
Compuestos policíclicos
Los compuestos policíclicos son moléculas orgánicas que contienen múltiples anillos interconectados. Estos compuestos incluyen hidrocarburos aromáticos policíclicos y otros sistemas de anillos complejos. Son significativos en la ciencia de materiales, productos farmacéuticos y electrónica orgánica. En CymitQuimica, ofrecemos compuestos policíclicos de alta calidad para apoyar sus investigaciones y aplicaciones industriales, asegurando resultados confiables y efectivos en sus proyectos.
Subcategorías de "Compuestos policíclicos"
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Se han encontrado 4574 productos de "Compuestos policíclicos"
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4,4'-Diamino-2,2'-bipyridine
CAS:<p>4,4'-Diamino-2,2'-bipyridine (DABP) is a redox-active compound that is synthesized to be used as a single-stranded DNA probe. It has been shown to have high affinity for nucleic acids and can be used in many applications including the detection of mutations in human ovarian carcinoma cells. DABP can also be used as a model protein for studying interactions with other biomolecules. The immobilization of DABP on an electrode surface allows for the study of its electrochemical properties. This includes the correlation between the redox potential and luminescence intensity and the dependence on pH or ionic strength. DABP can also be used to detect oxygen concentration or ATP levels in mitochondria through its ability to absorb light at wavelengths from 400 nm to 800 nm which is then converted into light at lower wavelengths by uv irradiation.</p>Fórmula:C10H10N4Pureza:Min. 97 Area-%Forma y color:White PowderPeso molecular:186.21 g/mol4-Chloro-6-methoxyquinoline
CAS:<p>4-Chloro-6-methoxyquinoline is an inhibitor of bacterial DNA gyrase. It has antibacterial activity against Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Pseudomonas aeruginosa. 4-Chloro-6-methoxyquinoline is a synthetic compound that was reinvestigated for its antibacterial activity. It has been shown to be effective in the treatment of Staphylococcal infections. The mechanism of action may involve inhibition of topoisomerase II or interference with the synthesis of DNA by binding to the enzyme bacterial DNA gyrase. Quinidine and cinchonidine are quinine derivatives that have been found to inhibit bacterial DNA gyrase. These compounds are found in the bark of Cinchona species, which includes Cinchona ledgeriana, Cinchona officinalis, and Cinchona succirub</p>Fórmula:C10H8ClNOPureza:Min. 95%Peso molecular:193.02944tert-Butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate
CAS:<p>Please enquire for more information about tert-Butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C13H24N2O3Pureza:Min. 95%Peso molecular:256.34 g/mol5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)indoline
CAS:<p>Please enquire for more information about 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)indoline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Pureza:Min. 95%2,2,4-Trimethyl-1,2-dihydroquinoline
CAS:<p>2,2,4-Trimethyl-1,2-dihydroquinoline is a chemical compound with the formula C8H10N2. It is a white solid that is insoluble in water but soluble in nonpolar solvents such as benzene, toluene and hexane. 2,2,4-Trimethyl-1,2-dihydroquinoline has been shown to induce liver lesions in rats at doses of 1.25 g/kg/day. It also reacts with hydrogen fluoride to form calcium stearate. This compound is also used as a precursor for the synthesis of diazonium salts and has been shown to be carcinogenic in animal studies.</p>Fórmula:C12H15NPureza:Min. 95%Forma y color:Clear Viscous LiquidPeso molecular:173.25 g/mol8-Quinolinesulfonyl chloride
CAS:<p>8-Quinolinesulfonyl chloride (8QSC) is a quinoline derivative that has been shown to have anticancer activity. 8QSC binds to the receptor site of cells and inhibits the production of amines, which are important for cell growth and proliferation. It also binds to hydrogen bonds, which may be involved in the cytotoxicity observed in pancreatic cancer cells. 8QSC shows significant cytotoxicity against Panc-1 cells, but not against NIH 3T3 cells. This may be due to its ability to form supramolecular aggregates with copper ions and quinoline derivatives.</p>Pureza:Min. 95%5-Bromoquinolin-8-amine
CAS:<p>5-Bromoquinolin-8-amine is a topoisomerase inhibitor that can be used as an antitumor agent. It has been shown to inhibit the growth of tumor cell lines and suppress the growth of colon carcinoma cells in rats and human colon carcinomas in mice. 5-Bromoquinolin-8-amine interacts with DNA, specifically inhibiting the formation of supercoiled DNA. This interaction may lead to the inhibition of tumor cell growth. 5-Bromoquinolin-8-amine also inhibits protein synthesis by interacting with proteins at the ribosomal level, leading to inhibited cell growth.</p>Fórmula:C9H7BrN2Pureza:Min. 95%Peso molecular:223.07 g/mol(1,10-Phenanthroline)tris[4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionato]europium(III)
CAS:<p>(1,10-Phenanthroline)tris[4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionato]europium(III) is a luminescent europium complex that is used in the development of microcapsules for fluorescence microscopy. The (1,10-phenanthroline) ligand is a chelate molecule that can be exchanged with other ligands to change the optical properties of the complex. The fluorescence microscope detects the emitted light at 488 nm and 514 nm wavelengths. The luminescent europium complex emits light when it binds to an organic molecule such as vinyl alcohol or water vapor. Ternary complexes are formed between the europium ion and two different ligands. Optical properties depend on the type of ligands present in these ternary complexes. This product has been shown to have chemical structures that are similar to those</p>Pureza:Min. 95%2,9-Bis(2-Phenylethyl)anthra(2,1,9-def:6,5,10-d'e'f')diisoquinoline-1,3,8,10(2H,9H)-tetrone
CAS:<p>2,9-Bis(2-phenylethyl)anthraquinone (BPAQ) is a synthetic compound that is used as an fluorescent probe to study biological processes. BPAQ binds to peptides and inhibits their binding to the surface of cells. This property has been used in diagnostic tests for stenosis, infantum, and other conditions. BPAQ has also been shown to inhibit HIV-1 replication in human cells by binding to the HIV-1 envelope protein gp120 and blocking its interaction with CD4 receptors on host cells. The discovery of the antiviral activity of BPAQ was based on its ability to inhibit leishmania growth in animals.</p>Fórmula:C40H26N2O4Pureza:Min. 95%Forma y color:PowderPeso molecular:598.65 g/molN2-(2-Tricyclo[3.3.1.13,7]dec-1-ylacetyl)-D-arginyl-L-arginyl-L-prolyl-(4R)-4-hydroxy-L-prolylglycyl-3-(2-thienyl)-L-alanyl-L-seryl- D-phenylalanyl-3-(2-thienyl)-L-alanyl-L-arginine
CAS:<p>Please enquire for more information about N2-(2-Tricyclo[3.3.1.13,7]dec-1-ylacetyl)-D-arginyl-L-arginyl-L-prolyl-(4R)-4-hydroxy-L-prolylglycyl-3-(2-thienyl)-L-alanyl-L-seryl- D-phenylalanyl-3-(2-thienyl)-L-alanyl-L-arginine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C68H99N19O14S2Pureza:Min. 95%Peso molecular:1,470.77 g/mol6,7-Dihydro-5H-quinolin-8-one
CAS:<p>6,7-Dihydro-5H-quinolin-8-one is a quinoline derivative that can be used to treat cancer. It is an inhibitor of topoisomerase II, which is an enzyme that catalyzes the formation of single stranded breaks in DNA and then reseals them. The inhibition of topoisomerase II leads to the accumulation of single strand breaks, which causes cell death. 6,7-Dihydro-5H-quinolin-8-one has been shown to have inhibitory activity against cancer cells in laboratory tests and also inhibits the growth of breast cancer cells in mice. This compound also has a number of other biological effects including being a ligand for some receptors and amine oxidases as well as having antihistamine properties.</p>Fórmula:C9H9NOPureza:Min. 95%Forma y color:White PowderPeso molecular:147.17 g/moltert-Butyl 4,7-diazaspiro[2.5]octane-4-carboxylate
CAS:<p>Please enquire for more information about tert-Butyl 4,7-diazaspiro[2.5]octane-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Pureza:Min. 95%5-Fmoc-amino-10,11-dihydro-5H-dibenzo[a,d]-cycloheptenyl-2-oxyacetyl-DL-Nle-4- methyl-benzhydrylamide resin
<p>Please enquire for more information about 5-Fmoc-amino-10,11-dihydro-5H-dibenzo[a,d]-cycloheptenyl-2-oxyacetyl-DL-Nle-4- methyl-benzhydrylamide resin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Pureza:Min. 95%10H-[1,2,5,8,11,14,17,20,23,26,29,32,35]Dithiaundecaazacyclooctatriacontino[11,10-b]isoquinoline,cyclic peptide derivative
CAS:<p>Please enquire for more information about 10H-[1,2,5,8,11,14,17,20,23,26,29,32,35]Dithiaundecaazacyclooctatriacontino[11,10-b]isoquinoline,cyclic peptide derivative including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C69H116N26O15S2Pureza:Min. 95%Peso molecular:1,613.96 g/mol7-Chloro-4-piperazinylquinoline
CAS:<p>7-Chloro-4-piperazinylquinoline is a quinoline derivative that belongs to the group of organic solvents. It has anticancer activity and is used as a medicine. 7-Chloro-4-piperazinylquinoline is used as an intermediate in the preparation of sorafenib, which is a potent inhibitor of the protein tyrosine kinase. Sorafenib inhibits cancer cell proliferation and tumor growth by blocking the activity of tyrosine kinases, which are necessary for cellular proliferation and survival. It also inhibits phospholipase A2, which leads to cell death by apoptosis.</p>Fórmula:C13H14ClN3Pureza:Min. 95%Peso molecular:247.72 g/mol1,5,7-Triazabicyclo[4.4.0]dec-5-ene
CAS:<p>1,5,7-Triazabicyclo[4.4.0]dec-5-ene is a model system for the reaction mechanism of protonated amines and nucleophilic addition reactions. It has been used as a solid catalyst for the synthesis of crystalline polymorphs of azabenzene from trifluoroacetic acid. The crystal structures of 1,5,7-triazabicyclo[4.4.0]dec-5-ene have been studied by X-ray diffraction data and nitrogen atoms were identified in the molecule. This molecule is stable in a wide range of conditions and can be handled without special precautions because it does not react with atmospheric moisture or oxygen.</p>Fórmula:C7H13N3Pureza:Min. 95%Forma y color:PowderPeso molecular:139.2 g/mol6-Bromoisoquinoline
CAS:<p>6-Bromoisoquinoline is a tetradentate ligand that can be used as a molecular model to study the binding of metal ions and organic molecules. 6-Bromoisoquinoline has been shown to bind covalently and noncovalently with phosphate groups on the surface of Caco-2 cells and to induce surface-enhanced Raman spectroscopy. This ligand has a high nucleophilicity and reacts readily with chloride, which is an acidic functional group. The reaction products are hydrochloric acid, trifluoroacetic acid, or both. 6-Bromoisoquinoline can also act as an allosteric modulator in some enzymes, such as phosphofructokinase in glycolysis.</p>Fórmula:C9H6BrNPureza:Min. 95%Peso molecular:208.05 g/molMethyl isoindoline-5-carboxylate HCl
CAS:<p>Please enquire for more information about Methyl isoindoline-5-carboxylate HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C10H12ClNO2Pureza:Min. 95%Peso molecular:213.66 g/molPyridoxal-5-phosphate monohydrate
CAS:<p>Bioavailable form of vitamin B6; coenzyme; food supplement</p>Fórmula:C8H10NO6P·H2OPureza:Min. 98.5 Area-%Forma y color:Off-White Slightly Yellow PowderPeso molecular:265.16 g/mol2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester
CAS:<p>2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester is a synthetic compound that can be used as a reagent in the synthesis of polynucleotides and polypeptides. It can also be used as an inhibitor of ketoreductase, which is an enzyme involved in the synthesis of fatty acids and ketones. 2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester has been shown to inhibit the growth of wild type and mutant strains of E. coli. The molecular weight of this compound is 439.</p>Fórmula:C28H24ClNO3Pureza:Min. 95%Peso molecular:457.95 g/mol
