| Cat.No. | Name | Information |
|---|---|---|
| M1959 | Oseltamivir | Oseltamivir is a potent and selective inhibitor of influenza virus neuraminidase enzyme. |
| M5055 | Peramivir | Peramivir is a transition-state analogue and a potent, specific influenza viral neuraminidase inhibitor with an IC50 of median 0.09 nM. |
| M1707 | Entecavir Monohydrate | Entecavir Hydrate is a class of antiviral compounds. |
| M3357 | Telbivudine | Telbivudine (Epavudine) is an orally active, potent antiviral inhibitor of hepatitis B virus (HBV) replication. Telbivudine is an antiviral compound used in hepatitis B research. |
| M1695 | Cidofovir | Cidofovir (Vistide) is an injectable antiviral medication for the treatment of cytomegalovirus (CMV) retinitis. |
| M4718 | Dendrobine | Dendrobine is an alkaloid isolated from Dendrobium nobile. Dendrobine has antiviral activity against influenza A virus, IC50 values for A/FM-1/1/47 (H1N1), A/Puerto Rico/8/34 H274Y (H1N1) and A/Aichi/2/68 (H3N2) were 3.39 μM, 2.16 μM and 5.32 μM, respectively. |
| M3222 | Peramivir Trihydrate | Peramivir Trihydrate is a trihydrate of the anti-infection agent peramivir (RWJ-270201,BCX-1812) which is a transition-state analogue and a potent, specific influenza viral neuraminidase inhibitor with an IC50 of median 0.09 nM. |
| M4789 | Isoscopoletin | Isoscopoletin (6-Hydroxy-7-methoxycoumarin) is an active ingredient in artemisia argyi leaves. Isoscopoletin showed significant inhibition of cell proliferation, with IC50 values of 4.0 μM and 1.6 μM against human CCRF-CEM leukemia cells and CEM/ADR5000 drug-resistant subline, respectively. Isoscopoletin (6-Hydroxy-7-methoxycoumarin) has the activity of inhibiting HBV replication. |
| M10082 | Amodiaquine | Amodiaquine is a 4-aminoquinoline compound related to chloroquine, used as an antimalarial and anti-inflammatory agent. |
| M7775 | 3-Deazaadenosine | 3-Deazaadenosine is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 µM, possesses antiviral activity inhibitor of leukocyte adhesion to TNF-treated endothelial cells. |
| M55849 | Riamilovir | Riamilovir is an antiviral drug whose activity is primarily directed against RNA viruses. |
| M55848 | Bofutrelvir | Bofutrelvir (FB2001) is a SARS-CoV-2 main protease Mpro inhibitor with an IC50 value of 53 nM and an EC50 value of 0.53 μM. |
| M55847 | Merafloxacin | Merafloxacin (CI-934), a fluoroquinolone antibacterial agent, is a selective programmed -1 ribosomal frameshifting (-1 PRF) inhibitor of beta coronaviruses. |
| M55846 | SARS-CoV-2-IN-6 | SARS-CoV-2-IN-6 is a SARS-CoV-2 3CLpro inhibitor that shows the most potent enzyme inhibitory IC50 value of 73 nM. |
| M55845 | Simnotrelvir | SARS-CoV-2-IN-41 is a potent SARS-CoV-2 3CLpro inhibitor with an IC50 value of 0.022 µM. |
| M55824 | IM-250 | IM-250 is an orally active helicase-primase inhibitor. |
| M55823 | PYR01 | PYR01 is a potent HIV-1 nonnucleoside reverse transcriptase inhibitor. |
| M55822 | PF-3450074 | PF-3450074 (PF-74) is a specifical inhibitor of HIV-1 capsid protein (CA) and displays a broad-spectrum inhibition of HIV isolates with submicromolar potency (EC50=8-640 nM). |
| M55821 | Letrazuril | Letrazuril is an anti-HIV agent. |
| M55820 | Elsulfavirine | Elsulfavirine is a reverse transcriptase inhibitors for HIV-1 infection and is a new anti-HIV agent. |
| M55819 | Emtricitabine | Emtricitabine is a nucleoside reverse transcriptase inhibitor (NRTI) with an EC50 of 0.01 μM in PBMC cell. |
| M55818 | Tenofovir diphosphate disodium | Tenofovir diphosphate disodium is an antiretroviral agent and an inhibitor of DNA polymerases. |
| M55817 | Glycolithocholic acid 3-sulfate | Glycolithocholic acid 3-sulfate (SLCG) is a cholic acid derivative and a metabolite of glycolithocholic acid. |
| M55816 | Glycolithocholic acid 3-sulfate disodium | Glycolithocholic acid 3-sulfate (disodium) inhibits replication of HIV-1 in vitro. |
| M55814 | Bemnifosbuvir | Bemnifosbuvir (AT-511) is a potent and orally active HCV viral replication inhibitor. |
| M55813 | RO-9187 | RO-9187 is a potent inhibitor of HCV virus replication with an IC50 of 171 nM. |
| M55812 | Tegobuvir | Tegobuvir is a specific, covalent inhibitor of the HCV NS5B polymerase. |
| M55811 | PSI-7409 tetrasodium | PSI-7409 tetrasodium is an active 5'-triphosphate metabolite of sofosbuvir (PSI-7977), inhibiting HCV NS5B polymerases, with IC50s of 1.6, 2.8, 0.7 and 2.6 μM for GT 1b_Con1, GT 2a_JFH1, GT 3a, and GT 4a NS5B polymerases, respectively. |
| M55810 | AB-836 | AB-836 is an orally active HBV capsid inhibitor. |
| M55809 | AB-452 | AB-452, a Dihydroquinolizinone (DHQ) analogue, is a potent and orally active HBV RNA destabilizer. |
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