Proteasa del VIH
Los inhibidores de la proteasa del VIH son una clase de fármacos antirretrovirales que atacan específicamente la enzima proteasa del virus de la inmunodeficiencia humana (VIH). Al inhibir esta enzima, estos compuestos evitan que el virus procese sus poliproteínas en proteínas maduras y funcionales, bloqueando así la producción de nuevos viriones infecciosos. Los inhibidores de la proteasa del VIH son una piedra angular de la terapia antirretroviral altamente activa (TARGA) utilizada para manejar el VIH/SIDA. En CymitQuimica, ofrecemos una variedad de inhibidores de la proteasa del VIH para apoyar su investigación en el tratamiento del VIH, la resistencia a los medicamentos y la virología.
Se han encontrado 447 productos de "Proteasa del VIH"
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Aurothioglucose
CAS:<p>Aurothioglucose is a active-site TrxR1 inhibitor.</p>Fórmula:C6H11AuO5SPureza:98%Forma y color:Yellow Crystals SolidPeso molecular:392.18BMS-378806
<p>BMS-378806 is an HIV inhibitor with EC50: 0.85-26.5nM for various strains.</p>Fórmula:C22H22N4O4Pureza:98%Forma y color:SolidPeso molecular:406.43Cyclotriazadisulfonamide
CAS:<p>Cyclotriazadisulfonamide (CADA) is a specific inhibitor of HIV entry that targets CD4 by preventing the co-translational translocation of human CD4 (huCD4) into the endoplasmic reticulum (ER) lumen through a signal peptide (SP)-dependent mechanism.</p>Fórmula:C31H39N3O4S2Forma y color:SolidPeso molecular:581.793-Deazaadenosine
CAS:<p>3-Deazaadenosine, an inhibitor of S-adenosylhomocysteine hydrolase with a Ki of 3.9 μM, exhibits anti-inflammatory, anti-proliferative, and anti-HIV activity.</p>Fórmula:C11H14N4O4Pureza:98%Forma y color:SolidPeso molecular:266.25Loviride
CAS:<p>Loviride, a reverse transcriptase inhibitor with IC50 of 0.3 μM, blocks HIV-1/2 and SIV in MT-4 cells.</p>Fórmula:C17H16Cl2N2O2Forma y color:SolidPeso molecular:351.23Ref: TM-T15776
Producto descatalogadoOxindole
CAS:<p>Oxindole (Indolin-2-one) is an aromatic heterocyclic building block. 2-indolinone derivatives have become lead compounds in the research of kinase inhibitors.Oxindole structure has been used in receptor tyrosine kinases (RTKs) inhibitors such as SU4984 and intedanib, the RTK family represents an important therapeutic target for anti-cancer drug development.</p>Fórmula:C8H7NOPureza:99.34%Forma y color:Off-White Crystalline PowderPeso molecular:133.15HIV-1 integrase inhibitor
CAS:<p>Hiv-1 integrase inhibitor is an effective anti-HIV drug.</p>Fórmula:C11H9N3O4Pureza:98%Forma y color:SolidPeso molecular:247.21
