Date published: 2026-1-11

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TMEM196 Activators

TMEM196 Activators encompass a variety of chemical compounds that indirectly stimulate the functional activity of TMEM196 by manipulating diverse signaling pathways and cellular processes. For instance, Forskolin and 8-Bromo-cAMP function by increasing cAMP levels, which in turn activate PKA. This kinase has the potential to phosphorylate TMEM196, thereby enhancing its cellular function. Similarly, PMA, an activator of PKC, may also indirectly stimulate TMEM196 by promoting its phosphorylation, a common regulatory mechanism for protein activation. Calcium ionophores like Ionomycin raise intracellular calcium levels, which could activate calcium-dependent kinases that might target TMEM196 for activation through phosphorylation. Conversely, Okadaic Acid prevents the dephosphorylation of proteins by inhibiting phosphatases PP1 and PP2A, potentially maintaining TMEM196 in an active state. Epigallocatechin gallate (EGCG) adds another layer of regulation by inhibiting competing kinases, potentially shifting the equilibrium toward pathways that activate TMEM196.

PI3K inhibitors, LY294002 and Wortmannin, disrupt AKT signaling, potentially inducing cellular responses that activate TMEM196 through intricate compensatory mechanisms. The presence of essential metal ions like Zinc and Magnesium may also modulate TMEM196 activity, especially if its function is contingent upon these ions as cofactors. Sphingosine-1-phosphate (S1P) activates G protein-coupled receptors, leading to signaling events that could culminate in the activation of TMEM196 via downstream effectors. Lastly, Thapsigargin, by hindering the SERCA pump, causes an increase in cytosoliccalcium, a condition that can trigger calcium-dependent kinases and potentially enhance the activity of TMEM196. Collectively, these chemical activators orchestrate a symphony of biochemical signals that converge to elevate the functional activity of TMEM196, ensuring that it performs its cellular role more effectively without the need for upregulation at the transcriptional or translational level.

SEE ALSO...

Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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 raises intracellular cAMP levels, which can lead to the activation of PKA (protein kinase A). PKA then phosphorylates target proteins, potentially including TMEM196, thereby enhancing its function within the cell.

8-Bromo-cAMP

76939-46-3sc-201564
sc-201564A
10 mg
50 mg
$126.00
$328.00
30
(1)

8-Bromo-cAMP acts as a cAMP analog, resisting enzymatic degradation and thus sustaining PKA activation. Sustained PKA activity could enhance the phosphorylation and activation of TMEM196 if it is a PKA substrate.

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
$41.00
$132.00
$214.00
$500.00
$948.00
119
(6)

PMA is a potent activator of protein kinase C (PKC), which can phosphorylate a wide array of proteins. TMEM196 might be activated by PKC-mediated phosphorylation, which could regulate its cellular functions.

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, potentially activating calcium-dependent protein kinases that may phosphorylate and activate TMEM196.

Okadaic Acid

78111-17-8sc-3513
sc-3513A
sc-3513B
25 µg
100 µg
1 mg
$291.00
$530.00
$1800.00
78
(4)

Okadaic Acid is a potent inhibitor of protein phosphatases PP1 and PP2A. Inhibition of these phosphatases prevents dephosphorylation of proteins, which could lead to sustained activation of TMEM196 if it is regulated by phosphorylation.

(−)-Epigallocatechin Gallate

989-51-5sc-200802
sc-200802A
sc-200802B
sc-200802C
sc-200802D
sc-200802E
10 mg
50 mg
100 mg
500 mg
1 g
10 g
$43.00
$73.00
$126.00
$243.00
$530.00
$1259.00
11
(1)

EGCG is known to inhibit certain protein kinases. By inhibiting competitive pathways, it may shift the signaling balance towards pathways that activate TMEM196.

LY 294002

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

LY294002 is a PI3K inhibitor that alters AKT signaling. Disruption of this pathway can result in compensatory responses in the cell that might activate TMEM196.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

Wortmannin is another PI3K inhibitor, similar in function to LY294002, and may indirectly lead to TMEM196 activation through the same compensatory cellular mechanisms.

Zinc

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

Zinc is a divalent cation that can act as a cofactor for several enzymes and may be involved in the direct or indirect activation of TMEM196 if it requires such a cofactor for its activity.

D-erythro-Sphingosine-1-phosphate

26993-30-6sc-201383
sc-201383D
sc-201383A
sc-201383B
sc-201383C
1 mg
2 mg
5 mg
10 mg
25 mg
$165.00
$322.00
$570.00
$907.00
$1727.00
7
(1)

S1P engages with G protein-coupled receptors to activate downstream signaling cascades. Such cascades could lead to the activation of TMEM196 through complex signal transduction mechanisms.