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Compound Detail

CHEMBL3098605

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Cc1ccc(NC(=O)CCCCCCC(=O)NO)cc1
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL3098605
Phase Preclinical
Structure Type MOL
InChI Key WFNAWUGSMGCUGF-UHFFFAOYSA-N
8
Targets
8
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

278.4
MW (Da)
2.78
ALogP
3
HBA
3
HBD
78.4
PSA (Ų)
0.39
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C15H22N2O3
MW 278.35
Aromatic Rings 1
Heavy Atoms 20
NP-Likeness -0.73

Activity Summary

IC50 8 meas. best 7.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histone deacetylase 6
CHEMBL1865
 IC50 7.92 7.92 12.0 1
Histone deacetylase 11
CHEMBL3310
 IC50 7.11 7.11 78.6 1
Histone deacetylase 1
CHEMBL325
 IC50 6.7 6.7 200.0 1
Histone deacetylase 8
CHEMBL3192
 IC50 6.47 6.47 336.0 1
Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)
CHEMBL2111363
 IC50 6.34 6.34 452.0 1
Histone deacetylase 2
CHEMBL1937
 IC50 6.23 6.23 589.0 1
Polyamine deacetylase HDAC10
CHEMBL5103
 IC50 6.19 6.19 649.0 1
NON-PROTEIN TARGET
CHEMBL3879801
 IC50 5.39 5.39 4100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Histone deacetylase 6 IC50 = 12.0 nM 7.92 Inhibition of human HDAC6 using RHKK(Ac) as substrate by fluorimetric analysis 24345446
Histone deacetylase 11 IC50 = 78.6 nM 7.11 Inhibition of human HDAC11 using RHKK(Ac) as substrate by fluorimetric analysis 24345446
Histone deacetylase 1 IC50 = 200.0 nM 6.7 Inhibition of human HDAC1 using RHKK(Ac) as substrate by fluorimetric analysis 24345446
Histone deacetylase 8 IC50 = 336.0 nM 6.47 Inhibition of human HDAC8 using RHK(Ac)K(Ac) as substrate by fluorimetric analys... 24345446
Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2) IC50 = 452.0 nM 6.34 Inhibition of human HDAC3/NCOR2 using RHKK(Ac) as substrate by fluorimetric anal... 24345446
Histone deacetylase 2 IC50 = 589.0 nM 6.23 Inhibition of human HDAC2 using RHKK(Ac) as substrate by fluorimetric analysis 24345446
Polyamine deacetylase HDAC10 IC50 = 649.0 nM 6.19 Inhibition of human HDAC10 using RHKK(Ac) as substrate by fluorimetric analysis 24345446
NON-PROTEIN TARGET IC50 = 4100.0 nM 5.39 Cytotoxicity against human H460 cells 24345446

Literature References

PubMed DOI Target Context # Activities
24345446 10.1016/j.bmcl.2013.11.072 NON-PROTEIN TARGET 1
24345446 10.1016/j.bmcl.2013.11.072 Histone deacetylase 11 1
24345446 10.1016/j.bmcl.2013.11.072 Polyamine deacetylase HDAC10 1
24345446 10.1016/j.bmcl.2013.11.072 Histone deacetylase 8 1
24345446 10.1016/j.bmcl.2013.11.072 Histone deacetylase 6 1
24345446 10.1016/j.bmcl.2013.11.072 Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2) 1
24345446 10.1016/j.bmcl.2013.11.072 Histone deacetylase 2 1
24345446 10.1016/j.bmcl.2013.11.072 Histone deacetylase 1 1

Data from ChEMBL 36 via Core Engine