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Assay Detail

CHEMBL784807

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Functional
Effective concentration was measured for the release of accumulated [3H]NE from chopped cortex of rat
10
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Rattus norvegicus
Confidence 1 — Organism
Curated By Intermediate

Target

Rattus norvegicus (CHEMBL376)
Type ORGANISM
Organism Rattus norvegicus

Publication

Pronounced pharmacological differences arising from minor structural changes in conformationally defined amphetamine analogues. Comparative evaluation of endo- and exo-2-amino- and endo- and exo-2-(methylamino)benzobicyclo[2.2.1]heptene and -benzobicylco[2.2.2]octene analogues. Conformationally defined adrenergic agents. 4.
Grunewald GL, Reitz TJ, Hallett A, Rutledge CO, Vollmer S, Archuleta JM, Ruth JA.
J Med Chem (1980) 23 : 614 -620
PubMed 7392028 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 10 5.56 6.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL612 DEXTROAMPHETAMINE 4.0 1 6.10
CHEMBL19393 LEVAMFETAMINE 4.0 1 5.77
CHEMBL49263 1 4.80
CHEMBL157518 2 -
CHEMBL301289 1 -
CHEMBL154758 2 -
CHEMBL157748 2 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL612 DEXTROAMPHETAMINE EC50 = 800.0 nM 6.10
CHEMBL19393 LEVAMFETAMINE EC50 = 1700.0 nM 5.77
CHEMBL49263 EC50 = 16000.0 nM 4.80
CHEMBL157518 EC50 = 1000000.0 nM -
CHEMBL301289 EC50 = 630000.0 nM -
CHEMBL154758 EC50 = 450000.0 nM -
CHEMBL157748 EC50 > 1000000.0 nM -
CHEMBL154758 EC50 > 1000000.0 nM -
CHEMBL157748 EC50 = 178000.0 nM -
CHEMBL157518 EC50 = 147000.0 nM -