Antiviral agent 83
Antiviral agent 83 is a boronic acid-modified Neocryptolepine (HY-E70250) derivative and is an anti-HPV agent. Antiviral agent 83 bind to the viral capsid protein and/or envelope protein, inducing conformational changes that effectively obstruct the interaction between the virus and host cell receptors. Antiviral agent 83 exhibits inhibitory activity against multiple high-risk HPV strains. Antiviral agent 83 inhibits HPV infection in vitro and in vaginal tract in vivo.
For research use only. We do not sell to patients.
- Formula: C29H25BN4O2
- Molecular Weight:472.35
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Antiviral agent 83 (Compound 13B) (10 μM; 48 h) inhibits HPV-16 PsVs infection in HeLa cells with high efficacy and low cytotoxicity, the virus inhibition rate is 83.33%, and the cytotoxicity is 5.71%[1].
Antiviral agent 83 (48 h) inhibits HPV-16 PsVs with an IC50 of 8.84 μM and exhibits low cytotoxicity in HeLa and VK2/E6E7 cells, with CC50 values of 62.14 μM and 89.08 μM, respectively, resulting in high selectivity indices of 7.03 and 10.08[1].
Antiviral agent 83 (0.625-10 μM; 48 h) potently inhibits infection by high-risk HPV-16, -18, -31, and -45 PsVs in HeLa cells with IC50 values ranging from 7.80 to 12.45 μM[1].
Antiviral agent 83 (5-20 μM; 1 h or 4 h preincubation; 48 h total incubation) directly inactivates HPV-45 PsVs in a dose- and time-dependent manner, with increased inhibition observed with longer pre-treatment durations[1].
Antiviral agent 83 (10 μM; 4 h) disrupts the morphological integrity of HPV-45 PsVs when incubated at 10 μM for 4 h[1].
Antiviral agent 83 binds specifically and with high affinity to HPV-16 L1 protein, with a Kd of 93.6 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:HPV-infected in HeLa cells.
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Concentration:0.625, 1.25, 2.5, 5, 8, 10 μM
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Incubation Time:48 h
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Result:Showed IC50 values of 8.84, 8.31, 12.45 and 7.8 μM against HPV-16, -18, -31, and -45 PsVs in HeLa cells.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:HPV-infected Nude mice (female, 6-8 weeks old)[1]
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Dosage:20 μM; 40 μM
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Administration:intravaginal injection; daily; 3 days
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Result:Decreased the luciferase signals in the murine vaginas from day 2.
Only very weak luciferase signals were observed in all the murine vaginas on day 4 at 40 μM.
Chemical Information
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Molecular Weight 472.35
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Formula C29H25BN4O2
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SMILES
CN1C2=NC3=CC=CC=C3C2=C(NC4=CC(NCC5=CC(B(O)O)=CC=C5)=CC=C4)C6=C1C=CC=C6
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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)