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Merck

SBR00041

Sigma-Aldrich

Cefiderocol

Sinónimos:

S-649266

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About This Item

Fórmula empírica (notación de Hill):
C30H34ClN7O10S2
Número de CAS:
Peso molecular:
752.21
Número MDL:
Código UNSPSC:
12352111
NACRES:
NA.76

Ensayo

≥95% (HPLC)

Nivel de calidad

Formulario

solid

idoneidad de la reacción

reagent type: chelator

espectro de actividad antibiótica

Gram-negative bacteria

Modo de acción

protein synthesis | inhibits

temp. de almacenamiento

−20°C

cadena SMILES

NC1=NC(/C(C(N[C@@H]2C(N3[C@@H]2SCC(C[N+]4(CCCC4)CCNC(C5=CC=C(O)C(O)=C5Cl)=O)=C3C([O-])=O)=O)=O)=N/OC(C(O)=O)(C)C)=CS1

InChI

1S/C30H34ClN7O10S2/c1-30(2,28(46)47)48-36-19(16-13-50-29(32)34-16)24(42)35-20-25(43)37-21(27(44)45)14(12-49-26(20)37)11-38(8-3-4-9-38)10-7-33-23(41)15-5-6-17(39)22(40)18(15)31/h5-6,13,20,26H,3-4,7-12H2,1-2H3,(H7-,32,33,34,35,36,39,40,41,42,44,45,46,47)/t20-,26-/m1/s1

Clave InChI

DBPPRLRVDVJOCL-FQRUVTKNSA-N

Descripción general

Cefiderocol has been shown to be effective in preventing the emergence of resistant mutants but is not active against methicillin-resistant Staphylococcus aureus (MRSA) or colistin-resistant bacteria. This versatile compound finds applications in cell biology and biochemical research.
Cefiderocol is a novel injectable siderophore cephalosporin, which was formerly known as S-649266. It has a catechol-type siderophore and cephalosporin core and side chains. Cefiderocol has structural similarity with both ceftazidime and cefepime, besides the chlorocatechol group on the end of the C-3 chain.

Aplicación

Cefiderocol has been used:
  • study bacterial infections and tracking their uptake in vivo
  • the study of the activity of Cefiderocol against gram-negative bacteria

Acciones bioquímicas o fisiológicas

Mode of Action: Cefiderocol binds to specific proteins called penicillin-binding proteins (PBPs) located on the bacterial cell wall. This binding affinity inhibits the synthesis of the bacterial cell wall, leading to cell lysis and bacterial death.

Antimicrobial Spectrum: Cefiderocol has strong antimicrobial properties, especially against a wide spectrum of Gram-negative pathogens. Due to its siderophore core it is also a natural iron-chelator, which adds to its antibacterial activities.

Características y beneficios

  • High-quality antibiotic suitable for multiple research applications
  • Ideal for Cell Biology and Biochemical research

Otras notas

For additional information on our range of Biochemicals, please complete this form.

Cláusula de descargo de responsabilidad

The product is not intended for use as a biocide under global biocide regulations, including but not limited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR) and others.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Certificados de análisis (COA)

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Justin J Choi et al.
Expert opinion on investigational drugs, 27(2), 193-197 (2018-01-11)
The emergence of multidrug-resistant bacterial pathogens has led to a global public health emergency and novel therapeutic options and drug-delivery systems are urgently needed. Cefiderocol is a siderophore cephalosporin antibiotic that has recently been developed to combat a variety of
Takafumi Sato et al.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 69(Suppl 7), S538-S543 (2019-11-15)
The emergence of antimicrobial resistance is a significant public health issue worldwide, particularly for healthcare-associated infections caused by carbapenem-resistant gram-negative pathogens. Cefiderocol is a novel siderophore cephalosporin targeting gram-negative bacteria, including strains with carbapenem resistance. The structural characteristics of cefiderocol

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