
Antivirals
Found 766 products of "Antivirals"
3,4-Difluoroaniline-2,6-d2
CAS:Controlled ProductApplications 3,4-Difluoroaniline-2,6-d2 (CAS# 1061566-62-8) can be used in its derivative form as an antiviral agent for Hepatitis B.
References Qiu, Y.L., et.al., U.S. Pat. Appl. Publ., 187,(2019);Formula:C6H3D2F2NColor and Shape:NeatMolecular weight:131.121-Boc-2-[4-(2-pyridinyl)benzylidene]hydrazine
CAS:Controlled ProductImpurity Atazanavir Impurity B
Applications An intermediate for the preparation of antiviral protease inhibitors. Atazanavir Impurity B
References Fassler, A., et al.: J. Med. Chem., 39, 3203 (1996), Bold, G., et al.: J. Med. Chem., 41, 3387 (1998).Formula:C17H21N3O2Color and Shape:NeatMolecular weight:299.37(3S,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-yl Acetate
CAS:Controlled ProductApplications Darunavir intermediate.
References Ghosh, A., et al.: J. Med. Chem., 39, 3278 (1996), Ghosh, A., et al.: Bioorg. Med. Chem. Lett., 1998, 8, 687 (1998), Richman, D., et al.: Nature, 410, 995 (2001), Koh, Y., et al.: Antimicrob. Agents Chemother., 47, 3123 (2003),Formula:C8H12O4Color and Shape:NeatMolecular weight:172.18[(3R,3aS,6aR)-Hydroxyhexahydrofuro[2,3-b]furanyl Succinimidyl Carbonate
CAS:Controlled ProductApplications Darunavir intermediate.
References Ghosh, A., et al.: J. Med. Chem., 39, 3278 (1996), Ghosh, A., et al.: Bioorg. Med. Chem. Lett., 1998, 8, 687 (1998), Richman, D., et al.: Nature, 410, 995 (2001), Koh, Y., et al.: Antimicrob. Agents Chemother., 47, 3123 (2003),Formula:C11H13NO7Color and Shape:NeatMolecular weight:271.224-(2-Pyridinyl)benzaldehyde
CAS:Controlled ProductImpurity Atazanavir Impurity (Pyridinyl Benzaldehyde)
Applications Reactive metabolite of atazanavir. Atazanavir Impurity; Pyridinyl Benzaldehyde impurity
References F. Li et al., Drug Metabolism and Disposition 39, 294 (2011)Formula:C12H9NOColor and Shape:NeatMolecular weight:183.21(2'R)-2'-Deoxy-2'-fluoro-2'-methyl-uridine 5'-Triphosphate Triethylammonium Salt
CAS:Controlled ProductStability Hygroscopic
Applications (2'R)-2'-Deoxy-2'-fluoro-2'-methyl-uridine 5'-Triphosphate Tetrasodium Salt is an impurity of Sofosbuvir (P839640) which is a prodrug that is metabolized to the active antiviral agent 2'-deoxy-2'-α-fluoro-β-C-methyluridine-5'-monophosphate.
References Lam, A.M.,et al.: Antimicrob. Agents. Chemotherapy., 56, 3359 (2012); Lam, A.M., et al.: J. Virol., 85, 12334 (2011); Sofia, M.J., et al.: J. Medn. Chem., 53, 7202 (2010);Formula:C28H61FN5O14P3Color and Shape:Off White SolidMolecular weight:803.73Tenofovir-O-((R)-9-(2-Hydroxypropyl)adenine)-phosphate ester
CAS:Controlled ProductFormula:C17H23N10O4PColor and Shape:Off-WhiteMolecular weight:462.42-Fluoro-3-methoxyaniline
CAS:Controlled ProductApplications 2-Fluoro-3-methoxyaniline is a reagent that is used in the structure-activity relationship studies on a series of cyclopentane-containing macrocyclic inhibitors of hepatitis C virus NS3/4A protease leading to the discovery of TMC435350.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Raboisson, R., et al.: Bioorg. Med. Chem. Lett., 18, 4853 (2008)Formula:C7H8FNOColor and Shape:NeatMolecular weight:141.14α-Bromoacetosyringone
CAS:Controlled ProductFormula:C10H11BrO4Color and Shape:NeatMolecular weight:275.1Zanamivir Azide Methyl Ester
CAS:Controlled ProductApplications An intermediate used in the preparation of Zanamivir derivatives.
References Andrews, D., et al.: Eur. J. Med. Chem., 34, 563 (1999), Altamore, T., et al.: Bioorg. Med. Chem., 14, 1126 (2006),Formula:C12H18N4O7Color and Shape:NeatMolecular weight:330.29(S)-Methyl 3-(4,4-difluorocyclohexanecarboxamido)-3-phenylpropanoate
CAS:Controlled ProductFormula:C17H21F2NO3Color and Shape:NeatMolecular weight:325.355S-2-Amino-5-dibenzylamino-4-oxo-1,6-diphenylhex-2-ene
CAS:Controlled ProductApplications An intermediate in the synthesis of Ritonavir.
References Sham, H., et al.: Bioorg. Med. Chem. Lett., 12, 3101 (2002),Formula:C32H32N2OColor and Shape:NeatMolecular weight:460.61Ivermectin 8α-hydroperoxide
**Ivermectin 8α-hydroperoxide** is a derivative of the antiparasitic agent ivermectin, which is synthesized through chemical modification. Ivermectin originally derives from the fermentation products of the bacterium *Streptomyces avermitilis*. The modification to form 8α-hydroperoxide involves the addition of a hydroperoxide group, potentially altering its biological properties.Formula:C48H74O16Purity:Min. 95%Molecular weight:907.09 g/molBalapiravir
CAS:Balapiravir is an antiviral agent, which is a synthetic derivative based on natural compounds, specifically designed to inhibit the replication of various viral pathogens. The source of Balapiravir integrates bio-based elements with modifications to enhance its therapeutic efficacy.Formula:C21H30N6O8Purity:Min. 95%Molecular weight:494.5 g/molSofosbuvir - Bio-X ™
CAS:Sofosbuvir is an antiviral agent that is used for the treatment of hepatitis C infections and is used in combination with other antiviral agents. This drug is an inhibitor of viral RNA polymerase called non-structural protein 5B (NS5B). As a result, it inhibits viral RNA replication.
Formula:C22H29FN3O9PPurity:Min. 95%Color and Shape:PowderMolecular weight:529.45 g/molFaldaprevir
CAS:Hepatitis C virus protease inhibitorFormula:C40H49BrN6O9SPurity:Min. 95%Color and Shape:White PowderMolecular weight:869.82 g/molLobucavir
CAS:Lobucavir is an antiviral compound with a mode of action that inhibits viral DNA polymerase. It is used for treating infections caused by herpesviruses and hepatitis B virus.
Formula:C11H15N5O3Purity:Min. 95%Molecular weight:265.27 g/mol8-epiAtazanavir
CAS:8-epiAtazanavir is a stereoisomer of the antiretroviral drug Atazanavir, which is derived from synthetic sources. It acts as an HIV-1 protease inhibitor, where it binds to the active site of the viral protease enzyme, thereby preventing the cleavage of precursor proteins required for the maturation of infectious viral particles. This interference with viral replication is achieved by the structural mimicry of the natural substrate of the protease, allowing it to competitively inhibit the enzyme's activity.Formula:C38H52N6O7Purity:Min. 95%Molecular weight:704.38975Foscarnet sodium
CAS:Foscarnet sodium is a pyrophosphate analog antiviral agent with action on viral DNA polymerase and is used for treating cytomegalovirus and herpes simplex virus infections.
Formula:CNa3O5PPurity:Min. 95%Color and Shape:White PowderMolecular weight:191.95 g/molIndinavir monohydrate
CAS:Indinavir monohydrate is an antiretroviral medication, which is a synthetic pharmaceutical compound, specifically a protease inhibitor, used in the treatment of HIV infection. It is derived from chemical synthesis processes that follow rigorous standards to produce a pharmacologically active compound. Indinavir functions by selectively inhibiting the HIV-1 protease enzyme, which is crucial for the viral replication cycle. By binding to the active site of the enzyme, indinavir prevents the cleavage of viral polypeptides, leading to the production of immature and non-infectious viral particles.Purity:Min. 95%Darunavir-D9
CAS:Darunavir-D9 is a prodrug of darunavir, which is an HIV protease inhibitor. Darunavir-D9 has been shown to be bioequivalent in pharmacokinetic parameters to darunavir given as a tablet. The drug exhibits a low plasma concentration profile and high clearance values. This may be due to rapid absorption and distribution of the drug, with a short elimination half-life. Darunavir-D9 also has little effect on the matrix effect and reproducibility of the reaction monitoring assay, making it an ideal candidate for use in clinical trials.Formula:C27H28D9N3O7SPurity:Min. 95%Molecular weight:556.72 g/molVicriviroc
CAS:Vicriviroc is an investigational pharmaceutical compound, specifically classified as an HIV entry inhibitor. It originates from a synthetic source, designed to target the CCR5 co-receptor on human immune cells. The mode of action involves blocking this co-receptor, thereby preventing the HIV virus from binding and fusing with the host cell membrane. This inhibition effectively obstructs the virus's ability to enter and infect the host cells, particularly those within the chemokine receptor family.
Formula:C28H38F3N5O2Purity:Min. 95%Molecular weight:533.63 g/molViramidine hydrochloride
CAS:Viramidine hydrochloride is an antiviral prodrug with action as a precursor to ribavirin, targeting viral RNA synthesis and is used for research on hepatitis C and other viral infections.Formula:C8H14ClN5O4Purity:Min. 95%Molecular weight:279.68 g/molVicriviroc malate
CAS:Vicriviroc malate is a CCR5 antagonist with action on blocking HIV entry into cells by targeting the CCR5 receptor and is used for research on HIV treatment.Formula:C28H38F3N5O2•C4H6O5Purity:Area-% Min. 90 Area-%Color and Shape:PowderMolecular weight:667.72 g/molPeramivir
CAS:Selective and potent inhibitor of sialidases (neuraminidases) in influenza A and B viruses. The compound binds tightly to the viral neuraminidase active site in late stages of viral life-cycle. It inhibits shedding sialic acids from host cell surface glycans, which interact with viral hemagglutinin, and consequently prevents release of new viral particles from the host cell surface.
Formula:C15H28N4O4Purity:Min. 95%Color and Shape:PowderMolecular weight:328.41 g/molGalidesivir dihydrochloride
CAS:Galidesivir dihydrochloride is an investigational antiviral drug, which is a synthetic nucleoside analogue with broad-spectrum activity. It is derived from a modified adenosine analog structure, targeting viral RNA-dependent RNA polymerases. Galidesivir functions through the incorporation into viral RNA, leading to premature termination of RNA synthesis, effectively inhibiting viral replication. This mechanism aligns with its utility in combating various RNA viruses.Formula:C11H15N5O3•(HCl)2Purity:Min. 95%Molecular weight:338.19 g/molBCX 4430 hydrochloride
CAS:RNA polymerase (RdRp) inhibitor
Formula:C11H15N5O3Purity:Min. 95%Molecular weight:265.27 g/molZiresovir
CAS:Respiratory syncytial virus (RSV) fusion (F) protein inhibitorFormula:C22H25N5O3SPurity:Min. 95%Color and Shape:PowderMolecular weight:439.53 g/molBET-BAY 002
CAS:BET-BAY 002 is an effective BET bromodomain inhibitor demonstrating efficacy in vivo and in vitro against multiple myeloma and leukaemia models.Formula:C22H18ClN5OColor and Shape:SolidMolecular weight:403.86UC-781
CAS:UC-781, a potent NNRTI, inhibits HIV-1 with a C50 of 5 nM and is stable across pH and temperatures.Formula:C17H18ClNO2SPurity:92.17%Color and Shape:SolidMolecular weight:335.85SARS-CoV-2 nsp13-IN-1
CAS:SARS-CoV-2 nsp13-IN-1 (C1) inhibits nsp13 ssDNA+ATPase (IC50: 6 μM), not ssDNA-ATPase; useful for COVID-19 research.
Formula:C27H20N4O2Purity:99.44%Color and Shape:SolidMolecular weight:432.47AMC-01
CAS:AMC-01 has potential antiviral activity and induces dose- and time-dependent inactivation of eIF2-α via phosphorylation of serine residue 51.Formula:C27H27BrN2O6Purity:99.95%Color and Shape:SolidMolecular weight:555.42WIN 54954
CAS:WIN 54954 is an orally available antiviral agent that inhibits Coxsackievirus and may be used in the study of small ribonucleic acid virus infections.Formula:C18H20Cl2N2O3Purity:98.98%Color and Shape:SolidMolecular weight:383.27Ref: TM-T61652
1mg49.00€5mg101.00€10mg165.00€25mg289.00€50mg465.00€100mg745.00€1mL*10mM (DMSO)113.00€HDAC3-IN-T247
CAS:HDAC3-IN-T247 (HDAC3 inhibitor T247) is a histone deacetylase 3 (HDAC3) inhibitor with antiviral activity that inhibits the proliferation of cancer cells.Formula:C21H19N5OSPurity:98.11% - 98.94%Color and Shape:SolidMolecular weight:389.47Ref: TM-T24131
1mg87.00€5mg178.00€10mg295.00€25mg610.00€50mg867.00€100mg1,153.00€1mL*10mM (DMSO)203.00€IND24
CAS:IND24 has anti-prion activity and can be used to study neurodegenerative diseases.Formula:C21H17N3SPurity:99.8%Color and Shape:SolidMolecular weight:343.44(R,1R)-Tenofovir amibufenamide
CAS:(R,1R)-Tenofovir amibufenamide ((R,1R)-HS-10234) can be used as a Tenofovir prodrug, which can be taken orally and has antiviral activity.Formula:C22H31N6O5PPurity:98.79% - 99.02%Color and Shape:SolidMolecular weight:490.49Ref: TM-T63290
1mg58.00€5mg133.00€10mg190.00€25mg328.00€50mg442.00€100mg598.00€200mg792.00€1mL*10mM (DMSO)145.00€Tenofovir exalidex
CAS:Tenofovir exalidex (CMX 157) is a lipid-conjugated acyclic nucleotide analog of Tenofovir, demonstrating efficacy against wild-type and antiretroviral-resistantFormula:C28H52N5O5PPurity:99.83%Color and Shape:SolidMolecular weight:569.72DDX3-IN-2
CAS:DDX3-IN-2 is a potent DDX3 inhibitor with an IC50 of 0.3 μM and shows broad antiviral effects, including against HIV resistance.Formula:C20H23N5OColor and Shape:SolidMolecular weight:349.43Paritaprevir
CAS:Paritaprevir is an antiviral medication, which is derived from chemical synthesis with its action targeting the hepatitis C virus (HCV). It operates primarily as a protease inhibitor, specifically targeting the NS3/4A protease, an essential enzyme for HCV replication. By inhibiting this protease, Paritaprevir effectively disrupts the viral life cycle, preventing the virus from maturing and proliferating within the host cells.Purity:Min. 95%CMP-5
CAS:CMP-5 is a PRMT5 inhibitor with antiviral activity, inhibits PRMT5 methyltransferase activity, and can be used in the study of SARS virus infection.Formula:C21H21N3Purity:98.68%Color and Shape:SolidMolecular weight:315.41Ref: TM-T10850
1mg44.00€5mg92.00€10mg137.00€25mg225.00€50mg334.00€100mg494.00€500mg1,054.00€1mL*10mM (DMSO)101.00€YM-53403
CAS:YM-53403: Antiviral that combats both RSV subgroup A/B, treats respiratory infections.
Formula:C36H29N3O3SPurity:98.49% - 98.85%Color and Shape:SolidMolecular weight:583.7R 61837
CAS:R 61837 is a novel rhinovirus inhibitor, a substituted phenylpyridazinamine, with antiviral activity.Formula:C16H20N4OPurity:99.53%Color and Shape:SolidMolecular weight:284.36Alamifovir
CAS:Alamifovir is an antiviral agent, which is synthetically derived. The mode of action of Alamifovir involves the inhibition of viral replication within host cells by targeting specific viral enzymes crucial for the replication process. This interference with the viral life cycle diminishes the ability of the virus to propagate and spread within the host organism.Formula:C19H20F6N5O5PSPurity:Min. 95%Molecular weight:575.42 g/molIQP-0528
CAS:IQP-0528: Potent NNRTI, blocks HIV entry, microbicidal gel, EC50: 0.2 nM for HIV-1, 100 nM for HIV-2.Formula:C20H24N2O3Purity:98.29% - 98.53%Color and Shape:SolidMolecular weight:340.42Ref: TM-T27625
1mg50.00€5mg105.00€10mg156.00€25mg254.00€50mg351.00€100mg465.00€200mg625.00€1mL*10mM (DMSO)109.00€ABI-1968
CAS:ABI-1968 has antiviral and antitumor activity and can be used to study immune system diseases.Formula:C35H58N5O6PPurity:98.54%Color and Shape:SolidMolecular weight:675.839Epetirimod
CAS:Epetirimod (S-30563) is a small molecule immunomodulator with antitumor and anti-infective activity for the study of papillomavirus infections.
Formula:C13H15N5Purity:99.08% - 99.53%Color and Shape:SolidMolecular weight:241.29DDG-39
CAS:DDG-39 (1-(2,3-dideoxy-2-fluoropentofuranosyl)cytosine) possesses antiviral activity with potent and selective anti-HIV-1 and HBV activity in cell culture.Formula:C9H12FN3O3Purity:99.17% - >99.99%Color and Shape:SolidMolecular weight:229.21Ref: TM-T67797
1mg180.00€5mg447.00€10mg655.00€25mg1,026.00€50mg1,388.00€100mg1,863.00€1mL*10mM (DMSO)401.00€Rociclovir
CAS:Rociclovir has antiviral activity and is used to treat viral infections.
Formula:C15H25N5O3Purity:99.19%Color and Shape:SolidMolecular weight:323.39BIT225
CAS:BIT225 is an HIV-1 Vpu inhibitor with antiviral activity that inhibits HIV-1 replication in myeloid dendritic cells.Formula:C16H15N5OPurity:98.8%Color and Shape:SolidMolecular weight:293.32



