1. Metabolic Enzyme/Protease
  2. HIV Integrase
  3. D719

D719 is an HIV-1 integrase inhibitor. D719 binds to the hydrophobic pocket of HIV-1 integrase CCD dimer, disrupts interaction with LEDGF/P75, and prevents integrase nuclear translocation. D719 reduces HIV-1 p24 antigen production in acute infection of human T cells. D719 can be used for the research of HIV infection.

For research use only. We do not sell to patients.

D719

D719 Chemical Structure

CAS No. : 384361-09-5

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Description

D719 is an HIV-1 integrase inhibitor. D719 binds to the hydrophobic pocket of HIV-1 integrase CCD dimer, disrupts interaction with LEDGF/P75, and prevents integrase nuclear translocation. D719 reduces HIV-1 p24 antigen production in acute infection of human T cells. D719 can be used for the research of HIV infection[1].

In Vitro

D719 (1 μM; from 5 h post-transfection until fixation the next day) inhibits nuclear translocation of EGFP-tagged HIV-1 integrase in HeLa Tet-Off Advanced Cells[1].
D719 (10 μM; from 5 h post-transfection until fixation the next day) inhibits nuclear translocation of native HIV-1 integrase in HeLa Tet-Off Advanced Cells[1].
D719 (0.5-20 μM; 3 days post-infection) inhibits HIV-1 replication in acutely infected C8166 T cells, reducing p24 antigen production with an EC50 of 4.33 μM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Immunofluorescence[1]

Cell Line: HeLa Tet-Off Advanced Cells
Concentration: 10 μM
Incubation Time: from 5 h post-transfection until fixation the next day
Result: Prevented native integrase from localizing to the nucleus, confirming inhibition of nuclear translocation independent of EGFP interactions.
Molecular Weight

412.46

Formula

C21H20N2O5S

CAS No.
SMILES

O=C1OC2=C(CN(CCO)CCO)C(O)=CC=C2C=C1C3=NC4=C(S3)C=CC=C4

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Please store the product under the recommended conditions in the Certificate of Analysis.

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D719
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HY-183926
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