ORCTL2 Inhibitors would belong to a class of chemical compounds designed to selectively modulate the activity or interactions of ORCTL2. These inhibitors would be developed with the goal of influencing the transport of organic cations facilitated by ORCTL2. Given that ORCTL2 plays a role in the uptake of cationic compounds, inhibitors might be designed to target specific binding sites or functional domains within ORCTL2 that are essential for its transport function. These compounds could be engineered to competitively bind to active sites within the transporter, potentially disrupting the transport of organic cations across the cell membrane.
Chemically, ORCTL2 Inhibitors could encompass a diverse range of structures, such as small molecules or potentially larger molecules, including peptides. These inhibitors might be designed to mimic the structure of organic cations or other ligands that ORCTL2 transports, effectively competing for binding and affecting the transport process. Alternatively, they could interact with regulatory elements of ORCTL2, such as allosteric sites, altering the transporter's conformation and impacting its transport activity. Designing effective ORCTL2 Inhibitors would necessitate a detailed understanding of the structural biology of ORCTL2, including the specific sites responsible for cation binding and transport. Given ORCTL2's involvement in cellular processes related to organic cation uptake, these inhibitors could offer insights into the complex molecular mechanisms underlying this type of transport without immediate reference to applications. Please note that research in this area is ongoing.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $78.00 $153.00 $740.00 $1413.00 $2091.00 | 73 | |
Derived from the plant Coleus forskohlii, Forskolin is known for its ability to increase cyclic AMP (cAMP) levels in cells, potentially influencing ORCTL2 activity indirectly. | ||||||
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $260.00 $350.00 $500.00 | 34 | |
IBMX is a non-specific inhibitor of phosphodiesterases, leading to increased levels of cAMP and cGMP in cells, which can indirectly affect the activity of transporters like ORCTL2. | ||||||
(−)-Epinephrine | 51-43-4 | sc-205674 sc-205674A sc-205674B sc-205674C sc-205674D | 1 g 5 g 10 g 100 g 1 kg | $41.00 $104.00 $201.00 $1774.00 $16500.00 | ||
As a hormone and neurotransmitter, Epinephrine can influence transporter activity through adrenergic receptors, potentially affecting ORCTL2. | ||||||
L-Noradrenaline | 51-41-2 | sc-357366 sc-357366A | 1 g 5 g | $326.00 $485.00 | 3 | |
Similar to Epinephrine, Norepinephrine affects adrenergic receptors and can modulate various cellular processes, potentially influencing ORCTL2 activity. | ||||||
PGE2 | 363-24-6 | sc-201225 sc-201225C sc-201225A sc-201225B | 1 mg 5 mg 10 mg 50 mg | $57.00 $159.00 $275.00 $678.00 | 37 | |
PGE2 is involved in modulating inflammatory responses and can affect various cellular signaling pathways, possibly impacting ORCTL2 activity. | ||||||
Sodium nitroprusside dihydrate | 13755-38-9 | sc-203395 sc-203395A sc-203395B | 1 g 5 g 100 g | $43.00 $85.00 $158.00 | 7 | |
Nitric oxide donors release nitric oxide, a signaling molecule that can modulate various cellular functions, including transporter activity, potentially influencing ORCTL2. | ||||||
Caffeine | 58-08-2 | sc-202514 sc-202514A sc-202514B sc-202514C sc-202514D | 50 g 100 g 250 g 1 kg 5 kg | $33.00 $67.00 $97.00 $192.00 $775.00 | 13 | |
Caffeine, a known phosphodiesterase inhibitor, increases cAMP levels, potentially affecting ORCTL2 activity through altered cellular signaling. | ||||||
Adenosine | 58-61-7 | sc-291838 sc-291838A sc-291838B sc-291838C sc-291838D sc-291838E sc-291838F | 1 g 5 g 100 g 250 g 1 kg 5 kg 10 kg | $34.00 $48.00 $300.00 $572.00 $1040.00 $2601.00 $4682.00 | 1 | |
Adenosine interacts with its receptors to modulate cellular signaling pathways, potentially affecting transporters like ORCTL2. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $28.00 $38.00 | 5 | |
As a beta-adrenergic agonist, Isoproterenol influences adrenergic receptors and could indirectly impact ORCTL2 activity through changes in intracellular signaling. | ||||||
Rolipram | 61413-54-5 | sc-3563 sc-3563A | 5 mg 50 mg | $77.00 $216.00 | 18 | |
Rolipram, a selective inhibitor of phosphodiesterase 4 (PDE4), leads to increased cAMP levels, which may indirectly influence ORCTL2. | ||||||