Date published: 2025-12-24

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GPR141 Inhibitors

GPR141 inhibitors pertain to a specialized class of chemical compounds designed to impede the activity of G protein-coupled receptor 141 (GPR141). This receptor, part of the extensive G protein-coupled receptor (GPCR) family, plays a role in various intracellular signaling cascades. GPR141 inhibitors work by binding to the receptor, thereby blocking its interaction with endogenous ligands. The action of these inhibitors is highly specific, targeting the unique conformational site of GPR141, which prevents the receptor from undergoing the conformational changes necessary for the activation of associated G proteins. By doing so, these inhibitors effectively arrest the GPR141-mediated signal transduction process, which can influence a range of downstream biological processes. This halt in signaling is crucial for the regulation of events that are normally modulated by the receptor's activity, making these inhibitors powerful tools for dissecting the physiological functions of GPR141. The specificity of GPR141 inhibitors means that they are adept at modulating a singular pathway without affecting the myriad of other GPCR-mediated pathways, thus ensuring minimal off-target effects. These inhibitory compounds typically exhibit high binding affinity, which ensures that they maintain receptor occupancy and exert sustained inhibitory effects. The binding of these inhibitors can be either reversible or irreversible, depending on the chemical nature of the compound and the duration of its interaction with GPR141. The inhibitors usually have well-characterized pharmacokinetic and pharmacodynamic profiles, providing predictable in vivo behavior. The ability to selectively inhibit GPR141 allows researchers to study the physiological and pathological roles of the receptor with precision. By understanding the receptor's involvement in cellular signaling mechanisms, it becomes possible to elucidate the broader implications of GPR141's activity within various biological systems.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

GW 9662

22978-25-2sc-202641
5 mg
$68.00
30
(2)

GW9662 is a selective PPARγ antagonist. By inhibiting PPARγ, GW9662 may reduce the transcription of multiple genes, including those that encode for GPCRs such as GPR141, potentially leading to reduced protein expression.

Pertussis Toxin (islet-activating protein)

70323-44-3sc-200837
50 µg
$442.00
3
(1)

Pertussis toxin irreversibly disables Gi/o proteins. As GPR141 is potentially coupled to Gi/o proteins, the toxin indirectly inhibits GPR141 signaling by preventing its ability to modulate adenylate cyclase activity.

NF 449

389142-38-5sc-203159
10 mg
$308.00
5
(1)

NF449 is a potent, selective antagonist of Gsα subunit of G proteins. If GPR141 interacts with Gsα proteins, NF449 could indirectly reduce GPR141's ability to modulate cAMP levels, thereby inhibiting its function.

YM 254890

568580-02-9sc-507356
1 mg
$500.00
(0)

YM-254890 is a selective inhibitor of Gq/11 proteins. If GPR141 signals through the Gq/11 pathway, this compound would inhibit GPR141 activity by blocking its ability to activate phospholipase C (PLC).

L-NG-Nitroarginine Methyl Ester (L-NAME)

51298-62-5sc-200333
sc-200333A
sc-200333B
1 g
5 g
25 g
$47.00
$105.00
$322.00
45
(1)

L-NAME is a nitric oxide synthase inhibitor. Nitric oxide can modulate GPCR activity; therefore, reducing its synthesis could indirectly affect GPR141 signaling pathways, leading to decreased activation.

JTE 907

282089-49-0sc-203616
sc-203616A
10 mg
50 mg
$283.00
$1100.00
(0)

JTE-907 is an inverse agonist of the CB2 receptor. By inhibiting CB2, it may indirectly modulate GPR141 activity in tissues where both receptors are expressed and potentially engage in cross-talk.

Clozapine

5786-21-0sc-200402
sc-200402A
50 mg
500 mg
$68.00
$357.00
11
(1)

Clozapine, an atypical antipsychotic, has broad receptor antagonist properties, including several GPCRs. It could indirectly inhibit GPR141 by modulating the cellular environment in which GPR141 operates.

Ketanserin

74050-98-9sc-279249
1 g
$700.00
(0)

Ketanserin is a serotonin receptor antagonist that can influence GPCR signaling pathways. As GPR141 is a GPCR, ketanserin may indirectly inhibit GPR141 by altering the serotonin-mediated regulatory pathways it participates in.