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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T82297 | GluN1(356-385) | ||
GluN1 (356-385) is an antigenic peptide implicated in N-methyl-D-aspartate receptor (NMDAR) encephalitis and has been shown to decrease the density of NMDAR surface clusters in hippocampal neurons. It serves as a tool to... | |||
T82296 | GluN1(359-378) | ||
GluN1 (359-378) is an antibody targeting the N-methyl-D-aspartate receptor (NMDAR) capable of crossing the blood-brain barrier and is utilized in researching therapies for anti-NMDAR encephalitis that focus on the immune... | |||
T7870 | TCN 201 | TCN-201 | NMDAR , iGluR |
TCN 201 is a selective antagonist of NMDA receptors containing the NR2A subunit. | |||
T16801 | (RS)-(Tetrazol-5-yl)glycine | LY 285265,D,L-(tetrazol-5-yl)glycine | NMDAR , iGluR |
(RS)-(Tetrazol-5-yl)glycine (LY 285265) (D,L-(tetrazol-5-yl)glycine) is an effective and selective N-methyl-D-aspartate receptor agonist. (RS)-(Tetrazol-5-yl)glycine has EC50s of 99 nM, 1.7 μM for GluN1/GluN2D, and GluN1... | |||
T15684 | L-689560 | NMDAR , iGluR | |
L-689560 is widely used as a radiolabeled ligand in binding studies and used to study the roles of NMDA receptors in normal neurological processes as well as in diseases. At the GluN1 glycine binding site, L-689560 is an... | |||
T10781 | CGP 78608 hydrochloride | PAMQX | NMDAR , iGluR |
CGP 78608 hydrochloride is a specific antagonist at the glycine binding site of the NMDA receptor (IC50 = 6 nM). CGP 78608 hydrochloride exhibits anticonvulsant activity. CGP 78608 hydrochloride potentiates GluN1/GluN3A-... | |||
T8450 | TCN 213 | TCN213 | NMDAR |
TCN 213 is an antagonist of NMDA receptor that has a selective for NR1/NR2A over NR1/NR2B | |||
T1186L | Ifenprodil | RC 61-91,RC-61-91,RC61-91,RC 6191 | Adrenergic Receptor , NMDAR |
Ifenprodil (RC61-91) is an inhibitor of the NMDA receptor, specifically of GluN1 (glycine-binding NMDA receptor subunit 1) and GluN2B (glutamate-binding NMDA receptor subunit 2) subunits. Additionally, Ifenprodil inhibit... | |||
T19881 | UBP608 | UBP-608,UBP 608 | |
UBP608 is an allosteric modulator of NMDA receptor family. It selectively inhibits GluN1/GluN2A receptors with a 23-fold selectivity compared to GluN1/GluN2D receptors. | |||
T24915 | UBP618 | UBP-618,UBP 618 | |
UBP618 is a GluN1/GluN2 receptors pan-inhibitor. | |||
T69906 | PEAQX sodium | ||
PEAQX, also known as NVP-AAM077; is a competitive antagonist at the NMDA receptor. Although originally described as 100-fold selective for GluN1/GluN2A receptors vs. GluN1/GluN2B receptors, more detailed studies of the K... | |||
T24551 | NSC339614 potassium | NSC 339614 potassium,NSC-339614 potassium,NSC339614 potassium salt | |
NSC339614 potassium is a selective GluN1/GluN2C and GluN1/GluN2D receptors potentiator. | |||
T24916 | UBP646 | UBP-646,UBP 646 | |
UBP646 is a GluN1/GluN2 receptors potentiator. | |||
T24917 | UBP684 | UBP-684,UBP 684 | |
UBP684 is an NMDAR pan-PAM. UBP684 increases the maximal l-glutamate/glycine response while having minor subunit-specific effects on agonist potency. It robustly potentiates responses at all GluN1/GluN2 subtypes and at n... | |||
T71290 | EVT-101 HCl | ||
EVT-101 is a GluN2B antagonist, binding at the same GluN1/GluN2B dimer interface as ifenprodil but adopting a remarkably different binding mode involving a distinct subcavity and receptor interactions. | |||
T62376 | GNE-9278 | ||
GNE-9278 is a highly selective NMDAR orthosteric modulator that acts on the GluN1 transmembrane structural domain (TMD).GNE-9278 acts on activated NMDAR and increases peak current and agonist affinity. | |||
T61227 | NAB-14 | ||
NAB-14 is a powerful and selective chemical compound that acts as a non-competitive antagonist for GluN2C and GluN2D receptors. With an IC50 value of 580 nM for GluN1/GluN2D, NAB-14 demonstrates high potency. This compou... | |||
T79569 | AChE/Aβ-IN-1 | ||
AChE/Aβ-IN-1 (compound 32) is a potent, orally active acetylcholinesterase (AChE) inhibitor with an IC50 of 86 nM and an NMDA receptor antagonist targeting the GluN1-1b/GluN2B subunit combination with an IC50 of 3.876 μM... | |||
T79571 | AChE/Aβ-IN-2 | ||
AChE/Aβ-IN-2 (compound 33) is a powerful, orally active acetylcholinesterase (AChE) inhibitor with an IC50 of 135 nM. It also functions as an NMDA receptor antagonist (GluN1-1b/GluN2B subunit combination) with an IC50 of... |