Penicillin G Kaliumsalz

Lieferant: MP Biomedicals
Achtung

Synonyme: Kalium-[2S-(2α,5α,6β)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylat, (2S,5R,6R)-3,3-Dimethyl-7-oxo-6- (2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptan-2-carbonsäure Kaliumsalz, 6-(2-Phenylacetamido)penicillansäure Kaliumsalz, [2S-(2α,5α,6β)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptan-2-carbonsäure Kaliumsalz, Benzylpenicillin Kaliumsalz

0210054325 0210054380 0210054310
ICNA0210054325EA 62 EUR
ICNA0210054325 ICNA0210054380 ICNA0210054310
Penicillin G Kaliumsalz
Penicillin G Kaliumsalz

Penicillin G is a narrow spectrum antibiotic.


Penicillin G is active against gram-positive and gram-negative aerobic and anaerobic bacteria. Penicillin G inhibits cell wall synthesis by binding to penicillin binding proteins (PBPs) which inhibits peptidoglycan chain cross-lining. Penicillin G is stable against hydrolysis by β-lactamases, such as penicillinases and cephalosporinases.


It is the drug of choice for Streptococcus pneumoniae, groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridans group streptococci, and non-penicillinase producing staphylococcus. Penicillin G potassium salt is used to study murosomes of staphylococci and the penicillin-induced lysis of Streptococcus mutans.


Mode of Action: Penicillin G acts by inhibiting cell wall synthesis through binding to penicillin binding proteins (PBPs), inhibiting peptidoglycan chain cross-linking..


Soluble in water (100 mg/ml) clear,colourless to light yellow.

Formel: C₁₆H₁₇KN₂O₄S
Molecular Weight: 372,49 g/mol
Schmelzpunkt: 214…217 °C
Dichte: 1,359 g/cm³ (20 °C)
Lagertemperatur: Kühlschrank
MDL: MFCD00036193
CAS-Nummer: 113-98-4
EINECS: 204-038-0
Merck Index: 12,07225

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