|source\Analogue Sets||Semi-synthetic | Erythromycin Analogue Set|
|Description||A semi-synthetic analogue of erythromycin prepared by reduction of erythromycin oxime; a potent antibiotic|
|B1335-476239||50 mg||$399||In stock|
|Purity||>98% by HPLC|
|Synonyms||9(S) Erythromycylamin A, BRL 42852ER, LY 024410|
|Solubility||Soluble in ethanol, methanol, DMF or DMSO. Good water solubility.|
One of the new generation erythromycins introduced in the 1980s. Improved acid stability was achieved by converting the 9-keto group to the more stable oxime an...
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...
Represents the first member of the current generation of erythromycin descendants, belonging to the ketolide class; acid stabile; has good activity against eryt...
Dihydrostreptomycin sulfate (1:x)
An irreversible base degradation product of ivermectin found in animals treated with ivermectin and in the environment
A semi-synthetic, ring-expanded erythromycin, produced by a beckmann rearrangement of erythromycin oxime and reduction to the imine ether, followed by reductive...
A semi-synthetic macrocyclic lactone prepared by the oxidation; used therapeutically for the prevention of intestinal parasites in dogs
A macrolide antibiotic active against a broad range of gram positive bacteria; enhance acid stability and improve oral bioavailability compared with erythromyci...
A degradation product of chlorotetracycline formed by acid-catalysed isomerisation of the dimethylamino group at C4
An early semi-synthetic erythromycin, prepared by reaction of the 9-keto moiety to methyl oxime; shows broad spectrum antibacterial and antiprotozoan activity a...
The salt prepared from valnemulin; the preferred formulation for pharmaceutical applications; a broad spectrum antibiotic used to control gastrointestinal infec...
Erythromycin A oxime
A semi-synthetic analogue of erythromycin; pivotal in the development of the ring expanded aza-erythromycins (e.g. Azithromycin) and the oxime ethers (e.g. Roxi...
A semi-synthetic cyclic lipopeptide belonging to the echinocandin class; not derived from echinocandin but rather from FR901379 which contains a phenolic sulpha...
An acid degradation product produced by selective hydrolysis of the more labile forosamine saccharide in the 17-position of 3-ethoxy-5,6-dihydrospinosyn J, the ...
A degradation product of oxytetracycline formed under acidic conditions; an initial dehydration to anhydrooxytetracycline then undergoes an internal cyclisation...
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...
Alvespimycin, a synthetic Geldanamycin derivative, has been found to be a potent, H2O-soluble Hsp90 inhibitor. IC50: 62 nM.
An acid degradation product produced by selective hydrolysis of the terminal saccharide unit of doramectin; a potent inhibitor of nematode larval development; a...
A semi-synthetic analogue of erythromycin prepared by reduction of erythromycin oxime; a potent antibiotic
A member of the extended spectrum beta-lactam family; similar in structure to penicillin