Date published: 2025-12-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

PKC δ Inhibitors

PKC δ inhibitors belong to a class of chemical compounds designed to target and modulate the activity of the protein kinase C delta (PKC δ) enzyme. This enzyme is a member of the protein kinase C (PKC) family, which plays a pivotal role in cell signaling processes, including cellular growth, differentiation, and apoptosis. PKC δ is specifically involved in mediating various cellular responses, including those related to oxidative stress, immune responses, and cell survival. These inhibitors are meticulously designed molecules that aim to selectively bind to the active site of the PKC δ enzyme, thereby impeding its enzymatic activity. By doing so, these compounds can influence downstream signaling pathways and cellular behaviors that are associated with PKC δ's function.

Structurally, PKC δ inhibitors often possess distinct chemical features that enable them to interact specifically with the active site of the enzyme. This active site is responsible for facilitating the transfer of phosphate groups from ATP to substrate proteins, a process that is central to the transmission of cellular signals. The inhibitors' interaction with the active site disrupts the normal phosphorylation cascade, leading to a cascade of downstream effects on cellular processes. Researchers and drug developers have invested substantial efforts in designing PKC δ inhibitors that exhibit high selectivity and potency, aiming to ensure minimal off-target effects and optimal modulation of the enzyme's activity. In conclusion, PKC δ inhibitors constitute a chemical class that is intricately involved in regulating the activity of the protein kinase C delta enzyme. These compounds are carefully designed to interact with the enzyme's active site, with the goal of influencing cellular signaling pathways and responses that are associated with PKC δ.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Rottlerin

82-08-6sc-3550
sc-3550B
sc-3550A
sc-3550C
sc-3550D
sc-3550E
10 mg
25 mg
50 mg
1 g
5 g
20 g
$82.00
$163.00
$296.00
$2050.00
$5110.00
$16330.00
51
(2)

Rottlerin inhibits PKC δ by binding to its ATP-binding site, preventing substrate phosphorylation and downstream signaling.

Gö 6983

133053-19-7sc-203432
sc-203432A
sc-203432B
1 mg
5 mg
10 mg
$103.00
$293.00
$465.00
15
(1)

Gö 6983 is a bisindolylmaleimide inhibitor that targets various PKC isoforms, including PKC δ, by competing with ATP for kinase binding.

5-(3-Chlorophenyl)-N-[4-morpholin-4-ymethyl)phenyl]furan-2-carboxamide

sc-501188
5 mg
$300.00
(0)

CID 2011756 selectively inhibits PKC δ by targeting its ATP-binding pocket, disrupting downstream cellular processes that rely on its activity.

Bisindolylmaleimide I (GF 109203X)

133052-90-1sc-24003A
sc-24003
1 mg
5 mg
$103.00
$237.00
36
(1)

Bisindolylmaleimide I is a broad-spectrum PKC inhibitor that targets PKC δ, interfering with its phosphorylation and modulating cell functions.

DAPH-7

145915-60-2sc-200699
1 mg
$71.00
1
(1)

CGP 53353 is a selective PKC δ inhibitor that hinders ATP binding, leading to reduced PKC δ activity and downstream signaling pathways.

Gö 6976

136194-77-9sc-221684
500 µg
$223.00
8
(1)

Gö 6976 is a pyrrole-indole compound that targets PKC δ, blocking its substrate phosphorylation and affecting processes dependent on its activity.

Bisindolylmaleimide IV

119139-23-0sc-3543
1 mg
$75.00
2
(1)

Bisindolylmaleimide IV is a selective PKC δ inhibitor that suppresses its kinase activity, leading to alterations in cellular signaling pathways.

Enzastaurin

170364-57-5sc-364488
sc-364488A
sc-364488B
10 mg
50 mg
200 mg
$254.00
$600.00
$1687.00
3
(1)

Enzastaurin is a PKC β and δ inhibitor that competes with ATP binding, disrupting PKC δ-mediated signaling cascades and influencing cell behavior.

PKR Inhibitor

608512-97-6sc-204200C
sc-204200
sc-204200D
sc-204200E
sc-204200A
sc-204200B
1 mg
5 mg
10 mg
25 mg
50 mg
100 mg
$64.00
$150.00
$300.00
$600.00
$800.00
$1800.00
5
(1)

C16 is a diacylglycerol (DAG) analog that selectively inhibits PKC δ by interfering with its activation and downstream modulation of cellular processes.