Penicillin G, Potassium (Potassium Benzylpenicillin)

Kirschbaum, Joel

doi:10.1016/s0099-5428(08)60421-9

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Transport Of Hydrophobic Penicillins1

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1990

2014

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Cited by 9 publications

(1 citation statement)

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“…Aromatic penicillins synthesized by P. chrysogenum are amphipathic, moderately hydrophobic, and negatively charged compounds [ 103 ]. These characteristics promote secretion by diffusion mechanisms through the peroxisomal and plasma membranes.…”

Section: Transport Of Hydrophobic Penicillinsmentioning

confidence: 99%

Penicillins

Garcı́a-Estrada¹,

Martı́n²

2014

Fungal Biology

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Section: Transport Of Hydrophobic Penicillinsmentioning

confidence: 99%

Penicillins

Garcı́a-Estrada¹,

Martı́n²

2014

Fungal Biology

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(2R,4S)‐2‐Aminomethyl‐5,5‐dimethyl‐1,3‐thiazolidine‐4‐carboxylic Acid Dihydrochloride: Synthesis, Epimerization, and Derivatives

Imming¹

1995

Archiv der Pharmazie

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(2R,4S)-2-AminomethyI-5,5-dimethyl-1,3-thiazolidin-4-carbonsaure dihydrochlorid: Synthese, Epimerisierung und Derivate Die Synthese der Titelverbindung 6a aus Penicillamin 5 oder aus Penicillinen 7, ihre spektroskopischen Daten und Stereochemie werden beschrieben. 6a epimerisiert in verdunnter waariger Losung schnell an C-2. Aukrdem wurden die amino-und carboxylgeschutzten Derivate 10-13 aus 6 hergestellt.

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Elks¹,

Ganellin²

1990

Dictionary of Drugs

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Penicillin G, Potassium (Potassium Benzylpenicillin)

Cited by 9 publications

References 257 publications

Penicillins

Penicillins

(2R,4S)‐2‐Aminomethyl‐5,5‐dimethyl‐1,3‐thiazolidine‐4‐carboxylic Acid Dihydrochloride: Synthesis, Epimerization, and Derivatives

B

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