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 765 productos de "Antivirales"
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Doravirine
CAS:<p>Non-nucleoside inhibitor of reverse transcriptase; anti-viral</p>Fórmula:C17H11ClF3N5O3Pureza:Min. 97 Area-%Forma y color:White PowderPeso molecular: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>Fórmula:C38H52N6O7Pureza:Min. 95%Forma y color:PowderPeso molecular: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>Fórmula:C8H14N3O6PPureza:Min. 95%Forma y color:PowderPeso molecular: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>Fórmula:C9H13N3O6Pureza:Min. 98 Area-%Forma y color:White Off-White PowderPeso molecular:259.22 g/molSaquinavir mesylate
CAS:Anti-viral; HIV protease inhibitorFórmula:C38H50N6O5•CH4O3SPureza:Min. 95%Forma y color:PowderPeso molecular:766.95 g/molLersivirine
CAS:<p>Anti-viral; non-nucleoside reverse transcriptase inhibitor</p>Fórmula:C17H18N4O2Pureza:Min. 95%Forma y color:SolidPeso molecular: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>Fórmula:C31H39FN4O7Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:598.28028Entecavir hydrate
CAS:<p>Nucleoside reverse transcriptase inhibitor; anti-Hepatitis B virus</p>Fórmula:C12H15N5O3·xH2OPureza:Min. 98 Area-%Forma y color:White PowderPeso molecular: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>Fórmula:C12H13N5O4Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:291.26 g/molGS 331007
CAS:<p>Anti-viral; RNA polymerase inhibitor; sofosbuvir metabolite</p>Fórmula:C10H13FN2O5Pureza:Min. 95%Forma y color:Off-White PowderPeso molecular: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.Fórmula:C22H29FN3O9PPureza:Min. 95%Forma y color:Off-White PowderPeso molecular: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>Fórmula:C9H13N3O3Pureza:Min. 95%Forma y color:PowderPeso molecular:211.22 g/molAtazanavir sulfate
CAS:<p>Anti-viral; HIV protease inhibitor</p>Fórmula:C38H52N6O7·H2SO4Pureza:Min. 95%Forma y color:PowderPeso molecular:802.94 g/molRaltegravir - 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>Fórmula:C20H21FN6O5Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:444.42 g/mol6-Fluoro-3-hydroxypyrazine-2-carboxamide
CAS:6-Fluoro-3-hydroxypyrazine-2-carboxamide is a potent RNA polymerase inhibitor, active against both RNA viruses in vitro and in vivo. A four-step approach to the synthesis of 6-Fluoro-3-hydroxypyrazine-2-carboxamide was reported in 2014. 6-Fluoro-3-hydroxypyrazine-2-carboxamide is commercialized and has recently been suggested for the treatment of mild cases of COVID-19.Fórmula:C5H4FN3O2Pureza:Min. 97 Area-%Forma y color:PowderPeso molecular:157.1 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>Fórmula:C16H28N2O4Pureza:Min. 95 Area-%Forma y color:PowderPeso molecular: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>Fórmula:C53H60F2N8O12Pureza:Min. 95%Peso molecular:1,039.1 g/molLedipasvir
CAS:Anti-viral; inhibitor of NS5A proteinFórmula:C49H54F2N8O6Pureza:Min. 98 Area-%Forma y color:Off-White PowderPeso molecular:889.00 g/molLetermovir
CAS:<p>Anti-viral; inhibitor of cytomegalovirus-terminase complex</p>Fórmula:C29H28F4N4O4Pureza:Min. 98 Area-%Forma y color:Yellow PowderPeso molecular:572.55 g/molN-Boc-protected -Guanidino Oseltamivir
CAS:<p>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.</p>Fórmula:C26H44N4O8Pureza:Min. 95%Forma y color:PowderPeso molecular:540.31591
