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Compound Detail

CHEMBL2042300

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CCNC(=O)[C@H]1O[C@@H](n2cnc3c(N)nc(NCCc4ccc(Br)cc4)nc32)[C@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL2042300
Phase Preclinical
Structure Type MOL
InChI Key IGMOGRIYXGJZIA-QCUYGVNKSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

506.4
MW (Da)
0.58
ALogP
10
HBA
5
HBD
160.4
PSA (Ų)
0.31
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H24BrN7O4
MW 506.36
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -0.17

Activity Summary

EC50 2 meas. best 7.38
IC50 2 meas. best 6.59

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A2a
CHEMBL251
EC50 7.38 7.38 42.0 1
Adenosine receptor A3
CHEMBL256
IC50 6.59 6.59 259.0 1
Adenosine receptor A2b
CHEMBL255
EC50 6.45 6.45 355.0 1
Adenosine receptor A1
CHEMBL226
IC50 5.68 5.68 2082.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22432713 10.1021/jm300206u Unchecked 2
22432713 10.1021/jm300206u Adenosine receptor A2a 1
22432713 10.1021/jm300206u Adenosine receptor A2b 1
22432713 10.1021/jm300206u Adenosine receptor A1 1
22432713 10.1021/jm300206u Adenosine receptor A3 1

Data from ChEMBL 36 via Core Engine