|Description||A second generation cephalosporin antibiotic|
|Appearance||White or off-white powder|
|Solubility||DMSO: Soluble Methanol: Soluble Water: Soluble|
The minor component (<20%) of the commercial anthelmintic, ivermectin; potent insecticide; in vitro, the B1b (25-iso-propyl) analogue is slightly more potent th...
KT5823, a benzodiazocine compound, has been found to be a PKG inhibitor and could promote the expression of TSH-induced NIS in thyroid cells.
A salt of the semi-synthetic tetracycline analogue, pirlimycin; a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans by binding t...
Azlocillin sodium salt
An extended spectrum beta-lactam antibiotic derived from ampicillin
A semi-synthetic analogue of lincomycin, prepared by chloride substitution of the exocyclic sugar hydroxy group; a broad spectrum antibiotic with activity again...
Milbemycin A3 oxime
A semi-synthetic macrocyclic lactone prepared by the oxidation and oximation of a mixture of milbemycin A3; the minor component (~30%) in the commercial product...
A semi-synthetic 4-epimethylamino analogue of avermectin B1b; prepared by oxidation of the 4-hydroxy moiety and reductive amination
A cephamycin beta-lactam antibiotic grouped with the second generation cephalosporins
A semi-synthetic 4”-epimethylamino analogue of avermectin B1b prepared by oxidation of the 4”-hydroxy moiety and reductive amination; members of the avermectin/...
A sparingly soluble (4.1 mg/ml) fungicidal polyene antifungal
A first generation cephalosporin antibiotic; slightly soluble in aqueous solution (1.789 mg/ml)
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 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 tetracycline, formed by dehydration at the C6 position under acidic conditions to aromatise the B ring; an important standard for monit...
A degradation product of chlorotetracycline formed by acid-catalysed isomerisation of the dimethylamino group at C4
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 semi-synthetic tetracycline prepared by dehydration of the 6-hydroxy group of oxytetracycline; shows broad spectrum antibacterial and antiprotozoan activity b...
A semi-synthetic, ring-expanded erythromycin, produced by a beckmann rearrangement of erythromycin oxime and reduction to the imine ether, followed by reductive...
A first generation cephalosporin antibiotic; sparingly soluble in aqueous solution (0.47 mg/ml)
A semi-synthetic paraherquamide analogue prepared by removal of the 2-oxo group in a four-step sequence of N-protection; a potent nematocide; induces a flaccid ...