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Assay Detail

CHEMBL4478033

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

Functional
Cytotoxicity against mouse L1210 cells assessed as cell growth inhibition
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Mus musculus
Cell Type L1210
Confidence 1 — Organism
Curated By Autocuration

Target

L1210 (CHEMBL386)
Type CELL-LINE
Organism Mus musculus

Publication

Synthesis and evaluation of duocarmycin SA analogs incorporating the methyl 1,2,8,8a-tetrahydrocyclopropa[c]imidazolo[4,5-e]indol-4-one-6-carboxylate (CImI) alkylation subunit.
Chanda PB, Boyle KE, Brody DM, Shukla V, Boger DL.
Bioorg Med Chem (2016) 24 : 4779 -4786
PubMed 27221071 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 8.90 11.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL308086 DUOCARMYCIN 1 11.00
CHEMBL4583938 1 10.40
CHEMBL4578928 1 10.30
CHEMBL146774 1 10.00
CHEMBL4520221 1 9.82
CHEMBL4546940 1 9.15
CHEMBL4544619 1 8.66
CHEMBL293412 1 8.22
CHEMBL1081390 1 7.22
CHEMBL4520945 1 7.16
CHEMBL4524401 1 5.96
CHEMBL4589036 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL308086 DUOCARMYCIN IC50 = 0.01 nM 11.00
CHEMBL4583938 IC50 = 0.04 nM 10.40
CHEMBL4578928 IC50 = 0.05 nM 10.30
CHEMBL146774 IC50 = 0.1 nM 10.00
CHEMBL4520221 IC50 = 0.15 nM 9.82
CHEMBL4546940 IC50 = 0.7 nM 9.15
CHEMBL4544619 IC50 = 2.2 nM 8.66
CHEMBL293412 IC50 = 6.0 nM 8.22
CHEMBL1081390 IC50 = 60.0 nM 7.22
CHEMBL4520945 IC50 = 70.0 nM 7.16
CHEMBL4524401 IC50 = 1100.0 nM 5.96
CHEMBL4589036 IC50 = 0.004 nM -