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.
- CAS No.: 384361-09-5
- Formula: C21H20N2O5S
- Molecular Weight:412.46
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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.
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Cell Line:HeLa Tet-Off Advanced Cells
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Concentration:10 μM
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Incubation Time:from 5 h post-transfection until fixation the next day
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Result:Prevented native integrase from localizing to the nucleus, confirming inhibition of nuclear translocation independent of EGFP interactions.
Chemical Information
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CAS No. 384361-09-5
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Molecular Weight 412.46
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Formula C21H20N2O5S
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SMILES
O=C1OC2=C(CN(CCO)CCO)C(O)=CC=C2C=C1C3=NC4=C(S3)C=CC=C4
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)