DNA and RNA polymerase enzymes. 3,4-Dihydro-6,7-isoquinolinediol is also used as a biochemical probe for studying the structure and function of proteins in solution.

Br-Mmc (4-Bromomethyl-7-methoxycoumarin) is used as a new fluorescence label for fatty acids. It is used for the determination of fatty acids by HPLC or TLC.

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Ethyl 5-[4-(difluoromethoxy)phenyl]-3-methyl-7-oxo-8-oxa-2-azabicyclo[4.3.0]nona-3,10-diene-4carboxylate (EFD) is a synthetic compound that interacts with calcium channels in the muscle cell membrane and modulates the flow of calcium ions through the channel. This interaction leads to an increase in intracellular calcium concentrations, which can activate protein kinase C and modify ion transport system function. EFD has been shown to be effective against neuroblastoma cells, as well as reticulum and sarcoplasmic reticulum cells. It also has an antagonistic effect on the ryanodine receptors in these cells, leading to increased release of calcium from storage sites within the cell.

2-Amino-9H-pyrido[2,3-b]indole is a potent inducer of human cytochrome P450 enzymes. It has been shown to be genotoxic and carcinogenic in animal models. 2-Amino-9H-pyrido[2,3-b]indole binds to DNA duplexes, forming covalent adducts with guanine bases. The enzyme responsible for the metabolism of this compound is glucuronide conjugate. This drug's pharmacokinetic properties are dependent on its reactive nature and the concentration-time curve that it produces.

4-Amino isoquinoline is a synthetic chemical that has a pyridine ring and chlorine atom. It can be synthesized by reacting 2,4-dichlorobenzene with acetaldehyde and hydrochloric acid. 4-Amino isoquinoline binds to the receptor that it interacts with, such as the ligand, dimethyl acetylenedicarboxylate, or taraxasterol acetate. This binding process can be used for treatment purposes. The ligand is usually introduced into the body through injection or ingestion of a drug. The ligand can also be attached to an antibody in order to target specific cells. The ligand has shown efficacy in treating cancerous tumors and other diseases like Parkinson's disease and Alzheimer's disease.

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Applications 1,2,3,4,5,6,7,8-OCTAHYDROPHENANTHRENE (cas# 5325-97-3) is a useful research chemical.

2-Mercaptopurine (2MP) is a thiopurine drug that is used to treat bowel disease. 2MP inhibits the activity of methyltransferase, which is an enzyme that converts 6-mercaptopurine to 6-thioguanine. This process prevents the conversion of 6-thioguanine into 6-thiouric acid, which is an intermediate in the synthesis of thymine nucleotides. 2MP also inhibits the binding of atp-binding cassette transporter proteins to DNA and blocks the incorporation of purines into RNA and DNA. The drug has been shown to be effective in treating squamous cell carcinoma and other diseases with a high level of activity. 2MP has been shown to be metabolized by erythrocyte polymerase chain reaction and can be detected in biological samples.

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Methyl 4-methoxy-2-indolecarboxylate is a natural product that has been shown to have cytotoxic and anticancer activity. It was first isolated from the leaves of Picrasma excelsa, which is a plant native to Southeast Asia. Methyl 4-methoxy-2-indolecarboxylate has been found to be effective against breast cancer cell lines and human cancer cells in culture. The anticancer effects may be due to its ability to inhibit protein synthesis by inhibiting the ribosome. This compound also inhibits dehydrocrenatine, which is a precursor of the hormone crenatine, thus leading to decreased production of this hormone.

Applications Protected nucleoside. References Elzein, E., et al.: Bioorg. Med. Chem. Lett., 17, 161 (2007), Franchetti, P., et al.: J. Med. Chem., 52, 2393 (2009),

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8-Aminopurine is an aminopurine that is used as a research tool in magnetic resonance spectroscopy. The proton magnetic resonance spectrum of 8-aminopurine shows two characteristic peaks at 3.0 and 4.2 ppm, which are assigned to the aminopurine tautomers (3-HPA, 4-HPA). The kinetic stability of 8-aminopurine in water is pH dependent and has been shown to be strongly dependent on the presence of aldehyde oxidase (AO) activity. AO activity can be inhibited by the addition of dimethylformamide or other non-specific inhibitors such as 2,6-dichloroisonicotinic acid.

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Applications 5,6,7,8-Tetrahydroquinoline (cas# 10500-57-9) is a useful research chemical.

4-Bromo-7-azaindole is a synthetic amine that has been shown to have anticancer activity. It has been shown to induce significant cytotoxicity in vitro against human ovarian carcinoma cell lines as well as lung fibroblasts. The mechanism of action of 4-bromo-7-azaindole is believed to be due to its ability to interact with hydrogen bonding and nitrogen atoms. Its cytotoxic activity was observed when the compound was in the cis form, but not when it was in the trans form. This may be due to steric interactions between the bromine atom and the benzene ring. 4-Bromo-7-azaindole can be synthesized by a cross coupling reaction using 2,6-lutidine and ethyl acetate.

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7-Chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid is a carboxyl group with a 3-chloroperoxybenzoic acid. It has been shown to be an effective antimicrobial agent against gram positive and gram negative bacteria, as well as fungi. 7CQCA is not active against mycoplasma or spirochetes. This compound is synthesized in the presence of 1% hydrochloric acid (HCl) and 10% trifluoride. The synthesis proceeds through the following steps: (1) chlorination of ethyl acetate (EtOAc), (2) dehydrogenation of the resultant 7CQCA, (3) hydrolysis of the resultant carboxylic acid, and (4) acetone reduction of the resultant quinoline ring to produce 7CQCA.

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8-Hydroxybergapten may have anti-wrinkle activity.