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Compound Detail

CHEMBL239497

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CCc1nc(N)nc(N)c1-c1ccc2c(c1)N(CCCOC)C(=O)C(CC)(c1cc(F)cc(F)c1)O2

Basic Information

ChEMBL ID CHEMBL239497
Phase Preclinical
Structure Type MOL
InChI Key ICDYHYNUXPDZEQ-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
1
PK Parameters
7
Publications
0
Known Names

Molecular Properties

497.6
MW (Da)
4.22
ALogP
7
HBA
2
HBD
116.6
PSA (Ų)
0.45
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 C26H29F2N5O3
MW 497.55
Aromatic Rings 3
Heavy Atoms 36
NP-Likeness -0.78

Activity Summary

IC50 4 meas. best 6.76

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Renin
CHEMBL286
IC50 6.76 6.76 175.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 6.34 6.34 460.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.48 5.48 3300.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 5.31 5.31 4900.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 0.3 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Renin IC50 = 175.0 nM 6.76 Inhibition of human renin by fluorescent tGFP assay 17574423
Cytochrome P450 3A4 IC50 = 460.0 nM 6.34 Inhibition of CYP3A4 17574423
Cytochrome P450 2D6 IC50 = 3300.0 nM 5.48 Inhibition of CYP2D6 17574423
Cytochrome P450 2C9 IC50 = 4900.0 nM 5.31 Inhibition of CYP2C9 17574423

Literature References

PubMed DOI Target Context # Activities
17574423 10.1016/j.bmc.2007.05.069 Renin 1
17574423 10.1016/j.bmc.2007.05.069 Liver microsomes 1
17574423 10.1016/j.bmc.2007.05.069 No relevant target 1
17574423 10.1016/j.bmc.2007.05.069 Caco-2 1
17574423 10.1016/j.bmc.2007.05.069 Cytochrome P450 3A4 1
17574423 10.1016/j.bmc.2007.05.069 Cytochrome P450 2D6 1
17574423 10.1016/j.bmc.2007.05.069 Cytochrome P450 2C9 1

Data from ChEMBL 36 via Core Engine