Date published: 2026-7-24

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p21-ARC Activators

p21-ARC Activators represent a diverse set of chemical compounds that indirectly enhance the functional activity of p21-ARC, a crucial component of the ARP2/3 complex involved in actin polymerization and cytoskeletal rearrangement. Jasplakinolide, by stabilizing actin filaments, potentially increases the demand for p21-ARC's activity in actin nucleation and stabilization. This is complemented by compounds like Latrunculin A, Latrunculia magnifica and Cytochalasin D, which disrupt actin polymerization and elongation, respectively, possibly leading to a compensatory upregulation of p21-ARC activity. Similarly, Swinholide A and Misakinolide A, by severing actin filaments, could indirectly enhance p21-ARC's role in actin nucleation and branching. Phalloidin influences actin dynamics, further underscoring the complex regulatory network influencing p21-ARC activity.

Additionally, broader cellular signaling modulators and metabolic influencers also play a role in modulating p21-ARC function. Bongkrekic Acid, by altering cellular energy status, could indirectly influence p21-ARC activity in cytoskeletal dynamics. Tyrphostin A23, a phosphatase inhibitor, can impact the phosphorylation state of proteins involved in actin dynamics, thereby potentially enhancing p21-ARC's functionality. Wortmannin, as a PI3K inhibitor, affects multiple signaling pathways, including those involved in actin dynamics, potentially leading to increased p21-ARC activity. Simvastatin, known for its cholesterol-lowering effects, also influences cytoskeletal organization, offering another avenue for indirectly enhancing p21-ARC's role in the ARP2/3 complex. Collectively, these p21-ARC Activators, through their targeted and diverse effects on cellular signaling and actin filament dynamics, play a crucial role in modulating the cytoskeletal functions associated with p21-ARC, highlighting the intricate interplay of biochemical pathways in cellular structure and movement.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Jasplakinolide

102396-24-7sc-202191
sc-202191A
50 µg
100 µg
$184.00
$305.00
59
(1)

Jasplakinolide stabilizes actin filaments, potentially enhancing the activity of p21-ARC in actin polymerization and stabilization within the ARP2/3 complex.

Latrunculin A, Latrunculia magnifica

76343-93-6sc-202691
sc-202691B
100 µg
500 µg
$265.00
$815.00
36
(2)

Latrunculin A, Latrunculia magnifica binds to monomeric G-actin, preventing its polymerization. This disruption can enhance p21-ARC activity in actin nucleation as a compensatory mechanism.

Cytochalasin D

22144-77-0sc-201442
sc-201442A
1 mg
5 mg
$165.00
$486.00
64
(4)

Cytochalasin D binds to the barbed ends of actin filaments, inhibiting elongation and potentially increasing p21-ARC activity in actin nucleation and branching.

Phalloidin

17466-45-4sc-202763
1 mg
$234.00
33
(1)

Phalloidin stabilizes actin filaments, potentially enhancing p21-ARC activity in the ARP2/3 complex to support actin filament formation and stabilization.

Bongkrekic acid

11076-19-0sc-205606
100 µg
$400.00
10
(1)

Bongkrekic Acid inhibits mitochondrial adenine nucleotide translocator, potentially altering cellular energy status and indirectly influencing p21-ARC activity in actin dynamics.

Tyrphostin A23

118409-57-7sc-3554
10 mg
$112.00
13
(1)

Tautomycin A23, as a PP1 and PP2A phosphatase inhibitor, could alter the phosphorylation state of proteins involved in actin dynamics, indirectly influencing p21-ARC 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, a PI3K inhibitor, could affect actin dynamics by altering signaling pathways, potentially leading to enhanced p21-ARC activity in actin nucleation and branching.

Simvastatin

79902-63-9sc-200829
sc-200829A
sc-200829B
sc-200829C
50 mg
250 mg
1 g
5 g
$31.00
$89.00
$135.00
$443.00
13
(1)

Simvastatin, by inhibiting HMG-CoA reductase, can influence cytoskeletal organization, potentially enhancing p21-ARC's role in actin polymerization within the ARP2/3 complex.