Page last updated: 2024-08-05 15:22:52

excitatory amino acid antagonist

Any substance which inhibits the action of receptors for excitatory amino acids.

ChEBI ID: 60798

Members (2)

MemberDefinitionClass
lamotrigineA member of the class of 1,2,4-triazines in which the triazene skeleton is substituted by amino groups at positions 3 and 5, and by a 2,3-dichlorophenyl group at position 6.lamotrigine
phenobarbitalA member of the class of barbiturates, the structure of which is that of barbituric acid substituted at C-5 by ethyl and phenyl groups.phenobarbital

Research

Studies (20,182)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-199011,790 (58.42)18.7374
1990's3,094 (15.33)18.2507
2000's2,621 (12.99)29.6817
2010's2,025 (10.03)24.3611
2020's652 (3.23)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials1,120 (5.12%)5.53%
Reviews1,389 (6.35%)6.00%
Case Studies1,698 (7.76%)4.05%
Observational65 (0.30%)0.25%
Other17,614 (80.48%)84.16%

Protein Targets (33)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
AR proteinHomo sapiens (human)Potency28.384222
Bloom syndrome protein isoform 1Homo sapiens (human)Potency89.125122
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency0.316211
cytochrome P450 2D6Homo sapiens (human)Potency38.901811
cytochrome P450 2D6 isoform 1Homo sapiens (human)Potency6.309611
D(1A) dopamine receptorHomo sapiens (human)Potency0.231111
euchromatic histone-lysine N-methyltransferase 2Homo sapiens (human)Potency4.229612
EWS/FLI fusion proteinHomo sapiens (human)Potency34.295444
GALC proteinHomo sapiens (human)Potency0.707911
gemininHomo sapiens (human)Potency7.810623
mitogen-activated protein kinase 1Homo sapiens (human)Potency35.716822
muscarinic acetylcholine receptor M1Rattus norvegicus (Norway rat)Potency2.511911
nuclear factor erythroid 2-related factor 2 isoform 2Homo sapiens (human)Potency29.092911
peripheral myelin protein 22 isoform 1Homo sapiens (human)Potency84.921411
potassium voltage-gated channel subfamily H member 2 isoform dHomo sapiens (human)Potency31.622811
thioredoxin reductaseRattus norvegicus (Norway rat)Potency28.425433

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Bile salt export pumpHomo sapiens (human)IC50134.000022
Dihydrofolate reductaseEscherichia coli K-12IC50348.900011
Dihydrofolate reductaseEscherichia coli K-12Ki15.240011
Potassium voltage-gated channel subfamily E member 1Homo sapiens (human)IC50158.489011
Potassium voltage-gated channel subfamily H member 2Homo sapiens (human)IC501,452.781767
Potassium voltage-gated channel subfamily KQT member 1Homo sapiens (human)IC50158.489011
Sigma non-opioid intracellular receptor 1Rattus norvegicus (Norway rat)IC5010.000011
Sodium channel protein type 1 subunit alphaHomo sapiens (human)IC5010.000011
Sodium channel protein type 1 subunit alphaRattus norvegicus (Norway rat)IC5082.633323
Sodium channel protein type 10 subunit alphaHomo sapiens (human)IC5097.000022
Sodium channel protein type 2 subunit alphaHomo sapiens (human)IC5034.250044
Sodium channel protein type 2 subunit alphaRattus norvegicus (Norway rat)IC5063.580045
Sodium channel protein type 3 subunit alphaHomo sapiens (human)IC5013.500022
Sodium channel protein type 3 subunit alphaRattus norvegicus (Norway rat)IC5082.633323
Sodium channel protein type 4 subunit alphaHomo sapiens (human)Ki17.000011
Sodium channel protein type 5 subunit alphaHomo sapiens (human)IC5067.270233
Sodium channel protein type 9 subunit alphaHomo sapiens (human)IC5017.000011
Voltage-dependent L-type calcium channel subunit alpha-1CHomo sapiens (human)IC501,421.910022

Other Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Sodium channel protein type 4 subunit alphaHomo sapiens (human)Kr1,440.000011