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Assay Detail

CHEMBL709040

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

Functional
Tested in vitro for inhibition after 144 hr exposure against human colon carcinoma LoVo cell line
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type LoVo
Confidence 1 — Organism
Curated By Expert

Target

LoVo (CHEMBL614721)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and antitumor activity of a new class of pyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepinone analogues of pyrrolo[1,4][2,1-c]benzodiazepines.
Baraldi PG, Leoni A, Cacciari B, Manfredini S, Simoni D, Bergomi M, Menta E, Spinelli S.
J Med Chem (1994) 37 : 4329 -4337
PubMed 7996544 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.00 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL137702 1 8.05
CHEMBL53463 DOXORUBICIN 4.0 1 7.24
CHEMBL852 MELPHALAN 4.0 1 5.39
CHEMBL335927 1 4.82
CHEMBL137476 1 4.57
CHEMBL538159 1 4.52
CHEMBL137657 1 4.43
CHEMBL436566 1 4.40
CHEMBL82340 1 4.38
CHEMBL137603 1 4.34
CHEMBL137629 1 4.32
CHEMBL342020 1 4.27
CHEMBL337104 1 4.27
CHEMBL137503 1 -
CHEMBL300842 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL137702 IC50 = 9.0 nM 8.05
CHEMBL53463 DOXORUBICIN IC50 = 57.0 nM 7.24
CHEMBL852 MELPHALAN IC50 = 4090.0 nM 5.39
CHEMBL335927 IC50 = 15000.0 nM 4.82
CHEMBL137476 IC50 = 27000.0 nM 4.57
CHEMBL538159 IC50 = 30000.0 nM 4.52
CHEMBL137657 IC50 = 37000.0 nM 4.43
CHEMBL436566 IC50 = 40000.0 nM 4.40
CHEMBL82340 IC50 = 42000.0 nM 4.38
CHEMBL137603 IC50 = 46000.0 nM 4.34
CHEMBL137629 IC50 = 48400.0 nM 4.32
CHEMBL342020 IC50 = 54000.0 nM 4.27
CHEMBL337104 IC50 = 54000.0 nM 4.27
CHEMBL137503 IC50 > 215000.0 nM -
CHEMBL300842 IC50 > 162000.0 nM -