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Compound Detail

CHEMBL4856029

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O=C(O)c1cc2c(oc1=O)c(Br)cc1cc(-c3nnn[nH]3)c(=O)oc12

Basic Information

ChEMBL ID CHEMBL4856029
Phase Preclinical
Structure Type MOL
InChI Key DZXMQNKIZBOASB-UHFFFAOYSA-N
1
Targets
5
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

405.1
MW (Da)
1.54
ALogP
8
HBA
2
HBD
152.2
PSA (Ų)
0.37
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H5BrN4O6
MW 405.12
Aromatic Rings 4
Heavy Atoms 25
NP-Likeness -0.51

Activity Summary

IC50 3 meas. best 7.8
EC50 2 meas. best 7.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
G-protein coupled receptor 35
CHEMBL1293267
IC50 7.8 7.21 15.9 3
G-protein coupled receptor 35
CHEMBL1293267
EC50 7.75 7.67 18.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
33630609 10.1021/acs.jmedchem.0c01624 G-protein coupled receptor 35 5
33630609 10.1021/acs.jmedchem.0c01624 Muscarinic acetylcholine receptor M3 1
33630609 10.1021/acs.jmedchem.0c01624 D(2) dopamine receptor 1
33630609 10.1021/acs.jmedchem.0c01624 Mu-type opioid receptor 1
33630609 10.1021/acs.jmedchem.0c01624 Histamine H3 receptor 1
33630609 10.1021/acs.jmedchem.0c01624 Free fatty acid receptor 4 1

Data from ChEMBL 36 via Core Engine