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Assay Detail

CHEMBL4349442

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

Binding
Inhibition of TRK (unknown origin)
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Targeting tropomyosin receptor kinase for cancer therapy.
Miao Q, Ma K, Chen D, Wu X, Jiang S.
Eur J Med Chem (2019) 175 : 129 -148
PubMed 31077998 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 7.18 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3989939 LAROTRECTINIB SULFATE 4.0 1 8.70
CHEMBL4436198 1 8.30
CHEMBL457608 1 8.10
CHEMBL457393 1 8.00
CHEMBL4444276 1 7.23
CHEMBL3686124 1 7.20
CHEMBL456986 1 7.17
CHEMBL4513841 1 7.06
CHEMBL3686122 1 6.96
CHEMBL4450111 1 6.37
CHEMBL3686123 1 6.21
CHEMBL4471757 1 6.07
CHEMBL4546320 1 5.91
CHEMBL4587619 1 -
CHEMBL1289115 1 -
CHEMBL4297627 SELITRECTINIB 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3989939 LAROTRECTINIB SULFATE IC50 = 2.0 nM 8.70
CHEMBL4436198 IC50 = 5.0 nM 8.30
CHEMBL457608 IC50 = 8.0 nM 8.10
CHEMBL457393 IC50 = 10.0 nM 8.00
CHEMBL4444276 IC50 = 59.0 nM 7.23
CHEMBL3686124 IC50 = 63.0 nM 7.20
CHEMBL456986 IC50 = 67.0 nM 7.17
CHEMBL4513841 IC50 = 87.0 nM 7.06
CHEMBL3686122 IC50 = 109.0 nM 6.96
CHEMBL4450111 IC50 = 426.0 nM 6.37
CHEMBL3686123 IC50 = 611.0 nM 6.21
CHEMBL4471757 IC50 = 859.0 nM 6.07
CHEMBL4546320 IC50 = 1240.0 nM 5.91
CHEMBL4587619 IC50 > 1000.0 nM -
CHEMBL1289115 IC50 > 1000.0 nM -
CHEMBL4297627 SELITRECTINIB IC50 > 1000.0 nM -