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Assay Detail

CHEMBL5330475

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

Functional
Cytotoxicity against human K562 cells assessed as cell growth inhibition measured after 72 hrs by MTT assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type K562
Confidence 1 — Organism
Curated By Autocuration

Target

K562 (CHEMBL385)
Type CELL-LINE
Organism Homo sapiens

Publication

New aryl-/heteroarylpiperazine derivatives of 1,7-dimethyl-8,9-diphenyl-4-azatricyclo[5.2.1.0<sup>2,6</sup>]dec-8-ene-3,5,10-trione: Synthesis and preliminary studies of biological activities.
Napiórkowska M, Kurpios-Piec D, Kiernozek-Kalińska E, Leśniak A, Klawikowska M, Bujalska-Zadrożny M.
Bioorg Med Chem (2023) 96 : 117518 -117518
PubMed 37951135 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.43 6.68

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL53463 DOXORUBICIN 4.0 1 6.68
CHEMBL5435378 1 5.40
CHEMBL5409943 1 5.36
CHEMBL5395179 1 5.25
CHEMBL5422403 1 5.17
CHEMBL5403228 1 5.09
CHEMBL5437394 1 5.05

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL53463 DOXORUBICIN IC50 = 210.0 nM 6.68
CHEMBL5435378 IC50 = 4010.0 nM 5.40
CHEMBL5409943 IC50 = 4380.0 nM 5.36
CHEMBL5395179 IC50 = 5650.0 nM 5.25
CHEMBL5422403 IC50 = 6760.0 nM 5.17
CHEMBL5403228 IC50 = 8080.0 nM 5.09
CHEMBL5437394 IC50 = 8860.0 nM 5.05