L-731988
L-731988 is an inhibitor targeting HIV-1 integrase. L-731988 inhibits HIV-1 replication by blocking integrase function. L-731988 exhibits ED50 values ranging from 0.5 μM to 3.14 μM against various HIV-1 isolates. L-731988 can be used for the research of human immunodeficiency virus type 1 (HIV-1) infection.
For research use only. We do not sell to patients.
- CAS No.: 251922-77-7
- Formula: C15H12FNO4
- Molecular Weight:289.26
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HCT-116 | CC50 |
10 μM
Compound: L-731988
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Cytotoxicity against human HCT116 cells expressing p53 after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells expressing p53 after 72 hrs by MTT assay
|
[PMID: 19026554] |
L-731988 (0.5-5.0 μM) suppresses RT activity of HIV-1 primary isolates in PBLs in a dose-dependent manner[1].
L-731988 inhibits replication of diverse primary HIV-1 isolates in PBLs, with ED50 values ranging from 0.544 to 3.14 μM; most isolates show less-than-twofold differences in susceptibility relative to HIVLAI, while HIV92RW009 exhibits a sixfold reduction in susceptibility[1].
L-731988 inhibits HIV-1 replication in MT-2 cells with ED50 values ranging from 0.505 to 1.6 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 251922-77-7
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Molecular Weight 289.26
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Formula C15H12FNO4
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SMILES
O=C(C(CC(C1=CC=CN1CC2=CC=C(C=C2)F)=O)=O)O
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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)