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Compound Detail

CHEMBL406650

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O=C(CCCCCC(=O)N(CC(=O)Nc1cccc2cccnc12)CC(=O)Nc1cccc2cccnc12)NO

Basic Information

ChEMBL ID CHEMBL406650
Phase Preclinical
Structure Type MOL
InChI Key SBMGJAVTUPAYSP-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

542.6
MW (Da)
3.64
ALogP
7
HBA
4
HBD
153.6
PSA (Ų)
0.12
QED
1
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H30N6O5
MW 542.60
Aromatic Rings 4
Heavy Atoms 40
NP-Likeness -0.85

Activity Summary

IC50 2 meas. best 7.58

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histone deacetylase 1
CHEMBL325
IC50 7.58 7.58 26.5 1
Unchecked
CHEMBL612545
IC50 4.28 4.28 52000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Histone deacetylase 1 IC50 = 26.5 nM 7.58 Inhibition of human HDAC1 18247554
Unchecked IC50 = 52000.0 nM 4.28 Inhibition of mouse SC9 cells 18247554

Literature References

PubMed DOI Target Context # Activities
18247554 10.1021/jm7011408 Histone deacetylase 1 1
18247554 10.1021/jm7011408 Unchecked 1

Data from ChEMBL 36 via Core Engine