Chemical inhibitors of LLGL1 can impede its function by targeting various signaling pathways and cellular processes that are essential for maintaining cell polarity. Bisindolylmaleimide I and Gö 6983, for instance, are potent inhibitors of Protein Kinase C (PKC). Inhibition of PKC by these chemicals can lead to changes in the phosphorylation state of proteins, disrupting the balance that affects LLGL1's localization and stability, hence its functional capacity in cells. Staurosporine, another multi-kinase inhibitor, can also obstruct PKC among other kinases, which can result in the functional inhibition of LLGL1 by altering cell polarity and cytoskeletal dynamics. Similarly, Y-27632 selectively inhibits ROCK kinases, and since ROCK is implicated in actin cytoskeleton regulation, its inhibition can affect LLGL1 by altering the cytoskeletal architecture that LLGL1 relies on to exert its function. ML-7 and Blebbistatin target the actomyosin components by inhibiting myosin light chain kinase and myosin II ATPase activity, respectively. These inhibitions can result in changes to cell shape and contractility, processes in which LLGL1 is inherently involved.
PD 98059 and U0126 specifically inhibit the MEK enzymes within the MAPK/ERK pathway, a pathway known for its role in cell growth and differentiation. Disrupting this pathway can interfere with LLGL1's function in cell polarity since the MEK enzymes are upstream regulators that can affect LLGL1's activity. SP600125 impairs the JNK pathway, which is another regulator of cell morphology and polarity. By inhibiting JNK, SP600125 can impede the signaling pathways that LLGL1 is a part of, leading to its functional inhibition. LY294002 and Wortmannin, both PI3K inhibitors, disrupt PI3K signaling that is crucial for cell survival and growth. Since PI3K is also involved in regulating cell polarity, its inhibition can hinder LLGL1 function. Lastly, SB203580 serves as a specific inhibitor of p38 MAPK, a pathway that responds to stress stimuli and is involved in cell differentiation. By blocking this pathway, SB203580 can negatively affect the role LLGL1 plays in maintaining cell polarity. Collectively, these chemicals target various kinases and signaling pathways that directly or indirectly impinge upon LLGL1's role in cell polarity maintenance.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Bisindolylmaleimide I (GF 109203X) | 133052-90-1 | sc-24003A sc-24003 | 1 mg 5 mg | $103.00 $237.00 | 36 | |
Bisindolylmaleimide I inhibits Protein Kinase C (PKC), which is involved in cell polarity where LLGL1 functions. Inhibiting PKC can disrupt the phosphorylation state that affects LLGL1's localization and stability, leading to its functional inhibition. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Staurosporine is a potent kinase inhibitor affecting multiple kinases including PKC. By inhibiting PKC, it can lead to the functional inhibition of LLGL1 due to altered cell polarity and cytoskeletal dynamics. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Y-27632 is a selective inhibitor of ROCK kinases. ROCK is implicated in regulating the actin cytoskeleton, and since LLGL1 is involved in cell polarity which relies on cytoskeletal dynamics, inhibition of ROCK can functionally inhibit LLGL1. | ||||||
ML-7 hydrochloride | 110448-33-4 | sc-200557 sc-200557A | 10 mg 50 mg | $89.00 $262.00 | 13 | |
ML-7 is an inhibitor of myosin light chain kinase (MLCK), which is crucial for actin-myosin contraction. By inhibiting MLCK, ML-7 can affect cell shape and polarity, thereby inhibiting LLGL1 action in maintaining cell polarity. | ||||||
(±)-Blebbistatin | 674289-55-5 | sc-203532B sc-203532 sc-203532A sc-203532C sc-203532D | 5 mg 10 mg 25 mg 50 mg 100 mg | $179.00 $307.00 $455.00 $924.00 $1689.00 | 7 | |
Blebbistatin inhibits myosin II ATPase activity. Myosin II is involved in cell contractility and polarity. By inhibiting myosin II, Blebbistatin can disrupt cell polarity processes in which LLGL1 is functionally involved. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD 98059 is an inhibitor of MEK, which is part of the MAPK/ERK pathway. Since LLGL1 is implicated in cell polarity and the MAPK/ERK pathway is involved in cell growth and differentiation, inhibiting MEK can functionally inhibit LLGL1. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of JNK, which participates in the regulation of cell morphology and polarity. Inhibition of JNK can functionally inhibit LLGL1 by disrupting signaling pathways involved in maintaining cell polarity. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a PI3K inhibitor. PI3K signaling is essential for cell survival and growth, processes that are linked to cell polarity controlled by LLGL1. Inhibition of PI3K can therefore disrupt LLGL1's function in cell polarity. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
U0126 is a selective inhibitor of MEK1/2. By inhibiting MEK1/2, part of the MAPK/ERK pathway, U0126 can disrupt the signaling required for cell differentiation and polarity, thereby functionally inhibiting LLGL1. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is a specific inhibitor of p38 MAPK. The p38 MAPK pathway is implicated in stress responses and cell differentiation. Inhibition of p38 MAPK can lead to the functional inhibition of LLGL1, affecting its role in cell polarity. | ||||||