Olfr566, like other olfactory receptors, is a member of the G-protein-coupled receptor (GPCR) family, responsible for recognizing and transducing odorant signals. These receptors play a pivotal role in initiating neuronal responses that lead to the perception of smells. Olfr566, being part of the largest gene family in the genome, contributes to the diversity and specificity of odorant detection. The potential inhibition of Olfr566 involves targeting specific signaling pathways associated with its function. Tetrodotoxin, a voltage-gated sodium channel blocker, modulates olfactory signaling pathways by disrupting ion channel activity. Nifedipine, a voltage-dependent L-type calcium channel blocker, influences Olfr566 indirectly by disrupting calcium homeostasis. Pertussis toxin inhibits Olfr566 through G protein interference, disrupting the normal functioning of the receptor.
H-89, a protein kinase A (PKA) inhibitor, disrupts the cAMP/PKA signaling cascade, leading to altered expression and function of Olfr566. LY294002, a PI3K inhibitor, affects Olfr566 through the PI3K/Akt pathway, interfering with downstream effectors crucial for its normal functioning. Rolipram, a phosphodiesterase (PDE4) inhibitor, elevates cAMP levels, affecting olfactory signaling and altering the expression and function of Olfr566. Amiloride, a sodium channel blocker, influences Olfr566 by modulating ion homeostasis. Verapamil, a calcium channel blocker, indirectly influences Olfr566 by disrupting calcium homeostasis. TAK-733 and U0126 are MEK inhibitors affecting Olfr566 through the MAPK/ERK pathway, disrupting the signaling cascade and altering expression and function. Wortmannin, a PI3K inhibitor, modulates Olfr566 activity through the PI3K/Akt pathway. Thapsigargin, a SERCA inhibitor, disrupts calcium homeostasis, potentially leading to decreased expression and function of Olfr566. In summary, the potential inhibition of Olfr566 involves targeting specific biochemical and cellular pathways associated with olfactory signal transduction. Modulating these pathways using various inhibitors may provide insights into understanding and controlling the function of Olfr566 in the complex process of odorant perception.
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $58.00 $170.00 | 15 | |
Voltage-dependent L-type calcium channel blocker influencing Olfr566 indirectly. Nifedipine disrupts calcium homeostasis, modulating olfactory signaling pathways and consequently leading to decreased expression and function of Olfr566. | ||||||
Pertussis Toxin (islet-activating protein) | 70323-44-3 | sc-200837 | 50 µg | $442.00 | 3 | |
ADP-ribosylating agent inhibiting Olfr566 through G protein interference. Pertussis toxin disrupts GPCR-mediated transduction, leading to altered expression and function of Olfr566 as a downstream consequence of G protein inhibition. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
PI3K inhibitor affecting Olfr566 through the PI3K/Akt pathway. LY294002 disrupts the PI3K pathway, modulating Olfr566 activity by interfering with downstream effectors crucial for its normal functioning. | ||||||
Rolipram | 61413-54-5 | sc-3563 sc-3563A | 5 mg 50 mg | $75.00 $212.00 | 18 | |
Phosphodiesterase (PDE4) inhibitor affecting Olfr566 through cAMP regulation. Rolipram elevates cAMP levels, modulating olfactory signaling pathways and consequently leading to altered expression and function of Olfr566. | ||||||
Amiloride | 2609-46-3 | sc-337527 | 1 g | $290.00 | 7 | |
Sodium channel blocker influencing Olfr566 by modulating ion homeostasis. Amiloride disrupts cellular ionic balance, indirectly suppressing Olfr566 expression and signaling by altering the intracellular environment. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $367.00 | ||
Calcium channel blocker influencing Olfr566 indirectly. Verapamil disrupts calcium homeostasis, modulating olfactory signaling pathways and consequently leading to decreased expression and function of Olfr566. | ||||||
TAK-733 | 1035555-63-5 | sc-364630 sc-364630A | 5 mg 10 mg | $340.00 $640.00 | 1 | |
MEK inhibitor affecting Olfr566 through the MAPK/ERK pathway. TAK-733 disrupts the MAPK/ERK signaling cascade, resulting in altered expression and function of Olfr566 as a downstream consequence of pathway inhibition. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
PI3K inhibitor influencing Olfr566 through the PI3K/Akt pathway. Wortmannin disrupts the PI3K pathway, modulating Olfr566 activity by interfering with downstream effectors crucial for its normal functioning. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
MEK inhibitor affecting Olfr566 through the MAPK/ERK pathway. U0126 disrupts the MAPK/ERK signaling cascade, resulting in altered expression and function of Olfr566 as a downstream consequence of pathway inhibition. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $94.00 $349.00 | 114 | |
SERCA inhibitor indirectly inhibiting Olfr566. Thapsigargin disrupts calcium homeostasis, modulating olfactory signaling pathways and consequently leading to decreased expression and function of Olfr566. | ||||||