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. |
M41201 | Tirfipiravir | Tirfipiravir is a nucleoside compound and antiviral agent, against the novel coronavirus or influenza virus. |
M41200 | Viral polymerase-IN-1 hydrochloride | Viral polymerase-IN-1 hydrochloride, a Gemcitabine derivative, potently inhibits influenza A and B viruses infection with IC90 values of 11.4-15.9 μM. |
M41199 | Influenza virus-IN-7 | Influenza virus-IN-7 is an orally active cap-dependent endonuclease inhibitor that can be used for the research of influenza viral infectious diseases. |
M41198 | Neuraminidase-IN-16 | Neuraminidase-IN-16 is a potent neuraminidase inhibitor with IC50s of 0.031, 0.15, 0.25, 0.60, 0.63 and 10.08 μM against neuraminidase of H5N1, H5N8, H1N1, H3N2, H5N1-H274Y and H1N1-H274Y, respectively. |
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. |
M41176 | TMC647055 | TMC647055 is a potent nonnucleoside NS5B polymerase inhibitor of HCV replication. |
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