Sulfonamidas y derivados
Las sulfonamidas son compuestos que contienen un grupo funcional sulfonamida (-SO₂NH₂), en el que un átomo de azufre está unido a un grupo amino. Fueron de los primeros antibióticos sintéticos utilizados en medicina, inhibiendo la síntesis de ácido fólico en bacterias, lo que les confiere propiedades antimicrobianas. Se utilizan principalmente para tratar infecciones bacterianas, aunque hoy en día su uso se ha visto reducido debido a la resistencia antimicrobiana. Además de su uso en antibióticos, las sulfonamidas también tienen aplicaciones en el tratamiento de enfermedades como la malaria y enfermedades inflamatorias intestinales.
En CymitQuimica ofrecemos sulfonamidas y sus derivados con alto grado de pureza para investigación en microbiología y desarrollo farmacéutico.
Se han encontrado 2589 productos de "Sulfonamidas y derivados"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Tiafenacil
CAS:<p>Applications Tiafenacil is a uracil herbicide used as a pesticide for the prevention and control of plants.<br>References Peng, X., et al. Faming Zhuanli Shenqing, 68pp Patent 2018 CODEN:CNXXEV<br></p>Fórmula:C19H18ClF4N3O5SForma y color:Off White SolidPeso molecular:511.87Indomethacin 1-Glycerin Ester
CAS:<p>Applications Indometacin 1-Glycerin Ester was synthesized and evaluated for anti-flammatory activity in the rate paw carrageenin edema essay.<br>References Paris, Gerard. , et al.: J. Med. Chem, 23, 9 (1980)<br></p>Fórmula:C22H22ClNO6Forma y color:NeatPeso molecular:431.87Metolazone
CAS:Producto controlado<p>Applications A diruetic. An antihypertensive.<br>References Curry, C.L., et al.: Clin. Ther., 9, 47 (1986), Kiyingi, A., et al.: Lancet, 335, 29 (1990)<br></p>Fórmula:C16H16ClN3O3SForma y color:NeatPeso molecular:365.83Sulfadiazine Silver Salt
CAS:Producto controlado<p>Applications Coordination compound. Antibacterial.<br>References Bohni, et al.: Chemotherapy, 14, 195 (1969), Carr, et al.: Antimicrob. Agents Chemother., 4, 585 (1973), Stober, H., et al.: Anal. Profiles Drug Subs., 11, 523 (1982),<br></p>Fórmula:C10H9N4O2S·AgForma y color:NeatPeso molecular:357.14Benzeneacetonitrile
CAS:Producto controlado<p>Applications Benzeneacetonitrile is a volatile compound released from apple trees infested with light brown apple moth larvae. It is also used in the synthesis of phenobarbital (P316760), methylphenidate (M325880), and other amphetamines.<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 Suckling, D. et al.: J. Agr. Food. Chem., 60, 9562 (2012); Cuevas-G. et al.: Int. J. Food. Sci. Technol., 47, 1378 (2012)<br></p>Fórmula:C8H7NForma y color:NeatPeso molecular:117.15(4R,6S)-5,6-Dihydro-6-methyl-4H-thieno[2,3-b]thiopyran-4-ol 7,7-Dioxide
CAS:Producto controlado<p>Applications (4R,6S)-4H-Thieno[2,3-b]thiopyran-4-ol, 5,6-dihydro-6-methyl-,7,7-dioxide is an analog of topically-active carbonic anhydrase inhibitor MK-507 also commonly known as Dorzolamide (D535100).<br>References Blacklock, T., et al.: J. Org. Chem., 58, 1672 (1993); Tempkin, O., et al.: Tetrahedron: Asym., 7, 2721 (1996)<br></p>Fórmula:C8H10O3S2Forma y color:NeatPeso molecular:218.29Sulfamethizole-d4
CAS:Producto controlado<p>Applications Isotope Labelled Sulfamethizole is a sulfonamide based antibiotic that exhibit bactericidal activities towards gram-negative bacteria. Sulfamehizole was shown to be effective in treating gram-negative Bacillus AmpC enzyme in elderly patients with lower respiratory tract infection and as well as against microbs responsible for tuberculosis.<br>References Mondelli, M., et al.: J. Molec. Struct., 1036, 180 (2013); Leelakrishnana, S., et al.: Adv. App. Sci. Res., 3, 3502 (2012); Ghoreishi, S.M., et al.: Anal. Lett., 46, 323 (2012);<br></p>Fórmula:C92H4H6N4O2S2Forma y color:NeatPeso molecular:274.36N-Nitroso Aceclofenac
Producto controladoFórmula:C16H12Cl2N2O5Forma y color:NeatPeso molecular:383.183N-Nitroso Furosemide-d5
Producto controladoFórmula:C12D5H5ClN3O6SForma y color:NeatPeso molecular:364.7738-Isopropyl Etodolac
CAS:Producto controlado<p>Impurity Etodolac EP Impurity D<br>Applications 8-Isopropyl Etodolac (Etodolac EP Impurity D) is an impurity in the synthesis of Etodolac (E933100), may have use in the treatment of myeloma. COX-1/COX-2/β-catenin inhibitors, or anti-inflammatory agent.<br>References Humber, L.G., et al.: Med. Res. Rev., 7, 1 (1987); Balfour, J.A, et al.: Drugs, 42, 274 (1991); Kato, et al.: J. Pharm. Pharmacol., 53 1679 (2001);<br></p>Fórmula:C18H23NO3Forma y color:NeatPeso molecular:301.38Benzoxazolemethanesulfonamide-N-(6-methyl-hexanoate)
CAS:Producto controlado<p>Applications Intermediate of Zonisamide-N-(6-hexanoic acid).<br></p>Fórmula:C15H20N2O5SForma y color:NeatPeso molecular:340.394-Hydroxy Triamterene Sulfate-d4, Sodium Salt
CAS:Producto controlado<p>Applications Isotope labelled 4-hydroxy triamterene sulfate sodium salt a metabolite of Triamterne, a diuretic agent.<br>References Vollmer, G., et al.: Arzneim.-Forsch., 31, 529 (1981), Gilfrich, H.J., et al.: Eur. J. Clin. Pharmacol., 25, 237 (1983),<br></p>Fórmula:C12H6D4N7NaO4SForma y color:NeatPeso molecular:375.333-Azabicyclo[3.3.0]octane Hydrochloride
CAS:Producto controlado<p>Applications 3-Azabicyclo[3.3.0]octane Hydrochloride is a reactant in the preparation of substituted pyrimidines derivatives as novel hedgehog signaling pathway inhibitors.<br>References Xin, M. et al.: Med. Chem. Res., 23, 3784 (2014); Xin, M. et al.: Bioorg. Med. Chem. Lett., 24, 983 (2014);<br></p>Fórmula:C7H13N·ClHForma y color:White To Light YellowPeso molecular:147.651-[1-(4-Chlorobenzoyl)-5-hydroxy-2-methyl-1H-indole-3-acetate]β-D-Glucopyranuronic Acid
CAS:Producto controlado<p>Stability Hygroscopic, Moisture Sensitive<br>Applications 1-[1-(4-Chlorobenzoyl)-5-hydroxy-2-methyl-1H-indole-3-acetate]β-D-Glucopyranuronic Acid is an analog of Indomethacin Acyl-β-D-glucuronide a metabolite of Indomethacin (I641000). Acyl glucuronides have been implicated in the toxicity of many xenobiotics and marketed drugs.<br>References Abid, A., et al.: Biochem. Pharmacol., 50, 557 (1995), Gamage, N., et al.: Toxicol. Sci., 90, 5 (2006), Cerveny, L., et al.: Drug Metab. Dispos., 35, 1032 (2007), Hayeshi, R., et al.: Eur. J. Pharm. Sci., 35, 383 (2008),<br></p>Fórmula:C24H22ClNO10Forma y color:NeatPeso molecular:519.894-Amino-4'-chlorodiphenyl Sulfone
CAS:Producto controlado<p>Applications 4-Amino-4'-chlorodiphenyl sulfone is a substituted 4-aminodiphenylsulfone as Escherichia coli dihydropteroate synthase inhibitor.<br>References Lopez de Compadre, R.L., et al.: J. Med. Chem., 31, 2315 (1988),<br></p>Fórmula:C12H10ClNO2SForma y color:Off-White To Light YellowPeso molecular:267.73rac-trans Dorzolamide Hydrochloride
CAS:Producto controlado<p>Applications rac-trans Dorzolamide is an impurity of Dorzolamide (D535100).<br>References Casini, A., et al.: Bioorg. Med. Chem. Lett., 13, 841 (2003), Clare, B., et al.: Bioorg. Med. Chem., 13, 2197 (2005),<br></p>Fórmula:C10H17ClN2O4S3Forma y color:NeatPeso molecular:360.9Dapsone N-β-D-Glucuronide Sodium Salt
CAS:Producto controlado<p>Stability Hygroscopic, unstable in solution<br>Applications Dapsone N-β-D-Glucuronide is the glucuronide conjugate and main urinary metabolite of the antibacterial Dapsone (D193250).<br>References Andoh, B.Y.A. et al.: Xenobiotica, 4, 571 (1974); Ogiya, S. et al.: Yakug. Zas., 81, 349 (1961);<br></p>Fórmula:C18H19N2NaO8SForma y color:NeatPeso molecular:446.41Indomethacin 1-Menthol ester
CAS:Producto controlado<p>Applications Indomethacin terpenoids' esters were synthesized and assessed both in vitro and in vivo as indomethacin dermal prodrugs.<br>References Bonina,, Francesco. , et al.: European Journal of Pharmaceutical Sciences, 14, 123 (2001),<br></p>Fórmula:C29H34ClNO4Forma y color:NeatPeso molecular:496.0385-Amino-3-(4-sulfonylphenyl)salicyclic Acid Sodium Salt
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications 5-Amino-3-(4-sulfonylphenyl)salicyclic Acid Sodium Salt is an impurity of mesalamine (M258100), which is the active metabolite of Sulfasalazine (S699084). Anti-inflammatory (gastrointestinal).<br>References Friedman, G., et al.: Am. J. Gastroenterol., 81, 141 (1986); Tursi A., Expert Opin. Pharmacother., 6, 69 (2005);<br></p>Fórmula:C13H11NO6S•x(Na)Forma y color:NeatPeso molecular:309.29 + x(22.99)8-Propyl Etodolac
CAS:Producto controlado<p>Impurity Etodolac EP Impurity E<br>Applications 8-Propyl Etodolac (Etodolac EP Impurity E) is an impurity in the synthesis of Etodolac (E933100), may have use in the treatment of myeloma. COX-1/COX-2/β-catenin inhibitors.<br>References Humber, L.G., et al.: Med. Res. Rev., 7, 1 (1987); Balfour, J.A, et al.: Drugs, 42, 274 (1991); Kato, et al.: J. Pharm. Pharmacol., 53 1679 (2001);<br></p>Fórmula:C18H23NO3Forma y color:NeatPeso molecular:301.38
![(4R,6S)-5,6-Dihydro-6-methyl-4H-thieno[2,3-b]thiopyran-4-ol 7,7-Dioxide](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FT344510.webp&w=3840&q=75)
![3-Azabicyclo[3.3.0]octane Hydrochloride](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FA795340.webp&w=3840&q=75)
![1-[1-(4-Chlorobenzoyl)-5-hydroxy-2-methyl-1H-indole-3-acetate]β-D-Glucopyranuronic A…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FC429115.webp&w=3840&q=75)
