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Compound Detail

CHEMBL2042312

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CNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(NCCc4ccc(NC(=O)c5cc(C(C)(C)C)c(O)c(C(C)(C)C)c5)cc4)nc32)[C@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL2042312
Phase Preclinical
Structure Type MOL
InChI Key OPDLTDYIRKUEAX-YHEPOBCMSA-N
3
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

841.0
MW (Da)
6.64
ALogP
12
HBA
7
HBD
195.8
PSA (Ų)
0.07
QED
4
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C48H56N8O6
MW 841.03
Aromatic Rings 6
Heavy Atoms 62
NP-Likeness -0.29

Activity Summary

EC50 2 meas. best 5.65
IC50 2 meas. best 5.76

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A3
CHEMBL256
IC50 5.76 5.76 1721.0 1
Adenosine receptor A2a
CHEMBL251
EC50 5.65 5.65 2242.0 1
Adenosine receptor A2b
CHEMBL255
EC50 5.17 5.17 6694.0 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