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Compound Detail

CHEMBL486479

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CCCn1c(=O)[nH]c2nc(-c3ccc(S(=O)(=O)N4CCN(Cc5ccc(C(F)(F)F)cc5)CC4)cc3)[nH]c2c1=O

Basic Information

ChEMBL ID CHEMBL486479
Phase Preclinical
Structure Type MOL
InChI Key RHBLXAUMNGSRMA-UHFFFAOYSA-N
5
Targets
6
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

576.6
MW (Da)
3.02
ALogP
7
HBA
2
HBD
124.2
PSA (Ų)
0.35
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 C26H27F3N6O4S
MW 576.60
Aromatic Rings 4
Heavy Atoms 40
NP-Likeness -1.60

Activity Summary

Ki 5 meas. best 9.52
IC50 1 meas. best 8.79

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A2b
CHEMBL255
Ki 9.52 9.52 0.3 1
Adenosine receptor A2b
CHEMBL255
IC50 8.79 8.79 1.6 1
Adenosine receptor A2a
CHEMBL251
Ki 6.84 6.84 145.0 1
Adenosine receptor A1
CHEMBL318
Ki 6.33 6.33 463.0 1
Adenosine receptor A2a
CHEMBL302
Ki 5.81 5.81 1540.0 1
Adenosine receptor A1
CHEMBL226
Ki 5.25 5.25 5630.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19569717 10.1021/jm900413e Adenosine receptor A1 2
19569717 10.1021/jm900413e Adenosine receptor A2a 2
19569717 10.1021/jm900413e Adenosine receptor A2b 2
19569717 10.1021/jm900413e Adenosine receptor A3 2

Data from ChEMBL 36 via Core Engine