| 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. |
| M55507 | Amantadine-d6 | Amantadine-d6 |
| M55503 | Ganciclovir-d5 | Ganciclovir-d5 |
| M55439 | Pyrazinamide-d3 | Pyrazinamide-d3 |
| M54850 | Sulfogaiacol | Sulfogaiacol is a antitussive agent. Sulfogaiacol is used for acute respiratory tract infections, cough and other conditions. |
| M54845 | 2,4-Dichlorobenzyl alcohol | 2,4-Dichlorobenzyl alcohol is a mild antiseptic, with a broad spectrum for bacterial and virus associated with mouth and throat infections. |
| M53488 | TAT | TAT (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1) and is a cell-penetrating peptide. |
| M53483 | HIV gag peptide (197-205) | HIV gag peptide (197-205) is a H-2Kd-restricted epitope derived from the p24 portion of the HIV-1 gag protein, consists of amino acids 197-205 (AMQMLKETI). |
| M45102 | ML188 | ML188 is a first-in-class probe and also a selective non-covalent SARS-CoV 3CLpro inhibitor with an IC50 of 1.5 μM. antiviral activity. |
| M44973 | Phloretic acid | Desaminotyrosine is a microbially associated metabolite protecting from influenza through augmentation of type I interferon signaling. |
| M44828 | Cyclo(Phe-Pro) | Cyclo(Phe-Pro) (Cyclo(phenylalanylprolyl)) inhibits retinoic acid-inducible gene-I (RIG-I) polyubiquitination, through its specific interaction with RIG-I, to blunt IRF-3 activation and type-I IFN production. |
| M44678 | 11-Oxomogroside II A1 | 11-Oxomogroside II A1 is an oxidized cucurbitin. |
| M43911 | Tachyplesin I | Tachyplesin I is a cationic antimicrobial peptide containing 17 amino acid residues. |
| 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. |
| 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. |
| M40724 | 3-Chloro-L-alanine | 3-Chloro-L-alanine is an inhibitor of kynureninase as well as an inhibitory amino acid analog that inhibits the activity of several enzymes (e.g. threonine deaminase, alanine racemase). |
| M40629 | Calcium trinatrium diethylenetriaminepentaacetic acid hydrate | Calcium trinatrium diethylenetriaminepentaacetic acid hydrate is a cytomegalovirus CMV replication inhibitor, chelator, heavy metal detoxifier (e.g., acute cadmium toxicity), and radioactivity promoter, which improves solubility by forming water-soluble chelates with polyvalent cations. |
| M40613 | Methylenedisalicylic acid | Methylenedisalicylic acid is a potent inhibitor of MarR family transcription factor A (MgrA) and Ser/Thr kinase (Stp1) that enhances SarA/MgrA phosphorylation through inhibition of Staphylococcus aureus Stp1, with an IC50 value of 9.68 ± 0.52 μM when acting on Stp1.In addition, Methylenedisalicylic acid can also be used as a lead compound in the study of methods to reduce staphylococcal toxicity. |
| M38807 | Umifenovir | Umifenovir is a potent, orally active broad-spectrum antiviral agent with activity against a number of enveloped and non-enveloped viruses. Umifenovir is an efficient inhibitor of SARS-CoV-2 in vitro. |
| M38767 | Abyssinone V | Abyssinone V is a prenylated flavonoid with predicted anti-viral activity. Abyssinone V is predicted to be antivirals including anti-herpes (HSV) agent, with mechanisms comprising inhibition of polymerase, ATPase and membrane integrity. |
| M38764 | Indinavir | Indinavir (MK-639 free base) is an orally active and selective HIV-1 protease inhibitor with a Ki of 0.54 nM for PR. Indinavir exhibits anticancer activity by inhibiting the activation of MMPs-2 hydrolysis, anti-angiogenesis and inducing apoptosis. Indinavir is also a SARS-CoV 3CLpro inhibitor. |
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