Antivíricos
Os antivirais são compostos especificamente projetados para inibir a replicação e a propagação de vírus, desempenhando um papel crítico no tratamento e na prevenção de infecções virais. Nesta categoria, você encontrará uma seleção abrangente de agentes antivirais destinados exclusivamente a fins de pesquisa laboratorial. Esses produtos são essenciais para estudar os mecanismos virais, desenvolver novas terapias antivirais e compreender os padrões de resistência. Pesquisadores podem utilizar esses antivirais para investigar a eficácia e a segurança de tratamentos potenciais, contribuindo para o avanço da ciência médica e o desenvolvimento de medicamentos antivirais inovadores. A disponibilidade de diversos agentes antivirais apoia a pesquisa de ponta em virologia e aprimora nossa capacidade de combater doenças virais.
Foram encontrados 764 produtos de "Antivíricos"
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Ganciclovir - Bio-X ™
CAS:<p>Ganciclovir is an acyclovir analog that is used in the treatment of cytomegalovirus and herpetic keratitis of the eye. This drug is a DNA polymerase inhibitor and exhibits its anti-viral properties by inhibiting viral replication.</p>Fórmula:C9H13N5O4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:255.23 g/molPS 3061
CAS:<p>PS 3061 is a type of biostimulant, which is derived from activated charcoal. Activated charcoal serves as the source of this biostimulant, providing a unique substrate that interacts with soil and plant roots. Its mode of action involves enhancing nutrient uptake and improving soil microbial activity, thereby facilitating better plant growth and development.</p>Fórmula:C53H75BrN8O8Pureza:Min. 95%Peso molecular:1,032.12 g/molCytarabine hydrochloride - Bio-X ™
CAS:Cytarabine is a pyrimidine nucleoside analogue that is used to treat leukaemia especially, non-lymphocytic leukaemia. This drug also has anti-viral and immunosuppressant properties. Cytarabine is cytotoxic and acts through direct DNA damage. Although its mechanism of action is not fully understood, it is said to inhibit DNA polymerase.Fórmula:C9H13N3O5•HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:279.68 g/molNevirapine
CAS:<p>Nevirapine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) with action on HIV reverse transcriptase to block viral replication and is used for treating HIV/AIDS in combination therapies.</p>Fórmula:C15H14N4OPureza:Min. 95%Cor e Forma:White PowderPeso molecular:266.3 g/molIndinavir sulfate
CAS:<p>Anti-viral; HIV-1 protease inhibitor</p>Fórmula:C36H47N5O4•H2O4SPureza:Min. 95%Cor e Forma:White To Off-White SolidPeso molecular:711.87 g/molGrazoprevir
CAS:<p>Anti-viral; inhibits Hepatitis C virus NS3/4a protease</p>Fórmula:C38H50N6O9SPureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:766.9 g/molFilociclovir
CAS:<p>Filociclovir is a novel antiviral agent, which is synthesized from small-molecule pharmaceutical compounds. It functions primarily by inhibiting viral DNA polymerase, thereby halting viral replication within infected host cells. This mechanism of action is particularly effective against certain herpesviruses, as it targets the polymerase enzyme that is critical for viral DNA synthesis and proliferation.</p>Fórmula:C11H13N5O3Pureza:Min. 95%Peso molecular:263.25 g/molDarunavir
CAS:<p>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.</p>Fórmula:C27H37N3O7SPureza:Min. 95%Cor e Forma:White PowderPeso molecular:547.66 g/molBoceprevir
CAS:<p>Boceprevir is a peptidomimetic, covalent inhibitor of NS3/4A serine protease from hepatitis C virus (HCV). Boceprevir also inhibits and acts as a substrate in the cytochrome P450 3A4 (CYP3A) metabolic pathway. Boceprevir was recently shown to inhibit the main protease Mpro (3CLpro) from SARS-CoV-2 with IC50 of 4.13 μM and EC50 of 1.31 μM.</p>Fórmula:C27H45N5O5Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:519.68 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-%Cor e Forma:PowderPeso molecular:444.42 g/molDolutegravir
CAS:<p>Dolutegravir is an HIV-1 integrase inhibitor. Dolutegravir is used in the treatment of HIV-1 infections as it hampers the integration of the viral genome into the host DNA (Katlama, 2012). Active on a wide number of HIV-1 phenotypes, dolutegravir is highly bioavailable with an IC90 of more than 30 hours (Cottrell, 2013).</p>Fórmula:C20H19F2N3O5Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:419.40 g/molPeramivir trihydrate
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:C15H28N4O4·3H2OPureza:Min. 95%Cor e Forma:PowderPeso molecular:382.45 g/molAmprenavir
CAS:<p>Anti-retroviral; HIV protease inhibitor</p>Fórmula:C25H35N3O6SPureza:Min. 98 Area-%Cor e Forma:White Off-White PowderPeso molecular:505.63 g/molLopinavir - Bio-X ™
CAS:<p>Chemically derived from ritonavir, Lopinavir belongs to the amphetamines. Lopinavir is clinically used in the prevention and treatment of HIV infections as it acts as HIV-1 protease inhibitor. In 2020, lopinavir was tested to treat COVID-19 patients and although it led to a higher rate of gastrointestinal side effects, the Lopinavir-treated group had a lower incidence of severe complications. Overall it was deemed not to work as a treatment.</p>Fórmula:C37H48N4O5Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:628.8 g/molN-[5-[3-[(4-Hydroxyphenyl)sulfamoyl]-4-methoxyphenyl]-4-methyl-1,3-thiazol-2-yl]-2,2-dimethylpropanamide
CAS:<p>PI4KIII beta inhibitor</p>Fórmula:C22H25N3O5S2Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:475.58 g/molVelpatasvir
CAS:<p>Antiviral; Hepatitis C virus NS5A antagonist</p>Fórmula:C49H54N8O8Pureza:Min. 95 Area-%Cor e Forma:White PowderPeso molecular:883 g/molFamciclovir - Bio-X ™
CAS:<p>Famciclovir is a guanosine analogue antiviral agent that is used for the treatment of various herpesvirus infections, most commonly for herpes zoster. It works by inhibiting the replication of the herpes virus. Famciclovir prevents viral DNA synthesis by inhibiting the viral DNA polymerase and by blocking viral DNA replication. Its active form is penciclovir.</p>Fórmula:C14H19N5O4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:321.33 g/molSaquinavir - Bio-X ™
CAS:<p>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.</p>Fórmula:C38H50N6O5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:670.84 g/molDarunavir Ethanolate
CAS:<p>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.</p>Fórmula:C27H37N3O7S·C2H6OPureza:Min. 95%Cor e Forma:White PowderPeso molecular:593.73 g/molAbacavir - Bio-X ™
CAS:<p>Abacavir is an antiviral nucleoside reverse transcriptase inhibitor that is used for the treatment of HIV. This drug inhibits the activity of HIV-1 reverse transcriptase (RT) both by competing with dGTP and by its incorporation into viral DNA.</p>Fórmula:C14H18N6OPureza:Min. 95%Cor e Forma:PowderPeso molecular:286.33 g/mol
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