Date published: 2025-11-24

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CB1 Inhibitors

CB1 inhibitors represent a distinct chemical class comprising compounds meticulously designed to selectively target the cannabinoid receptor type 1 (CB1 receptor). Predominantly located in the central nervous system, the CB1 receptor stands as a G-protein coupled receptor pivotal to an array of physiological processes, including neurotransmission, pain perception, appetite regulation, and emotional responses. The fundamental role of CB1 receptors in mediating cannabinoid-mediated effects underscores their significance in orchestrating diverse biological functions. CB1 inhibitors, through their specific interaction with CB1 receptors, disrupt the normal functioning of these receptors by binding to them. This interference leads to the modulation of signaling pathways associated with CB1-mediated effects. The precision of CB1 inhibitors lies in their selective interaction with CB1 receptors, enabling the exertion of inhibitory effects on CB1 activity while sparing significant impact on other receptor systems. Characterized by high affinity and specificity for CB1 receptors, these inhibitors offer a nuanced approach to the precise modulation of CB1-mediated signaling pathways. The ongoing development and scientific scrutiny of CB1 inhibitors contribute substantially to advancing our comprehension of the intricate workings of the endocannabinoid system and its nuanced involvement in an array of physiological processes.

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Items 21 to 22 of 22 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Pimozide

2062-78-4sc-203662
100 mg
$102.00
3
(1)

Pimozide is an antipsychotic drug that has been reported to have CB1 receptor antagonistic properties.

Rimonabant-d10 Hydrochloride

158681-13-1 (unlabeled)sc-219975
1 mg
$360.00
(0)

Rimonabant-d10 Hydrochloride is a selective CB1 receptor antagonist, characterized by its deuterated structure which alters isotopic mass and may influence metabolic stability. This compound engages in unique van der Waals interactions, enhancing its binding specificity. Its distinct isotopic labeling can affect reaction kinetics, potentially leading to altered degradation pathways. Furthermore, the compound's lipophilicity may modulate membrane permeability, impacting cellular uptake and distribution.