Date published: 2026-5-30

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SR-7 Inhibitors

SR-7 inhibitors belong to a distinctive chemical class recognized for their specific molecular function within biological systems. Characterized by their ability to modulate SR-7, these inhibitors exert their effects through intricate interactions at the molecular level. SR-7, short for a substrate receptor 7, is an integral component of a cellular machinery crucial for various physiological processes. This chemical class has garnered attention due to its unique mechanism of action in targeting SR-7, thereby influencing downstream cellular events. The inhibitors typically exhibit a high degree of selectivity for SR-7, demonstrating a specificity that distinguishes them from other compounds. SR-7 inhibitors often feature well-defined molecular motifs that facilitate their binding to SR-7, disrupting its normal function. The binding affinity between the inhibitor and SR-7 is a pivotal determinant of their effectiveness. These inhibitors may interfere with the substrate recognition and binding process of SR-7, thereby influencing the subsequent signaling cascades or cellular responses. Understanding the structural nuances of SR-7 inhibitors has become imperative in elucidating their impact on cellular processes and holds promise for further applications in the field of molecular biology.

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Items 11 to 15 of 15 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Methiothepin mesylate salt

74611-28-2sc-253005
100 mg
$141.00
1
(0)

Methiothepin mesylate salt functions as an SR-7 inhibitor, characterized by its ability to disrupt specific protein-protein interactions within signaling pathways. This compound exhibits a unique affinity for certain receptor subtypes, facilitating conformational changes that influence downstream signaling cascades. Its reaction kinetics suggest a biphasic binding pattern, where initial rapid association is followed by a prolonged engagement, potentially altering receptor desensitization and internalization processes.

Vortioxetine Hydrobromide

960203-27-4sc-475775
5 mg
$220.00
(0)

Vortioxetine Hydrobromide acts as an SR-7 inhibitor, distinguished by its selective modulation of serotonin receptors. This compound engages in unique allosteric interactions, enhancing receptor activity while simultaneously stabilizing inactive conformations. Its kinetic profile reveals a complex binding mechanism, characterized by a gradual onset of action that may influence receptor recycling and signaling efficiency. The compound's solubility properties further facilitate its interaction dynamics within biological systems.

Clozapine

5786-21-0sc-200402
sc-200402A
sc-200402B
sc-200402C
50 mg
500 mg
5 g
10 g
$69.00
$364.00
$2500.00
$4100.00
11
(1)

Antagonizes HTR7 receptor among other activities, leading to decreased receptor signaling.

Risperidone

106266-06-2sc-204881
sc-204881A
sc-204881B
sc-204881C
10 mg
50 mg
1 g
5 g
$174.00
$719.00
$1020.00
$2040.00
1
(1)

Acts on HTR7 receptors as an antagonist, inhibiting serotonin-mediated effects.

Lurasidone-d8 hydrochloride

367514-88-3 (unlabeled)sc-491073
1 mg
$480.00
(0)

Antagonizes HTR7 receptor, among others, leading to inhibition of serotonin signaling.