Date published: 2025-11-1

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LOC100041378 Inhibitors

inhibitors of LOC100041378 like Wortmannin and LY294002 inhibit the PI3K/AKT pathway, a crucial signal transduction route that governs cell growth, survival, and metabolism. By inhibiting PI3K, these compounds prevent the phosphorylation and activation of AKT, which can lead to changes in protein activity, including those potentially regulated by LOC100041378. PD0325901 and SB203580 target the MAPK signaling pathway; PD0325901 specifically inhibits MEK1/2, preventing the activation of ERK1/2, while SB203580 selectively impedes p38 MAPK. These actions can alter the phosphorylation state of proteins, influencing their activity, stability, and interaction with other cellular components.

SP600125, PP2, and Gefitinib affect different aspects of kinase regulation. SP600125 reduces JNK activity, thereby influencing proteins regulated by stress-activated pathways. PP2 blocks Src family kinases, which are involved in multiple signaling pathways, including those that regulate cell adhesion, growth, and differentiation. Gefitinib's inhibition of EGFR tyrosine kinase can lead to reduced activation of downstream signaling molecules that are important for cellular responses. ZM447439 and VX-680 are Aurora kinase inhibitors, disrupting cell cycle progression and mitotic spindle formation, which can impact the phosphorylation and function of proteins associated with cell division. Palbociclib's inhibition of CDK4/6 alters the cell cycle, potentially affecting the synthesis and degradation of proteins. Olaparib and Nutlin-3a target DNA repair and tumor suppressor pathways. By inhibiting PARP, Olaparib affects DNA damage responses,which may influence protein stability, including potentially LOC100041378. Nutlin-3a disrupts p53-MDM2 interaction, which can alter p53-mediated transcriptional regulation of genes involved in cell cycle control and apoptosis, processes that can indirectly affect protein functions.

Items 1 to 10 of 11 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$66.00
$219.00
$417.00
97
(3)

Wortmannin is a covalent inhibitor of phosphatidylinositol 3-kinase (PI3K), which can affect downstream signaling impacting protein activity, including LOC100041378.

SP600125

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

SP600125 is an inhibitor of c-Jun N-terminal kinase (JNK), altering transcription factor activity and protein expression.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$88.00
$342.00
284
(5)

SB203580 is a p38 MAP kinase inhibitor, modifying the kinase activity that can control protein function and cell responses.

PP 2

172889-27-9sc-202769
sc-202769A
1 mg
5 mg
$92.00
$223.00
30
(1)

PP2 is a selective inhibitor of Src family tyrosine kinases, affecting signaling pathways and potentially the activity of proteins like LOC100041378.

ZM-447439

331771-20-1sc-200696
sc-200696A
1 mg
10 mg
$150.00
$349.00
15
(1)

ZM447439 is an Aurora kinase inhibitor, which can disrupt cell cycle progression and thus protein activity and stability.

Gefitinib

184475-35-2sc-202166
sc-202166A
sc-202166B
sc-202166C
100 mg
250 mg
1 g
5 g
$62.00
$112.00
$214.00
$342.00
74
(2)

Gefitinib selectively inhibits the epidermal growth factor receptor (EGFR) tyrosine kinase, which can regulate protein signal transduction.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

LY294002 inhibits PI3K, altering the AKT signaling pathway and potentially affecting protein activity, including LOC100041378.

Olaparib

763113-22-0sc-302017
sc-302017A
sc-302017B
250 mg
500 mg
1 g
$206.00
$299.00
$485.00
10
(1)

Olaparib is a PARP inhibitor, influencing DNA repair processes and can impact protein stability and function.

Tozasertib

639089-54-6sc-358750
sc-358750A
25 mg
50 mg
$61.00
$85.00
4
(1)

VX-680 is an Aurora kinase inhibitor, potentially altering phosphorylation patterns that affect protein function.

Palbociclib

571190-30-2sc-507366
50 mg
$315.00
(0)

Palbociclib is a CDK4/6 inhibitor, which can arrest cell cycle progression impacting protein synthesis and turnover.