
Antivirals
Found 767 products of "Antivirals"
Indinavir sulfate
CAS:Anti-viral; HIV-1 protease inhibitorFormula:C36H47N5O4•H2O4SPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:711.87 g/molBMS 806 - Bio-X ™
CAS:BMS 806 is used as an anti-viral agent. It has been shown to inhibit the replication of HIV. BMS 806 inhibits viral life by binding to the surface glycoproteins and inhibiting viral entry into cells. The drug also inhibits viral replication by preventing DNA transcription and translation.Formula:C22H22N4O4Purity:Min. 95%Color and Shape:PowderMolecular weight:406.43 g/molLedipasvir
CAS:Anti-viral; inhibitor of NS5A proteinFormula:C49H54F2N8O6Purity:Min. 98 Area-%Color and Shape:Off-White PowderMolecular weight:889.00 g/molLetermovir
CAS:Anti-viral; inhibitor of cytomegalovirus-terminase complex
Formula:C29H28F4N4O4Purity:Min. 98 Area-%Color and Shape:Yellow PowderMolecular weight:572.55 g/molElvitegravir
CAS:HIV-1 integrase inhibitor; inhibits DNA strand transferFormula:C23H23ClFNO5Purity:Min. 95%Color and Shape:PowderMolecular weight:477.88 g/molN-Boc-protected -Guanidino Oseltamivir
CAS:N-Boc-protected -Guanidino Oseltamivir is a fine chemical that belongs to the group of versatile building blocks. It is a complex compound that has been used in research as a reagent and speciality chemical. N-Boc-protected -Guanidino Oseltamivir is an important intermediate for the synthesis of a variety of useful compounds, such as pharmaceuticals and natural products. This compound is also used as a reaction component in organic syntheses, especially for the preparation of high quality and useful scaffolds.
Formula:C26H44N4O8Purity:Min. 95%Color and Shape:PowderMolecular weight:540.31591Tenofovir diphosphate triethylamine(mixture of diastereomers)
CAS:Tenofovir diphosphate triethylamine (mixture of diastereomers) is an antiviral compound, which is a synthetic chemical product derived from the parent compound, tenofovir. This formulation includes a mixture of diastereomers to enhance its solubility and bioavailability. The compound primarily functions as a nucleotide reverse transcriptase inhibitor (NRTI). It targets viral reverse transcriptase enzymes, inhibiting DNA synthesis and subsequent viral replication by causing premature chain termination.Formula:C9H16N5O10P3•(C6H15N)xPurity:Min. 95%2',3'-Dideoxy-5-fluoro-3'-thiacytidine
CAS:Emtricitabine is a nucleoside analog that is an antiviral drug used to treat HIV/AIDS. It is a synthetic nucleoside analog of cytidine, in which the 3' phosphate and 5' hydroxyl groups have been replaced with a fluorine atom and a methoxy group, respectively. Emtricitabine has been shown to inhibit the synthesis of viral DNA by competing for incorporation into the viral DNA strand during the elongation phase of viral replication. Emtricitabine also has anticancer activity, but no other known therapeutic uses.Formula:C8H10FN3O3SPurity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:247.25 g/molDoravirine
CAS:Non-nucleoside inhibitor of reverse transcriptase; anti-viral
Formula:C17H11ClF3N5O3Purity:Min. 97 Area-%Color and Shape:White PowderMolecular weight:425.75 g/molRaltegravir potassium - Bio-X ™
CAS:Raltegravir is an antiretroviral agent that is used for the treatment of HIV infections. It inhibits HIV integrase in order to prevent viral genome from being inserted into the human genome. It binds to the active site of the enzyme and prevents it from binding to a target sequence on the viral DNA. This drug is metabolized by glucuronidation.Formula:C20H21FN6O5•KPurity:Min. 95%Color and Shape:PowderMolecular weight:483.51 g/molLamivudine - Bio-X ™
CAS:Lamivudine (commonly called 3TC) is a potent nucleoside analogue reverse transcriptase inhibitor. It is one of the front line treatments for HIV. It is an analogue of cytidine, and can inhibit both types (1 and 2) of HIV reverse transcriptase as well as the reverse transcriptase of hepatitis B. It needs to be phosphorylated to its triphosphate form before it is active.Formula:C8H11N3O3SPurity:Min. 95%Molecular weight:229.26 g/molFosamprenavir calcium
Fosamprenavir calcium is an antiretroviral medication, which is derived from the prodrug of amprenavir. It is synthesized through chemical processes to enhance oral bioavailability and improve pharmacokinetic properties. Through its mode of action, fosamprenavir is converted in vivo to amprenavir, which acts as an inhibitor of the HIV-1 protease enzyme. By inhibiting this enzyme, it prevents the cleavage of the Gag-Pol polyprotein, disrupting viral replication and processing, ultimately leading to the production of immature, non-infectious viral particles.Formula:C25H34CaN3O9PSPurity:Min. 95%Molecular weight:623.67 g/molSaquinavir mesylate - Bio-X ™
CAS:Saquinavir is a HIV protease inhibitor drug that is used with other antiretroviral drugs for the treatment of HIV-1. As this drug prevents HIV protease activity, it prevents the proteolysis of the Gag polyprotein and thus results in non-infectious virus particles.
Formula:C38H50N6O5•CH4O3SPurity:Min. 95%Color and Shape:PowderMolecular weight:766.95 g/molRilpivirine
CAS:Anti-viral; non-nucleoside reverse transcriptase inhibitorFormula:C22H18N6Purity:Min. 95%Color and Shape:PowderMolecular weight:366.42 g/molDarunavir
CAS:Darunavir is a HIV-1 protease inhibitor used orally in the treatment of patients with multi-drug resistant HIV-1 infection (Ghosh, 2007). It has also been shown to be effective against other infectious diseases such as hepatitis C virus and SARS coronavirus. Metabolized by cytochrome P450 3A (CYP3A) isoenzymes, darunavir is often administered together with ritonavir that prolongs its bioavaiability, giving a terminal elimination half-life (t1/2) of 15 hours (Back, 2008). The effect of darunavir on natural compounds such as matrix proteins and toll-like receptor activity has also been studied via high performance liquid chromatography (HPLC) experiments.
Formula:C27H37N3O7SPurity:Min. 95%Color and Shape:White PowderMolecular weight:547.66 g/molBaloxavir marboxil
CAS:Baloxavir marboxil is a selective inhibitor of the cap-dependent endonuclease of RNA polymerase, an acidic protein in influenza A and B viruses. In patients, baloxavir marboxil reduces the time to recovery by alleviating the symptoms of the influenza A and B infection, in both adults and children.Formula:C27H23F2N3O7SPurity:Min. 95%Color and Shape:PowderMolecular weight:571.55 g/molAtazanavir - Bio-X ™
CAS:Atazanavir is an antiviral protease inhibitor, used in the anti-retroviral therapy of adult and sometimes paediatric patients infected with HIV. This drug inhibits the processing of viral Gag and Gag-pol polyproteins in HIV-1 infected cells by binding to the HIV-1 protease active site.
Formula:C38H52N6O7Purity:Min. 95%Color and Shape:PowderMolecular weight:704.86 g/molTenofovir - Bio-X ™
CAS:Tenofovir is an acyclic nucleoside phosphonate that exhibits anti-viral properties through its inhibition of reverse transcriptases. In particular, Tenofovir is a potent inhibitor of Human Immunodeficiency Virus (HIV) and chronic Hepatitis B Virus (HBV) reverse transcriptases, thus preventing the replication of genetic viral material. This property is beneficial in virus research areas and developing antiviral treatments. Once inside the body tenofovir is metabolized into its active form, tenofovir diphosphate, by the lysosomal protease cathepsin A, nucleotide kinases and adenylate kinases.
Tenofovir is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready to use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.Formula:C9H14N5O4PPurity:Min. 98.5 Area-%Color and Shape:White To Off-White SolidMolecular weight:287.21 g/molGS 441524
CAS:Nucleoside analog with antiviral activity against zoonotic feline infectious peritonitis virus (FIPV) and severe acute respiratory syndrome (SARS) virus from Coronaviridae family. The compound is a pro-drug and undergoes intracellular phosphorylation resulting in the active triphosphate metabolite. The triphosphorylated GS 441524 analog competes with natural nucleoside triphosphates and interferes with viral RNA synthesis. In previous studies it was tested in vitro as well as in experimental animals and showed good safety profile.Formula:C12H13N5O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:291.26 g/molSaquinavir mesylate
CAS:Anti-viral; HIV protease inhibitorFormula:C38H50N6O5•CH4O3SPurity:Min. 95%Color and Shape:PowderMolecular weight:766.95 g/mol
