Antibiotics

Virustomycin A is a 18-membered macrolide antibiotic originally isolated from Streptomyces sp. AM-2604. It is effective against infectious and plant pathogenic fungi. It is active against trichomonads and various RNA and DNA viruses.

Cephradine monohydrate is the first generation cephalosporin, which is active against a wide range of Gram-positive and Gram-negative bacteria.

Sultriecin is a dominant analogue in the family of triene antibiotic isolated from Streptomyces. It is a phosphate ester of fostriecin and displays potent antifungal and antitumour activity.

A semi-synthetic pleuromutilin formed by selective reduction of the ethene to ethyl. It exhibits comparable antibiotic potency to pleuromutilin.

A secondary degradation product formed by dehydration of epichlortetracycline at the C6 position to aromatise the B ring. It is an important standard for monitoring tetracycline stability.

A minor co-metabolite of erythromycin produced by saccharopolyspora erythreae. It exhibits a narrow spectrum of antibacterial activity, and it is much less active than erythromycin A and B.

It is a broad-spectrum aminoglycoside antibiotic produced by the strain of Micromonospora spp. One of several components of the gentamicin C complex which comprises approximately 80% gentamicin and exhibits the most potent antimicrobial activity.

It is a broad-spectrum aminoglycoside antibiotic produced by the strain of Micromonospora spp. One of several components of the gentamicin C complex which comprises approximately 80% gentamicin and exhibits the most potent antimicrobial activity.

It is an aminoglycoside antibiotic produced by the strain of Micromonospora spp. One of several components of the gentamicin C complex which can comprise 25-55% gentamicin depending on the manufacturer or manufacturing process.

A salt of the semi-synthetic tetracycline analogue, pirlimycin. It is a broad spectrum lincosaminide antibiotic with activity against anaerobic bacteria and protozoans by binding to the 23S ribosomal subunit, blocking protein synthesis. It is also an impurity of Clindamycin.

The hydrochloride salt of a rare semi-synthetic tetracycline. It is prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of declomycin. It inhibits protein translation by reversibly binding to the 30S ribosomal subunit and blocking the entry of aminoacyl tRNA into the ribosomal A site. It is a semi-synthetic antibiotic with activity against tetracycline-resistant E. coli, S. aureus and E. faecalis.

Citromycin, an antibiotic, is isolated from the cultures of two strains of Streptomyces.

One of several different components found in standard grade Gentamicin. Gentamicin is an aminoglycoside antibiotic.

17-AAG is an antibiotic with antineoplastic activity that inhibits heat shock protein 90 (HSP90). It was shown to induce apoptosis of mouse lymphoma cancer stem cells (CSCs) and human acute myeloid leukemia (AML) CSCs.

A broad spectrum third generation cephalosporin targeting a wide range of gram-positive and gram-negative organisms. It is especially useful against pathogens responsible for causing ear, nose, and throat infections such as haemophilus influenzae and moraxella.

Sulfapyridine is a short-acting sulfonamide antibiotic used in the treatment of dermatitis herpetiformis. It has antibacterial activity.

JBIR-15 is an aspochracin derivative metabolized from Aspergillus sclerotiorum. It exhibits antifungal activity against C. albicans.

Neohydroxyaspergillic acid is an antibiotic produced by Aspergillus sckrotiorum, which is active against some bacteriophages and fungus.

Penicolinate A is a metabolite produced by Penicillium species, displaying antimalarial and antituberculosis activity. It exhibits potent cytotoxic activity against the human ovarian cancer cell line A2780 with an IC50 value of 4.1μM.

Meclocycline is a tetracycline antibiotic derived from methacycline. It has a broad-spectrum antibacterial and antiprotozoan activity.