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. |
|