Date published: 2025-11-1

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Ccdc163 Activators

Ccdc163 Activators are a specialized set of chemical compounds that enhance the activity of Ccdc163 through distinct biochemical pathways. Ccdc163, being a relatively understudied protein, may be indirectly influenced by chemicals that modulate the cellular environment in which Ccdc163 operates. For instance, compounds that alter the redox state of cells could affect the conformation and function of Ccdc163 if it is sensitive to changes in oxidative stress. Similarly, if Ccdc163 is involved in ciliary function or structure within cells, chemicals that stabilize microtubules or enhance tubulin acetylation might indirectly enhance the functional activity of Ccdc163 by improving the structural integrity of cilia where Ccdc163 is localized. Membrane-permeable cyclic nucleotides or their analogs could also play a role, assuming that Ccdc163 activity is modulated by cyclic nucleotide-dependent signaling pathways. Phosphodiesterase inhibitors that elevate intracellular levels of cyclic nucleotides might thus have an indirect activating effect on Ccdc163.

Furthermore, if Ccdc163 is part of a signaling cascade that involves calcium signaling, ionophores that increase intracellular calcium concentration could indirectly enhance Ccdc163 activity. Modulators of intracellular calcium stores, such as SERCA inhibitors, may also influence the activity of Ccdc163 by altering calcium dynamics within the cell. Additionally, if Ccdc163 has a role in cellular response to hypoxia, compounds that simulate hypoxic conditions or stabilize HIF-1 alpha could indirectly increase Ccdc163 activity by engaging the cellular hypoxic response. Compounds that influence the cellular energy state, such as AMPK activators, may also modulate Ccdc163 activity if it is linked to cellular energy sensing pathways. Similarly, molecules that affect lipid signaling pathways, potentially involving Ccdc163, could be considered indirect activators; for instance, agonists of PPAR receptors that play a role in lipid metabolism and signaling. Given the complexity of cellular signaling and the potential for cross-talk between pathways, these chemicals provide a starting point for exploring the activation mechanisms of Ccdc163, even in the absence of direct activators or a fully understood functional context.

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
$76.00
$150.00
$725.00
$1385.00
$2050.00
73
(3)

Forskolin activates adenylyl cyclase, increasing the levels of cyclic AMP (cAMP) within the cell. If Ccdc163 is regulated by cAMP-dependent pathways, forskolin could enhance its activity.

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
$40.00
$129.00
$210.00
$490.00
$929.00
119
(6)

PMA is a diacylglycerol (DAG) analog that activates protein kinase C (PKC). If Ccdc163 is influenced by PKC signaling, PMA could lead to an increase in its functional activity.

Ionomycin

56092-82-1sc-3592
sc-3592A
1 mg
5 mg
$76.00
$265.00
80
(4)

Ionomycin is a calcium ionophore that increases intracellular calcium levels, potentially affecting proteins regulated by calcium signaling, possibly including Ccdc163.

AICAR

2627-69-2sc-200659
sc-200659A
sc-200659B
50 mg
250 mg
1 g
$60.00
$270.00
$350.00
48
(2)

AICAR activates AMP-activated protein kinase (AMPK), which is involved in energy sensing. Activation of AMPK could lead to cellular responses that indirectly enhance Ccdc163 activity.

Rosiglitazone

122320-73-4sc-202795
sc-202795A
sc-202795C
sc-202795D
sc-202795B
25 mg
100 mg
500 mg
1 g
5 g
$118.00
$320.00
$622.00
$928.00
$1234.00
38
(1)

Rosiglitazone is a PPARγ agonist that modulates lipid metabolism and signaling. If Ccdc163 activity is linked to lipid signaling, rosiglitazone could indirectly enhance its activity.

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$65.00
$319.00
$575.00
$998.00
28
(1)

Retinoic acid influences gene expression through retinoic acid receptors. If Ccdc163 is responsive to retinoid signaling, retinoic acid could indirectly increase its functional activity.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$94.00
$349.00
114
(2)

Thapsigargin inhibits the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA), disrupting calcium homeostasis. This could indirectly activate Ccdc163 if it is calcium-dependent.

8-Bromoadenosine 3′,5′-cyclic monophosphate

23583-48-4sc-217493B
sc-217493
sc-217493A
sc-217493C
sc-217493D
25 mg
50 mg
100 mg
250 mg
500 mg
$106.00
$166.00
$289.00
$550.00
$819.00
2
(1)

8-Br-cAMP is a cAMP analog that activates cAMP-dependent pathways. This can indirectly enhance Ccdc163 activity if it functions within these pathways.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$56.00
$260.00
$980.00
163
(3)

MG132 is a proteasome inhibitor that can influence protein turnover. If Ccdc163 stability is affected by proteasomal degradation, MG132 could enhance its cellular activity.

Metformin

657-24-9sc-507370
10 mg
$77.00
2
(0)

Metformin activates AMPK and can influence cellular metabolism. If Ccdc163 activity is linked to metabolic pathways, metformin could indirectly enhance its activity.