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Assay Detail

CHEMBL5114020

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

Binding
Inhibition of telomerase derived from human K562 cell extract incubated for 30 mins by TRAP assay
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type K562
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Telomerase reverse transcriptase (CHEMBL2916)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Role of basic aminoalkyl chains in the lead optimization of Indoloquinoline alkaloids.
Nuthakki VK, Mudududdla R, Bharate SB.
Eur J Med Chem (2022) 227 : 113938 -113938
PubMed 34710743 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.00 6.36

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL219728 1 6.36
CHEMBL225340 1 6.26
CHEMBL222205 1 5.95
CHEMBL376497 1 5.81
CHEMBL222885 1 5.63
CHEMBL224248 QUINDOLINE 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL219728 IC50 = 440.0 nM 6.36
CHEMBL225340 IC50 = 550.0 nM 6.26
CHEMBL222205 IC50 = 1120.0 nM 5.95
CHEMBL376497 IC50 = 1550.0 nM 5.81
CHEMBL222885 IC50 = 2350.0 nM 5.63
CHEMBL224248 QUINDOLINE IC50 > 138000.0 nM -