Assay Detail
Functional
CHEMBL698624
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In vitro anticellular activity expressed as inhibitory concentration for the growth of human uterine cervix carcinoma HeLa S3 cells for a period of 1 hour
26
Total Activities
26
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | HeLa |
| Confidence | 1 — Organism |
| Curated By | Expert |
Publication
Synthesis and antitumor activity of duocarmycin derivatives: A-ring pyrrole compounds bearing cinnamoyl groups.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 26 | 7.38 | 9.30 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL35670 | — | — | 1 | 9.30 |
| CHEMBL178034 | — | — | 1 | 8.70 |
| CHEMBL174057 | — | — | 1 | 8.68 |
| CHEMBL441114 | — | — | 1 | 8.60 |
| CHEMBL177739 | — | — | 1 | 8.40 |
| CHEMBL177453 | — | — | 1 | 8.23 |
| CHEMBL101995 | — | — | 1 | 8.15 |
| CHEMBL368460 | — | — | 1 | 8.13 |
| CHEMBL177211 | — | — | 1 | 8.02 |
| CHEMBL174560 | — | — | 1 | 7.92 |
| CHEMBL177461 | — | — | 1 | 7.89 |
| CHEMBL368387 | — | — | 1 | 7.72 |
| CHEMBL367886 | — | — | 1 | 7.50 |
| CHEMBL175415 | — | — | 1 | 7.48 |
| CHEMBL177493 | — | — | 1 | 7.41 |
| CHEMBL177254 | — | — | 1 | 7.29 |
| CHEMBL173665 | — | — | 1 | 7.29 |
| CHEMBL554372 | — | — | 1 | 6.54 |
| CHEMBL552523 | — | — | 1 | 6.54 |
| CHEMBL558389 | — | — | 1 | 6.37 |
| CHEMBL557159 | — | — | 1 | 6.00 |
| CHEMBL537143 | — | — | 1 | 5.92 |
| CHEMBL559176 | — | — | 1 | 5.75 |
| CHEMBL535140 | — | — | 1 | 5.68 |
| CHEMBL175422 | — | — | 1 | 5.00 |
| CHEMBL174857 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL35670 | — | IC50 | = | 0.5 | nM | 9.30 |
| CHEMBL178034 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL174057 | — | IC50 | = | 2.1 | nM | 8.68 |
| CHEMBL441114 | — | IC50 | = | 2.5 | nM | 8.60 |
| CHEMBL177739 | — | IC50 | = | 4.0 | nM | 8.40 |
| CHEMBL177453 | — | IC50 | = | 5.9 | nM | 8.23 |
| CHEMBL101995 | — | IC50 | = | 7.0 | nM | 8.15 |
| CHEMBL368460 | — | IC50 | = | 7.4 | nM | 8.13 |
| CHEMBL177211 | — | IC50 | = | 9.5 | nM | 8.02 |
| CHEMBL174560 | — | IC50 | = | 12.0 | nM | 7.92 |
| CHEMBL177461 | — | IC50 | = | 13.0 | nM | 7.89 |
| CHEMBL368387 | — | IC50 | = | 19.0 | nM | 7.72 |
| CHEMBL367886 | — | IC50 | = | 32.0 | nM | 7.50 |
| CHEMBL175415 | — | IC50 | = | 33.0 | nM | 7.48 |
| CHEMBL177493 | — | IC50 | = | 39.0 | nM | 7.41 |
| CHEMBL177254 | — | IC50 | = | 51.0 | nM | 7.29 |
| CHEMBL173665 | — | IC50 | = | 51.0 | nM | 7.29 |
| CHEMBL554372 | — | IC50 | = | 290.0 | nM | 6.54 |
| CHEMBL552523 | — | IC50 | = | 290.0 | nM | 6.54 |
| CHEMBL558389 | — | IC50 | = | 430.0 | nM | 6.37 |
| CHEMBL557159 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL537143 | — | IC50 | = | 1200.0 | nM | 5.92 |
| CHEMBL559176 | — | IC50 | = | 1800.0 | nM | 5.75 |
| CHEMBL535140 | — | IC50 | = | 2100.0 | nM | 5.68 |
| CHEMBL175422 | — | IC50 | = | 10000.0 | nM | 5.00 |
| CHEMBL174857 | — | IC50 | > | 100.0 | nM | - |