![(6R,7R)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F28043-6r-7r-7-amino-3-hydroxymethyl-8-oxo-5-thia-1-azabicyclo-4-2-0-oct-2-ene-2-carboxylic-acid.webp&w=3840&q=75)
CAS 15690-38-7
:ácido (6R,7R)-7-amino-3-(hidroximetil)-8-oxo-5-tia-1-azabiciclo[4.2.0]oct-2-eno-2-carboxílico
Descripción:
La sustancia química conocida como ácido (6R,7R)-7-amino-3-(hidroximetil)-8-oxo-5-tia-1-azabiciclo[4.2.0]oct-2-eno-2-carboxílico, con el número CAS 15690-38-7, es un compuesto bicíclico que presenta una estructura de anillo de tiazolidina. Este compuesto se caracteriza por la presencia de un grupo amino, un grupo hidroximetilo y un grupo funcional ácido carboxílico, lo que contribuye a su potencial actividad biológica. La estereoquímica indicada por la configuración (6R,7R) sugiere disposiciones espaciales específicas de átomos que pueden influir en las interacciones del compuesto con objetivos biológicos. Su grupo oxo y el componente tiazolidina sugieren una reactividad potencial e interacciones con varios sistemas biológicos. Este compuesto es de interés en la química medicinal, particularmente en el desarrollo de antibióticos, debido a sus similitudes estructurales con agentes antibióticos conocidos. La estructura bicíclica única también puede conferir propiedades farmacológicas específicas, convirtiéndolo en un tema de investigación en el diseño y desarrollo de fármacos.
Fórmula:C8H10N2O4S
InChI:InChI=1S/C8H10N2O4S/c9-4-6(12)10-5(8(13)14)3(1-11)2-15-7(4)10/h4,7,11H,1-2,9H2,(H,13,14)/t4-,7-/m1/s1
Clave InChI:InChIKey=BQIMPGFMMOZASS-CLZZGJSISA-N
SMILES:C(O)(=O)C=1N2[C@@]([C@H](N)C2=O)(SCC1CO)[H]
Sinónimos:- (6R,7R)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
- (6R,7R)-7-Amino-3-hydroxymethylceph-3-em-4-carboxylic acid
- 3-Hydroxymethyl-7-aminoceph-3-em-4-carboxylic acid
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-3-(hydroxymethyl)-8-oxo-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-3-(hydroxymethyl)-8-oxo-, (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-3-(hydroxymethyl)-8-oxo-, (6R-trans)-
- 7-Amino-3-(Hydroxymethyl)-8-Oxo-5-Thia-1-Azabicyclo[4.2.0]Oct-2-Ene-2-Carboxylic Acid
- 7-Amino-3-hydoxymethyl-3-cephem-carboxylic acid
- 7-Amino-3-hydroxymethyl-3-cephem-4-carboxylic acid
- 7-Amino-deacetylcephalosporanic acid
- 7β-Amino-3-(hydroxymethyl)-3-cephem-4-carboxylic acid
- Deacetyl-7-aminocephalosporanic acid
- Ver más sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 9 productos.
(6R,7R)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS:Fórmula:C8H10N2O4SPureza:95%Forma y color:SolidPeso molecular:230.2410(6R,7R)-7-Amino-3-Hydroxymethyl-8-Oxo-5-Thia-1-Aza-Bicyclo[4.2.0.]Oct-2-Ene-2-Carboxylic Acid
CAS:(6R,7R)-7-Amino-3-Hydroxymethyl-8-Oxo-5-Thia-1-Aza-Bicyclo[4.2.0.]Oct-2-Ene-2-Carboxylic AcidPureza:98%Peso molecular:230.24g/molDeacetyl-7-aminocephalosporanic acid
CAS:Deacetyl-7-aminocephalosporanic acid serves as a crucial intermediate in the production of β-lactam broad-spectrum cephalosporin antibiotics.Fórmula:C8H10N2O4SPureza:99.97%Forma y color:SolidPeso molecular:230.247-Aminodeacetylcephalosporanic Acid
CAS:Fórmula:C8H10N2O4SPureza:>97.0%(T)(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:230.247-Amino-deacetylcephalosporanic Acid
CAS:Producto controladoApplications Intermediate in the semi-synthetic cephalosporins synthesis. Found in Acremonium chrysogenum.
References Fukagawa, M. et al.; Agr. Biol. Chem. 55, 2163 (1991)Fórmula:C8H10N2O4SForma y color:NeatPeso molecular:230.24(6R,7R)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS:Fórmula:C8H10N2O4SPureza:95%Forma y color:SolidPeso molecular:230.247-Amino-3-(hydroxymethyl)-cephem-4-carboxylic acid
CAS:Cefepime is a broad-spectrum antibiotic that belongs to the group of β-lactam antibiotics. It inhibits the growth of bacteria by binding to the 50S ribosomal subunit, which prevents bacterial protein synthesis. Cefepime hydrochloride is a prodrug that is hydrolyzed in vivo to cefepime, its active form. Cefepime hydrochloride has been shown to inhibit the production of subtilisin and acylase, enzymes involved in the digestion of proteins and fats. The hydrolysis reaction also increases the solubility of cefepime. The crystallization process for cefepime hydrochloride involves heating with organic solvents such as methanol and ethanol. This process can be used for purification and isolation from impurities.Fórmula:C8H10N2O4SPureza:Min. 95%Peso molecular:230.24 g/mol
![(6R,7R)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA007HQ7.jpg&w=3840&q=75)
![(6R,7R)-7-Amino-3-Hydroxymethyl-8-Oxo-5-Thia-1-Aza-Bicyclo[4.2.0.]Oct-2-Ene-2-Carboxylic Acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F54%2Fthumb%2FOR1029784.jpg&w=3840&q=75)
![(6R,7R)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb%2FF243053.jpg&w=3840&q=75)
