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Assay Detail

CHEMBL4265678

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Functional
Antiproliferative activity against human MCF7 cells after 72 hrs by MTT assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MCF7
Confidence 1 — Organism
Curated By Intermediate

Target

MCF7 (CHEMBL387)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and in vitro antitumor activity of novel alkenyl derivatives of pyridoxine, bioisosteric analogs of feruloyl methane.
Pavelyev RS, Bondar OV, Nguyen TNT, Ziganshina AA, Al Farroukh M, Karwt R, Alekbaeva GD, Pugachev MV, Yamaleeva ZR, Kataeva ON, Balakin KV, Shtyrlin YG.
Bioorg Med Chem (2018) 26 : 5824 -5837
PubMed 30429098 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.39 5.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4295033 1 5.96
CHEMBL4281914 1 5.89
CHEMBL53463 DOXORUBICIN 4.0 1 5.85
CHEMBL4294345 1 5.66
CHEMBL4287109 1 5.62
CHEMBL4288205 1 5.54
CHEMBL4292030 1 5.41
CHEMBL4279876 1 5.39
CHEMBL4283750 1 5.34
CHEMBL4284361 1 5.18
CHEMBL4285673 1 5.14
CHEMBL4291615 1 4.57
CHEMBL106509 DEHYDROZINGERONE 1 4.51
CHEMBL4280299 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4295033 IC50 = 1100.0 nM 5.96
CHEMBL4281914 IC50 = 1300.0 nM 5.89
CHEMBL53463 DOXORUBICIN IC50 = 1400.0 nM 5.85
CHEMBL4294345 IC50 = 2200.0 nM 5.66
CHEMBL4287109 IC50 = 2400.0 nM 5.62
CHEMBL4288205 IC50 = 2900.0 nM 5.54
CHEMBL4292030 IC50 = 3900.0 nM 5.41
CHEMBL4279876 IC50 = 4100.0 nM 5.39
CHEMBL4283750 IC50 = 4600.0 nM 5.34
CHEMBL4284361 IC50 = 6600.0 nM 5.18
CHEMBL4285673 IC50 = 7200.0 nM 5.14
CHEMBL4291615 IC50 = 27000.0 nM 4.57
CHEMBL106509 DEHYDROZINGERONE IC50 = 31000.0 nM 4.51
CHEMBL4280299 IC50 = 398000.0 nM -