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Compound Detail

CHEMBL489324

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Cc1nnc(C(C)C)n1C1CCN(C(C)C[C@H](NC(=O)C2CCC(F)(F)CC2)c2ccccc2)CC1.Cl

Basic Information

ChEMBL ID CHEMBL489324
Phase Preclinical
Structure Type MOL
InChI Key YNPNDZCAIVVHTC-ANXYTEBKSA-N
Parent Compound CHEMBL522259
Active Moiety CHEMBL522259
2
Targets
2
Activities
1
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

501.7
MW (Da)
5.81
ALogP
5
HBA
1
HBD
63.0
PSA (Ų)
0.50
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H42ClF2N5O
MW 538.13
Aromatic Rings 2
Heavy Atoms 36
NP-Likeness -1.27

Activity Summary

IC50 2 meas. best 7.21

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
C-C chemokine receptor type 5
CHEMBL274
IC50 7.21 7.21 62.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.68 5.68 2100.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 16.0 mL.min-1.g-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19185490 10.1016/j.bmcl.2009.01.008 No relevant target 1
19185490 10.1016/j.bmcl.2009.01.008 Liver microsomes 1
19185490 10.1016/j.bmcl.2009.01.008 C-C chemokine receptor type 5 1
19185490 10.1016/j.bmcl.2009.01.008 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine