| 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. |
| M41191 | HIV-1 inhibitor-57 | HIV-1 inhibitor-57 is a HIV inhibitor. |
| M41190 | C34 peptide | C34 peptide is a biological active peptide. |
| M41189 | Fipravirimat dihydrochloride | Fipravirimat dihydrochloride is a potent HIV-1 inhibitor. |
| M41188 | TAT-GluR23A Fusion Peptide | TAT-GluR23A Fusion Peptide is a biological active peptide. |
| M41187 | MK-4965 | MK-4965 is a nonnucleoside reverse transcriptase inhibitor (NNRTI). |
| M41186 | HIV-IN petide | HIV-IN petide is a competitive inhibitor of HIV-1 protease (Ki=50 nM). |
| M41185 | L-870810 | L-870810 is a potent HIV-1 IN chain transfer inhibitor with antiviral activity. |
| M41184 | Bavtavirine | Bavtavirine is a potent non-nucleoside reverse transcriptase inhibitors (NNRTIs). |
| M41183 | HIV-1 protease-IN-3 | HIV-1 protease-IN-3 is a potent inhibitor of HIV-1 protease (IC50=71 nM; EC50=0.86 μM). |
| M41182 | HIV-1 capsid inhibitor 1 | HIV-1 capsid inhibitor 1 is a potent HIV-1 Capsid inhibitor with an EC50 value of 3.13 µM. |
| M41181 | GS-9822 | GS-9822 is a potent antivira agent with nanomolar activity against wild-type HIV-1 viruses. |
| M41180 | Clavirolide L | Clavirolide L is a dolabellane-type diterpenoid that can be isolated from Clavularia viridis. |
| M41179 | Rhuscholide A | Rhuscholide A is a benzofuran lactone that shows significant anti-HIV-1 activity, with an EC50 of 1.62 μM. |
| M41178 | HIV-1 inhibitor-59 | HIV-1 inhibitor-59 is a HIV-1 inhibitor, with EC50s of 5.62-171 nM against the wild-type (WT) and mutant HIV-1 strains. |
| M41177 | NNRTIs-IN-1 | NNRTIs-IN-1 is a potent non-nucleoside reverse transcriptase inhibitor featuring significantly anti-resistance efficacy. |
| M41175 | HCV-IN-44 | HCV-IN-44 is an HCV NS5B protein inhibitor that can effectively inhibit the replication of HCV virus. |
| M41174 | HCV-IN-43 | HCV-IN-43 is an HCV NS5B protein inhibitor that can effectively inhibit the replication of HCV virus. |
| M41173 | BILB 1941 | BILB 1941 is a potent and specific nonnucleoside inhibitor of the hepatitis C virus (HCV) RNA polymerase in vitro. |
| M41172 | HBV-IN-35 | HBV-IN-35 is a HBV inhibitor. |
| M41171 | HBV-IN-40 | HBV-IN-40 is a HBV inhibitor (IC50: 0.7 μM). |
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