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

CHEMBL2011126

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
CC(=O)N1CCN(c2nc(NCc3cc4ccccc4cn3)c3c(n2)C(=O)N(C(C)C)C3)CC1

Basic Information

ChEMBL ID CHEMBL2011126
Phase Preclinical
Structure Type MOL
InChI Key KDIZLZUNMOJKHK-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
1
PK Parameters
5
Publications
0
Known Names

Molecular Properties

459.6
MW (Da)
2.67
ALogP
7
HBA
1
HBD
94.6
PSA (Ų)
0.63
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 C25H29N7O2
MW 459.55
Aromatic Rings 3
Heavy Atoms 34
NP-Likeness -1.13

Activity Summary

IC50 2 meas. best 7.62

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
P2X purinoceptor 3
CHEMBL2998
IC50 7.62 7.62 24.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 5.16 5.16 7000.0 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
22370269 10.1016/j.bmcl.2012.01.124 P2X purinoceptor 3 1
22370269 10.1016/j.bmcl.2012.01.124 No relevant target 1
22370269 10.1016/j.bmcl.2012.01.124 Cytochrome P450 2C9 1
22370269 10.1016/j.bmcl.2012.01.124 Liver microsomes 1
22370269 10.1016/j.bmcl.2012.01.124 Caco-2 1

Data from ChEMBL 36 via Core Engine