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Assay Detail

CHEMBL1924909

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

Binding
Inhibition of His-tagged catalytic domain Trypanosoma brucei brucei PDEB2 expressed in baculovirus infected insect Sf21 cells
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Trypanosoma brucei brucei
Cell Type Sf21
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Pharmacological validation of Trypanosoma brucei phosphodiesterases B1 and B2 as druggable targets for African sleeping sickness.
Bland ND, Wang C, Tallman C, Gustafson AE, Wang Z, Ashton TD, Ochiana SO, McAllister G, Cotter K, Fang AP, Gechijian L, Garceau N, Gangurde R, Ortenberg R, Ondrechen MJ, Campbell RK, Pollastri MP.
J Med Chem (2011) 54 : 8188 -8194
PubMed 22023548 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 4.89 5.41

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL372575 1 5.41
CHEMBL1922284 1 5.03
CHEMBL1922286 1 4.95
CHEMBL42126 PICLAMILAST 2.0 1 4.94
CHEMBL297555 1 4.84
CHEMBL285913 TREQUINSIN 2.0 1 4.59
CHEMBL1922283 1 4.47
CHEMBL1922282 LIRIMILAST 2.0 1 -
CHEMBL48017 1 -
CHEMBL1922285 1 -
CHEMBL1922287 1 -
CHEMBL1922288 1 -
CHEMBL1922289 1 -
CHEMBL1922290 1 -
CHEMBL1922291 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL372575 IC50 = 3900.0 nM 5.41
CHEMBL1922284 IC50 = 9400.0 nM 5.03
CHEMBL1922286 IC50 = 11200.0 nM 4.95
CHEMBL42126 PICLAMILAST IC50 = 11400.0 nM 4.94
CHEMBL297555 IC50 = 14300.0 nM 4.84
CHEMBL285913 TREQUINSIN IC50 = 25400.0 nM 4.59
CHEMBL1922283 IC50 = 34000.0 nM 4.47
CHEMBL1922282 LIRIMILAST IC50 > 10000.0 nM -
CHEMBL48017 IC50 > 100000.0 nM -
CHEMBL1922285 IC50 > 30000.0 nM -
CHEMBL1922287 IC50 - -
CHEMBL1922288 IC50 - -
CHEMBL1922289 IC50 - -
CHEMBL1922290 IC50 - -
CHEMBL1922291 IC50 - -