
Chinoni e Derivati
I chinoni sono composti aromatici che contengono un sistema ad anelli benzenici con due gruppi carbonilici in posizioni specifiche, formando una struttura cicloesenica con ossigeno. Derivano da composti come l’antrachinone e la 1,4-benzochinone, che svolgono importanti funzioni biologiche, tra cui il trasferimento di elettroni nei processi metabolici. I derivati dei chinoni, come le idrochinoni e gli agenti antireumatici, trovano applicazione nell’industria farmaceutica grazie alle loro proprietà antiossidanti, antimicrobiche e anticancerogene. Inoltre, i chinoni sono impiegati nella produzione di coloranti e prodotti cosmetici.
Presso CymitQuimica, offriamo chinoni e i loro derivati per applicazioni in chimica organica, farmaceutica e nell’industria cosmetica.
Trovati 24351 prodotti di "Chinoni e Derivati"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
3,5-Di-tert-butyl-4-Hydroxybenzaldehyde
CAS:Formula:C15H22O2Colore e forma:White To Off-White SolidPeso molecolare:234.34Lubiprostone Related Compound 8
CAS:Formula:C20H32F2O5Colore e forma:White To Off-White SolidPeso molecolare:390.47(-)-Citrinin
CAS:<p>Stability Hygroscopic<br>Applications Antibiotic substance produced by a white spore aspergilus which has been placed under the species name Aspergillus niveus. Also produced in small quantities by Penicillium citrinum.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Ciegler, A., et al.: Appl. Microbiol., 26, 271 (1973), Creppy, E., et al.: Toxicol. Lett., 28, 29 (1985), DeGroene, E., et al.: Cancer Res., 56, 299 (1996),<br></p>Formula:C13H14O5Colore e forma:YellowPeso molecolare:250.25Podophyllotoxin 4-O-Glucoside
CAS:Prodotto controllato<p>Applications Podophyllotoxin 4-O-glucoside is the glucoside derivative of Podophyllotoxin (P681000), a skin treatment for genital warts caused by some types of HPVs.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Marques, J.V., et al.: J. Biol. Chem., 288, 466 (2013); Kelly, M.G. & Hartwell, J.L.; J. of the Nat'l Cancer Inst., 14, 967 (1954); Gupta, R.S.; Somatic Cell Genetics, 7, 59 (1981); Gupta, R.S.; Cancer Research, 43, 505 (1983)<br></p>Formula:C35H36O13Colore e forma:NeatPeso molecolare:664.654'-Demethylepipodophyllotoxin
CAS:Prodotto controllato<p>Applications A potent inhibitor of microtubule assembly.<br></p>Formula:C21H20O8Colore e forma:NeatPeso molecolare:400.38Patulin
CAS:<p>Stability Hygroscopic<br>Applications Patulin (PAT), a mycotoxin produced by certain species of Penicillium, Aspergillus, and Byssochlamys, is mainly found in ripe apple and apple products. Patulin-induced genotoxicity and modulation of glutathione in Hep G2 cells. Patulin is an antibiotic. Patulin-induced nephropathy and gastrointestinal tract malfunction have been demonstrated in several animal models. The oral LD50 value of patulin ranges between 29 and 55 mg/kg body weight in rodents and 170 mg/kg body weight in poultry. The World Health Organization considers patulin cytotoxic and established a safety level of patulin in apple juice at 50 μM. At 100-200 μM, patulin can directly increase intracellular oxidative stress in HEK293 and HL-60 cells. In 1944, this compound was tested in a clinical trial for potential antibiotic<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Scott, P., et al.: J. Agric. Food Chem., 20, 450 (1972), Aden, D., et al.: Nature, 282, 615 (1979), Surralles, J., et al.: Mutat. Res., 341, 169 (1995), Alves, I., et al.: Mutagenesis, 15, 229 (2000), Liu, B., et al.: Toxicol. Appl. Pharmacol., 191, 255 (2003), Puel, O., Galtier, P., and Oswald, I.P. Biosynthesis and toxicological effects of patulin. Toxins 2(4) 613-631 (2010). Liu, B., Wu, T., Yu, F., et al. Induction of oxidative stress response by the mycotoxin patulin in mammalian cells. Toxicol Sci 95(2) 340-347 (2007). Chalmers, I., and Clarke, M. Commentary: The 1994 patulin trial: The first properly controlled multicentre trial conducted under the aegis of the British Medical Research Council. Int J Epidemiol 32 253-260 (2004).<br></p>Formula:C7H6O4Colore e forma:Off-White To YellowPeso molecolare:154.12Ref: TR-P206500
Prodotto fuori produzione3-[6-Chloro-4-(trifluoromethyl)pyridin-2-yl]benzoic acid
CAS:Purezza:95.0%Colore e forma:SolidPeso molecolare:301.6499938964844N1,N1'-(Ethane-1,2-diyl)bis(N1-methylbenzene-1,4-diamine)
CAS:Purezza:95.0%Peso molecolare:270.38000488281255-Biphenyl-4-yl-1H-pyrazole-3-carboxylic acid methyl ester
Purezza:95.0%Peso molecolare:278.3110046386719



