Date published: 2026-2-14

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BKS Inhibitors

Chemical inhibitors of BKS can disrupt its signaling functions through a variety of molecular mechanisms. Wortmannin and LY294002, for instance, target phosphoinositide 3-kinases (PI3Ks), key enzymes in the PI3K/Akt signaling pathway which is often crucial for protein functions related to cell survival, proliferation, and metabolism. By inhibiting PI3K, these chemicals prevent the phosphorylation of phosphatidylinositol 4,5-bisphosphate (PIP2) to phosphatidylinositol 3,4,5-trisphosphate (PIP3). This inhibition can impede the activation of downstream targets that BKS may act upon or with, thereby impeding BKS's functionality in cellular signaling. Similarly, specific kinase inhibitors such as Dasatinib and PP2 interfere with Src family kinases. Since Src kinases are involved in various signaling pathways, their inhibition by these chemicals can disrupt the functional activity of BKS if it is associated with Src-mediated signaling pathways.

Further inhibitory effects on BKS come from chemicals like U0126, PD98059, SB203580, and SP600125, which target different mitogen-activated protein kinases (MAPKs). U0126 and PD98059 specifically inhibit MEK1/2, thereby blocking the activation of extracellular signal-regulated kinases (ERKs), which could be necessary for BKS's role in certain signaling pathways. SB203580, on the other hand, inhibits p38 MAPK, and SP600125 inhibits c-Jun N-terminal kinase (JNK), both of which are part of the MAPK family. These inhibitors can disrupt the MAPK signaling cascade, leading to a decrease in BKS's activity if it is regulated by MAPK. Additionally, GF109203X and Go6983, as inhibitors of protein kinase C (PKC), can impede signaling pathways where BKS's functionality is contingent upon PKC-mediated phosphorylation. Finally, mTOR inhibitors like Rapamycin and AZD8055 can have a substantial effect on BKS by blocking the mTOR pathway, which is critical for cell growth and proliferation. AZD8055 specifically targets both mTORC1 and mTORC2 complexes, which could be essential for BKS's activity in related signaling networks. Each of these chemicals, by targeting specific kinases or signaling pathways, can significantly alter the functional landscape in which BKS operates within the cell.

SEE ALSO...

Items 1 to 10 of 12 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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 a steroidal metabolite of Penicillium funiculosum and acts as a potent inhibitor of phosphoinositide 3-kinases (PI3K), which can lead to the downstream inhibition of pathways and proteins, potentially including BKS, that rely on PI3K signaling.

LY 294002

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

LY294002 is a synthetic molecule that inhibits PI3K, preventing the phosphorylation of PIP2 to PIP3. This action disrupts signal transduction pathways associated with PI3K, which could include those involving BKS if it is part of the PI3K pathway.

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$70.00
$145.00
51
(1)

Dasatinib is a small molecule inhibitor targeting multiple tyrosine kinases, including Src family kinases and BCR-ABL. It could inhibit BKS if BKS is a kinase or is part of a pathway that requires kinase activity suppressed by Dasatinib.

PP 2

172889-27-9sc-202769
sc-202769A
1 mg
5 mg
$94.00
$227.00
30
(1)

PP2 is a selective inhibitor of Src family tyrosine kinases. It would inhibit BKS if BKS is a Src family member or is functionally dependent on Src kinase signaling.

U-0126

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

U0126 is an inhibitor of MEK1/2, which blocks the activation of MAPK/ERK kinase. If BKS functions downstream of the MEK/ERK pathway, U0126 could inhibit its activity by disrupting upstream signaling.

SB 203580

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

SB203580 is a pyridinyl imidazole compound that inhibits p38 MAP kinase. If BKS is involved in a pathway that is regulated by p38 MAPK, then SB203580 could inhibit its activity.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

SP600125 is an anthrapyrazolone inhibitor that selectively inhibits JNK. If BKS is a JNK substrate or involved in JNK-mediated signaling, SP600125 could lead to its functional inhibition.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

PD98059 is a non-competitive inhibitor of MEK1/2 activation and kinase activity, which could inhibit BKS if BKS relies on the MEK/ERK pathway for its function.

Bisindolylmaleimide I (GF 109203X)

133052-90-1sc-24003A
sc-24003
1 mg
5 mg
$105.00
$242.00
36
(1)

GF109203X, also known as Bisindolylmaleimide I, is a potent and selective PKC inhibitor. If BKS activity is PKC-dependent, GF109203X could result in functional inhibition of BKS.

Gö 6983

133053-19-7sc-203432
sc-203432A
sc-203432B
1 mg
5 mg
10 mg
$105.00
$299.00
$474.00
15
(1)

Go6983 is a pan-PKC inhibitor that could inhibit BKS if BKS is regulated by PKC or is part of PKC-mediated signaling pathways.