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

CHEMBL2040569

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
O=C(NCC1CC1)c1nc(-c2cnccn2)[nH]c(=O)c1O

Basic Information

ChEMBL ID CHEMBL2040569
Phase Preclinical
Structure Type MOL
InChI Key OKJFDVHTIVXZEU-UHFFFAOYSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

287.3
MW (Da)
0.07
ALogP
6
HBA
3
HBD
120.9
PSA (Ų)
0.73
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C13H13N5O3
MW 287.28
Aromatic Rings 2
Heavy Atoms 21
NP-Likeness -1.03

Activity Summary

EC50 1 meas. best 5.44
Ki 1 meas. best 6.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Polymerase acidic protein
CHEMBL1169598
Ki 6.0 6.0 990.0 1
Polymerase acidic protein
CHEMBL1169598
EC50 5.44 5.44 3660.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Polymerase acidic protein Ki = 990.0 nM 6.0 Binding affinity to PA N-terminal domain (Competitive) 22211528
Polymerase acidic protein EC50 = 3660.0 nM 5.44 Plaque growth inhibition 22211528

Literature References

PubMed DOI Target Context # Activities
22211528 10.1021/cb200439z Polymerase acidic protein 2
22211528 10.1021/cb200439z Influenza A virus 1

Data from ChEMBL 36 via Core Engine