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Compound Detail

CHEMBL429459

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

Basic Information

ChEMBL ID CHEMBL429459
Phase Preclinical
Structure Type MOL
InChI Key NAJFOBIBNBUZAN-UHFFFAOYSA-N
3
Targets
3
Activities
1
Assay Types
6
PK Parameters
7
Publications
0
Known Names

Molecular Properties

483.5
MW (Da)
3.56
ALogP
7
HBA
3
HBD
127.6
PSA (Ų)
0.44
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H27F2N5O3
MW 483.52
Aromatic Rings 3
Heavy Atoms 35
NP-Likeness -0.52

Activity Summary

IC50 3 meas. best 7.37

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Renin
CHEMBL286
IC50 7.37 7.37 43.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 5.32 5.32 4790.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.16 5.16 6960.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 22.0 mL.min-1.kg-1 Rattus norvegicus
Cmax 384.68 nM Rattus norvegicus
F 7.0 % Rattus norvegicus
T1/2 0.2333 hr Homo sapiens
T1/2 0.1167 hr Rattus norvegicus
T1/2 1.6 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Renin IC50 = 43.0 nM 7.37 Inhibition of human renin by fluorescent tGFP assay 17574423
Cytochrome P450 3A4 IC50 = 4790.0 nM 5.32 Inhibition of CYP3A4 17574423
Cytochrome P450 2D6 IC50 = 6960.0 nM 5.16 Inhibition of CYP2D6 17574423

Literature References

PubMed DOI Target Context # Activities
17574423 10.1016/j.bmc.2007.05.069 Rattus norvegicus 5
17574423 10.1016/j.bmc.2007.05.069 Liver microsomes 2
17574423 10.1016/j.bmc.2007.05.069 Renin 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

Data from ChEMBL 36 via Core Engine