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Microbiology/Virology

Chemical Structure Cat. No. Product Name CAS No.
RV 521 Chemical Structure
 BCP37534 RV 521 1903763-82-5
RV 521 is a highly potent fusion inhibitor designed to treat RSV disease through target of a surface protein that mediates RSV binding to cellular receptors .
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.
L742001 hydrochloride Chemical Structure
 BCP37304 L742001 hydrochloride 174605-64-2
L-742001 is an inhibitor of the influenza virus RNA polymerase PA subunit, implicated in several roles, including endonuclease and protease activities as well as viral RNA/complementary RNA promoter binding.
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.
Oxyclozanide Chemical Structure
 BCP36971 Oxyclozanide 2277-92-1
Oxyclozanide is a salicylanilide anthelmintic drug that mainly acts by uncoupling oxidative phosphorylation in flukes.
Diminazene aceturate Chemical Structure
 BCP36970 Diminazene aceturate 908-54-3
Diminazene aceturate is a ACE activator, inhibiting MAPKs and STAT phosphorylation.
Vebicorvir Chemical Structure
 BCP36939 Vebicorvir 2090064-66-5
Vebicorvir is a first-generation hepatitis B virus (HBV) core protein inhibitor, has demonstrated effective antiviral activity.
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.
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