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Compound Detail

CHEMBL2011123

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CCOc1ccc([C@@H](C)Nc2nc(N3CCN(C(C)=O)CC3)nc3c2CN(C(C)C)C3=O)cc1F

Basic Information

ChEMBL ID CHEMBL2011123
Phase Preclinical
Structure Type MOL
InChI Key UWGMYBLNCMZZFK-MRXNPFEDSA-N
2
Targets
2
Activities
1
Assay Types
1
PK Parameters
6
Publications
0
Known Names

Molecular Properties

484.6
MW (Da)
3.22
ALogP
7
HBA
1
HBD
90.9
PSA (Ų)
0.65
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 C25H33FN6O3
MW 484.58
Aromatic Rings 2
Heavy Atoms 35
NP-Likeness -1.54

Activity Summary

IC50 2 meas. best 7.42

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
P2X purinoceptor 3
CHEMBL2998
IC50 7.42 7.42 38.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 4.96 4.96 11000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 17.0 mL.min-1.g-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL3301361 ADMET 2
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