| 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. |
| M5083 | β-Cyclodextrin | β-Cyclodextrin affects the formation of isomerization products during peptide deamidation. |
| M1707 | Entecavir Monohydrate | Entecavir Hydrate is a class of antiviral compounds. |
| M3357 | Telbivudine | 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. |
| M10421 | Sodium citrate (dihydrate) | Sodium citrate dehydrate is an anticoagulant and also used as a buffer and food preservatives. |
| 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. |
| M41168 | Xalnesiran | Xalnesiran is siRNA for the treatment of chronic hepatitis B (HBV). |
| M41167 | Isothiafludine | Isothiafludine is an orally active non-nucleosidic anti-HBV compound. |
| M41166 | Xalnesiran sodium | Xalnesiran (sodium) is siRNA for the treatment of chronic hepatitis B (HBV).. |
| M41165 | HBV-IN-36 | HBV-IN-36 is a HBV inhibior (IC50=2 μM), showing anti-HBV activity with EC50 of 0.58 μM. |
| M41164 | HEC72702 | HEC72702 is a potent and orally active hepatitis B virus capsid inhibitor with an EC50 values of 0.039 µM. |
| M41163 | HBV-IN-33 | HBV-IN-33, a HBV inhibitor, notably suppresses HBV replication in HepAD38, HepG2-HBV1.3 and HepG2-NTCP cells. |
| M41162 | Oxynitidine | Oxynitidine is an HBV inhibitor (ID50=30.8 µg/mL), which can effectively inhibit the DNA replication activity of HBV. |
| M41161 | Helioxanthin | Helioxanthin (ACH126447) and its analogues exhibit significant in vitro antiviral activity against hepatitis B virus (HBV, EC50=1 uM) and flavivirus. |
| M41126 | DENV-IN-10 | DENV-IN-10 is a potent tetravalent dengue inhibitor, with EC50s of 1.36, 0.87, 0.94, and 0.95 μM against DENV-1-4 serotypes, respectively. |
| M41125 | EBOV/MARV-IN-3 | EBOV/MARV-IN-3 is a potent EBOV and MARV inhibitor with IC50 values of 0.5, 1.2 µM, respectively. |
| M41124 | VK-1727 | VK-1727 is a selective small molecule inhibitor of EBNA1. |
| M40994 | Uprifosbuvir | Uprifosbuvir is a nucleic acid NS5b polymerase inhibitor with antiviral activity and may be used in hepatitis C related studies. |
| M40944 | Fomivirsen | Fomivirsen is a phosphorothioate oligonucleotide derivative that binds to and degrades the mRNA of the CMV immediate-early 2 protein, thereby inhibiting viral proliferation, and can be used in studies related to cytomegalovirus retinitis (CMV). |
| M40860 | Bucillamine | Bucillamine is an orally active endogenous cysteine derivative of the amino acid that also acts as a sulfhydryl donor with antiangiogenic, antioxidant, and anti-inflammatory activities, and is used in rheumatoid arthritis (RA), cystinuria, and gout studies. |
| M40808 | β-Amyrin acetate | β-Amyrin acetate is a triterpenoid natural product that localizes to HMG CoA reductase and inhibits its activity, with potent anti-inflammatory, anti-fungal, anti-diabetic, and anti-hyperlipidemic activities. |
| M40761 | Rabbit defensin NP-1 | Rabbit defensin NP-1, a defensin isolated from rabbit neutrophils, consists of 33 amino acids rich in arginine and cysteine residues and has antimicrobial activity. |
| M40760 | Human β-defensin-3 | Human β-defensin-3 is an antimicrobial peptide produced by epithelial cells that reduces inflammatory cytokine responses, as well as inhibits microbial growth, and has immunomodulatory activity with IC90 values ranging from 6-25 μg/ml. |
| M40759 | Human β-defensin 1 | Human β-defensin 1 is a member of a family of naturally occurring antimicrobial peptides produced by epithelial cells that have antimicrobial activity and can be used in studies related to autoimmune diseases. |
| M40757 | Human β-defensin-2 | Human β-defensin-2 is a cysteine-rich cationic skin antimicrobial peptide (SAP) produced by epithelial cells and a member of the cationic host defense peptide (HDP) family. Antibacterial activity against Gram-negative bacteria and Candida (LD90: 25 μg/ml). Can be used in studies related to colitis. |
| M40503 | Lugdunin | Lugdunin is a class of non-ribosomal peptides (NRPs) with good antimicrobial activity and inhibits methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE) and Listeria monocytogenes. |
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