Date published: 2026-5-30

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ENSMUSG00000074179 Inhibitors

Chemical inhibitors of ENSMUSG00000074179 utilize diverse molecular mechanisms to impede the protein's activity within cellular processes. Alizarin, for example, can directly bind to the protein's active site, which competes with its natural substrates. This competition effectively prevents the substrates from interacting with ENSMUSG00000074179 and carrying out its normal enzymatic functions. Similarly, Quercetin can inhibit the protein by stabilizing its inactive form, thus preventing the structural changes that are necessary for its activation. This stabilization not only inhibits ENSMUSG00000074179 itself but also can disrupt its interaction with other cellular molecules that are essential for its function.

Other inhibitors interfere with signaling pathways that are crucial for the protein's activity. Genistein, for instance, can inhibit ENSMUSG00000074179 by blocking the phosphorylation it requires for activation, acting as a tyrosine kinase inhibitor. PD 98059 and U0126 both target the MAP kinase pathway, with PD 98059 specifically inhibiting MEK, thereby preventing the activation of MAP kinase, and U0126 preventing necessary phosphorylation steps. LY294002 and Wortmannin exert their effects by inhibiting PI3K, an upstream regulator in pathways that involve ENSMUSG00000074179, leading to a reduction in the protein's signaling activities. SB203580 and SP600125 inhibit the p38 MAP kinase and JNK, respectively, each contributing to a decrease in ENSMUSG00000074179 activity by impeding different components of the MAP kinase signaling pathways. SB431542 selectively inhibits the TGF-β type I receptor ALK5, reducing signaling through pathways that involve ENSMUSG00000074179, while Gefitinib targets the EGFR, which is another significant player in the regulatory pathways of ENSMUSG00000074179. Each of these inhibitors, through their unique interactions with different molecules and pathways, can reduce the functional activity of ENSMUSG00000074179.

Items 1 to 10 of 12 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Alizarin

72-48-0sc-214519
sc-214519A
1.5 g
100 g
$21.00
$51.00
(0)

Alizarin directly inhibits ENSMUSG00000074179 by binding to the active site where it competes with the natural substrates of the enzyme, preventing their interaction and subsequent catalytic activity. This inhibition process specifically disrupts the enzyme's ability to carry out its normal metabolic functions within the cell.

Genistein

446-72-0sc-3515
sc-3515A
sc-3515B
sc-3515C
sc-3515D
sc-3515E
sc-3515F
100 mg
500 mg
1 g
5 g
10 g
25 g
100 g
$45.00
$164.00
$200.00
$402.00
$575.00
$981.00
$2031.00
46
(1)

Genistein inhibits ENSMUSG00000074179 by interfering with the phosphorylation process that the protein relies on for its activation. This compound acts as a tyrosine kinase inhibitor, and since phosphorylation is a common post-translational modification that can activate enzymes, its inhibition can result in decreased activity of ENSMUSG00000074179.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$110.00
$250.00
$936.00
$50.00
33
(2)

Quercetin inhibits ENSMUSG00000074179 by stabilizing the inactive form of the protein and preventing its conformational change required for activation. This binding also potentially disrupts the protein's interaction with other cellular molecules necessary for its function.

PD 98059

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

PD 98059 inhibits ENSMUSG00000074179 by blocking the MAP kinase pathway, which is a signaling pathway that the protein is part of. This chemical specifically inhibits MEK, which in turn prevents the activation of MAP kinase that could be downstream of ENSMUSG00000074179 activity.

LY 294002

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

LY294002 inhibits ENSMUSG00000074179 by acting as a PI3K inhibitor, which is an upstream regulator in pathways that ENSMUSG00000074179 is involved in. Inhibition of PI3K leads to a reduction in downstream signaling activities, which includes the functional processes of ENSMUSG00000074179.

SB 203580

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

SB203580 inhibits ENSMUSG00000074179 by impeding the p38 MAP kinase pathway. Since this signaling pathway has a role in the regulation of ENSMUSG00000074179, the inhibition of p38 MAP kinase directly reduces the functional activity of the protein.

U-0126

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

U0126 functions as an inhibitor of MEK, which is also part of the MAP kinase pathway that ENSMUSG00000074179 operates within. By inhibiting MEK, U0126 effectively reduces the protein's activity by preventing the necessary phosphorylation and activation steps.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

Wortmannin inhibits ENSMUSG00000074179 by irreversibly inhibiting PI3K. Given that PI3K is crucial for several cellular signaling pathways, the inhibition of PI3K by Wortmannin results in a decrease in the activity of ENSMUSG00000074179 as it interrupts the signaling cascades in which the protein is involved.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Rapamycin inhibits ENSMUSG00000074179 by binding to FKBP12 and forming a complex that inhibits the mTOR pathway, which is a key regulator of cell growth and metabolism that the protein is associated with. The inhibition of mTOR leads to a reduction in the activity of downstream proteins including ENSMUSG00000074179.

SP600125

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

SP600125 inhibits ENSMUSG00000074179 by acting as an inhibitor of JNK, another kinase within the MAP kinase signaling pathways. As JNK activity is reduced, the subsequent signaling events that lead to the activation of ENSMUSG00000074179 are also inhibited.