penicillin g

Penicillin G sodium(Benzylpenicillin sodium) salt is a penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.

Penicillin G potassium (Benzylpenicillin potassium) is the potassium salt form of penicillin G, a broad-spectrum penicillin antibiotic.

Penicillin G Benzathine Tetrahydrate (Benzathine Benzylpenicillin Tetrahydrate) serves as an antibiotic effective against numerous bacterial infections [1].

Penicillin-G-CoA (Penicillin G-coenzyme A) is a derivative of coenzyme A.

Penicillin G benzathine has anti-bacterial infectious activity and can be used to study early syphilis.

Penicillin G procaine hydrate is a compound formulation combining the antibiotic Penicillin G and the local anaesthetic procaine, serving to release the drug slowly and alleviate pain, with inhibitory activity against Gram-positive bacteria.

Procaine penicillin G (Duphapen) (procaine benzylpenicillin) is an antibiotic useful for the treatment of a number of bacterial infections. Specifically, it is used for syphilis, anthrax, mouth infections, pneumonia, diphtheria, cellulitis, and animal bites.

Penicillin G-d5 potassium salt is a deuterated form of penicillin G potassium and serves as a stable isotope internal standard for penicillin G. Penicillin G potassium is a fast-acting antibiotic belonging to the penicillin family.

Penicillin G Benzathine Tetrahydrate (Standard) is the standard substance of Penicillin G Benzathine Tetrahydrate, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Penicillin G Benzathine Tetrahydrate (Benzathine Benzylpenicillin Tetrahydrate) serves as an antibiotic effective against numerous bacterial infections .

Penicillin G potassium (Standard) is the standard substance of Penicillin G potassium, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Penicillin G potassium (Benzylpenicillin potassium) is the potassium salt form of penicillin G, a broad-spectrum penicillin antibiotic.

Penicillin G sodium salt (Standard) is the analytical standard of Penicillin G sodium salt (T0958) and is intended for research and analytical applications. Penicillin G sodium salt is a representative β-lactam antibiotic. Penicillin G sodium salt (Standard) supports analytical method development, quantitative determination, quality control procedures, and pharmacological research involving β-lactam compounds.

Penicillin G-D5 Potassium Salt (Standard) is a reference standard of Penicillin G-D5 Potassium Salt intended for quantitative analysis, quality control, and related biochemical research applications. Penicillin G-d5 potassium salt is a deuterated compound of Penicillin G potassium salt. Penicillin G potassium salt has a CAS number of 113-98-4. Benzylpenicillin potassium is the potassium salt form of penicillin G, a broad-spectrum penicillin antibiotic.

Penicillin G-BSA is a hapten-carrier protein conjugate formed by coupling Penicillin G to bovine serum albumin (BSA). As a hapten, Penicillin G alone cannot induce an immune response and must be conjugated to a large molecular protein to become a complete antigen with immunogenicity. Penicillin G-BSA may be supplied as a lyophilized powder or as a solution. The solution is prepared in 0.01 M TBS (pH 7.4) buffer at a typical concentration of 1 mg/mL.

Penicillin G-OVA is a hapten-carrier protein conjugate formed by coupling Penicillin G to chicken ovalbumin (OVA). As a hapten, Penicillin G alone cannot induce an immune response and must be conjugated to a large molecular protein to become a complete antigen with immunogenicity.Penicillin G-OVA may be supplied as a lyophilized powder or as a solution. The solution is prepared in 0.01 M TBS (pH 7.4) buffer at a typical concentration of 1 mg/mL.

AMK-GX (Immobilized Penicillin G acylase) is a stabilized form of penicillin acylase with enhanced temperature and pH resistance. It exhibits high recovery rates and maintains most of its original activity even after 12 cycles of use. AMK-GX catalyzes the conversion of Penicillin G (PG) into 6-aminopenicillanic acid (6-APA) and 7-amino-desacetoxycephalosporanic acid, which are crucial intermediates in the production of β-lactam antibiotics.

Ephenamine penicilline is a bioactive chemical.

TunR1 is an antibiotic and derivative of tunicamycin .1It is active againstB. subtilis(MIC = 0.3 μg/ml) and increases the efficacy of the β-lactam antibiotics oxacillin , methicillin , and penicillin G againstB. subtiliswhen used at a concentration of 0.4 μg/ml. TunR1 (5 μg/ml) is cytotoxic to MDA-MB-231 breast cancer cells and non-cancerous CHO cells. Unlike tunicamycin, TunR1 does not inhibit glycosylation in a protein N-glycosylation assay. 1.Price, N.P., Hartman, T.M., Li, J., et al.Modified tunicamycins with reduced eukaryotic toxicity that enhance the antibacterial activity of β-lactamsJ. Antibiot. (Tokyo)70(11)1070-1077(2017)

TunR2 is an antibiotic and derivative of tunicamycin .1It is active againstB. subtilis(MIC = 0.3 μg/ml) and increases the efficacy of the β-lactam antibiotics oxacillin , methicillin , and penicillin G againstB. subtiliswhen used at a concentration of 0.4 μg/ml. Unlike tunicamycin, TunR2 is non-toxic toS. cerevisiae(MIC = >10 μg/ml) and does not inhibit glycosylation in a protein N-glycosylation assay. TunR2 also has reduced antiproliferative activity against MDA-MB-231 and CHO cells compared with tunicamycin. 1.Price, N.P., Hartman, T.M., Li, J., et al.Modified tunicamycins with reduced eukaryotic toxicity that enhance the antibacterial activity of β-lactamsJ. Antibiot. (Tokyo)70(11)1070-1077(2017)

Phenylacetyl-coenzyme A (CoA) is a key intermediate in aerobic catabolism of phenylacetate in bacteria such asPseudomonas, when cultured in minimal media using phenylacetate as the sole carbon source.1It is a precursor in the synthesis of the antibiotic penicillin G found in industrial strains ofP. chrysogenum. Phenylacetyl-CoA also acts as an effector molecule of the TetR family transcriptional repressor PaaR inT. thermophilusand the GntR family transcriptional regulator PaaX inE. coliandPseudomonas, binding to each protein to induce derepression of various genes.2