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Antibiotic

Chemical Structure Cat. No. Product Name CAS No.
Pradofloxacin Chemical Structure
 BCP37544 Pradofloxacin 195532-12-8
Pradofloxacin is a 3rd generation fluoroquinolone antibiotic developed by Bayer HealthCare AG, Animal Health GmBH.
Pefloxacin mesylate dihydrate Chemical Structure
 BCP37535 Pefloxacin mesylate dihydrate 149676-40-4
Pefloxacin Mesylate Dihydrate is the third generation of fluoroquinolone class of antibacterials, which inhibits Topoisomerase II activity and DNA replication.
Calicheamicin Chemical Structure
 BCP37119 Calicheamicin 113440-58-7
Calicheamicin is a potent DNA-damaging cytotoxic agent.
Amrubicin hydrochloride Chemical Structure
 BCP37110 Amrubicin hydrochloride 92470-31-0
Amrubicin Hydrochloride is the hydrochloride salt of a third-generation synthetic 9-amino-anthracycline with antineoplastic activity. Amrubicin intercalates into DNA and inhibits the activity of topoisomerase II, resulting in inhibition of DNA replication, and RNA and protein synthesis, followed by cell growth inhibition and cell death.
HQNO Chemical Structure
 BCP36896 HQNO 341-88-8
HQNO is a natural quinolone secreted by P. aeruginosa. HQNO is a potent inhibitor of the electron transport chain with Kd of 64 nM for the ubiquinol-ferricytochrome c oxidoreductase segment (Complex III) of the respiratory chain. HQNO is also an inhibitor of bacterial and mitochondrialType II NADH : quinone oxidoreductase (NDH-2) with IC50 of 7.3 μM in the presence of 50μM menadione.
Avibactam sodium hydrate Chemical Structure
 BCP36679 Avibactam sodium hydrate AVH
Avibactam sodium hydrate is a covalent and reversible non-β-lactam β-lactamase inhibitor which inhibits β-lactamase TEM-1 and CTX-M-15 with IC50s of 8 nM and 5 nM, respectively.
Lefamulin Chemical Structure
 BCP24164 Lefamulin 1061337-51-6
Lefamulin is a new and relatively unique antibiotic used for treatment of community acquired pneumonia. Lefamulin has not been linked to an increased rate of transient serum liver test abnormalities during treatment or to instances of clinically apparent liver injury.
Hypothemycin Chemical Structure
 BCP36594 Hypothemycin 76958-67-3
Hypothemycin is a macrolide that is isolated from the cultured broth of Hypomyces subiculosus and shows antifungal activity and inhibits the growth of some human cancer cells. It has a role as an EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor, an antineoplastic agent, a fungal metabolite and an antifungal agent. It is a macrolide, an enone, an aromatic ether, an epoxide, a diol, a polyketide, a member of phenols and a secondary alpha-hydroxy ketone.
Thienamycin Chemical Structure
 BCP36562 Thienamycin 59995-64-1
Thienamycin is one of the most potent naturally produced antibiotics known thus far.
Hygromycin B Chemical Structure
 BCP36504 Hygromycin B 8052-93-5
Hygromycin B is an aminoglycoside antibiotic produced by the bacterium Streptomyces hygroscopicus which kills bacteria, fungi and higher eukaryotic cells by inhibiting protein synthesis.
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