Penicillin G potassium

CAS: 113-98-4

Ref. 3D-AP18307

Produktinformation

• Name: Penicillin G potassium
• Synonyme: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid potassium saltBenzylpen icillin potassiumBenzyl penicillinate potassium salt, 3,3-Dimethyl-7-oxo-6-[(phenylacetyl)amino]-[2S-(2α,5α,6.beta]).-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monopotassium salt, 4-Thia-1-azabicyclo, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-, monopotassium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]- (2S,5R,6R)-, potassium salt (1:1), 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- (2S,5R,6R)-, monopotassium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]- [2S-(2α,5α,6β)]-, monopotassium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-, [2S-(2alpha,5alpha,6beta)]-, monopotassium salt, Benzylpenicillin potassium salt, Benzylpenicillinic acid potassium salt, Cosmopen, Cristapen, Crytapen, Dixocillin, Eskacillin, Falapen, Forpen, Hipercilina, Hyasorb, Hylenta, Kalium-[2S-(2α,5α,6β)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylat, Liquapen, M-cillin, Megacillin tablets, Monopen, Monopotassium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1 -azabicyclo, Notaral, Novocillin vet., Novopen-G, Nsc 131815, Orpeneed, Pen-G, Penicillin G Potassium Salt, Pentid, Pentids, Pfizerpen, Potassium 2,2-dimethyl-6β-phenylacetamidopenam-3α-carboxylate, Potassium 3,3-Dimethyl-7-Oxo-6-[(Phenylacetyl)Amino]-4-Thia-1-Azabicyclo[3.2.0]Heptane-2-Carboxylate, Potassium 6-(phenylacetamido)penicillanate, Potassium benzylpenicillin, Potassium benzylpenicillinate, Potassium penicillin G, R-Pen, Scotcil, Sugracillin, Tabilin, Truxcillin, Unilab Penicillin G, [2S-(2α,5α,6β)]-3,3-Dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate de potassium, [2S-(2α,5α,6β)]-6-(fenilacetamido)-3,3-dimetil-7-oxo-4-tia-1-azabiciclo[3.2.0]heptano-2-carboxilato de potasio, potassium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, potassium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, potassium [2S-(2alpha,5alpha,6beta)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, potassium [2S-(2α,5α,6β)]-3,3-dimethyl-7-oxo-6-(phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

Beschreibung

Penicillin G potassium is an antibiotic that belongs to the penicillin family of beta-lactam antibiotics. It is used as a first-line drug for the treatment of serious infections caused by bacteria, including some strains which are resistant to other antibiotics. Penicillin G potassium blocks bacterial cell wall synthesis by inhibiting the cross-linking of peptidoglycan, an essential component in bacterial cell walls. Penicillin G potassium binds to penicillin-binding proteins (PBPs) on the surface of bacteria and inhibits transpeptidation reactions in bacterial cell walls. This binding prevents the formation of an antibiotic-inhibitor complex with PBPs, preventing transpeptidation reactions and synthesis of peptidoglycan, leading to cell death.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 372.48 g/mol
• Formel: C₁₆H₁₇KN₂O₄S
• Reinheit: Min. 95 Area-%
• Farbe/Form: Powder