| 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. |
| M53450 | Influenza HA (110-119) | Influenza HA (110-119) is the 110-119 fragment of influenza virus hemagglutinin that can stimulate Treg cells proliferation. |
| M53449 | Influenza NP (147-155) | Influenza NP (147-155) is a Kd restricted epitope from influenza nucleoprotein. |
| M53448 | CEF1, Influenza Matrix Protein M1 (58-66) | CEF1, Influenza Matrix Protein M1 (58-66) is an epitope derived from the matrix protein of the influenza A virus. |
| M53447 | CEF7, Influenza Virus NP (380-388) | CEF7, Influenza Virus NP (380-388) is a HLA-B*08 restricted influenza virus nucleoprotein epitope. |
| M53446 | CEF8, Influenza Virus NP (383-391) | CEF8, Influenza Virus NP (383-391), an influenza A virus nucleoprotein containing residues 383 to 391, is the most important HLA-B*2705-restricted epitope in the nucleoprotein of influenza A viruses. |
| M53445 | Fusion Inhibitory Peptide | Fusion Inhibitory Peptide (Z-D-Phe-Phe-Gly-OH, FIP, Virus Replication Inhibitory Peptide) is a potent inhibitor of the virus replication, by inhibiting the membrane fusing activity of a viral glycoprotein. |
| M53444 | PA (224-233), Influenza | PA (224-233), Influenza is a 10-aa peptide, a fragment of polymerase 2 protein in influenza A virus. |
| M53443 | Influenza HA (307-319) | Influenza HA (307-319) is 13 amino acids 307 to 319 fragment of Influenza HA. |
| M53442 | Influenza HA (518-526) | Influenza HA (518-526) is an H-2Kd-restricted epitope of the influenza virus hemagglutinin comprised amino acids 533 to 541. |
| M53441 | Urumin | Urumin has antiviral activity against the human influenza A virus. |
| M53440 | CEF6 | CEF6 is a 9-aa-long peptide corresponding to aa 418-426 of the influenza A virus (H1N1) nucleocapsid protein. |
| M53433 | RVG-Cys | RVG-Cys (RVG29-Cys) is based on rabies virus glycoprotein (RVG29) peptide and connected to Cys to facilitate subsequent coupling. |
| M53432 | Antioxidant agent-9 | Antioxidant agent-9 is a peptide with the sequence Asp-Trp. |
| M53431 | Z-Arg-Leu-Arg-Gly-Gly-AMC | Z-Arg-Leu-Arg-Gly-Gly-AMC is a peptide substrate of SARS-CoV PLpro. |
| M53430 | Herpes virus inhibitor 1 | Herpes virus inhibitor 1 is a herpes virus inhibitor and disrupts herpes virus ribonucleotide reductase quaternary structure. |
| M50231 | CMX990 | CMX990 is a SARS-CoV-2 3CL protease inhibitor that inhibits the EC90s of SARS-CoV-2 in human bronchial epithelial cells (HBECs) and HeLa-ACE2 cells at 9.6 nM and 101 nM, respectively. |
| M49843 | 5-Hydroxymethyl-2'-deoxyuridine | 5-Hydroxymethyl-2'-deoxyuridine is a nucleoside analog. 5-Hydroxymethyl-2'-deoxyuridine inhibits the replication of multiple human leukemia cell lines with IC50 values of 1.7-5.8 μM. 5-Hydroxymethyl-2'-deoxyuridine can be used for the research of cell replication and leukemia. |
| M49834 | HIV-1 inhibitor-6 | HIV-1 inhibitor-6 is a potent HIV-1 pre-mRNA alternative splicing inhibitor. HIV-1 inhibitor-6 blocks HIV replication. HIV-1 inhibitor-6 is active against wild-type HIV-1IIIB (subtype B, X4-tropic) and HIV-1 97USSN54 (subtype A, R5-tropic) with EC50s of 0.6 μM and 0.9 μM, respectively. |
| M49500 | 18BIOder | 18BIOder is a neuroprotective GSK-3β inhibitor, highly selectively inhibiting HIV-1. |
| M45228 | ALG-000184 | ALG-000184 is a precursor compound to ALG-001075 and a pan-genotypic type II capsid assembly modifier (CAM) for use in studies related to chronic hepatitis B. |
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