|Description||A second generation cephalosporin antibiotic|
A secondary degradation product formed by epimerisation of tetracycline and dehydration at the C6 position to aromatise the B ring; an important standard for mo...
KT5555, a benzodiazocin compound, has been found to be a tyrosine kinase inhibitor of multi target like JAK2, FLT3 and TrkA. It was also found to exhibit effect...
A semi-synthetic tetracycline formed by a mannich condensation of formaldehyde and 4-hydroxyethylpiperazine with tetracyclin; used commercially as a salt in com...
A degradation product of erythromycin formed by a complex internal rearrangement of erythromycin A on exposure to acidic conditions; in acid forms the enol ethe...
Cefamandole sodium salt
A second generation cephalosporin antibiotic
A macrolide antibiotic active against a broad range of gram positive bacteria; enhance acid stability and improve oral bioavailability compared with erythromyci...
Aa semi-synthetic pleuromutilin prepared by sequential reaction of dihydropleuromutilin tosylate with 2-amino-1,2,4-triazole-5-thiol; a broad spectrum antibioti...
A semi-synthetic erythromycin belonging to the ring expanded aza–erythromycins; regarded as the first of the triamilides
A cephamycin antibiotic grouped with the second generation cephalosporins
17-AAG,an analog of geldanamycin, is a potent heat shock protein 90 (Hsp90) inhibitor (IC50= 5 nM) with a 100-fold higher binding affinity for HSP90 derived fro...
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...
A degradation product of chlorotetracycline formed by acid-catalysed isomerisation of the dimethylamino group at C4
Prepared by acylation of chloramphenicol with succinic anhydride to provide a water soluble pro-drug; represents an alternative pro-drug strategy for chloramphe...
A cephamycin beta-lactam antibiotic grouped with the second generation cephalosporins
Semi-synthetic, slightly more hydrophobic, analogue of lovastatin; a specific inhibitor of HMG-coa reductase
A degradation product of oxytetracycline, formed under acidic conditions. An initial dehydration to anhydrooxytetracycline then undergoes an internal cyclisatio...
A salt of clindamycin, a semi-synthetic lincosamide; prepared by selective phosphorylation of the 2-hydroxy moiety of the sugar of clindamycin; a broad spectrum...
A semi-synthetic glycopeptide prepared from A40926
Erythromycin A enol ether
A degradation product of erythromycin formed under acidic conditions by C6–OH internal attack on the C9 ketone to produce a cyclic enol ether; an important stan...
Amoxicillin sodium salt
An extended spectrum beta-lactam antibiotic; similar in structure to ampicillin