Date published: 2026-3-13

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D5DR Inhibitors

The chemical class of D5DR Inhibitors consists of a diverse group of compounds primarily characterized by their ability to antagonize dopamine receptor activity, either directly or indirectly. These inhibitors interact with the dopaminergic system in various ways. Some, like SCH-23390, are selective and bind directly to D5DR, blocking its activation. Others, such as fluphenazine, haloperidol, and chlorpromazine, are less selective and antagonize multiple dopamine receptor subtypes, including D5DR. The action of these drugs results in decreased dopaminergic signaling, which in turn reduces D5DR activity. Furthermore, some compounds in this class, like domperidone, L-741,626, sulpiride, and amisulpride, are known for their specificity towards D2-like receptors but may indirectly affect D5DR due to the intricate interplay within the dopamine receptor family. The interconnectedness of these receptor subtypes means that antagonizing one subtype can have ripple effects on the function of others, including D5DR.

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Items 11 to 15 of 15 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

(RS)-(±)-Sulpiride

15676-16-1sc-205494
100 mg
$70.00
(0)

A dopamine D2 antagonist, which may indirectly affect D5DR activity through modulating dopaminergic signaling pathways.

Amisulpride

71675-85-9sc-203510
50 mg
$116.00
(1)

A selective dopamine antagonist, primarily at D2 and D3 receptors, but may influence D5DR indirectly.

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)

antagonizes multiple dopamine receptors, potentially affecting D5DR activity.

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)

An atypical antipsychotic with a broad receptor antagonist profile, including possible effects on D5DR.

Olanzapine

132539-06-1sc-212469
100 mg
$133.00
6
(1)

An antipsychotic with a wide range of receptor targets, potentially leading to indirect inhibition of D5DR.