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Compound Detail

CHEMBL505914

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CN1CC(C)(NC(=O)Nc2cccc(-c3nnnn3C)c2)C(CN2CCC[C@@H](Cc3ccc(F)cc3)C2)OC1=O.Cl

Basic Information

ChEMBL ID CHEMBL505914
Phase Preclinical
Structure Type MOL
InChI Key YCFVYJUGRZBNKN-UNRBIGBYSA-N
Parent Compound CHEMBL518571
Active Moiety CHEMBL518571
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

550.6
MW (Da)
3.30
ALogP
8
HBA
2
HBD
117.5
PSA (Ų)
0.46
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H36ClFN8O3
MW 587.10
Aromatic Rings 3
Heavy Atoms 40
NP-Likeness -1.31

Activity Summary

IC50 4 meas. best 9.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Eosinophil
CHEMBL614636
IC50 9.89 9.89 0.1 1
C-C chemokine receptor type 3
CHEMBL3473
IC50 9.82 9.82 0.1 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.8 4.8 15700.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 4.77 4.77 17000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19010676 10.1016/j.bmcl.2008.11.002 C-C chemokine receptor type 3 1
19010676 10.1016/j.bmcl.2008.11.002 Eosinophil 1
19010676 10.1016/j.bmcl.2008.11.002 Cytochrome P450 2D6 1
19010676 10.1016/j.bmcl.2008.11.002 Voltage-gated inwardly rectifying potassium channel KCNH2 1
19010676 10.1016/j.bmcl.2008.11.002 Liver microsomes 1

Data from ChEMBL 36 via Core Engine