| 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. |
| 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. |
| M3640 | BAY 57-1293 | BAY 57-1293 is a potent helicase primase inhibitor that exhibites antiviral effect on herpes simplex virus (HSV) with IC50 of 20 nM for both HSV-1 and HSV-2. |
| M3433 | Nitazoxanide | Nitazoxanide is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent (IC50 for canine influenza virus ranges from 0.17 to 0.21 μM). |
| M3406 | Quinidine | Quinidine is a pharmaceutical agent that acts as a class I antiarrhythmic agent. |
| M3340 | Aciclovir | Aciclovir is a synthetic nucleoside analogue active against herpesviruses. |
| M3336 | Moroxydine hydrochloride | Moroxydine hydrochloride is a synthetic antiviral compound chemically belonging to the series of the heterocyclic biguanidines. |
| M3299 | Pyrazinamide | Pyrazinamide is a pyrazine that is used therapeutically as an antitubercular agent. |
| M3298 | Levofloxacin | Levofloxacin is a synthetic fluoroquinolone (fluoroquinolones) antibacterial agent. |
| M3277 | VCH-916 | VCH-916 is a novel nonnucleoside HCV RNA polymerase inhibitor. |
| M3270 | Docosanol | Docosanol is a saturated fatty alcohol. (ED50=2.5 mg/ml for plaque inhibition, and ED50=1.7 mg/ml for inhibition of virus production) |
| M3204 | Oseltamivir phosphate | Oseltamivir phosphate (Tamiflu) is a competitive neuraminidase inhibitor. |
| M3183 | Quinacrine dihydrochloride | Quinacrine dihydrochloride is a non-selective MAO-A/B inhibitor. Quinacrine (Mepacrine) dihydrochloride is an orally bioavailable antimalarial agent, suppresses NF-κB and activate p53 signaling, which results in the induction of the apoptosis. |
| M3178 | Auranofin | Auranofin is an inhibitor of thioredoxin reductase (TrxR) (IC50 = 20 nM; Ki = 4 nM for the NADPH-reduced form of human cytosolic TrxR). |
| M3113 | Valganciclovir hydrochloride | Valganciclovir HCl is a precursor compound of ganciclovir with antiviral activity for studies related to cytomegalovirus infections. |
| M3067 | Thonzonium Bromide | Thonzonium bromide is a monocationic detergent that promotes tissue contact by dispersion and penetration of the cellular debris and exudate of the containing solution. |
| M3018 | Sodium ascorbate | Sodium Ascorbate (L-Ascorbic acid sodium salt) is a more bioavailable form of vitamin C that is an alternative to taking ascorbic acid as a supplement. |
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