| 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. |
| M9029 | Cefathiamidine | Cefathiamidine is the first generation of cephalosporin antibacterial used for the treatment of respiratory, liver, five senses, urinary tract infections, endocarditis and sepsis. |
| M9028 | Nifuratel | Nifuratel is a local antiprotozoal and antifungal agent used in gynecology. |
| M9027 | Piroctone Olamine | Piroctone Olamine is a wide spectrum antibacterial and antifungal agent used in the treatment of dandruff, fungal infections. |
| M8981 | Triadimenol | Triadimenol (Triademenol) is a triazole-type fungicide that was identified as weak estrogen receptor agonists, Triademenol is reported as a potent exosome inhibitor which can block the activity of exosomes. |
| M8980 | Neticonazole Hydrochloride | Neticonazole Hydrochloride is an imidazole antifungal for the treatment of fungal skin infections, Neticonazole is reported as a potent exosome inhibitor which can block the activity of exosomes. |
| M8885 | Rafoxanide | Rafoxanide is a novel allosteric inhibitor of SPAK and OSR1. |
| M8868 | Zerumbone | Zerumbone is a TRAIL-induced apoptosis potentiator. Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes of Zingiber zerumbet Smith. Zerumbone potently inhibits the activation of Epstein-Barr virus with an IC50 of 0.14 mM. |
| M8836 | U18666A | U18666A is an intra-cellular cholesterol transport inhibitor. U18666A inhibits replication of Ebola virus, dengue virus, and human hepatitis C virus. |
| M8711 | Delafloxacin | Delafloxacin is a fluoroquinolone antibiotic active against both Gram-negative and Gram-positive bacteria such as MRSA. |
| M8438 | Retro-2 cycl | Retro-2 cycl is a non-toxic inhibitor of the endosome-to-Golgi retrograde transport that selectively protect cells from ricin, cholera toxin, and Shiga-like toxins, without affecting compartment morphology, endogenous retrograde cargos, or other trafficking steps. |
| M8420 | Camalexin | Camalexin is a phytoalexin isolated from cruciferous plants that exhibits antibacterial, antifungal, antiproliferative and cancer chemopreventive activities. |
| M8265 | Adefovir | Adefovir is an antiviral compound that inhibits hepatitis B virus (HBV) DNA polymerase (reverse transcriptase) after intracellular conversion to adefovir diphosphate. |
| M7997 | Palmitoylethanolamide | Palmitoylethanolamide (Palmidrol) is an active endogenous CB2 cannabinoid receptor agonist. |
| M7726 | Piperaquine tetraphosphate tetrahydrate | Piperaquine tetrahydrate is a research antimalarial compound highly active against chloroquine-resistant plasmodium falciparum and Plasmodium vivax . |
| M6718 | ESI 09 | ESI 09 is a novel ePAC inhibitor with IC50 values of 3.2 and 1.4 μM for EPAC1 and EPAC2, respectively. |
| M6603 | Cilastatin sodium | Cilastatin sodium is a reversible, competitive renal dehydropeptidase I inhibitor with IC50 of 0.1 μM, it inhibits the bacterial metallob-lactamase enzyme CphA with an IC50 of 178 μM. |
| M6394 | AC 45594 | AC 45594 is a sF-1 inverse agonist. 4-Heptyloxyphenol (AC 45594) has antibacterial activity agaisnt P. gingivalis, S. artemidis, Str. sobrinus (MIC: 0.10, 0.21, 0.14 mM). |
| M6204 | GC376 | GC376 is a 3CLpro inhibitor; inhibits the replication of viruses TGEV, FIPV and PTV with IC50 values of 0.15, 0.2 and 0.15 μM. |
| M6131 | Pristinamycin | Pristinamycin, produced by Streptomyces pristinaespiralis, is an orally active streptogramin-like antibiotic. The pristinamycins exhibit a strong synergistic antibacterial activity against a wide range of Gram-positive and some Gram-negative bacteria, including methicillin- and vancomycin-resistant strains. |
| M5969 | Sodium sulfadiazine | Sodium Sulfadiazine is a sodium salt form of sulfadiazine, an intermediate-acting bacteriostatic, synthetic sulfanilamide derivative. |
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