Date published: 2026-2-22

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5730455P16Rik Activators

5730455P16Rik activators encompass a diverse array of chemical compounds that facilitate the enhancement of the protein's functional activity through various intracellular signaling pathways. Compounds such as Forskolin and Epigallocatechin gallate elevate the activity of 5730455P16Rik by modulating levels of secondary messengers and kinase activity, respectively. Forskolin's ability to raise cAMP levels indirectly activates protein kinase A, which could phosphorylate 5730455P16Rik, thereby enhancing its activity. Epigallocatechin gallate, known for its kinase inhibitory properties, may reduce competitive or regulatory signaling, allowing for the increased activity of 5730455P16Rik. Similarly, Genistein, by inhibiting tyrosine kinases, and Staurosporine, through broad-spectrum kinase inhibition, may lift the restraints on 5730455P16Rik's activity imposed by these kinases.

5730455P16Rik activators encompass a diverse array of chemical compounds that facilitate the enhancement of the protein's functional activity through various intracellular signaling pathways. Compounds such as Forskolin and Epigallocatechin gallate elevate the activity of 5730455P16Rik by modulating levels of secondary messengers and kinase activity, respectively. Forskolin's ability to raise cAMP levels indirectly activates protein kinase A, which could phosphorylate 5730455P16Rik, thereby enhancing its activity. Epigallocatechin gallate, known for its kinase inhibitory properties, may reduce competitive or regulatory signaling, allowing for the increased activity of 5730455P16Rik. Similarly, Genistein, by inhibiting tyrosine kinases, and Staurosporine, through broad-spectrum kinase inhibition, may lift the restraints on 5730455P16Rik's activity imposed by these kinases. Compounds like PMA and Sphingosine-1-phosphate act on protein kinase C and sphingosine-1-phosphate receptors, respectively, which could lead to the phosphorylation and functional activation of 5730455P16Rik if it is part of their signaling cascades.

Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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)

Sphingosine-1-phosphate engages with its receptors to regulate cellular signaling pathways including those that might control the localization and function of 5730455P16Rik, consequently enhancing its activity.

(−)-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)

This compound is a kinase inhibitor that may reduce competitive signaling pathways, thereby freeing up 5730455P16Rik to be more active within its specific signaling axis.

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 activates protein kinase C (PKC), which may phosphorylate and enhance the activity of 5730455P16Rik if it is a PKC substrate.

LY 294002

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

LY294002 is a PI3K inhibitor that modulates the PI3K/AKT pathway, potentially allowing for the relief of inhibitory control over 5730455P16Rik, thereby enhancing its activity.

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 also a PI3K inhibitor that can enhance the activity of 5730455P16Rik by reducing PI3K/AKT pathway activity, which might otherwise sequester factors that activate 5730455P16Rik.

Thapsigargin

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

By increasing intracellular calcium levels, thapsigargin can activate calcium-dependent signaling pathways that may enhance the activity of 5730455P16Rik.

A23187

52665-69-7sc-3591
sc-3591B
sc-3591A
sc-3591C
1 mg
5 mg
10 mg
25 mg
$55.00
$131.00
$203.00
$317.00
23
(1)

A23187 is an ionophore that increases intracellular calcium concentration, potentially enhancing the activity of 5730455P16Rik through calcium signaling.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$64.00
$246.00
136
(2)

U0126 is a MEK inhibitor which could shift signaling dynamics in favor of pathways that activate 5730455P16Rik by inhibiting the MEK/ERK pathway.

SB 203580

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

This compound is a p38 MAPK inhibitor, potentially enhancing the activity of 5730455P16Rik by altering the signaling landscape to support pathways in which 5730455P16Rik is involved.

Genistein

446-72-0sc-3515
sc-3515A
sc-3515B
sc-3515C
sc-3515D
sc-3515E
sc-3515F
100 mg
500 mg
1 g
5 g
10 g
25 g
100 g
$45.00
$164.00
$200.00
$402.00
$575.00
$981.00
$2031.00
46
(1)

Genistein is a tyrosine kinase inhibitor that may relieve 5730455P16Rik from competitive or regulatory tyrosine kinase phosphorylation, thereby enhancing its activity.