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Assay Detail

CHEMBL1248460

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

Binding
Inhibition of human recombinant LAR after 30 mins by spectrophotometry
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Receptor-type tyrosine-protein phosphatase F (CHEMBL3521)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and evaluation of some novel dibenzo[b,d]furan carboxylic acids as potential anti-diabetic agents.
Lakshminarayana N, Prasad YR, Gharat L, Thomas A, Narayanan S, Raghuram A, Srinivasan CV, Gopalan B.
Eur J Med Chem (2010) 45 : 3709 -3718
PubMed 20627471 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.65 6.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1241315 OXALYLAMINOBENZOIC ACID 1 6.39
CHEMBL1242458 1 5.88
CHEMBL1242827 1 5.70
CHEMBL1242553 1 5.68
CHEMBL1242826 1 5.68
CHEMBL1241469 1 5.68
CHEMBL1242643 1 5.67
CHEMBL1242736 1 5.58
CHEMBL1242457 1 5.57
CHEMBL1242552 1 5.54
CHEMBL1242642 1 5.53
CHEMBL1242362 1 5.52
CHEMBL1242735 1 5.49
CHEMBL1241314 1 5.45
CHEMBL1242363 1 5.43

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1241315 OXALYLAMINOBENZOIC ACID IC50 = 410.0 nM 6.39
CHEMBL1242458 IC50 = 1323.0 nM 5.88
CHEMBL1242827 IC50 = 1981.0 nM 5.70
CHEMBL1242553 IC50 = 2067.0 nM 5.68
CHEMBL1242826 IC50 = 2102.0 nM 5.68
CHEMBL1241469 IC50 = 2065.0 nM 5.68
CHEMBL1242643 IC50 = 2144.0 nM 5.67
CHEMBL1242736 IC50 = 2647.0 nM 5.58
CHEMBL1242457 IC50 = 2686.0 nM 5.57
CHEMBL1242552 IC50 = 2872.0 nM 5.54
CHEMBL1242642 IC50 = 2942.0 nM 5.53
CHEMBL1242362 IC50 = 2989.0 nM 5.52
CHEMBL1242735 IC50 = 3248.0 nM 5.49
CHEMBL1241314 IC50 = 3574.0 nM 5.45
CHEMBL1242363 IC50 = 3752.0 nM 5.43