|Description||A beta-lactamase inhibitor used to increase potency of beta-lactam antibiotics|
|B1335-476743||5 g||$198||In stock|
|Appearance||White crystalline powder|
Semi-synthetic, slightly more hydrophobic, analogue of lovastatin; a specific inhibitor of HMG-coa reductase
A semi-synthetic avermectin derivative prepared by selective hydrolysis and oximation of doramectin; a potent nematocide used for the treatment of endo- and exo...
A cephamycin beta-lactam antibiotic grouped with the second generation cephalosporins
An extended spectrum beta-lactam antibiotic and resistant to many beta-lactamases
15-Acetoxyscirpenol, a semisyntheticmycotoxin, has been found to be a trichothecene class member.
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...
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 salt prepared from demeclocycline taking advantage of the basic dimethylamino group; shows broad spectrum antibacterial and antiprotozoan activity by binding ...
A degradation product of tetracycline, formed by dehydration at the C6 position under acidic conditions to aromatise the B ring; an important standard for monit...
A semi–synthetic analogue of pleuromutilin; a potent and highly selective antibiotic active against a range of gram positive bacteria; inhibits protein synthesi...
A freely soluble aminoglycoside antibiotic similar in structure to streptomycin
A fourth generation cephalosporin antibiotic
Dihydrospinosyn A aglycone
An acid degradation product produced by hydrolysis of both saccharide groups of 3-ethoxy-5,6-dihydrospinosyn J, the major component of the commercial insecticid...
A sparingly soluble (4.1 mg/ml) fungicidal polyene antifungal
The hydrochloride salt of a rare semi-synthetic tetracycline; prepared by hydrogenolysis of the chloro and benzylic hydroxy moieties of declomycin; acts by reve...
A semi-synthetic tetracycline; prepared by the introduction of a tert-butylaminoacetamido group into a previously unexplored and un-substituted region of existi...
A semi-synthetic produced by hydrolysing the disaccharide unit of ivermectin; a potent inhibitor of nematode larval development, but is devoid of paralytic acti...
Broad spectrum aminoglycoside antibiotic derived from its counterpart kanamycin A."
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...
The major component in the second generation spinosyn family of bio-insecticides marketed as spinetoram; a semi-synthetic compound prepared by selective ethylat...