1810020G14Rik Activators are a series of chemical compounds that indirectly stimulate the functional activity of the protein 1810020G14Rik by interacting with specific signaling pathways and biological processes. Forskolin, for instance, by raising cAMP levels, indirectly activates protein kinase A (PKA), affecting phosphorylation events that could enhance the activity of 1810020G14Rik. Similarly, Epigallocatechin gallate, by inhibiting various protein kinases, and LY294002, as a PI3K inhibitor, both impact signaling. 1810020G14Rik Activators encompass a spectrum of chemical compounds that indirectly enhance the functional activity of the 1810020G14Rik protein through modulation of distinct signaling pathways and cellular processes. Forskolin, for example, catalyzes the conversion of ATP to cAMP, ultimately activating PKA, which can phosphorylate a multitude of substrates, potentially leading to the upregulation of 1810020G14Rik activity in cAMP-responsive pathways.
Epigallocatechin gallate (EGCG) serves a critical role by inhibiting various protein kinases, which might reduce competitive phosphorylation or alter signaling cascades in a manner that indirectly favors 1810020G14Rik activation. Similarly, the PI3K inhibitors LY294002 and Wortmannin create a cellular context where downregulation of the PI3K/Akt pathway may shift cellular dynamics to enhance 1810020G14Rik's role in relevant processes. Inhibition of MEK by PD98059 and U0126, by disrupting the MAPK/ERK pathway, may redirect the flow of signaling to compensate through mechanisms that activate 1810020G14Rik. Furthermore, compounds like Sphingosine-1-phosphate and Phorbol 12-myristate 13-acetate (PMA) operate through sphingolipid and PKC-mediated signaling, respectively, potentially contributing to the functional activation of 1810020G14Rik by fine-tuning the cellular signaling milieu. SB203580's inhibition of p38 MAPK and Bisindolylmaleimide I's targeting of PKC may similarly induce a cellular environment that selectively enhances 1810020G14Rik activity by attenuating specific stress response and signaling pathways.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
EGCG is a potent antioxidant that inhibits various protein kinases. By modulating kinase activity, it could lead to the activation of 1810020G14Rik by altering the phosphorylation status of proteins within its signaling network. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a PI3K inhibitor. By inhibiting PI3K, it affects the PI3K/Akt pathway, which may indirectly lead to the functional activation of 1810020G14Rik if its activity is regulated by the downstream effects of this pathway. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 is an inhibitor of MEK, which is part of the MAPK/ERK pathway. Inhibition of MEK could lead to compensatory activation of alternative pathways that enhance the activity of 1810020G14Rik. | ||||||
D-erythro-Sphingosine-1-phosphate | 26993-30-6 | sc-201383 sc-201383D sc-201383A sc-201383B sc-201383C | 1 mg 2 mg 5 mg 10 mg 25 mg | $162.00 $316.00 $559.00 $889.00 $1693.00 | 7 | |
Sphingosine-1-phosphate binds to its receptors and activates intracellular signaling that could lead to the functional activation of 1810020G14Rik by modulating cellular processes such as migration and survival. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA is a potent activator of protein kinase C (PKC), which is involved in various signaling cascades. Activation of PKC could lead to the activation of 1810020G14Rik through PKC-mediated signaling events. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is an inhibitor of p38 MAPK. By inhibiting p38 MAPK, it could lead to the functional activation of 1810020G14Rik through the alteration of stress response signaling pathways. | ||||||
A23187 | 52665-69-7 | sc-3591 sc-3591B sc-3591A sc-3591C | 1 mg 5 mg 10 mg 25 mg | $54.00 $128.00 $199.00 $311.00 | 23 | |
A23187 is an ionophore that increases intracellular calcium levels. Elevated calcium levels can activate calcium-dependent proteins that could enhance the activity of 1810020G14Rik via calcium signaling pathways. | ||||||
Ionomycin | 56092-82-1 | sc-3592 sc-3592A | 1 mg 5 mg | $76.00 $265.00 | 80 | |
Ionomycin is a calcium ionophore that increases intracellular calcium, thereby activating calcium-dependent signaling pathways. These pathways could indirectly lead to the activation of 1810020G14Rik. | ||||||
Bisindolylmaleimide I (GF 109203X) | 133052-90-1 | sc-24003A sc-24003 | 1 mg 5 mg | $103.00 $237.00 | 36 | |
Bisindolylmaleimide I is a specific inhibitor of PKC. Inhibition of PKC can lead to changes in signaling networks, potentially enhancing the activity of 1810020G14Rik by shifting the balance of cellular signaling. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin is an inhibitor of PI3K, and by affecting the PI3K/Akt pathway, it may indirectly activate 1810020G14Rik by modulating cellular survival and growth signals. |