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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T6608 | NMDA | N-Methyl-D-aspartic acid | Endogenous Metabolite , NMDAR , iGluR |
N-Methyl-D-aspartic acid is an amino acid that, as the D-isomer, is the defining agonist for the NMDA (N-Methyl-D-aspartic acid) receptor subtype of glutamate receptors. | |||
T12234 | NMDA-IN-1 | NMDAR | |
NMDA-IN-1 is a potent and NR2B-selective antagonist of NMDA(NMDA Ki of 0.85 nM; NR2B Ca2+ influx IC50 is 9.7 nM). | |||
T23014 | MNI-caged-NMDA | Others | |
NMDA caged with the photosensitive 4-methoxy-7-nitroindolinyl group | |||
T40999 | NMDA receptor antagonist 2 | ||
NMDA receptor antagonist 2 is a highly potent and orally active NR2B subtype-selective antagonist of the N-methyl-D-aspartate (NMDA) receptor. It exhibits remarkable binding affinities, with an IC50 of 1.0 nM and a Ki va... | |||
T23165 | PMPA (NMDA antagonist) | Others | |
PMPA is a competitive NMDA receptor antagonist. | |||
T60513 | NMDA-IN-2 | ||
NMDA-IN-2 (compound 6b) is a Procaine derivative that is an inhibitor of NMDA receptor 2B subtype [1]. | |||
T60792 | NMDA receptor antagonist-3 | ||
NMDA receptor antagonist-3 is a NMDA receptor antagonist with a significan recovery rate (40.0%, at 100 μM) and safe toxicological characteristics in SH-SY5Y and human adipose mesenchymal stem cells. | |||
T79374 | NMDA receptor antagonist 7 | iGluR | |
Compound (S)-10a, a GluN2B subunit-selective NMDA receptor antagonist, exhibits a K i of 93 nM and an IC 50 of 72 nM. It is potentially useful for research into neurodegenerative diseases [1]. | |||
T79375 | NMDA receptor antagonist 8 | iGluR | |
Compound (R)-10a, an NMDA receptor antagonist, exhibits selectivity for the GluN2B subunit, possessing a Ki of 265 nM and an IC50 of 62 nM. This compound is utilized in research pertaining to neurodegenerative diseases [... | |||
T61924 | NMDA receptor modulator 6 | ||
NMDA receptor regulator 6 (Compound 183) is an effective NMDA receptor regulator and has research value in neurological disorders. | |||
T79273 | NMDA receptor antagonist 6 | iGluR | |
NMDA Receptor Antagonist 6 (Compound 13b) functions as an antagonist at the glycine-binding site of the NMDA receptor and demonstrates cytoneuroprotective efficacy. It safeguards PC12 cells from NMDA-induced damage and a... | |||
T60685 | NMDA receptor modulator 3 | ||
NMDA receptor modulator 3 (Compound 99) is a potent modulator of NMDA receptor that can be used in the research of neurological disorder [1]. | |||
T63003 | NMDA receptor potentiator-1 | ||
NMDA receptor potentiator-1 (Compound 1368) is a subunit-selective NMDA receptor enhancer with IC50 values of 4 μM and 5 μM for NR2C and NR2D expression, respectively. | |||
T61470 | NMDA receptor antagonist 5 | ||
NMDA receptor antagonist 5 (Compound 10e), a potent and non-toxic NMDA receptor antagonist, exhibits brain permeability. It is of significance in studying neurological disorders [1]. | |||
T61117 | NMDA receptor modulator 5 | ||
NMDA receptor modulator 5 (Compound 195), a potent NMDA receptor modulator, exhibits potential for neurological disorder research [1]. | |||
T60552 | NMDA receptor modulator 2 | ||
NMDA receptor modulator 2 (Compound 1) is a potent modulator of the NMDA receptor that can be used for neurological disorder research [1]. | |||
T60960 | NMDA receptor modulator 4 | ||
NMDA receptor modulator 4 (Compound 169) can be used for the research of neurological disorder that is a potent modulator of NMDA receptor [1]. | |||
T60306 | NMDA receptor antagonist 4 | ||
NMDA receptor antagonist 4 (IIc) is an uncompetitive, voltage-dependent, orally active NMDAR blocker, with an IC 50 of 1.93 μM. NMDA receptor antagonist 4 shows a positive predicted blood-brain-barrier (BBB) permeability... | |||
T9626 | Cycloleucine | NMDAR | |
Cycloleucine is an antagonist of NMDA receptor associated glycine receptor with a Ki of 600 μM. Cycloleucine is also a competitive inhibitor of S-adenosyl-methionine mediated methylation with anxiolytic and cytostatic ef... | |||
T1896 | Ro 61-8048 | Hydroxylase | |
Ro 61-8048 is a potent and selective inhibitor of kynurenine hydroxylase with an IC50 value of 37 nM. |