|Molecular Weight||585.60 (anhydrous basis)|
|Description||Broad spectrum aminoglycoside antibiotic derived from its counterpart kanamycin A."|
A semi-synthetic produced by selective hydrolysis of the terminal saccharide unit; a potent inhibitor of nematode larval development, but is devoid of paralytic...
A minor component of the zearalenone complex produced by several species of fusarium; causes estrogenic effects in domestic livestock; a metabolite of α-zearala...
A beta-lactamase inhibitor used to increase potency of beta-lactam antibiotics
A semi-synthetic glycopeptide prepared from A40926
A degradation product of oxytetracycline, formed under acidic conditions. An initial dehydration to anhydrooxytetracycline then undergoes an internal cyclisatio...
A salt prepared from minocycline; the preferred formulation for pharmaceutical applications; shows broad spectrum antibacterial and antiprotozoan activity and a...
A semi-synthetic pleuromutilin; prepared by sequential reaction of pleuromutilin tosylate with 2-amino-1,1-dimethylethylthiol, coupling the free amine with a pr...
Pseudoerythromycin A enol ether
A degradation product of erythromycin formed by a complex internal rearrangement of erythromycin A on exposure to neutral to weakly alkaline conditions; devoid ...
A semi-synthetic pleuromutilin prepared by reacting pleuromutilin tosylate with tropine-3-thiol; a broad spectrum antibiotic with no cross resistance to existin...
Standard Solution Aflatoxicol
The 2 ppm acetonitrile solution of aflatoxicol, a metabolite of aflatoxin, could be commonly used as standard solution.
A first generation semi-synthetic erythromycin; prepared by coupling the 11- and 12-OH groups to form a cyclic carbonate; shows comparable or better in vitro po...
Spinosyn D 17-pseudoaglycone
An acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position in spinosyn D; only weakly active as an...
Semi-synthetic, slightly more hydrophobic, analogue of lovastatin; a specific inhibitor of HMG-coa reductase
A polar metabolite first isolated from streptomyces sapporonensi with activity against gram negative bacteria; a veterinary antibiotic.
A rare semi-synthetic tetracycline prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of declomycin;acts by reversibly binding to the 30S ri...
A second generation cephalosporin antibiotic
A first generation cephalosporin antibiotic; has similar anti-bacterial spectrum of activity to cefalexin
4-Bromo-calcimycin, a halogenated analog of A-2318, is a non-Fluorescent Ca2+ ionophore which could be commonly used in fluorescent probes experiments as a modu...
A potent epithiodioxopiperazine mycotoxin produced by species of gliocladium, aspergillus and penicillium; at the cellular level inhibits a broad range of unrel...
An antimalarial 4-aminoquinoline compound; inhibits growth of malarial parasites and treat malarial infections