Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL2207167

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
N#CC1(n2cc([C@@H](NC(=O)c3cn[nH]c3)C3CCCCC3)nn2)CC1

Basic Information

ChEMBL ID CHEMBL2207167
Phase Preclinical
Structure Type MOL
InChI Key SYDGGPNMAZALGO-HNNXBMFYSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
2
Publications
0
Known Names

Molecular Properties

339.4
MW (Da)
2.07
ALogP
6
HBA
2
HBD
112.3
PSA (Ų)
0.87
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H21N7O
MW 339.40
Aromatic Rings 2
Heavy Atoms 25
NP-Likeness -1.12

Activity Summary

IC50 1 meas. best 7.64

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cathepsin S
CHEMBL2954
IC50 7.64 7.64 23.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.5 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Cathepsin S IC50 = 23.0 nM 7.64 Inhibition of cathepsin S using FR-aminoluciferin as substrate preincubated for ... 23084902

Literature References

PubMed DOI Target Context # Activities
23084902 10.1016/j.bmcl.2012.09.054 Liver microsomes 1
23084902 10.1016/j.bmcl.2012.09.054 Cathepsin S 1

Data from ChEMBL 36 via Core Engine