Antibióticos naturales y semisintéticos
Los antibióticos naturales y semisintéticos se caracterizan por estructuras químicas con anillos heterocíclicos y grupos funcionales activos que inhiben el crecimiento de microorganismos. Sus estructuras les permiten interactuar con los procesos vitales de las bacterias, lo que los hace útiles como tratamientos para infecciones bacterianas. Los antibióticos semisintéticos pueden ser modificados para mejorar el espectro de actividad o la resistencia a la degradación.
En CymitQuimica ofrecemos antibióticos naturales y semisintéticos de alta calidad para investigación en microbiología y desarrollo farmacéutico.
Se han encontrado 6347 productos de "Antibióticos naturales y semisintéticos"
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Producto descatalogadoLincomycin 2,4-Phosphate (Clindamycin Phosphate EP Impurity G)
Fórmula:C18H33N2O8PSForma y color:White To Off-White SolidPeso molecular:468.51Ref: 4Z-L-093006
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Producto descatalogadoRef: 4Z-E-2037
Producto descatalogadoBenzylpenicillin Potassium EP Impurity E (Benzylpenicillin (Benzathine) EP Impurity E, Benzylpenicillin (Procaine) EP Impurity B, Benzylpenicillin Sodium EP Impurity E) (S,R,R-Isomer) (5R,6R-Benzylpen
CAS:Fórmula:C16H20N2O5SForma y color:White To Off-White SolidPeso molecular:352.41Ref: 4Z-S-4314
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Producto descatalogadoRef: 4Z-P-8921
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Producto descatalogadoVancomycin EP Impurity J HCl (26-epi-Vancomycin B HCl )
CAS:Fórmula:C66H75Cl2N9O24·HClPeso molecular:1449.29 36.46Ref: 4Z-V-032011
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Producto descatalogadoN-Nitroso Benzylpenicillin Potassium EP Impurity E (N-Nitroso Benzylpenicillin (Benzathine), Benzylpenicillin Sodium EP Impurity E, N-Nitroso Benzylpenicillin (Procaine) EP Impurity B) (Mixture of Diastereomers)
Fórmula:C16H19N3O6SPeso molecular:381.40Ref: 4Z-P-0463
Producto descatalogadoSultamicillin EP Impurity C (Ampicillin, Piperacillin EP Impurity A)
CAS:Fórmula:C16H19N3O4SPeso molecular:349.41Ref: 4Z-S-081002
Producto descatalogadoRef: 4Z-P-0453
Producto descatalogadoDeoxynivalenol
CAS:Producto controlado<p>Applications Deoxynivalenol is a tricothecene mycotoxin and potent protein synthesis inhibitor. Deoxynivalenol exhibits cytotoxic activity in vivo via the ribotoxic stress response. Deoxynivalenol induces p38-mediated gene expression and apoptosis in leukocytes; activity results in systemic expression of interleukin-6 (IL-6) and other proinflammatory cytokines. Also induces migration of NF-κB into the nucleus.Environmental contaminants; Food contaminants<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 Bae, et al.: Toxicol. Sci., 105, 59 (2008), Shi, et al.: Toxicol. Sci., 109, 247 (2009), Krishnaswamy, et al.: Free Radic. Biol. Med., 49 50 (2010),<br></p>Fórmula:C15H20O6Forma y color:NeatPeso molecular:296.32Fumonisin B2
CAS:Producto controlado<p>Stability Hygroscopic, Toxic<br>Applications A mycotoxin produced by mold associated with corn. Inhibitor of sphingosine N-acyltransferase. Blocks the formation of ceramide from sphingosine.<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 Monbaliu, S., et al.: J. Agric. Food Chem., 58, 10475 (2010), Klosowski, G., et al.: Biores. Technol., 101, 9723 (2010), Soerensen, L., et al.: Anal. Bioanal. Chem., 398, 1535 (2010),<br></p>Fórmula:C34H59NO14Forma y color:Off-WhitePeso molecular:705.83Ref: TR-F862755
Producto descatalogadoFumonisin B3
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications Fumonisin B3 is a mycotoxin present in corn. Fungal metabolite believed to cause leukoencephalomalacia in horses.<br>References Azcona-Olivera, J. et al.: J. Agric. Food Chem., 40, 531 (1992); Hopmans, E. et al.: J. Agric. Food Chem., 41, 1655 (1993); Monbaliu, S., et al.: J. Agric. Food Chem., 58, 10475 (2010), Klosowski, G., et al.: Biores. Technol., 101, 9723 (2010), Soerensen, L., et al.: Anal. Bioanal. Chem., 398, 1535 (2010),<br></p>Fórmula:C34H59NO14Forma y color:BeigePeso molecular:705.83T-2 Toxin
CAS:Producto controlado<p>Applications T-2 Toxin is a tricothecene mycotoxin produced by fungi of the genus Fusarium. T-2 Toxin induces DNA damage and cell death on prolonged administration.Environmental contaminants; Food contaminants<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 Kim, C., et al.: Cancer Res., 57, 3115 (1997), Bottrel, R., et al.: Antimicrob. Agents Chemother., 1999, 43, 856 (1999), Murray, P., et al.: J. Immunol., 178, 2623 (2007), Choi, H., et al.: Toxicol. Appl. Pharmacol., 240, 46 (2009), Amuzie, C., et al.: Toxicol. Sci., 113, 412 (2010),<br></p>Fórmula:C24H34O9Forma y color:White SolidPeso molecular:466.52Fumonisin B1
CAS:<p>Stability Hygroscopic<br>Applications A mycotoxin produced by mold associated with corn. Fungal metabolite believed to cause leukoencephalomalacia in horses.Environmental contaminants; Food contaminants<br>References Monbaliu, S., et al.: J. Agric. Food Chem., 58, 10475 (2010), Klosowski, G., et al.: Biores. Technol., 101, 9723 (2010), Soerensen, L., et al.: Anal. Bioanal. Chem., 398, 1535 (2010),<br></p>Fórmula:C34H59NO15Forma y color:NeatPeso molecular:721.83Zearalenone 4-Sulfate Ammonium Salt
CAS:Producto controladoFórmula:C18H25NO8SForma y color:NeatPeso molecular:415.46α-Zearalenol-d4 (Major)
CAS:Producto controlado<p>Applications α-Zearalenol-d4 is the isotope labelled metabolite of Zearalenone (Z270500), an estrogenic mycotoxin produced by Fusarium fungi commonly found in grains.<br>References Olsen, M., et al.: Acta Pharmacol. Toxicol., 48, 15 (1981), Chang, W., et al.: Food Chem. Toxicol., 22, 887 (1984), El Golli, E., et al.: Toxicol Lett., 166, 122 (2006), Hassen, W., et al.: Toxicology, 232, 294 (2007), Benzoni, E., et al.: Reprod. Toxicol., 25, 461 (2008),<br></p>Fórmula:C18H20D4O5Forma y color:NeatPeso molecular:324.4HT-2 Toxin (>85%)
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications HT-2 Toxin is a trichothecene group mycotoxin. HT-2 Toxin is the 4-hydroxy analogue of T-2 Toxin (T002980) which has been shown to induce DNA damage and cell death on prolonged administration.Environmental contaminants; Food contaminants<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 Weidner, M. et al.: J. Agric. Food Chem., 60, 5676 (2012); Choi, H. et al.: Toxicol. Appl. Pharmacol., 240, 46 (2009); Amuzie, C. et al.: Toxicol. Sci., 113, 412 (2010);<br></p>Fórmula:C22H32O8Pureza:>85%Forma y color:Off-WhitePeso molecular:424.48Zearalenone
CAS:<p>Applications Estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones.Environmental contaminants; Food contaminants<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 Tanaka, T., et al.: J. Agric. Food Chem., 36, 979 (1988), Hamilton, S., et al.: Anticancer Res., 16, 3597 (1996), Hecht, S., et al.: Cancer Lett., 150, 49 (2000), Hussein, H., et al.: Toxicology, 167, 101 (2001), Lim, H., et al.: J. Immunol., 175, 4180 (2005),<br></p>Fórmula:C18H22O5Forma y color:White To Light BrownPeso molecular:318.36rac Zearalenone-d6
CAS:Producto controlado<p>Applications Estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones.Environmental contaminants; Food contaminants<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 Tanaka, T., et al.: J. Agric. Food Chem., 36, 979 (1988), Hamilton, S., et al.: Anticancer Res., 16, 3597 (1996), Hecht, S., et al.: Cancer Lett., 150, 49 (2000), Hussein, H., et al.: Toxicology, 167, 101 (2001), Lim, H., et al.: J. Immunol., 175, 4180 (2005),<br></p>Fórmula:C18H16D6O5Forma y color:BeigePeso molecular:324.40rac Zearalenone-d6 (major)
CAS:Producto controladoFórmula:C18H16D6O5Forma y color:NeatPeso molecular:324.40β-Zearalenol-d4 (Major)
CAS:Producto controlado<p>Stability Light Sensitive<br>Applications Isotope labelled β-Zearalenol is an more active metabolite of Zearalenone (Z270500), a estrogenic mycotoxin produced by Fusarium fungi commonly found in grains.<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 Olsen, M., et al.: Acta Pharmacol. Toxicol., 48, 15 (1981), Chang, W., et al.: Food Chem. Toxicol., 22, 887 (1984), El Golli, E., et al.: Toxicol Lett., 166, 122 (2006), Hassen, W., et al.: Toxicology, 232, 294 (2007), Benzoni, E., et al.: Reprod. Toxicol., 25, 461 (2008),<br></p>Fórmula:C18H20D4O5Forma y color:NeatPeso molecular:324.415-O-Demethyl Tacrolimus
CAS:<p>Tacrolimus is a macrolide that is used as an immunosuppressive drug. It has been shown to bind to the FK-binding protein, which in turn inhibits calcineurin. This prevents the release of IL-2, TNF-α and other cytokines. The immunosuppressive effects of tacrolimus have been evaluated using analytical methods such as coefficients, affinity, and monitoring techniques such as immunoassays and agglutination. These techniques are used to evaluate the plasma concentration of tacrolimus. Tacrolimus also binds to proteins in the blood samples and can be detected by turbidimetric or electrochemiluminescence immunoassay reagents.</p>Fórmula:C43H67NO12Pureza:Min. 95%Peso molecular:789.99 g/mol15-Acetyl Deoxynivalenol (~90%)
CAS:Producto controlado<p>Applications A mycotoxin produced by the fungi Fusarium culmorum and Fusarium graminearum, inhibits protein synthesis.Environmental contaminants; Food contaminants<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 Ashraf, A.; et al.: Int. J. Biol. Biotechnol., 4, 391 (2007), Burlakoti, R., et al.: App. Environ. Microbiol., 74, 6513 (2008), Steinmetz, W., et al.: Eur. J. Med. Chem., 44, 4485 (2009), Zhang, Y., et al.: Phytopathol., 99, 95 (2009),<br></p>Fórmula:C17H22O7Pureza:~90%Forma y color:WhitePeso molecular:338.353-Acetyldeoxynivalenol
CAS:Producto controlado<p>Stability Appears to decompose in DMSO<br>Applications 3-Acetyldeoxynivalenol is a trichothecene mycotoxin that is produced in a plant-pathogenic fungus, Fusarium graminearum Schwabe.Environmental contaminants; Food contaminants<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 Beyer, M., et al.: Int. J. Food. Microbiol., 119, 153 (2007); Schiefer, H.B., et al.: Can. J. Comp. Med., 49, 315 (1985); Mirocha, C.J., et al.: App. Enviro.Microbiol., 55, 1315 (1989);<br></p>Fórmula:C17H22O7Forma y color:WhitePeso molecular:338.354H-Furo[2,3-c]pyranyl Mupirocin Sodium Impurity
CAS:<p>Impurity Mupirocin EP Impurity D<br>Stability Hygroscopic<br>Applications Mupirocin (M794000) impurity. (Mupirocin EP Impurity D) The rearrangement isomer of Mupirocin is prepared using an enzyme-catalyzed, selective deesterification.<br>References Sime, J.T., et al.: Tetrahedron Lett., 28, 5169 (1987),<br></p>Fórmula:C26H43O9·NaForma y color:NeatPeso molecular:522.60
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