Date published: 2026-5-30

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NR3B Activators

NR3B activators are a category of chemical compounds that interact with the NR3B subunit, also known as GluN3B, which is a component of the N-methyl-D-aspartate receptor (NMDAR) complex. NMDARs are ionotropic glutamate receptors that play a crucial role in synaptic transmission and plasticity in the central nervous system. The receptor complex is a heterotetramer, usually composed of two obligatory GluN1 subunits and two regulatory subunits which can include GluN2 (A-D) and GluN3 (A-B) subunits. The inclusion of the NR3B subunit in this complex can modulate the receptor's ion channel properties. NR3B activators, therefore, influence the activity of the receptors by selectively binding to the NR3B subunit, which can alter the receptor's pharmacology, kinetics, and calcium permeability. The precise mechanism by which NR3B activators modulate the receptor function is complex and involves the alteration of NMDAR subunit composition and the consequent functional dynamics of the receptor.

The chemistry of NR3B activators is diverse, reflecting a range of structures that can engage with the NR3B subunit. The interaction between the activators and the receptor is highly specific, often involving direct binding to the modulatory sites distinct from the glutamate-binding site. These activators can be either synthetic or naturally occurring compounds, and they can vary greatly in terms of their molecular size, polarity, and overall shape. Their specificity for the NR3B subunit is of particular interest in the study of the pharmacological modulation of NMDARs because it allows for selective targeting of receptor subtypes with different subunit compositions. By modulating the activity of the NR3B subunit, these activators can affect the ion channel properties of the NMDARs, which in turn can influence the receptor's role in synaptic signaling. The development of NR3B activators contributes significantly to the understanding of the complex pharmacology of NMDARs and the structural-functional relationships within the receptor complexes.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Glycine

56-40-6sc-29096A
sc-29096
sc-29096B
sc-29096C
500 g
1 kg
3 kg
10 kg
$41.00
$71.00
$112.00
$357.00
15
(9)

Glycine acts as a co-agonist of NMDA receptors, which may contain NR3B subunits. Binding of glycine enhances the receptor's ion channel activity.

D-Serine

312-84-5sc-391671
sc-391671A
sc-391671B
5 g
25 g
100 g
$43.00
$128.00
$204.00
(0)

D-Serine is another co-agonist for NMDA receptors and can enhance the receptor activity by binding to the glycine site, potentially involving NR3B.

Spermine

71-44-3sc-212953A
sc-212953
sc-212953B
sc-212953C
1 g
5 g
25 g
100 g
$61.00
$196.00
$277.00
$901.00
1
(0)

Spermine can potentiate NMDA receptor activity by interacting with sites that may be modulated by the NR3B subunit, enhancing calcium permeability.

Ifenprodil hemitartrate

23210-58-4sc-203601B
sc-203601
sc-203601A
5 mg
10 mg
50 mg
$39.00
$61.00
$142.00
(0)

Ifenprodil selectively inhibits NR2B-containing NMDA receptors, which can lead to compensation by NR3B-containing receptors, indirectly enhancing their activity.

Zinc

7440-66-6sc-213177
100 g
$48.00
(0)

Zinc can modulate the activity of NMDA receptors by binding to a specific site, which may influence the activity of receptors containing NR3B.

Cyclothiazide

2259-96-3sc-202560
sc-202560A
10 mg
50 mg
$107.00
$227.00
3
(1)

Cyclothiazide, by preventing AMPA receptor desensitization, can increase synaptic glutamate, which may enhance NR3B-containing NMDA receptor activity.

Memantine hydrochloride

41100-52-1sc-203628
50 mg
$69.00
4
(2)

Memantine acts as an uncompetitive NMDA receptor antagonist with voltage-dependent block, which might lead to downstream regulatory effects on NR3B activity.

Pregnenolone

145-13-1sc-204860
sc-204860A
sc-204860B
sc-204860C
5 g
25 g
100 g
500 g
$87.00
$148.00
$347.00
$1122.00
(1)

Pregnenolone sulfate is a neurosteroid that can modulate NMDA receptor activity, potentially affecting NR3B subunit function.