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Compound Detail

CHEMBL186149

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CCCC[C@H](NC(=O)O[C@H](Cc1nnc(-c2ccc(F)cc2)o1)C(C)(C)C)C(=O)C(=O)Nc1cc[nH]n1

Basic Information

ChEMBL ID CHEMBL186149
Phase Preclinical
Structure Type MOL
InChI Key QCFNLTHDXRFFKG-ZWKOTPCHSA-N
1
Targets
5
Activities
1
Assay Types
3
PK Parameters
7
Publications
0
Known Names

Molecular Properties

514.6
MW (Da)
4.05
ALogP
8
HBA
3
HBD
152.1
PSA (Ų)
0.32
QED
1
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H31FN6O5
MW 514.56
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -1.10

Activity Summary

IC50 5 meas. best 5.31

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cathepsin K
CHEMBL268
IC50 5.31 5.31 4900.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 33.0 mL.min-1.kg-1 Rattus norvegicus
F 88.0 % Rattus norvegicus
T1/2 2.5 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cathepsin K IC50 = 4900.0 nM 5.31 Inhibition of 10 lM Cbz-Phe-Arg-AMC binding to human cathepsin K in fluorescence... 15982880

Literature References

Data from ChEMBL 36 via Core Engine