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Compound Detail

CHEMBL4212040

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C=CCN(CC(=O)NCc1ccccc1)C(=O)[C@]12CCC(C)(C)C[C@H]1C1=CC[C@@H]3[C@@]4(C)CC[C@H](O)C(C)(C)[C@@H]4CC[C@@]3(C)[C@]1(C)CC2

Basic Information

ChEMBL ID CHEMBL4212040
Phase Preclinical
Structure Type MOL
InChI Key ZKNNWJKXRMQITJ-DKLSOEIZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
7
Publications
0
Known Names

Molecular Properties

643.0
MW (Da)
8.48
ALogP
3
HBA
2
HBD
69.6
PSA (Ų)
0.29
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H62N2O3
MW 642.97
Aromatic Rings 1
Heavy Atoms 47
NP-Likeness 1.53

Activity Summary

EC50 1 meas. best 4.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
A2780
CHEMBL614004
EC50 4.89 4.89 12900.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
A2780 EC50 = 12900.0 nM 4.89 Cytotoxicity against human A2780 cells after 96 hrs by sulforhodamine-B assay 29529499

Literature References

Data from ChEMBL 36 via Core Engine