GPR171 inhibitors are a class of chemical compounds that target the GPR171 receptor, a member of the G protein-coupled receptor (GPCR) family. GPR171 is a relatively orphan receptor, meaning its endogenous ligands and biological roles have not been fully elucidated. However, it is thought to be involved in regulating specific signaling pathways, including those linked to neuropeptides. Inhibitors of GPR171 typically work by blocking the interaction between the receptor and its ligands or by altering the receptor's ability to trigger downstream signaling events. These inhibitors are often small molecules that have been designed or identified through screening to bind to the receptor's active or allosteric sites, effectively preventing its activation.
Structurally, GPR171 inhibitors exhibit diversity in their molecular frameworks but tend to share certain features that facilitate interaction with the transmembrane domains of GPCRs. These features often include hydrophobic moieties that enable the compounds to embed within the lipid bilayer, as well as polar or charged groups that interact with key amino acid residues within the receptor. The optimization of such inhibitors typically involves balancing properties like lipophilicity and binding affinity to achieve selective and potent inhibition of GPR171. These molecules are studied to understand GPR171's role in cellular signaling, where inhibition of the receptor can shed light on the pathways and physiological processes in which it participates. This exploration contributes to a greater understanding of GPCR function and the broad role of GPR171 in various biological contexts.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Clozapine | 5786-21-0 | sc-200402 sc-200402A sc-200402B sc-200402C | 50 mg 500 mg 5 g 10 g | $69.00 $364.00 $2500.00 $4100.00 | 11 | |
Clozapine, an atypical antipsychotic, may inhibit GPR171 expression by modulating various neurotransmitter receptors, potentially influencing GPCR signaling pathways. | ||||||
Haloperidol | 52-86-8 | sc-507512 | 5 g | $190.00 | ||
Haloperidol might affect GPR171 expression by antagonizing dopamine receptors, potentially altering GPCR-related cellular responses. | ||||||
Ritanserin | 87051-43-2 | sc-203681 sc-203681A | 10 mg 50 mg | $89.00 $312.00 | 2 | |
Ritanserin could inhibit GPR171 expression by targeting serotonin receptors, possibly affecting GPCR signaling networks. | ||||||
Yohimbine hydrochloride | 65-19-0 | sc-204412 sc-204412A sc-204412B | 1 g 5 g 25 g | $51.00 $171.00 $530.00 | 2 | |
Yohimbine may affect GPR171 expression by acting as an alpha-2 adrenergic receptor antagonist, influencing adrenergic signaling pathways. | ||||||
Tropisetron hydrochloride | 105826-92-4 | sc-204930 sc-204930A | 10 mg 50 mg | $96.00 $571.00 | 2 | |
Tropisetron could influence GPR171 expression by antagonizing the 5-HT3 receptor, affecting serotonin signaling pathways. | ||||||
Olanzapine | 132539-06-1 | sc-212469 | 100 mg | $133.00 | 6 | |
Olanzapine may modulate GPR171 expression by affecting multiple neurotransmitter receptors, influencing various GPCR signaling pathways. | ||||||
Atropine | 51-55-8 | sc-252392 | 5 g | $204.00 | 2 | |
Atropine could affect GPR171 expression by antagonizing muscarinic acetylcholine receptors, modulating cholinergic signaling. | ||||||
BQ 788 sodium salt | 156161-89-6 | sc-203534 sc-203534A sc-203534B | 1 mg 5 mg 25 mg | $318.00 $1297.00 $5000.00 | 2 | |
BQ-788 may inhibit GPR171 expression by selectively antagonizing the endothelin ETB receptor, influencing endothelin signaling pathways. | ||||||