Influenza Virus

CAS No.	Product Name	Inquiry
108729-21-1	Influenza-virus-IN-1 Influenza virus-IN-1 (compound 14) is a potent influenza A virus inhibitor with an EC50 of 2.46 µM and CC50 of >200 µM. Influenza virus-IN-1 shows a concentration dependent inhibition activity for PAN endonuclease with EC50 of 312.36 nM. Influenza virus-IN-1 shows shows anti-influenza A virus activities.
1093851-61-6	Oseltamivir-[Acetamide-d3] Oseltamivir-[Acetamide-d3] is the labelled analogue of Oseltamivir. Oseltamivir is an antiviral medication used to treat and prevent influenza A and influenza B.
109511-58-2	U0126 U0126 is a MAPK inhibitor with antitumor activity. It inhibits MEK1 and MEK2 with IC50 values of 72 nM and 58 nM, respectively. U0126 inhibits tumorigenicity of liver cancer stem cells.
11089-65-9	Tunicamycin Tunicamycin, a mixture of homologous nucleoside antibiotics, has been used to study the effect of N-linked glycosylation of human proton-coupled folate transporter (HsPCFT) in HeLa cells. Tunicamycin blocks the formation of N-glycosidic linkages by inhibiting the first step in glycoprotein synthesis. It exhibits a range of biological activities, including antimicrobial, antivirus, and antitumor effects. It is produced by certain bacteria, including Streptomyces lysosuperficus and Streptomyces chartreusis.
1111897-60-9	7,3',4'-Trihydroxy-3-benzyl-2H-chromene 7,3',4'-Trihydroxy-3-benzyl-2H-chromene is a natural flavonoid isolated from the heartwoods of Caesalpinia sappan L, it is a Potential xanthine oxidase inhibitor.
111393-84-1	Amitivir Amitivir is an inosine monophosphate dehydrogenase inhibitor with activity against several influenza A and B viruses and broad antiviral activity against orthomyxoviruses and paramyxoviruses.
112408-67-0	3-Deoxysappanchalcone 3-Deoxysappanchalcone, coming from the heartwood of Caesalpinia sappan Linn, may be an effective HO-1 inducer at the translational level that has anti-inflammatory effects, and a valuable compound for modulating inflammatory conditions. Anti-influenza virus mechanisms of 3-Deoxysappanchalcone involved anti-apoptosis and anti-inflammation activities in vitro. Moreover, 3-Deoxysappanchalcone could be a promising drug candidate for influenza treatment. The inhibitory activity of 3-Deoxysappanchalcone on MMP-9 expression and production in TNF-α-treated cells was found to be mediated by the suppression of AP-1 and NF-κB activation.
112430-64-5	Ganoderic acid T-N
112529-37-0	4-O-Methylepisappanol
112747-98-5	Clemastanin B Clemastanin B is found in the root of Clematis stans (Ranunculaceae), Eucommia sp. and Galium sinaicum, it has antioxidant and anti-inflammatory activities.
1149348-10-6	FGI-106-tetrahydrochloride FGI-106 tetrahydrochloride is a potent and broad-spectrum inhibitor with inhibitory activity against multiple viruses. FGI- 106 tetrahydrochloride is active against Ebola, Rift Valley and Dengue Fever viruses with EC50s of 100 nM, 800 nM and 400-900 nM, respectively. FGI-106 tetrahydrochloride also inhibits non-hemorrhagic fever viruses HCV and HIV-1 with EC50s of 200 nM and 150 nM, respectively.
1159908-45-8	Palmitoyl Ethanolamide-[7,7,8,8-d4] Palmitoyl Ethanolamide-[7,7,8,8-d4] is the labelled analogue of Palmitoylethanolamide, which is an endogenous CB2 cannabinoid receptor agonist and a selective GPR55 agonist.
1173097-76-1	U0126-EtOH U0126-EtOH is a highly selective inhibitor of MEK1/2 with IC50 of 0.07 μM/0.06 μM, 100-fold higher affinity for ΔN3-S218E/S222D MEK than PD98059.
117772-70-0	Azithromycin dihydrate Azithromycin dihydrate is the dihydrate form of azithromycin, an orally bioavailable azalide derived from erythromycin, and a member of a subclass of macrolide antibiotics, with anti-bacterial activity. Azithromycin is marginally less active than erythromycin in vitro against Gram-positive organisms, although this is of doubtful clinical significance as susceptibility concentration fall within the range of achievable tissue Azithromycin concentrations.
1190215-03-2	M2 ion channel blocker M2 ion channel blocker is an antiviral agent that works through blocking the activity of M2 ion channel.
1191921-01-3	Oseltamivir-acetate Oseltamivir-acetate is an impurity of Oseltamivir, which is an acetamido cyclohexene that is a structural homolog of sialic acid and inhibits neuraminidase.
121288-39-9	Loxoribine It is a small-molecule immunostimulant, toll-like receptor 7 (TLR7) agonist, TLR7 ligand and antitumor agent.
1216461-56-1	Cletoquine-d4-1 Cletoquine-d4-1 (Desethylhydroxychloroquine-d4-1) is the deuterium labeled Cletoquine. Cletoquine (Desethylhydroxychloroquine) is a major active metabolite of Hydroxychloroquine. Cletoquine is produced in the liver by CYP2D6, CYP3A4, CYP3A5, and CYP2C8 isoenzymes. Cletoquine is also a Chloroquine derivative and has the ability to against the chikungunya virus (CHIKV). Cletoquine has antimalarial effects and has the potential for autoimmune diseases treatment.
1242184-43-5	Oseltamivir Acid-[d3] Oseltamivir Acid-[d3] is the labelled analogue of Oseltamivir Acid, which is a metabolite of Oseltamivir. Oseltamivir is an antiviral medication used to treat and prevent influenza A and influenza B.
1246833-26-0	Curcumin-d6

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