CAS 26098-04-4: Gentamicina C1a
Descripción:
Gentamicina C1a es un antibiótico aminoglucósido derivado de la bacteria Micromonospora purpurea. Se utiliza principalmente para tratar diversas infecciones bacterianas, particularmente aquellas causadas por bacterias Gram-negativas. Gentamicina C1a exhibe un amplio espectro de actividad antibacteriana y actúa inhibiendo la síntesis de proteínas en las bacterias, lo que lleva a la muerte celular. La sustancia se caracteriza por su estructura compleja, que incluye múltiples azúcares amino y un núcleo de 2-deoxiestreptamina. Se administra típicamente por inyección debido a su baja biodisponibilidad oral. Gentamicina C1a es conocido por su potencial nefrotóxico y ototóxico, lo que requiere un monitoreo cuidadoso de la función renal y la audición durante el tratamiento. El fármaco a menudo se utiliza en combinación con otros antibióticos para mejorar su eficacia y reducir el riesgo de desarrollo de resistencia. Su farmacocinética implica una rápida distribución en los tejidos del cuerpo, con una vida media que puede variar según la función renal. En general, Gentamicina C1a sigue siendo una opción crítica en el arsenal contra infecciones graves, particularmente en entornos hospitalarios.
Fórmula:C19H39N5O7
InChI:InChI=1S/C19H39N5O7/c1-19(27)7-28-18(13(26)16(19)24-2)31-15-11(23)5-10(22)14(12(15)25)30-17-9(21)4-3-8(6-20)29-17/h8-18,24-27H,3-7,20-23H2,1-2H3/t8-,9+,10-,11+,12-,13+,14+,15-,16+,17+,18+,19-/m0/s1
Clave InChI:InChIKey=VEGXETMJINRLTH-BOZYPMBZSA-N
SMILES:O([C@@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CN)CC[C@H]2N)[C@@H](N)C[C@H]1N)[C@@H]3[C@H](O)[C@@H](NC)[C@@](C)(O)CO3
Sinónimos:- <span class="text-smallcaps">D</smallcap>-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-β-<smallcap>L</smallcap>-arabinopyranosyl-(1→6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-<smallcap>D</span>-erythro-hexopyranosyl-(1→4)]-2-deoxy-
- Geneticin C<sub>1a</sub>
- Gentamicin C1a
- Gentamicin C<sub>1a</sub>
- Gentamicin C<sub>3</sub>
- Gentamycin C<sub>1a</sub>
- O-3-Deoxy-4-C-methyl-3-(methylamino)-β-<span class="text-smallcaps">L</smallcap>-arabinopyranosyl-(1→6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-<smallcap>D</smallcap>-erythro-hexopyranosyl-(1→4)]-2-deoxy-<smallcap>D</span>-streptamine
- Gentamycin C1a
- Gentamicin C3
- O-3-Deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1→6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-erythro-hexopyranosyl-(1→4)]-2-deoxy-D-streptamine
- D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1→6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-erythro-hexopyranosyl-(1→4)]-2-deoxy-
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Encontrado 9 productos.
Gentamicin C1A Deuterated Pentaacetate Salt
CAS:Producto controladoFórmula:C19H39N5O7·C10H20O10Forma y color:NeatPeso molecular:449.54+(300.26)Gentamicin C1a Pentaacetate Salt
CAS:Stability Hygroscopic Applications Antibacterial. References Holt, H.A., et al.: J. Antimicrob. Chemother., 34, 747 (1994), Wilschanski, M., et al.: Am. J. Respir. Crit. Care Med., 161, 860 (2000),Fórmula:C29H59N5O17Forma y color:BeigePeso molecular:749.8Gentamicin C1a pentaacetate salt
CAS:Fórmula:C29H59N5O17Pureza:≥ 95%Forma y color:White to off-white crystalline powderPeso molecular:749.8D-Streptamine, O-3-deoxy-4-C-methyl-3-(methylamino)-β-L-arabinopyranosyl-(1→6)-O-[2,6-diamino-2,3,4,6-tetradeoxy-α-D-erythro-hexopyranosyl-(1→4)]-2-deoxy-
CAS:Fórmula:C19H39N5O7Pureza:%Forma y color:SolidPeso molecular:449.5423Gentamicin C1a
CAS:Gentamicin C1a is an aminoglycoside antibiotic, which is a secondary metabolite derived from the bacterium Micromonospora. This antibiotic functions through a mode of action that involves binding to the 30S subunit of bacterial ribosomes. This binding disrupts protein synthesis by causing misreading of the mRNA, ultimately leading to inhibition of bacterial growth and cellular death. Gentamicin C1a is primarily used in the treatment of severe infections caused by Gram-negative bacteria, including Pseudomonas aeruginosa, Escherichia coli, and Klebsiella species. It is widely employed in both clinical settings for treating complicated urinary tract infections, respiratory tract infections, and bloodstream infections, as well as in research applications to study bacterial protein synthesis mechanisms. Its potency and broad-spectrum activity make it a valuable tool in antimicrobial chemotherapy, although its use must be carefully monitored due to potential nephrotoxic and ototoxic side effects.Fórmula:C19H39N5O7Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:449.54 g/molGentamicin C1a
CAS:Gentamicin C1a, a major component with antibacterial activity, is the precursor to Etimicin.Fórmula:C19H39N5O7Forma y color:SolidPeso molecular:449.54Gentamicin C1a pentaacetate
CAS:Gentamicin C1a pentaacetate is an aminoglycoside antibiotic derivative, which is synthesized through the acetylation of the hydroxyl groups in gentamicin C1a. This compound is derived from the fermentation products of Micromonospora species, a genus of actinobacteria. Its mode of action is similar to that of standard aminoglycosides, primarily involving the binding to bacterial 30S ribosomal subunits. This binding interferes with protein synthesis by causing misreading of mRNA, ultimately leading to the inhibition of protein production and bacterial cell death. In scientific research, Gentamicin C1a pentaacetate is utilized in studies focusing on antibiotic resistance mechanisms, structure-activity relationships, and the development of new derivative antibiotics. Its modified structure offers opportunities to explore variations in bacterial susceptibility and efflux mechanisms. Understanding such interactions is vital for the design of potent antibiotic candidates and combating resistant bacterial strains. Given the growing concern over antibiotic resistance, studies involving Gentamicin C1a pentaacetate contribute to a broader comprehension of aminoglycoside modifications and their potential applications in clinical and laboratory settings.Fórmula:C29H59N5O17Pureza:Min. 95%Forma y color:Off-White PowderPeso molecular:749.8 g/mol
