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Proteasa del VIH

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 449 productos de "Proteasa del VIH"

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  • Cys-TAT(47-57)

    CAS:
    <p>Cys-TAT(47-57): arginine-rich peptide from HIV-1 TAT protein's transduction domain.</p>
    Fórmula:C67H124N34O14S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1661.99
  • Kuguacin N


    <p>Kuguacin N is a useful organic compound for research related to life sciences and the catalog number is T126345.</p>
    Fórmula:C30H46O4
    Forma y color:Solid
    Peso molecular:470.694
  • CTP518

    CAS:
    <p>CTP518, a deuterated Atazanivir derivative, is a HIV protease inhibitor.</p>
    Fórmula:C38H52N6O7
    Pureza:98%
    Forma y color:Solid
    Peso molecular:719.95
  • 12-Oxocalanolide A


    <p>12-Oxocalanolide A is a useful organic compound for research related to life sciences and the catalog number is T125675.</p>
    Fórmula:C22H24O5
    Forma y color:Solid
    Peso molecular:368.429
  • HIV gag peptide (197-205)

    CAS:
    <p>HIV gag peptide (197-205) is a H-2Kd-restricted epitope derived from the p24 portion of the HIV-1 gag protein and composed of the amino acid 197-205 (AMQMLKETI</p>
    Fórmula:C45H81N11O14S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1064.32
  • TAT peptide


    <p>TAT peptide, a CPP, delivers molecules into cells by traversing membrane barriers using aa49-57 of TAT protein.</p>
    Fórmula:C65H124N34O15
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1621.91
  • Kni 102

    CAS:
    <p>Kni 102 is a biochemical.</p>
    Fórmula:C31H41N5O7
    Forma y color:Solid
    Peso molecular:595.69
  • HIV-1 inhibitor-81


    <p>HIV-1inhibitor-81 (Compound 14g) is an HIV-1 protease inhibitor with a Ki of 1.6 nM. This compound exhibits antiviral activity against HIV-1, with an EC50 value of 250 nM.</p>
    Fórmula:C32H44N2O8S
    Forma y color:Solid
    Peso molecular:616.77
  • HIV-1 inhibitor-6 

    CAS:
    <p>HIV-1 inhibitor-6 (3-Pyridinecarboxamide, 1,4-dihydro-1-methyl-N-(5-nitro-1,2-benzisothiazol-3-yl)-4-oxo-) is a potent HIV-1 pre-mRNA selective splicing</p>
    Fórmula:C14H10N4O4S
    Pureza:99.33%
    Forma y color:Solid
    Peso molecular:330.32
  • Scirpusin A

    CAS:
    <p>Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.</p>
    Fórmula:C28H22O7
    Forma y color:Solid
    Peso molecular:470.47
  • Aureothin

    CAS:
    <p>Aureothin: a nitroaryl polyketide with antitumor, antifungal &amp; insecticidal properties; inhibits NADH:oxidoreductase (IC50s: 0.07-22 nmol/mg).</p>
    Fórmula:C22H23NO6
    Forma y color:Solid
    Peso molecular:397.42
  • NNRT-IN-6


    <p>NNRT-IN-6 (Compound 13a) is a non-nucleoside reverse transcriptase inhibitor (NNRT) used to inhibit HIV-1 reverse transcriptase (HIV-1RT), with an IC50 of 0.41 μM. It effectively suppresses both wild-type HIV-1 and mutants L100I, K103N, Y181C, Y188L, E138K, F227L/V106A, and RES056, with an EC50 range of 6.2-250 nM.</p>
    Fórmula:C32H31N9O3S
    Forma y color:Solid
    Peso molecular:621.71
  • (2S,5S)-Censavudine


    <p>(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.</p>
    Fórmula:C12H12N2O4
    Forma y color:Solid
    Peso molecular:248.23
  • Salvianan A

    CAS:
    <p>1,6,11-Trimethyl-1,2-dihydrofuro[2',3':1,2]phenanthro[4,3-d]oxazole (compound 1) serves as an effective anti-HIV-1 agent [1].</p>
    Fórmula:C20H17NO2
    Forma y color:Solid
    Peso molecular:303.35
  • Bictegravir Sodium

    CAS:
    <p>Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.</p>
    Fórmula:C21H17F3N3NaO5
    Pureza:99.97%
    Forma y color:Solid
    Peso molecular:471.36
  • NF279

    CAS:
    <p>P2X1 antagonist</p>
    Fórmula:C49H36N6Na6O23S6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1407.17
  • Decanoyl-RVKR-CMK

    CAS:
    <p>Inhibits all seven proprotein convertases; stops proET-1 processing; hinders VGF secretion in PC12 cells.</p>
    Fórmula:C34H66ClN11O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:744.42
  • HIV-IN-9


    <p>HIV-IN-9 (Compound 2b) is an HIV inhibitor with an IC50 value of 6.65 μg/mL, demonstrating high binding affinity for HIV-RT.</p>
    Forma y color:Odour Solid
  • HIV-1 protease-IN-14


    <p>HIV-1protease-IN-14 (compound 5ae) is an effective inhibitor of HIV-1protease, exhibiting Ki values of 0.28 nM and 56.9 nM against WTHIV-1PR and R41THIV-1PR, respectively. This compound also demonstrates low cytotoxicity.</p>
    Forma y color:Odour Solid
  • Carbovir triphosphate

    CAS:
    <p>Carbovir triphosphate (CBV-TP), a phosphorylated metabolite, serves as a research tool for studying human immunodeficiency virus (HIV) [1].</p>
    Fórmula:C11H16N5O11P3
    Forma y color:Solid
    Peso molecular:487.19