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Assay Detail

CHEMBL1942689

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Functional
Antiproliferative activity against human KARPAS299 cells after 96 hrs by cell counting assay
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type KARPAS-299
Confidence 1 — Organism
Curated By Autocuration

Target

KARPAS-299 (CHEMBL2366156)
Type CELL-LINE
Organism Homo sapiens

Publication

Design and synthesis of a highly selective, orally active and potent anaplastic lymphoma kinase inhibitor (CH5424802).
Kinoshita K, Asoh K, Furuichi N, Ito T, Kawada H, Hara S, Ohwada J, Miyagi T, Kobayashi T, Takanashi K, Tsukaguchi T, Sakamoto H, Tsukuda T, Oikawa N.
Bioorg Med Chem (2012) 20 : 1271 -1280
PubMed 22225917 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 7.48 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1738797 ALECTINIB 4.0 1 8.52
CHEMBL1940181 1 8.32
CHEMBL1823221 1 7.89
CHEMBL1940179 1 7.65
CHEMBL1940182 1 7.58
CHEMBL1940180 1 7.58
CHEMBL1940178 1 7.34
CHEMBL1940175 1 7.06
CHEMBL1940174 1 6.92
CHEMBL1940177 1 6.82
CHEMBL1940176 1 6.62

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1738797 ALECTINIB IC50 = 3.0 nM 8.52
CHEMBL1940181 IC50 = 4.8 nM 8.32
CHEMBL1823221 IC50 = 12.8 nM 7.89
CHEMBL1940179 IC50 = 22.4 nM 7.65
CHEMBL1940182 IC50 = 26.1 nM 7.58
CHEMBL1940180 IC50 = 26.5 nM 7.58
CHEMBL1940178 IC50 = 45.8 nM 7.34
CHEMBL1940175 IC50 = 86.9 nM 7.06
CHEMBL1940174 IC50 = 121.0 nM 6.92
CHEMBL1940177 IC50 = 151.0 nM 6.82
CHEMBL1940176 IC50 = 238.0 nM 6.62