OR1D5 inhibitors belong to a class of compounds that specifically target and inhibit the activity of the olfactory receptor 1D5 (OR1D5), which is a G-protein-coupled receptor (GPCR) involved in olfactory signaling. Olfactory receptors like OR1D5 are members of a larger family of receptors responsible for detecting odorant molecules in the environment, translating chemical signals into neural responses. The inhibition of OR1D5 function results in the disruption of specific odorant-receptor interactions, providing insight into the molecular mechanics of olfaction. Structurally, OR1D5 inhibitors can vary widely, with their design often centered around mimicking or blocking the natural ligand that activates OR1D5. By impeding the receptor's ability to bind to its target molecules, these inhibitors modulate receptor activity, leading to altered olfactory signal transduction pathways.
From a chemical perspective, the synthesis and development of OR1D5 inhibitors involve precise understanding of receptor-ligand binding dynamics, including hydrophobic interactions, hydrogen bonding, and spatial complementarity within the receptor's binding pocket. Researchers utilize structure-activity relationship (SAR) studies to determine key molecular features that enhance inhibitory potency, selectivity, and stability. Advanced techniques such as molecular docking and computational modeling play a significant role in designing novel inhibitors, providing theoretical predictions on binding affinity and orientation within the receptor. Additionally, chemical optimization through iterative synthesis and testing helps refine the properties of these compounds, ensuring they effectively target OR1D5 without off-target effects on other olfactory receptors or GPCRs. This focused approach in the chemical characterization of OR1D5 inhibitors enables a deeper understanding of olfactory receptor function and their broader roles in sensory systems.
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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 | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Activates adenylate cyclase, increasing cAMP levels, which can modulate the activity of various proteins including olfactory receptors like OR1D5. | ||||||
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $159.00 $315.00 $598.00 | 34 | |
Non-selective inhibitor of phosphodiesterases, increases intracellular cAMP by preventing its breakdown, indirectly affecting OR1D5 activity. | ||||||
KT 5720 | 108068-98-0 | sc-3538 sc-3538A sc-3538B | 50 µg 100 µg 500 µg | $97.00 $144.00 $648.00 | 47 | |
Inhibits protein kinase A (PKA), which is involved in the phosphorylation of proteins downstream of cAMP signaling, affecting OR1D5 indirectly. | ||||||
H-89 dihydrochloride | 130964-39-5 | sc-3537 sc-3537A | 1 mg 10 mg | $92.00 $182.00 | 71 | |
Another PKA inhibitor, can decrease the phosphorylation of cellular proteins involved in cyclic nucleotide signaling, thus influencing OR1D5. | ||||||
ODQ | 41443-28-1 | sc-200325 sc-200325A | 10 mg 50 mg | $76.00 $218.00 | 13 | |
Inhibits guanylyl cyclase, reducing cGMP levels, which can have various effects on cellular signaling pathways affecting OR1D5. | ||||||
L-NG-Nitroarginine Methyl Ester (L-NAME) | 51298-62-5 | sc-200333 sc-200333A sc-200333B | 1 g 5 g 25 g | $47.00 $105.00 $322.00 | 45 | |
Inhibits nitric oxide synthase, which can affect cGMP levels and therefore indirectly influence signaling pathways involving OR1D5. | ||||||
Ro 20-1724 | 29925-17-5 | sc-200709 sc-200709A sc-200709B | 100 mg 1 g 5 g | $85.00 $418.00 $1543.00 | 17 | |
Inhibitor of phosphodiesterase type 4, increases cAMP by preventing its breakdown, potentially modulating OR1D5. | ||||||
Rp-cAMPS | 151837-09-1 | sc-24010 | 1 mg | $199.00 | 37 | |
cAMP analog that inhibits PKA, can decrease phosphorylation of cellular proteins involved in cAMP signaling, therefore affecting OR1D5. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
Inhibits PI3K, potentially affecting downstream signaling pathways that can influence OR1D5 activity. | ||||||