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Assay Detail

CHEMBL3077880

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

Functional
Cytotoxicity against human melanoma cells
78
Total Activities
39
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Publication

Comparative QSAR and pharmacophore modeling of substituted 2-[2-(dimethylamino) ethyl]-1, 2-dihydro-3H-dibenz[de,h]isoquinoline-1,3-diones derivatives as anti-tumor activity
Sharma MC, Sharma S, Sharma P, Kumar A
Med Chem Res (2013) 22 : 5772 -5788
· DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 78 8.18 8.33

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL146315 2 8.33
CHEMBL147556 2 8.30
CHEMBL422843 2 8.29
CHEMBL178168 2 8.25
CHEMBL148229 2 8.24
CHEMBL147428 2 8.24
CHEMBL146516 2 8.23
CHEMBL149619 2 8.23
CHEMBL177706 2 8.22
CHEMBL148027 2 8.22
CHEMBL147216 2 8.22
CHEMBL149184 2 8.21
CHEMBL2281897 2 8.20
CHEMBL439632 2 8.20
CHEMBL343852 2 8.19
CHEMBL146559 2 8.18
CHEMBL358993 2 8.17
CHEMBL345020 2 8.17
CHEMBL439812 2 8.17
CHEMBL146037 2 8.16
CHEMBL290677 AZONAFIDE 2 8.15
CHEMBL344310 2 8.15
CHEMBL356785 2 8.15
CHEMBL148263 2 8.15
CHEMBL146104 2 8.15
CHEMBL147576 2 8.15
CHEMBL148344 2 8.15
CHEMBL149293 2 8.14
CHEMBL145826 2 8.14
CHEMBL148281 2 8.14

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL146315 IC50 = 4.69 nM 8.33
CHEMBL147556 IC50 = 5.06 nM 8.30
CHEMBL422843 IC50 = 5.12 nM 8.29
CHEMBL178168 IC50 = 5.61 nM 8.25
CHEMBL148229 IC50 = 5.69 nM 8.24
CHEMBL147428 IC50 = 5.73 nM 8.24
CHEMBL149619 IC50 = 5.92 nM 8.23
CHEMBL146516 IC50 = 5.92 nM 8.23
CHEMBL177706 IC50 = 6.01 nM 8.22
CHEMBL148027 IC50 = 6.02 nM 8.22
CHEMBL147216 IC50 = 6.08 nM 8.22
CHEMBL149184 IC50 = 6.2 nM 8.21
CHEMBL439632 IC50 = 6.27 nM 8.20
CHEMBL2281897 IC50 = 6.26 nM 8.20
CHEMBL343852 IC50 = 6.53 nM 8.19
CHEMBL146559 IC50 = 6.57 nM 8.18
CHEMBL345020 IC50 = 6.75 nM 8.17
CHEMBL439812 IC50 = 6.79 nM 8.17
CHEMBL358993 IC50 = 6.74 nM 8.17
CHEMBL146037 IC50 = 6.89 nM 8.16
CHEMBL290677 AZONAFIDE IC50 = 7.15 nM 8.15
CHEMBL148263 IC50 = 7.13 nM 8.15
CHEMBL344310 IC50 = 7.11 nM 8.15
CHEMBL146104 IC50 = 7.01 nM 8.15
CHEMBL147576 IC50 = 7.12 nM 8.15
CHEMBL356785 IC50 = 7.09 nM 8.15
CHEMBL148344 IC50 = 7.05 nM 8.15
CHEMBL148281 IC50 = 7.19 nM 8.14
CHEMBL145826 IC50 = 7.22 nM 8.14
CHEMBL146101 IC50 = 7.2 nM 8.14
CHEMBL422137 IC50 = 7.28 nM 8.14
CHEMBL149293 IC50 = 7.28 nM 8.14
CHEMBL343913 IC50 = 7.44 nM 8.13
CHEMBL147597 IC50 = 7.35 nM 8.13
CHEMBL148141 IC50 = 7.42 nM 8.13
CHEMBL146785 IC50 = 7.8 nM 8.11
CHEMBL145869 IC50 = 8.02 nM 8.10
CHEMBL147372 IC50 = 7.96 nM 8.10
CHEMBL144014 IC50 = 8.34 nM 8.08
CHEMBL146516 IC50 = 169044093.16 nM -
CHEMBL146785 IC50 = 128233058.27 nM -
CHEMBL356785 IC50 = 141253754.46 nM -
CHEMBL146101 IC50 = 138995263.12 nM -
CHEMBL148281 IC50 = 139315680.29 nM -
CHEMBL422137 IC50 = 137404197.5 nM -
CHEMBL147576 IC50 = 140604752.41 nM -
CHEMBL343913 IC50 = 134586035.41 nM -
CHEMBL147372 IC50 = 125892541.18 nM -
CHEMBL146104 IC50 = 142889395.85 nM -
CHEMBL2281897 IC50 = 159955802.86 nM -