Page last updated: 2024-08-05 15:31:38

EC 3.5.1.2 (glutaminase) inhibitor

Any EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitor that interferes with the activity of a glutaminase (EC 3.5.1.2) and thus the generation of glutamate from glutamine.

ChEBI ID: 60280

Members (2)

MemberDefinitionClass
compound 968A partially hydrogenated benzophenanthridine carrying an oxo group at C-4, geminal methyl groups at C-2 and a 3-bromo-4-(dimethylamino)phenyl group at C-5.5-[3-bromo-4-(dimethylamino)phenyl]-2,2-dimethyl-2,3,5,6-tetrahydrobenzo[a]phenanthridin-4(1H)-one
diazooxonorleucineA non-proteinogenic L-alpha-amino acid that is L-norleucine which is substituted at position 5 by an oxo group and at position 6 by a diazo group. It is as inhibitor of various glutamine-utilising enzymes.6-diazo-5-oxo-L-norleucine zwitterion; 6-diazo-5-oxo-L-norleucine

Research

Studies (347)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-1990168 (48.41)18.7374
1990's52 (14.99)18.2507
2000's35 (10.09)29.6817
2010's59 (17.00)24.3611
2020's33 (9.51)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials1 (0.28%)5.53%
Reviews15 (4.19%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other342 (95.53%)84.16%

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
EWS/FLI fusion proteinHomo sapiens (human)Potency23.576833
Fumarate hydrataseHomo sapiens (human)Potency37.221211
polyproteinZika virusPotency37.221211