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Assay Detail

CHEMBL1252159

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Functional
Cytotoxicity against human A431 cells
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A-431
Confidence 1 — Organism
Curated By Autocuration

Target

A-431 (CHEMBL614069)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and evaluation of 2-amino-4-m-bromoanilino-6-arylmethyl-7H-pyrrolo[2,3-d]pyrimidines as tyrosine kinase inhibitors and antiangiogenic agents.
Gangjee A, Zhao Y, Raghavan S, Ihnat MA, Disch BC.
Bioorg Med Chem (2010) 18 : 5261 -5273
PubMed 20558072 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 4.58 5.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1095464 1 5.92
CHEMBL1254285 1 4.55
CHEMBL499344 1 4.50
CHEMBL1254522 1 4.45
CHEMBL1254199 1 4.34
CHEMBL1254286 1 4.29
CHEMBL1254523 1 4.03
CHEMBL1095465 1 -
CHEMBL1254363 1 -
CHEMBL1254364 1 -
CHEMBL1254443 1 -
CHEMBL1254444 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1095464 IC50 = 1210.0 nM 5.92
CHEMBL1254285 IC50 = 27900.0 nM 4.55
CHEMBL499344 IC50 = 31800.0 nM 4.50
CHEMBL1254522 IC50 = 35600.0 nM 4.45
CHEMBL1254199 IC50 = 45700.0 nM 4.34
CHEMBL1254286 IC50 = 50900.0 nM 4.29
CHEMBL1254523 IC50 = 94100.0 nM 4.03
CHEMBL1095465 IC50 > 50000.0 nM -
CHEMBL1254363 IC50 > 500000.0 nM -
CHEMBL1254364 IC50 = 204300.0 nM -
CHEMBL1254443 IC50 = 226300.0 nM -
CHEMBL1254444 IC50 = 197400.0 nM -