penicillin

Methicillin sodium salt is the sodium salt form of methicillin, a semisynthetic beta-lactam penicillin antibiotic with beta-lactamase resistant activity.

Ceftobiprole medocaril (BAL5788), the parenteral prodrug of Ceftobiprole, is a broad-spectrum cephalosporin effective against Methicillin-resistant Staphylococcus aureus (MRSA).

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 V Potassium (Phenoxymethylpenicillin potassium salt) is an orally administered, broad-spectrum penicillin antibiotic used for treating mild to moderate infections caused by susceptible gram-positive organisms.

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

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

Penicillin G Procaine is a β-lactam antibiotic and is a crystalline complex produced by chemically combining penicillin G with procaine.

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 V (Phenoxymethylpenicillin) is an effective, orally-administered antibiotic with activity against Streptococci, Clostridium difficile, and Staphylococcus aureus. It holds potential for research into treatments for otitis, sinusitis, pharyngitis, and tonsillitis [1] [2] [3] [4].

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

Penicillin amidase (Penicillin acylase) is an enzyme utilized for cleaving the acyl side chains from penicillins. It facilitates the production of 6-aminopenicillanic acid and is also employed in resolving racemic mixtures, peptide synthesis, and the creation of semi-synthetic β-lactam antibiotics [1] [2] [3].

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 V-d5 is a deuterated compound of Penicillin V. Penicillin V has a CAS number of 87-08-1.

Penicillin OVA is a conjugate protein of penicillin and ovalbumin, utilized as an antigen in immunological studies. It induces IgE-dependent allergic reactions to penicillin in mice.

Penicillin G BSA is an antigen-adjuvant conjugate consisting of Penicillin G linked with bovine serum albumin (BSA). This conjugation enhances the generation of antigen-specific antibodies in vaccine models by linking the antigen with the protein adjuvant. The conjugate does not alter protein folding or disrupt major epitopes, while it enhances cross-presentation and the production of antigen-specific T cells.

Penicillin BSA is an antigen-adjuvant conjugate of Penicillin with Bovine Serum Albumin (BSA). By conjugating the antigen with a protein adjuvant, this compound enhances specific antibody production in vaccine models. The conjugate does not affect protein folding or destroy primary epitopes, and it also boosts cross-presentation and the generation of antigen-specific T cells.

Penicillin G OVA is an antigen-adjuvant conjugate composed of Penicillin G and ovalbumin (OVA). Conjugating the antigen with a protein adjuvant enhances the production of antigen-specific antibodies in vaccine models. This conjugation does not affect protein folding or alter major epitopes, while also enhancing cross-presentation and the generation of antigen-specific T cells.

Ephenamine penicilline is a bioactive chemical.

Benzylpenicillin 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.

Penicillinase, a beta-lactamase enzyme, inactivates beta-lactam antibiotics by hydrolyzing the peptide bond of the characteristic four-membered beta-lactam ring, rendering the antibiotic ineffective [1].

Ampicillin (Aminobenzylpenicillin) is a semi-synthetic penicillin belonging to the β-lactam group of antibiotics. Ampicillin has bactericidal activity against a wide range of Gram-positive and Gram-negative bacteria.

Penicillamine (Artamine), possessing antineoplastic properties, induces apoptosis by a p53-mediated mechanism and inhibits angiogenesis by chelating with copper, a cofactor for angiogenesis. Artamine is a beta dimethyl analog of the amino acid cysteine. As a degradation product of penicillin antibiotics, Artamine chelates with heavy metals and increases their urinary excretion.

Zidebactam (WCK-5107) is an effective β-lactamase inhibitor. Zidebactam also is a penicillin-binding protein2 inhibitor (IC50: 0.26 μg mL).

Cefixime (FR-17027) is a broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell wall synthesis by disrupting peptidoglycan synthesis, resulting in a reduction in bacterial cell wall stability and bacterial cell lysis. Stable in the presence of a variety of beta-lactamases, this agent is more active against gram-negative bacteria and less active against gram-positive bacteria compared to second-generation cephalosporins.