RGL2 inhibitors encompass a category of chemicals that modulate cellular signaling pathways in which RGL2 is a participant or has an influence. These inhibitors do not directly target RGL2 but rather the broader signaling cascades that RGL2 might affect, such as MAPK/ERK, PI3K/AKT, and Rho GTPase pathways. The inhibition strategies include the use of small molecules that interfere with kinases and other proteins that are either upstream or downstream of RGL2 in these pathways.
The inhibitors function by altering the activity of kinases like CDK4/6, MEK, and AKT or by disrupting the interactions of small GTPases, which are pivotal elements in signaling pathways regulated by RGL2. For instance, PD 0332991 and CCT128930 are kinase inhibitors that can arrest the cell cycle and prevent survival signals, respectively, thereby counteracting the cell proliferation and survival effects RGL2 may promote through these pathways. Other chemicals, such as LY294002 and Wortmannin, are PI3K inhibitors that can reduce AKT activation, thereby impeding any RGL2-mediated signaling through the PI3K/AKT pathway, which is often linked to cell growth and survival. Similarly, U0126 and PD 98059 are specific MEK inhibitors that prevent the activation of the ERK pathway, which could be critical in RGL2-related signaling mechanisms.
SEE ALSO...
Items 1 to 10 of 11 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $321.00 | ||
Inhibits CDK4/6, leading to cell cycle arrest; as RGL2 is implicated in GTPase signaling related to cell cycle progression, inhibition of CDK4/6 can impede RGL2-mediated effects. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A PI3K inhibitor that can reduce AKT phosphorylation, potentially diminishing RGL2-mediated signaling through the PI3K/AKT pathway. | ||||||
GW 5074 | 220904-83-6 | sc-200639 sc-200639A | 5 mg 25 mg | $106.00 $417.00 | 10 | |
Inhibits Raf kinase, which is upstream of MEK/ERK signaling; may reduce RGL2-mediated activation of the MAPK/ERK pathway. | ||||||
NSC 23766 | 733767-34-5 | sc-204823 sc-204823A | 10 mg 50 mg | $151.00 $609.00 | 75 | |
Disrupts Rac1 interaction with its guanine nucleotide exchange factors (GEFs), potentially attenuating RGL2-mediated Rac1 activation. | ||||||
IQ-1 | 331001-62-8 | sc-202665 | 10 mg | $180.00 | 2 | |
A selective inhibitor of Cdc42, a GTPase that RGL2 may interact with; inhibits GTPase signaling pathways involving RGL2. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $186.00 $707.00 | 88 | |
ROCK inhibitor that affects downstream Rho GTPase signaling; may indirectly lessen RGL2-mediated cytoskeletal dynamics and cell migration. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
Inhibits MEK1, a kinase in the MAPK/ERK pathway; could suppress the activation of downstream targets of RGL2 within this pathway. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
PI3K inhibitor, similar to LY294002, that can impact RGL2-related PI3K/AKT signaling pathways. | ||||||
XAV939 | 284028-89-3 | sc-296704 sc-296704A sc-296704B | 1 mg 5 mg 50 mg | $36.00 $117.00 $525.00 | 26 | |
Directly inhibits Cdc42-Rac1 interaction; may affect RGL2-mediated signaling by altering GTPase activity. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
Inhibits p38 MAPK, which is involved in stress responses; may modulate RGL2-related signaling under stress conditions. | ||||||