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Compound Detail

CHEMBL149800

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Clc1ccc(CCNc2ncnc3ccc(Cl)cc23)cc1

Basic Information

ChEMBL ID CHEMBL149800
Phase Preclinical
Structure Type MOL
InChI Key AOWWUEORXDGINB-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

318.2
MW (Da)
4.59
ALogP
3
HBA
1
HBD
37.8
PSA (Ų)
0.76
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H13Cl2N3
MW 318.21
Aromatic Rings 3
Heavy Atoms 21
NP-Likeness -1.22

Activity Summary

IC50 2 meas. best 6.46

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 6.46 6.46 344.0 1
Huntingtin
CHEMBL5514
IC50 5.46 5.46 3440.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 344.0 nM 6.46 Inhibition of NF-kappaB activation 19726185
Huntingtin IC50 = 3440.0 nM 5.46 Inhibition of Huntingtin protein aggregation by cell based assay 19243939

Literature References

PubMed DOI Target Context # Activities
11229767 10.1016/s0960-894x(00)00718-6 ADMET 2
11229767 10.1016/s0960-894x(00)00718-6 T-cell 1
19243939 10.1016/j.bmcl.2009.01.087 Huntingtin 1
19726185 10.1016/j.bmcl.2009.08.021 Unchecked 1
19854049 10.1016/j.bmcl.2009.10.024 Metabotropic glutamate receptor 5 1

Data from ChEMBL 36 via Core Engine