| 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. |
| M4330 | Paederoside | Paederoside is a monoterpene S-methyl thiocarbonate isolated from Paederia Pertomentosa. Paederoside showed high antitumor promotion and inhibited epstein-Barr virus activation. |
| M4283 | Usaramine | Usaramine |
| M4215 | Isomangiferin | Isomangiferin (Isomangiferin) is a natural compound with antiviral effects. |
| M4214 | Theaflavin | Theaflavin is a natural influenza A (H1N1) neuraminidase inhibitor. |
| M4182 | Isochlorogenic-acid-B | 3, 4-dicaffeoylquinic acid is naturally isolated and has antioxidant, DNA protective, neuroprotective and liver protective properties. 3, 4-dicaffeoylquinic acid has apoptosis-mediated cytotoxicity and α-glucosidase inhibition. 3, 4-dicaffeoylquinic acid has a unique antiviral mechanism, that is, by increasing TRAIL, the virus clearance rate can be improved. |
| M4150 | Glycitin | Soybean isoflavone (Glycitin) is a natural isoflavone isolated from beans that promotes the proliferation of bone marrow stromal cells and osteoblasts and inhibits the biological functions of bone conversion. Glycitin has antibacterial, antiviral and estrogenic effects. |
| M4113 | Alisol-F-24-acetate | Alisol-F-24-acetate |
| M4111 | Alisol-F | Alisol F is a triterpenoid isolated from Alisma alisma, which has immunosuppressive and antiviral functions. Alisol F showed inhibitory activity against the secretion of hepatitis B virus (HBV) surface antigen (HBsAg) in vitro with IC50 of 0.6 μM. |
| M4099 | Saikosaponin-B2 | Saikosaponin B2, an active ingredient isolated from Bupleurum chinense, is an invasion inhibitor of HCV virus infection. Anti-cancer effect. |
| M4065 | Ginsenoside-Rb2 | Ginsenoside Rb2 is one of the main bioactive components of ginseng extract. Ginsenoside Rb2 can up-regulate GPR120 gene expression. Ginsenoside Rb2 has antiviral effects. |
| M4062 | Punicalagin | Punicalagin is a species from Punica Granatum L. Or polyphenols isolated from the leaves of Terminalia catappa L. Punicalagin is a reversible, noncompetitive 3CLpro inhibitor that inhibits SARS-COV-2 replication in vitro. Punicalagin is an anti-hepatitis B virus (HBV) drug with antioxidant, anti-inflammatory and anticancer effects. Punicalagin has the potential to be used in COVID-19 research. |
| M3964 | Harringtonine | Harringtonine is a natural cephalotaxus alkaloid which blocks protein synthesis through translation elongation inhibition. Harringtonine inhibits protein synthesis. Harringtonine has anti-chikungunya virus (CHIKV) activities with an EC50 of 0.24 μM. |
| M3944 | Nimorazole | Nimorazole is a nitroimidazole anti-infective. |
| M3942 | Cephalotaxine | Cephalotaxine is a benzazepine alkaloid isolated from Cephalotaxus harringtonia. |
| M3878 | Salinomycin sodium salt | Salinomycin sodium salt is an anticoccidial compound with potent anti-bacterial activity and an novel anticancer agent targeting human cancer stem cells. |
| M3864 | Remdesivir | Remdesivir, also known as GS-5734, is a nucleoside analogue with in vitro activity against multiple RNA viruses, including Ebola and CoV. |
| M3794 | Tomeglovir | Tomeglovir is a novel nonnucleosidic inhibitor of human cytomegalovirus replication. Tomeglovir is a potent anti-CMV agent, inhibiting processing of viral DNA-concatemers, with IC50s of 0.34 μM and 0.039 μM for HCMV and MCMV. |
| M3726 | Caspofungin acetate | Caspofungin acetate is an echinocandin that inhibits the synthesis of β (1,3)-D-glucan, an integral component of the fungal cell wall. |
| M3724 | Caspofungin | Caspofungin is an echinocandin agent with fungicidal activity against candida species. |
| M3711 | Pirodavir | Pirodavir (R77975) is a capsid - bound anti-picornavirus compound that is active in vitro against most rhinovirus (RV) serotypes. |
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