Date published: 2025-12-18

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PKC Inhibitors

Santa Cruz Biotechnology now offers a broad range of PKC Inhibitors. Members of the protein kinase C (PKC) family play a key regulatory role in a variety of cellular functions including cell growth and differentiation, gene expression, hormone secretion and membrane function. PKC Inhibitors offered by Santa Cruz inhibit PKC and, in some cases, other cell growth and differentiation related proteins. View detailed PKC Inhibitor specifications, including PKC Inhibitor CAS number, molecular weight, molecular formula and chemical structure, by clicking on the product name.

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Items 1 to 10 of 110 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

HA-100 dihydrochloride

210297-47-5sc-203072
sc-203072A
5 mg
25 mg
$163.00
$418.00
39
(1)

HA-100 dihydrochloride (CAS 210297-47-5) is a chemical compound utilized as a potent inhibitor of PKC, a key enzyme in cellular signaling. It modulates PKC activity, impacting cellular processes. Notable for its inhibitory properties, it's employed in various research contexts to investigate signaling pathways.

Melittin

37231-28-0sc-200868
sc-200868A
sc-200868B
500 µg
1 mg
10 mg
$192.00
$332.00
$772.00
2
(1)

Melittin (CAS 37231-28-0) is a peptide found in bee venom. It acts as an inhibitor of PKC, a cellular signaling enzyme. Its impact on cellular processes makes it a subject of scientific interest.

1-(5-Isoquinolinesulfonyl)-3-methylpiperazine

84477-73-6sc-208552
5 mg
$78.00
(0)

1-(5-Isoquinolinesulfonyl)-3-methylpiperazine (CAS 84477-73-6) is a chemical compound known for its role as a PKC inhibitor. It modulates PKC activity without clinical connotations.

Suramin sodium

129-46-4sc-507209
sc-507209F
sc-507209A
sc-507209B
sc-507209C
sc-507209D
sc-507209E
50 mg
100 mg
250 mg
1 g
10 g
25 g
50 g
$149.00
$210.00
$714.00
$2550.00
$10750.00
$21410.00
$40290.00
5
(1)

Suramin sodium (CAS 129-46-4) is a compound acting as a PKC inhibitor, targeting cellular signaling pathways. It modulates PKC activity, impacting cellular processes.

rac Propranolol-d7

98897-23-5sc-212742
5 mg
$305.00
1
(0)

Rac Propranolol-d7 exhibits unique interactions with protein kinase C (PKC) through its isotopic labeling, which allows for precise tracking in biochemical assays. This compound influences the conformational dynamics of PKC, potentially altering its activation state and modulating downstream signaling cascades. Its distinct isotopic composition may enhance the resolution of kinetic studies, providing insights into the timing and efficiency of phosphorylation events within cellular pathways.

Myricetin 3-Rhamnoside

17912-87-7sc-221964
2 mg
$100.00
(0)

Myricetin 3-Rhamnoside (CAS 17912-87-7) is a compound known for its PKC inhibitory properties. It modulates PKC activity without involving clinical or therapeutic aspects, showing potential in cellular regulation.

Calphostin C

121263-19-2sc-3545
sc-3545A
100 µg
1 mg
$336.00
$1642.00
20
(1)

Calphostin C (CAS 121263-19-2) is a potent compound that acts as an inhibitor of PKC (Protein Kinase C). It influences cellular processes by targeting PKC activity modulation.

O-3M3FBS

313981-55-4sc-204142
sc-204142A
10 mg
50 mg
$140.00
$460.00
2
(1)

BIM-1 selectively inhibits PKCβ isoforms by targeting the ATP-binding site, reducing their kinase activity and downstream signaling cascades.

TLCK hydrochloride

4238-41-9sc-201296
200 mg
$160.00
2
(1)

TLCK hydrochloride acts as a selective inhibitor of protein kinase C (PKC), engaging in specific interactions that disrupt the enzyme's catalytic activity. Its unique structure allows for competitive binding at the active site, influencing the phosphorylation of target substrates. The compound's reactivity with cysteine residues in PKC can lead to conformational changes, affecting the enzyme's stability and function. This modulation of PKC activity can provide insights into its regulatory mechanisms in various cellular processes.

Chelerythrine

34316-15-9sc-507380
100 mg
$540.00
(0)

Chelerythrine interferes with PKC activation by binding to the catalytic domain, leading to reduced substrate phosphorylation and altered cellular responses.