Antivirales
Los antivirales son compuestos específicamente diseñados para inhibir la replicación y la propagación de virus, desempeñando un papel crítico en el tratamiento y la prevención de infecciones virales. En esta categoría, encontrará una selección completa de agentes antivirales destinados exclusivamente a fines de investigación en laboratorio. Estos productos son esenciales para estudiar los mecanismos virales, desarrollar nuevas terapias antivirales y comprender los patrones de resistencia. Los investigadores pueden utilizar estos antivirales para investigar la eficacia y la seguridad de tratamientos potenciales, contribuyendo al avance de la ciencia médica y al desarrollo de medicamentos antivirales innovadores. La disponibilidad de diversos agentes antivirales respalda la investigación de vanguardia en virología y mejora nuestra capacidad para combatir las enfermedades virales.
Se han encontrado 764 productos de "Antivirales"
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Zanamivir Azide Methyl Ester
CAS:Producto controlado<p>Applications An intermediate used in the preparation of Zanamivir derivatives.<br>References Andrews, D., et al.: Eur. J. Med. Chem., 34, 563 (1999), Altamore, T., et al.: Bioorg. Med. Chem., 14, 1126 (2006),<br></p>Fórmula:C12H18N4O7Forma y color:NeatPeso molecular:330.29Nelfinavir Sulfone
CAS:Producto controlado<p>Impurity Nelfinavir Sulphone Impurity<br>Applications Nelfinavir Sulfone is an impurity of Nelfinavir Mesylate (N389750). It is a COVID19-related research product.<br>References Aymard, G., et al.: J. Chromatogr. B, 744, 227 (2000), Jing, Q., et al.: J. Pharm. Biomed. Anal., 41, 1065 (2006),<br></p>Fórmula:C32H45N3O6SForma y color:NeatPeso molecular:599.785S-2-Amino-5-dibenzylamino-4-oxo-1,6-diphenylhex-2-ene
CAS:Producto controlado<p>Applications An intermediate in the synthesis of Ritonavir.<br>References Sham, H., et al.: Bioorg. Med. Chem. Lett., 12, 3101 (2002),<br></p>Fórmula:C32H32N2OForma y color:NeatPeso molecular:460.61Tenofovir-O-((R)-9-(2-Hydroxypropyl)adenine)-phosphate ester
CAS:Producto controladoFórmula:C17H23N10O4PForma y color:Off-WhitePeso molecular:462.43,4-Difluoroaniline-2,6-d2
CAS:Producto controlado<p>Applications 3,4-Difluoroaniline-2,6-d2 (CAS# 1061566-62-8) can be used in its derivative form as an antiviral agent for Hepatitis B.<br>References Qiu, Y.L., et.al., U.S. Pat. Appl. Publ., 187,(2019);<br></p>Fórmula:C6H3D2F2NForma y color:NeatPeso molecular:131.125,6,7,8-Tetrahydro-1-naphthalenol
CAS:Producto controlado<p>Applications 5,6,7,8-Tetrahydro-1-naphthalenol was used as a reagent in the synthesis of phosphonamidate and phosphonodiamidate prodrugs of adefovir and tenofovir which are used in the treatment of HIV infections. Also used in the synthesis of tetrahydronaphthalene-1-ol derivatives which were found to be promising potent antitumor agents.<br>References Pertusati, F., et al.: Eur. J. Med. Chem., 78, 259 (2014); Dong, Y., et al.: Bioorg. Med. Chem. Lett., 19, 6289 (2009);<br></p>Fórmula:C10H12OForma y color:NeatPeso molecular:148.2(2'R)-2'-Deoxy-2'-fluoro-2'-methyl-uridine 5'-Triphosphate Triethylammonium Salt
CAS:Producto controlado<p>Stability Hygroscopic<br>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.<br>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);<br></p>Fórmula:C28H61FN5O14P3Forma y color:Off White SolidPeso molecular:803.73Tromantadine hydrochloride
CAS:Producto controlado<p>Tromantadine hydrochloride is a synthetic antiviral compound, which is a derivative of adamantane. It originates from chemical synthesis, tailored specifically to target viral processes. Tromantadine hydrochloride primarily exerts its effects by inhibiting the penetration of virus particles into host cells and impeding the subsequent stages of viral replication. This mode of action effectively reduces the viral load and hinders the progression of the infection.</p>Fórmula:C16H28N2O2•HClPureza:Min. 95%Peso molecular:316.87 g/molFaldaprevir
CAS:Hepatitis C virus protease inhibitorFórmula:C40H49BrN6O9SPureza:Min. 95%Forma y color:White PowderPeso molecular:869.82 g/molPeramivir
CAS:<p>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.</p>Fórmula:C15H28N4O4Pureza:Min. 95%Forma y color:PowderPeso molecular:328.41 g/molVicriviroc
CAS:<p>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.</p>Fórmula:C28H38F3N5O2Pureza:Min. 95%Peso molecular:533.63 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.Pureza:Min. 95%Viramidine hydrochloride
CAS:<p>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.</p>Fórmula:C8H14ClN5O4Pureza:Min. 95%Peso molecular:279.68 g/molDarunavir-D9
CAS:<p>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.</p>Fórmula:C27H28D9N3O7SPureza:Min. 95%Peso molecular:556.72 g/mol8-epiAtazanavir
CAS:<p>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.</p>Fórmula:C38H52N6O7Pureza:Min. 95%Peso molecular:704.38975Ziresovir
CAS:<p>Respiratory syncytial virus (RSV) fusion (F) protein inhibitor</p>Fórmula:C22H25N5O3SPureza:Min. 95%Forma y color:PowderPeso molecular:439.53 g/molSofosbuvir - Bio-X ™
CAS:<p>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.</p>Fórmula:C22H29FN3O9PPureza:Min. 95%Forma y color:PowderPeso molecular:529.45 g/molCarbovir triphosphate triethylamine
CAS:<p>Carbovir triphosphate triethylamine is a nucleotide analog, which is a derivative of nucleoside analogs designed for antiviral applications. It is synthesized through chemical modification of guanosine analogs, resulting in its active triphosphate form. This compound functions as a potent antiretroviral agent by mimicking natural nucleotides and interfering with viral DNA synthesis. The active triphosphate impedes the action of viral reverse transcriptase by incorporating itself into the viral DNA chain, causing premature termination and effectively halting viral replication.</p>Pureza:Min. 95%SE 563
CAS:<p>SE 563 is a biocontrol agent, which is an organism-based product derived from natural sources. It is sourced from a specific strain of entomopathogenic nematodes known for their effectiveness in targeting and controlling insect pests. The mode of action involves the nematodes seeking out their insect hosts in the soil, entering through natural openings, and releasing symbiotic bacteria that kill the host from within.</p>Fórmula:C22H17ClF3NO3Pureza:Min. 95%Peso molecular:435.08491
