Date published: 2026-5-30

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HPV 16-E5 Inhibitors

Chemical inhibitors of HPV 16-E5 have been identified, each employing distinct mechanisms to inhibit this viral protein's function within host cells. Imiquimod can enhance the immune response, particularly the production of cytokines like interferon-alpha, which targets cells expressing HPV 16-E5. This immune-mediated approach reduces the presence of HPV 16-E5, undermining its capability to function effectively. Similarly, Cidofovir disrupts the viral replication process by incorporating into the viral DNA, which prevents the proper assembly of viral proteins, including HPV 16-E5, thus impeding its function. Lopinavir leads to the accumulation of misfolded proteins in the endoplasmic reticulum, triggering an unfolded protein response that can diminish HPV 16-E5's function. Sirolimus and its counterpart, Rapamycin, inhibit the mTOR pathway, crucial for the synthesis of viral proteins; by doing so, they reduce the production of HPV 16-E5. Zinc sulfate can interfere with the conformation of HPV 16-E5, likely disturbing its activity, while Indole-3-carbinol modulates cellular proliferation and apoptosis pathways, which can alter the functioning environment of HPV 16-E5.

Further, Curcumin disrupts pathways that HPV 16-E5 might exploit, such as those involved in cell proliferation and apoptosis, altering the cellular environment to inhibit the protein's function. Etoposide exerts its effect by initiating a DNA damage response, leading to the apoptosis of cells harboring HPV 16-E5, which indirectly diminishes the protein's functional presence. Quercetin's antiviral effects include the suppression of protein synthesis and viral replication, which encompasses the inhibition of HPV 16-E5. Disulfiram modifies the cellular redox state, leading to oxidative stress that can disrupt the function of viral proteins, including HPV 16-E5. Lastly, Resveratrol influences signaling pathways related to cell proliferation and apoptosis, which can inhibit the environment conducive to HPV 16-E5's function, thereby inhibiting the protein. Each of these chemicals employs a unique mode of action to inhibit HPV 16-E5, ranging from direct interference with viral replication processes to modulation of the host cell environment.

Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Imiquimod

99011-02-6sc-200385
sc-200385A
100 mg
500 mg
$67.00
$284.00
6
(1)

Imiquimod, an immune response modifier, can inhibit HPV 16-E5 by enhancing the host's immune response to the virus-infected cells. By promoting the production of cytokines such as interferon-alpha, the immune system can more effectively target and eliminate cells expressing HPV 16-E5, thereby reducing the protein's presence and hindering its function.

Cidofovir

113852-37-2sc-482141
50 mg
$135.00
(0)

Cidofovir is an antiviral drug that, while primarily used to inhibit viral DNA polymerase, can also lead to the functional inhibition of HPV 16-E5 by incorporating into the viral DNA, thereby preventing the proper assembly of viral proteins, including HPV 16-E5, and leading to a reduction in its function within the host cell.

Lopinavir

192725-17-0sc-207831
10 mg
$132.00
6
(1)

Lopinavir, known as an HIV protease inhibitor, can inhibit HPV 16-E5 by causing misfolded protein accumulation in the endoplasmic reticulum, leading to an unfolded protein response that can diminish the viral protein's function and interfere with the viral life cycle, including the action of HPV 16-E5.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Sirolimus, a macrolide compound, can inhibit HPV 16-E5 by inhibiting the mTOR pathway which is crucial for the translation of viral proteins. By inhibiting mTOR, sirolimus reduces the synthesis of viral proteins, including HPV 16-E5, thereby reducing its functional presence in the host cell.

Zinc

7440-66-6sc-213177
100 g
$48.00
(0)

Zinc Sulfate can inhibit HPV 16-E5 by enhancing the host's antiviral response and potentially interfering with the protein's ability to alter cellular processes. Zinc ions can disrupt the protein conformation of HPV 16-E5, inhibiting its function.

Indole-3-carbinol

700-06-1sc-202662
sc-202662A
sc-202662B
sc-202662C
sc-202662D
1 g
5 g
100 g
250 g
1 kg
$39.00
$61.00
$146.00
$312.00
$1032.00
5
(1)

Indole-3-carbinol can modulate pathways involving cellular proliferation and apoptosis. By influencing these pathways, the compound can alter the environment in which HPV 16-E5 operates, potentially inhibiting the protein's ability to contribute to the pathogenesis caused by the virus.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Curcumin can inhibit HPV 16-E5 by disrupting cellular pathways that the protein utilizes for enhancing the virus's life cycle, including pathways involved in cell proliferation and apoptosis. The compound's anti-inflammatory and antioxidant properties can contribute to a cellular environment less conducive to the function of HPV 16-E5.

Etoposide (VP-16)

33419-42-0sc-3512B
sc-3512
sc-3512A
10 mg
100 mg
500 mg
$51.00
$231.00
$523.00
63
(1)

Etoposide, a topoisomerase inhibitor, can indirectly inhibit HPV 16-E5 by initiating DNA damage response pathways that can lead to apoptosis of cells expressing the viral proteins, including HPV 16-E5, thus inhibiting the protein's ability to assist in viral persistence and pathogenesis.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$110.00
$250.00
$936.00
$50.00
33
(2)

Quercetin can inhibit HPV 16-E5 by exerting antiviral effects that include the inhibition of protein synthesis and viral replication, which would encompass the suppression of HPV 16-E5 function.

Disulfiram

97-77-8sc-205654
sc-205654A
50 g
100 g
$53.00
$89.00
7
(1)

Disulfiram can inhibit HPV 16-E5 by modifying the redox state of the cell, leading to oxidative stress that can disrupt viral protein function, including HPV 16-E5, and potentially lead to the degradation or inactivation of the protein.