Olr87 inhibitors are a class of chemical compounds characterized by their ability to interact specifically with the olfactory receptor Olr87. These compounds typically exhibit a range of structural diversity, but they often share common features that facilitate their binding to the receptor's active site. The Olr87 receptor, being a member of the G-protein-coupled receptor (GPCR) family, is involved in the initial detection of odor molecules, translating external chemical signals into intracellular responses. Inhibitors of Olr87 may achieve their effect through competitive binding, where the inhibitor molecule occupies the binding site of the receptor, thus preventing the natural ligand from activating the receptor. Alternatively, they might interact allosterically, binding to a different part of the receptor and inducing a conformational change that reduces the receptor's ability to interact with its natural ligand. The design and synthesis of Olr87 inhibitors require an in-depth understanding of the receptor's three-dimensional structure and the dynamics of its ligand-binding domain.
From a chemical standpoint, Olr87 inhibitors often possess specific functional groups that enhance their affinity and specificity for the receptor. These functional groups might include aromatic rings, heterocycles, and various substituents that participate in hydrogen bonding, hydrophobic interactions, or Van der Waals forces with the receptor. Advanced techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and molecular modeling are typically employed to elucidate the binding interactions between Olr87 and its inhibitors. Moreover, structure-activity relationship (SAR) studies play a critical role in optimizing the inhibitory potency and selectivity of these compounds. By systematically modifying different parts of the inhibitor molecule and evaluating the resulting changes in activity, researchers can identify key structural elements that are crucial for binding and inhibition. The development of Olr87 inhibitors also involves rigorous in vitro assays to confirm their efficacy in blocking receptor activity, providing valuable insights into the fundamental mechanisms of olfactory signal transduction.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
BCR-ABL tyrosine kinase inhibitor, may indirectly affect Olr87 through kinase pathway modulation. | ||||||
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $62.00 $112.00 $214.00 $342.00 | 74 | |
EGFR inhibitor, could modulate EGFR pathways intersecting with Olr87's signaling. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Src family kinase inhibitor, potentially alters pathways influencing Olr87 activity. | ||||||
Erlotinib Hydrochloride | 183319-69-9 | sc-202154 sc-202154A | 10 mg 25 mg | $74.00 $119.00 | 33 | |
EGFR inhibitor, may impact signaling pathways related to Olr87 function. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
RAF inhibitor, potentially disrupts RAF/MEK/ERK signaling associated with Olr87. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $150.00 $920.00 | 5 | |
Multi-targeted receptor tyrosine kinase inhibitor, may affect pathways linked to Olr87 activity. | ||||||
BIBF1120 | 656247-17-5 | sc-364433 sc-364433A | 5 mg 10 mg | $180.00 $315.00 | 2 | |
Tyrosine kinase inhibitor, could affect various signaling pathways intersecting with Olr87. | ||||||
Lenvatinib | 417716-92-8 | sc-488530 sc-488530A sc-488530B | 5 mg 25 mg 100 mg | $178.00 $648.00 $1657.00 | 3 | |
Multi-kinase inhibitor, potentially modulates pathways involved in Olr87 regulation. | ||||||