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Antibiotics and Antivirals

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Cat. No. Product Name Field of Application Chemical Structure
DC9029 Abacavir Abacavir is a powerful nucleoside analog reverse transcriptase inhibitor (NRTI) used to treat HIV and AIDS.
DCAPI1273 Acyclovir (Aciclovir) Acyclovir (Aciclovir)
DC10513 AFN-1252(Debio 1452) Featured AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.
DC10303 Allopurinol riboside Allopurinol riboside, a metabolite of allopurinol, shows potent activities against parasites.
DC10621 Amenamevir Featured Amenamevir, also known as ASP2151, is a herpes virus helicase-primase inhibitor.
DC7058 Amprenavir Featured Amprenavir (Agenerase) is a HIV protease inhibitor(Ki=0.6 nM) used to treat HIV infection.
DC11738 SCYX-7158 An orally-active, CNS permeable benzoxaborole antiprotozoal agent.
DC7061 AN-2690(Tavaborole) AN-2690(Tavaborole), an antifungal agent with activity against Trichophyton species, in a topical solution formulation, for the potential treatment of onychomycosis.
DC9827 AN3365(Epetraborole) Featured AN3365 is a first-in-class antibiotic that demonstrates potent activity across a wide spectrum of Gram-negative bacteria, including those resistant to many other antibiotics.
DC10168 Anle138b Featured Anle138b is a novel oligomer modulator.
DC11088 Fosmanogepix antifungal.
DC11407 Asapiprant(BGE-175) Featured Asapiprant (BGE-175) is a potent and specific antagonist of human PGD2/PTGDR signaling with Ki of 0.44 nM. BGE-175 is currently in a Phase 2 clinical trial to test whether it can prevent disease progression and mortality in older patients hospitalized wit
DC3150 Atazanavir Featured Atazanavir is a HIV protease inhibitor with Ki of 2.66 nM.
DC9480 Atazanavir (sulfate) Atazanavir sulfate is a sulfate salt form of atazanavir that is an highly potent HIV-1 protease inhibitor.
DC10552 AU1235 Featured AU1235 is an adamantyl urea inhibitor of Mycobacterium tuberculosis.
DCAPI1362 Azithromycin (Zithromax) Azithromycin (Zithromax)
DC7541 Balapiravir Balapiravir (R1626, Ro 4588161) is the prodrug of a nucleoside analogue inhibitor of the hepatitis C virus (HCV) RNA-dependent RNA polymerase (R1479, RG1479).
DC11057 Baloxavir acid Featured Baloxavir acid (S-033447) is an anti-influenza compound that potently and selectively inhibits the cap-dependent endonuclease within the polymerase PA subunit of influenza A and B viruses.
DC11056 Baloxavir marboxil Featured Baloxavir marboxil is a prodrug of S-033447. S-033447 is a small molecule inhibitor of the cap-dependent endonuclease of influenza A and B viruses.
DC10294 Bay 41-4109 BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV) with an IC50 of 53 nM.
DC10085 Bay 41-4109 (racemate) Featured BAY 41-4109 racemate is a potent inhibitor of human hepatitis B virus (HBV) with an IC50 of 53 nM.
DC8809 Bedaquiline fumarate Featured Bedaquiline fumarate(TMC207; R207910) is an anti-tuberculosis drug which selectively inhibit the mycobacterial energy metabolism i.e. ATP synthesis and found to be effective against all states of Mycobacterium tuberculosis.
DC4143 Besifloxacin HCl Featured Besifloxacin HCl is a fourth-generation fluoroquinolone antibiotic.
DC21382 EIDD-1931(NHC) Featured EIDD-1931 (β-d-N4-Hydroxycytidine, NHC) inhibits both murine hepatitis virus (MHV) (EC50 of 0.17 μM) and Middle East respiratory syndrome CoV (MERS-CoV) (EC50 of 0.56 μM) with minimal cytotoxicity. It also inhibits SARS-CoV-2 and multiple 2 endemic, epide
DC10890 Bictegravir Featured Bictegravir is a novel, potent inhibitor of HIV-1 integrase with an IC50 of 7.5 nM.
DC10393 Bicyclomycin benzoate Bicyclomycin benzoate is an antibiotic exhibiting activity against a broad spectrum of Gram-negative bacteria and against the Gram-positive bacterium.
DC9853 BM212 Featured BM-212 is a potent antimycobacterial agent and MmpL3 inhibitor.
DC7007 BMS-538203 BMS-538203 is a highly efficient HIV integrase inhibitor and antiviral agent.
DC9700 BMS-707035 Featured BMS-707035 is a potent, specific, and reversible HIV-I integrase (IN) inhibitor that blocks HIV IN strand transfer activity.
DC5077 Boceprevir(EBP 520; SCH 503034 ) Featured Boceprevir(EBP 520; SCH 503034 ) is useful for Anti HCV.

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