Date published: 2026-4-24

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CD16-B Activators

CD16-B activators constitute a diverse group of chemical compounds that enhance the functional activity of the CD16-B protein through various intracellular signaling pathways. For instance, Bisindolylmaleimide, as a selective inhibitor of protein kinase C, impedes the phosphorylation-associated downregulation of CD16-B, thereby sustaining its activity levels. Similarly, the action of Forskolin, by increasing intracellular cAMP, can enhance CD16-B functionality through PKA-dependent mechanisms, ensuring an amplified response to ligand binding. ProstaglandinE2, engaging with the EP4 receptor, activates downstream PI3K/Akt pathways, which then act to stabilize and activate CD16-B, impeding its internalization and degradation. The calcium ionophore Ionomycin raises intracellular calcium levels, indirectly promoting CD16-B activity by simulating the activation of calcium-dependent pathways. Additionally, Thapsigargin, by inhibiting the SERCA pump, also elevates cytosolic calcium levels, leading to the enhancement of CD16-B signaling.

The modulation of CD16-B activity is further influenced by compounds that target specific kinases involved in its regulation. Piceatannol and U0126 work to inhibit Syk kinase and MEK1/2 respectively, removing negative regulation on CD16-B and allowing for an upregulated signaling response. Bryostatin 1, a modulator of PKC, uniquely prolongs CD16-B activation by altering phosphorylation patterns without triggering downregulation. SB 203580 and PD98059, both inhibitors of elements within the MAPK pathway, lift the suppression of CD16-B signaling, thus promoting its activity. Dibutyryl-cAMP, by mimicking the effect of elevated cAMP, activates PKA, which in turn enhances CD16-B signaling. Lastly, LY294002, while inhibiting PI3K, disrupts negative feedback loops, resulting in a net increase in CD16-B activity, exemplifying how inhibitors of signaling pathways can sometimes lead to the unexpected enhancement of downstream proteins such as CD16-B. All these compounds work in a concerted manner to amplify the functional activity of CD16-B, albeit through distinct biochemical routes, showcasing the complexity of intracellular signaling and regulation.

Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Bisindolylmaleimide I (GF 109203X)

133052-90-1sc-24003A
sc-24003
1 mg
5 mg
$105.00
$242.00
36
(1)

Bisindolylmaleimide is a potent and selective inhibitor of protein kinase C (PKC). By inhibiting PKC, it prevents the phosphorylation and subsequent downregulation of CD16-B. This leads to enhanced activity of CD16-B as it remains in a state conducive to binding immune complexes.

PGE2

363-24-6sc-201225
sc-201225C
sc-201225A
sc-201225B
1 mg
5 mg
10 mg
50 mg
$57.00
$159.00
$275.00
$678.00
37
(1)

Prostaglandin E2 (PGE2) engages the EP4 receptor, which in turn can lead to the activation of downstream signaling cascades such as the PI3K/Akt pathway. This activation can promote the stabilization and activation of CD16-B by preventing its internalization and degradation.

Forskolin

66575-29-9sc-3562
sc-3562A
sc-3562B
sc-3562C
sc-3562D
5 mg
50 mg
1 g
2 g
5 g
$78.00
$153.00
$740.00
$1413.00
$2091.00
73
(3)

Forskolin activates adenylyl cyclase, increasing intracellular cAMP levels. Elevated cAMP can enhance the functional activity of CD16-B through PKA-dependent signaling pathways, leading to increased affinity and/or avidity for its ligands.

Ionomycin

56092-82-1sc-3592
sc-3592A
1 mg
5 mg
$78.00
$270.00
80
(4)

Ionomycin is a calcium ionophore that increases intracellular calcium levels. This elevation can mimic signaling events leading to the activation of pathways that enhance the surface expression and function of CD16-B, facilitating its role in immune complex binding.

Piceatannol

10083-24-6sc-200610
sc-200610A
sc-200610B
1 mg
5 mg
25 mg
$51.00
$71.00
$199.00
11
(2)

Piceatannol inhibits the Syk kinase, which is involved in the negative regulation of CD16-B signaling. Inhibition of Syk can relieve its suppressive effects, resulting in the enhancement of CD16-B-mediated signaling.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$136.00
$446.00
114
(2)

Thapsigargin is a SERCA pump inhibitor that leads to increased cytosolic calcium levels, similar to ionomycin. It can potentiate signaling pathways that result in the functional upregulation of CD16-B, promoting its activity in immune response.

Bryostatin 1

83314-01-6sc-201407
10 µg
$245.00
9
(1)

Bryostatin 1 is a PKC modulator that can lead to the prolonged activation of CD16-B by altering the phosphorylation status of proteins involved in its signaling cascade, enhancing its activity without promoting downregulation typically associated with PKC activators.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

SB 203580 is a p38 MAPK inhibitor, which can indirectly enhance the activity of CD16-B by blocking negative regulatory elements within the MAPK pathway, thus allowing CD16-B signaling to proceed unimpeded.

Dibutyryl-cAMP

16980-89-5sc-201567
sc-201567A
sc-201567B
sc-201567C
20 mg
100 mg
500 mg
10 g
$47.00
$136.00
$492.00
$4552.00
74
(7)

Dibutyryl-cAMP is a cAMP analog that can permeate cell membranes and mimic the effects of elevated cAMP within the cell. By doing so, it can activate PKA and enhance CD16-B signaling through phosphorylation events that increase its functional activity in immune processes.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

LY294002 is a PI3K inhibitor that can paradoxically enhance CD16-B signaling by perturbing negative feedback mechanisms that usually restrain CD16-B activity. By inhibiting PI3K, LY294002 can lead to compensatory responses in cells that result in the activation of CD16-B.