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Compound Detail

CHEMBL521621

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CON(C)C(=O)[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)nc(Cl)nc32)[C@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL521621
Phase Preclinical
Structure Type MOL
InChI Key PWQJUKHXFSFTDU-MOROJQBDSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

574.8
MW (Da)
1.34
ALogP
10
HBA
3
HBD
134.9
PSA (Ų)
0.23
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C19H20ClIN6O5
MW 574.76
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -0.49

Activity Summary

Ki 2 meas. best 7.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A3
CHEMBL256
Ki 7.15 7.15 70.2 1
Adenosine receptor A1
CHEMBL226
Ki 6.6 6.6 252.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18752961 10.1016/j.bmc.2008.08.007 Adenosine receptor A1 2
18752961 10.1016/j.bmc.2008.08.007 Adenosine receptor A3 2
18752961 10.1016/j.bmc.2008.08.007 Adenosine receptors; A1 & A3 1
18752961 10.1016/j.bmc.2008.08.007 Adenosine receptor A2a 1

Data from ChEMBL 36 via Core Engine