Compostos Policiclícos
Os compostos policíclicos são moléculas orgânicas que contêm múltiplos anéis interconectados. Esses compostos incluem hidrocarbonetos aromáticos policíclicos e outros sistemas de anéis complexos. Eles são significativos na ciência dos materiais, produtos farmacêuticos e eletrônica orgânica. Na CymitQuimica, oferecemos compostos policíclicos de alta qualidade para apoiar suas pesquisas e aplicações industriais, garantindo resultados confiáveis e eficazes em seus projetos.
Subcategorias de "Compostos Policiclícos"
- Acridinas(97 produtos)
- Antraquinonas(533 produtos)
- Ácidos antraquinonasulfónicos(16 produtos)
- Azobenzenos(270 produtos)
- Azonaftalenos(98 produtos)
- Azoxibenzenos(12 produtos)
- Azulenos(11 produtos)
- Benzimidazóis(1.475 produtos)
- Benzodioxanos(27 produtos)
- Benzofuranos(924 produtos)
- Benzotiofenos(700 produtos)
- Benzotriazóis(438 produtos)
- Binaftil(133 produtos)
- Carbazóis(462 produtos)
- Cromanos, Cromenos(480 produtos)
- Cumarinas(1.122 produtos)
- Ciclofanos(11 produtos)
- Fluorenos e Fluorenonas(381 produtos)
- Imidazopiridinas(10 produtos)
- Indans(118 produtos)
- Indazóis(2.037 produtos)
- Indenos(22 produtos)
- Indóis(3.988 produtos)
- Indolinas(119 produtos)
- Isatinas(234 produtos)
- Isobenzofuranos(17 produtos)
- Ftalimidas N-Substituída(153 produtos)
- Naftalenos(2.437 produtos)
- Naftiridina(17 produtos)
- Naftoquinona(2 produtos)
- Perilenos(36 produtos)
- Fenazinas(25 produtos)
- Ftalazinas(33 produtos)
- Ftalimida(153 produtos)
- Hidrocarbonetos aromáticos policíclicos (PAHs)(270 produtos)
- Polifenol(261 produtos)
- Pteridinas(52 produtos)
- Pireno(87 produtos)
- Quinuclidina(1 produtos)
- Tetracenos(7 produtos)
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5-Hydroxyisoquinoline
CAS:5-Hydroxyisoquinoline is a quinoline derivative that is synthesized from aziridine. It has been shown to be a potent insulin sensitizing agent in mice with type 2 diabetes mellitus. 5-Hydroxyisoquinoline has been shown to inhibit the activity of purified enzymes preparations and show high selectivity for chloride channels, which are responsible for the transport of chloride ions across cell membranes. This inhibition leads to an influx of protons into the cell, which may lead to a change in the redox potential and changes in the molecular structure of the molecule. The reaction mechanism involves substitution at position 5 of the isoquinoline ring by hydroxy groups (OH).Fórmula:C9H7NOPureza:Min. 95%Cor e Forma:Yellow PowderPeso molecular:145.16 g/mol3-(2-Aminoethyl)-5-methoxy-1H-indole-2-carboxylic acid
CAS:3-(2-Aminoethyl)-5-methoxy-1H-indole-2-carboxylic acid is a fine chemical that is used as a building block for research chemicals, reagents, and specialty chemicals. It has the CAS No. 52648-13-2. 3-(2-Aminoethyl)-5-methoxy-1H-indole-2-carboxylic acid is also a versatile building block for synthesis of complex compounds with high quality and is a reaction component in many reactions. This compound can serve as an intermediate or scaffold in chemical synthesis.Fórmula:C12H14N2O3Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:234.25 g/mol1,10-Phenanthroline monohydrate
CAS:1,10-Phenanthroline monohydrate is a metal chelate that binds to DNA by hydrogen bonds. It has been shown to have an intramolecular hydrogen and a linear calibration curve with a coefficient of determination (r2) of 0.998. The rate constant for the reaction of 1,10-phenanthroline monohydrate with DNA is 5.00 x 10 M-1 s-1 at 25°C in water and pH 7.4 buffer. The coordination geometry for 1,10-phenanthroline monohydrate is octahedral with the axial ligands occupying the equatorial positions and the equatorial ligands occupying the axial positions. This compound has been shown to be active against HL-60 cells, which causes cancerous transformations in vitro. Fluorescence spectrometry data shows that 1,10-phenanthroline monohydrate can bind to DNA in vitro but not in vivo.Fórmula:C12H10N2OPureza:Min. 95%Cor e Forma:Off-White PowderPeso molecular:198.22 g/mol6-Bromo-1H-indole-3-carboxylic acid
CAS:6-Bromo-1H-indole-3-carboxylic acid is a natural product that is isolated from the marine sponge Smenospongia purpurea. It was first reported in 1979 and has been used for the synthesis of other compounds. 6-Bromoindole, a precursor to 6-bromo-1H-indole-3-carboxylic acid, is biosynthesized from methyl ester and NMR spectra indicate that it has a dihedral angle of 173°. This compound has been shown to have antibacterial activity against staphylococcus.Fórmula:C9H6BrNO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:240.05 g/mol3-Methylxanthine
CAS:Produto ControladoDiuretic; cardiac stimulant; smooth muscle relaxant; bronchodilatorFórmula:C6H6N4O2Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:166.14 g/mol4',6-Diamidino-2-phenylindole 2HCl
CAS:4',6-Diamidino-2-phenylindole 2HCl (DAB) is a chemical compound used as a histological stain to detect and identify different types of cancer cells. It has been shown to have cytotoxic activity against cancer cells in vitro, but not normal cells. DAB inhibits the growth of cancer cells by disrupting the mitochondrial membrane potential, leading to the release of cytochrome c and apoptosis. The use of this substance has shown that it is not toxic to maternal blood or embryonic tissues. DAB binds to nuclear DNA and polymerase chain reaction products, providing an accurate way to measure cancer cell proliferation.Fórmula:C16H17Cl2N5Pureza:Min. 97.5 Area-%Cor e Forma:Yellow PowderPeso molecular:350.25 g/mol5-(Trifluoromethoxy)-1H-indole-2,3-dione
CAS:5-(Trifluoromethoxy)-1H-indole-2,3-dione is a potent anticancer agent that inhibits the growth of cancer cells by inducing apoptosis. It binds to DNA, forming hydrogen bonds with guanine and adenine residues. This binding prevents the formation of hydrogen bonds between DNA bases, which are essential for maintaining the stability of DNA. The disruption of these bonds leads to chromosomal degradation and eventually cell death. 5-(Trifluoromethoxy)-1H-indole-2,3-dione has shown antifungal activity against Cryptococcus neoformans in vitro and in vivo. This drug also has an allosteric modulator effect on HL60 cells.Fórmula:C9H4F3NO3Pureza:Min. 95%Cor e Forma:Red PowderPeso molecular:231.13 g/mol4-Fluoroindole
CAS:4-Fluoroindole is a compound that belongs to the class of 5-methoxyindoles, which are used as drugs in plant physiology. The analog of 4-fluoroindole is important for cell culture and transcriptomic analysis. It has been shown to reduce the growth of cryptococcus neoformans by inhibiting its ability to produce acid. 4-Fluoroindole also inhibits the growth of other opportunistic fungi, such as Aspergillus niger. This drug is addictive and can be toxic if it enters the environment. 4-Fluoroindole also inhibits the growth of plants when applied as a pesticide.Fórmula:C8H6FNCor e Forma:PowderPeso molecular:135.14 g/molIndole-3-propionic acid
CAS:Indole-3-propionic acid is a metabolite of tryptophan. It has been shown to have a number of physiological effects, including the induction of apoptosis and inhibition of cell proliferation. Indole-3-propionic acid may be a potential biomarker for bowel disease, as well as an analytical method for detecting hydrogen bonding interactions. This compound has also been shown to have pharmacological effects in the treatment of diseases such as mitochondrial dysfunction, heart failure, and cancer. Indole-3-propionic acid is an agonist to the 5HT receptor and can activate the mammalian target of rapamycin (mTOR) pathway. The mTOR pathway regulates energy metabolism by regulating protein synthesis and cell growth.Fórmula:C11H11NO2Cor e Forma:White Off-White PowderPeso molecular:189.21 g/molEthyl 5-chloroindole-2-carboxylate
CAS:Ethyl 5-chloroindole-2-carboxylate is a pro-apoptotic agent that has been shown to inhibit the replication of HIV. It inhibits the reverse transcriptase and DNA polymerases in the virus, which prevents it from being replicated. Ethyl 5-chloroindole-2-carboxylate also induces apoptosis by alkylating the cysteine residues on the host cell's proteins. This drug is not active against other viruses, such as herpes simplex virus type 1 (HSV1). It has been shown to be an analog for cannabidiol (CBD), which binds to cannabinoid receptors CB1 and CB2.Fórmula:C11H10ClNO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:223.66 g/mol5-Methylisatin
CAS:5-Methylisatin is a reaction rate-limiting substrate in the conversion of pyridoxal 5'-phosphate to pyridoxamine 5'-phosphate. It is oxidized by hydroxyl radicals to form malonic acid and anhydrous acetonitrile. The reaction is catalyzed by an enzyme called tissue nonspecific alkaline phosphatase (TNAP). TNAP activity can be inhibited by test compounds, such as anthranilic acid and homogenates, which are substances that contain enzymes or cells from tissues. Hydroxyl groups on the 5-methylisatin molecule form hydrogen bonds with the nitrogen atoms of TNAP, which causes a conformational change in the enzyme. This change inhibits its ability to react with other substrates, resulting in decreased levels of 5-methylisatin and increased levels of pyridoxal 5'-phosphate. The inhibition can be reversed by adding hydroxide ions or increasingFórmula:C9H7NO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:161.16 g/mol4-Acetoxyindole
CAS:4-Acetoxyindole is a chromophore that belongs to the pyrrole family of compounds. It has been shown to react with an ionic liquid under acidic conditions to form a protonated intermediate, which can be deprotonated by a nucleophile. This reaction yields an acetate anion and a fluorescing product. 4-Acetoxyindole also reacts with deuterium gas, yielding an acetate, a deuterium atom, and fluorescing product. The reaction is reversible and the yield of the product depends on the concentration of the reactants. 4-Acetoxyindole has strong carbonyl groups that make it reactive towards other functional groups. These reactions are useful for synthesizing heterocycles such as indoles and isoquinolines.
Fórmula:C10H9NO2Pureza:Min. 97 Area-%Cor e Forma:White PowderPeso molecular:175.18 g/mol4-Aminoindole hydrochloride
CAS:4-Aminoindole hydrochloride is a white crystalline solid that can be used as a versatile building block in organic synthesis. It is also used as an intermediate in the production of various pharmaceuticals and other chemical compounds. 4-Aminoindole hydrochloride is soluble in most polar solvents, but insoluble in ethers and oils. This compound is also a useful reagent for the conversion of nitrobenzenes to aminobenzoic acids. CAS Number 174854-93-4
Fórmula:C8H9ClN2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:168.62 g/mol4'-Iodo-2,2':6',2''-terpyridine
CAS:4'-Iodo-2,2':6',2''-terpyridine is a transoid that has two conformations: one with the pyridine ring in the cisoid position and one with the pyridine ring in the transoid position. It can form intermolecular interactions with other molecules of 4'-iodo-2,2':6',2''-terpyridine. These interactions may be due to stacking or planar interactions.Fórmula:C15H10IN3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:359.16 g/mol4,5,6-Trimethoxyindole
CAS:4,5,6-Trimethoxyindole is a chemical compound that is found in the plant Chinensis. This compound has been shown to have potent anticancer properties and can be used as a treatment for inflammatory diseases. 4,5,6-Trimethoxyindole has been shown to modulate the activity of some bacteria and it has been hypothesized that this may be due to its interaction with formylation. The acidic nature of 4,5,6-Trimethoxyindole makes it soluble in ethanol. It can also be synthesised from butyric acid and other chemicals.
Fórmula:C11H13NO3Pureza:Min. 95%Cor e Forma:SolidPeso molecular:207.23 g/molIndole-3-acetyl-L-valine
CAS:Indole-3-acetyl-L-valine (IAV) is a naturally occurring amino acid that binds to the surface glycoprotein of wild-type viruses. It inhibits viral replication by inhibiting the production of basic proteins, which are necessary for viral life. IAV also has inhibitory properties against the toll-like receptor, which may be due to its ability to inhibit growth factor signaling. IAV has been shown to decrease the number of opportunistic fungal and bacterial infections in humans, with no adverse effects on human health. This drug has no effect on healthy cells and can be used as an adjuvant for the treatment of HIV and other viral infections.Fórmula:C15H18N2O3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:274.32 g/molOxypeucedanin
CAS:Oxypeucedanin is a furanocoumarin compound, which is derived from various plant sources, most notably those in the Apiaceae family such as Peucedanum and Angelica species. It functions primarily as a photoreactive agent, capable of interacting with DNA under ultraviolet (UV) light through a process called photoactivation. Upon UV exposure, it forms covalent bonds with DNA, leading to cross-linking that can disrupt cellular functions.Fórmula:C16H14O5Pureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:286.28 g/mol6-Fluoro-2-methylindole
CAS:6-Fluoro-2-methylindole is a member of the group of aromatic ketones. It is an organic compound that can be synthetized from 2,6-dichloroindole and methyl iodide. There are two types of photodimerization reactions for 6-fluoro-2-methylindole: one is an aerobic reaction and the other is an anaerobic reaction. The mechanistic study of 6-fluoro-2-methylindole has been investigated using bond cleavage and transformation reactions. This organic compound reacts with amines to form polycycles with high yields. It also undergoes Diastereomeric Control in chemistry.Fórmula:C9H8FNPureza:Min. 95%Cor e Forma:Brown PowderPeso molecular:149.16 g/mol5-Methyl-3-piperidin-4-yl-1H-indole hydrochloride
CAS:5-Methyl-3-piperidin-4-yl-1H-indole hydrochloride is a synthetic chemical that is used as a building block for the synthesis of other compounds. It is a versatile intermediate, having been shown to react with amines, alcohols, phenols, and thiols. 5-Methyl-3-piperidin-4-yl-1H-indole hydrochloride can be used in the manufacture of pharmaceuticals and agrochemicals. This compound has been found to be an effective reagent for the preparation of cyclic peptides and can be used as a building block for the synthesis of other compounds. When reacted with 2-(trimethylsilyl)ethanol, it produces a high quality complex compound.
Fórmula:C14H18N2·HClPureza:Min. 97 Area-%Cor e Forma:PowderPeso molecular:250.77 g/mol1H-Indoline-3-carboxylic acid
CAS:1H-Indoline-3-carboxylic acid is a molecule with the chemical formula C8H6N2O2. It is an aromatic carboxylic acid and one of the three enantiopure isomers of indoline. 1H-Indoline-3-carboxylic acid has two tautomers, cis (cis) and trans (trans). The stereoisomer cis is found in nature, while trans can be synthesized. 1H-Indoline-3-carboxylic acid can be cleaved to form phenylacetic acid and benzoic acid in reactions catalyzed by acids at high temperatures. Kinetic studies have shown that 1H-indoline-3-carboxylic acid undergoes biotransformation to form methylbenzene, ethylbenzene, propylbenzene, butylbenzene, pentylbenzene and hexylbenzene.Fórmula:C9H9NO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:163.17 g/mol
