Antiviraux
Les antiviraux sont des composés spécifiquement conçus pour inhiber la réplication et la propagation des virus, jouant un rôle crucial dans le traitement et la prévention des infections virales. Dans cette catégorie, vous trouverez une sélection complète d'agents antiviraux destinés uniquement à des fins de recherche en laboratoire. Ces produits sont essentiels pour étudier les mécanismes viraux, développer de nouvelles thérapies antivirales et comprendre les schémas de résistance. Les chercheurs peuvent utiliser ces antiviraux pour évaluer l'efficacité et la sécurité des traitements potentiels, contribuant ainsi à l'avancement de la science médicale et au développement de médicaments antiviraux innovants. La disponibilité de divers agents antiviraux soutient la recherche de pointe en virologie et améliore notre capacité à combattre les maladies virales.
765 produits trouvés pour "Antiviraux"
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Doravirine
CAS :<p>Non-nucleoside inhibitor of reverse transcriptase; anti-viral</p>Formule :C17H11ClF3N5O3Degré de pureté :Min. 97 Area-%Couleur et forme :White PowderMasse moléculaire :425.75 g/molAtazanavir - Bio-X ™
CAS :<p>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.</p>Formule :C38H52N6O7Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :704.86 g/molCidofovir anhydrous - Bio-X ™
CAS :<p>Cidofovir is an anti-viral agent that is used to treat Cytomegalovirus (CMV) retinitis in patients with AIDS. This drug suppresses CMV replication by inhibiting viral DNA synthesis.</p>Formule :C8H14N3O6PDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :279.19 g/molEIDD-1931
CAS :<p>Nucleoside analog with antiviral activity against coronaviruses, hepatitis and influenzas viruses. EIDD 1931 inhibited the Middle East Respiratory Syndrome coronavirus (MERS-CoV) and the murine hepatitis virus (MHV) replication in vitro at submicromolar concentrations. EIDD 1931 is able to evade the proofreading exonuclease ExoN and presents with high barrier to development of drug resistance.</p>Formule :C9H13N3O6Degré de pureté :Min. 98 Area-%Couleur et forme :White Off-White PowderMasse moléculaire :259.22 g/molSaquinavir mesylate
CAS :Anti-viral; HIV protease inhibitorFormule :C38H50N6O5•CH4O3SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :766.95 g/molLersivirine
CAS :Anti-viral; non-nucleoside reverse transcriptase inhibitorFormule :C17H18N4O2Degré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :310.14298Rupintrivir
CAS :<p>Rupintrivir is a peptidomimetic antiviral with action on rhinovirus 3C protease to inhibit viral replication and is used for research on rhinovirus and other viral infections.</p>Formule :C31H39FN4O7Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :598.28028Raltegravir - Bio-X ™
CAS :<p>Raltegravir is an antiretroviral agent used for the treatment of HIV infections in conjunction with other antiretrovirals. It inhibits the activity of HIV-1 integrase, which impedes the insertion of HIV-1 DNA into the host cell genome. Raltegravir also inhibits resistant mutants of HIV-1 that are associated with disease activity and progression.</p>Formule :C20H21FN6O5Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :444.42 g/molEntecavir hydrate
CAS :<p>Nucleoside reverse transcriptase inhibitor; anti-Hepatitis B virus</p>Formule :C12H15N5O3·xH2ODegré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :277.28 g/molGS 441524
CAS :<p>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.</p>Formule :C12H13N5O4Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :291.26 g/molGS 331007
CAS :<p>Anti-viral; RNA polymerase inhibitor; sofosbuvir metabolite</p>Formule :C10H13FN2O5Degré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :260.22 g/molSofosbuvir
CAS :Potent inhibitor of viral RNA polymerase called non-structural protein 5B (NS5B). This nucleotide analog is effective against Hepatitis C virus (HCV) infection since it inhibits viral RNA replication. Sofosbuvir is a prodrug and gets triphosphorylated in the liver cells, generating biologically active compound with anti-viral activity.Formule :C22H29FN3O9PDegré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :529.45 g/molZalcitabine - Bio-X ™
CAS :<p>Zalcitabine (also known as dideoxycytidine or ddC) is a nucleoside analogue reverse transcriptase inhibitor (NRTI) medication used in the treatment of human immunodeficiency virus (HIV) infections. It works by blocking reverse transcriptase, an enzyme essential for replication of the HIV virus, thereby preventing the virus from multiplying and spreading. Zalcitabine is often used in combination with other antiretroviral drugs to effectively treat HIV/AIDS.</p>Formule :C9H13N3O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :211.22 g/molAtazanavir sulfate
CAS :<p>Anti-viral; HIV protease inhibitor</p>Formule :C38H52N6O7·H2SO4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :802.94 g/molDarunavir ethanolate- Bio-X ™
CAS :<p>Darunavir is an HIV protease inhibitor that is used in the treatment of HIV-1 infection. This drug inhibits HIV-1 protease from binding and catalyzing by attaching to the enzyme and preventing HIV replication.</p>Formule :C27H37N3O7S·C2H6ODegré de pureté :Min. 99 Area-%Couleur et forme :PowderMasse moléculaire :593.73 g/molOmbitasvir
CAS :<p>Ombitasvir is a NS5A inhibitor antiviral agent with action on hepatitis C virus replication and is used for treating chronic hepatitis C in combination therapies.</p>Formule :C50H67N7O8Degré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :894.1 g/molOseltamivir
CAS :<p>Inhibitor of viral neuraminidase enzyme, effective against influenza A and B viruses. This antiviral compound inhibits neuraminidase-mediated cleavage of host cell sialic acids, which interact with newly synthesised virions from the host cell. This prevents virion budding from the host, resulting in inhibition of virion release and viral infection overall.</p>Formule :C16H28N2O4Degré de pureté :Min. 95 Area-%Couleur et forme :PowderMasse moléculaire :312.4 g/molLedipasvir D-tartrate
CAS :<p>Ledipasvir D-tartrate is an antiviral compound, which is a direct-acting antiviral agent used in the treatment of hepatitis C virus (HCV) infection. It originates from synthetic sources designed to inhibit the replication of specific viral proteins. Ledipasvir functions by targeting the NS5A protein of the hepatitis C virus, a key component necessary for viral replication. By binding to this protein, Ledipasvir disrupts and inhibits the HCV replication complex, effectively suppressing the viral load in patients.</p>Formule :C53H60F2N8O12Degré de pureté :Min. 95%Masse moléculaire :1,039.1 g/molLedipasvir
CAS :Anti-viral; inhibitor of NS5A proteinFormule :C49H54F2N8O6Degré de pureté :Min. 98 Area-%Couleur et forme :Off-White PowderMasse moléculaire :889.00 g/molLetermovir
CAS :<p>Anti-viral; inhibitor of cytomegalovirus-terminase complex</p>Formule :C29H28F4N4O4Degré de pureté :Min. 98 Area-%Couleur et forme :Yellow PowderMasse moléculaire :572.55 g/mol
