|Molecular Weight||585.60 (anhydrous basis)|
|Description||Broad spectrum aminoglycoside antibiotic derived from its counterpart kanamycin A."|
Amoxicillin sodium salt
An extended spectrum beta-lactam antibiotic; similar in structure to ampicillin
An irreversible base degradation product of ivermectin found in animals treated with ivermectin and in the environment
An insoluble broad spectrum anti-parasitic drug; considered a dangerous good
A base-catalysed intermediate in the decomposition of ivermectin; formed by epimerisation at the 2-position which ultimately rearranges irreversibly to the isom...
An acid degradation product produced by selective hydrolysis of the terminal saccharide unit of doramectin; a potent inhibitor of nematode larval development; a...
Cefepime hydrochloride hydrate
A fourth generation cephalosporin antibiotic.
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 lincosamide prepared from clindamycin by hydrolysing the propyl N-methylproline and re-annealing a 4-ethylpipecolic acid; a broad spectrum anti...
A mixture of eprinomectins B1a and B1b in a 9:1 ratio, produced from a mixture of avermectin B1a and B1b; is used commercially as a topical endectocide (insecti...
15-Acetoxyscirpenol, a semisyntheticmycotoxin, has been found to be a trichothecene class member.
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...
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 cephamycin antibiotic grouped with the second generation cephalosporins
A narrow spectrum beta-lactam antibiotic of the penicillin class
A semi-synthetic tetracycline prepared by dehydration of the 6-hydroxy group of chlortetracycline to yield an exocyclic 6-methylene; a close structural analogue...
A semi-synthetic 4”-epimethylamino analogue of avermectin B1a prepared by oxidation of the 4”-hydroxy moiety and reductive amination
A salt of the semi-synthetic tetracycline analogue, pirlimycin; a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans by binding t...
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...
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 analogue of ostreogrycin A (virginiamycin M, pristinamycin IIA, streptogramin A) formed by addition of diethylaminoethylthiol to the 2-pyrrolin...