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Compound Detail

CHEMBL3416808

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CCNC(=O)[C@H]1O[C@@H](n2cnc3c(N)nc(N4CCN(c5ccc(OCc6ccc(C(F)(F)F)cc6)cc5)CC4)nc32)[C@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL3416808
Phase Preclinical
Structure Type MOL
InChI Key FKJZJHHCFXKNFO-NLJXWPIHSA-N
4
Targets
5
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

642.6
MW (Da)
2.09
ALogP
12
HBA
4
HBD
164.1
PSA (Ų)
0.22
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H33F3N8O5
MW 642.64
Aromatic Rings 4
Heavy Atoms 46
NP-Likeness -0.63

Activity Summary

Ki 3 meas. best 8.35
EC50 2 meas. best 7.42

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A1
CHEMBL226
Ki 8.35 8.35 4.5 1
Adenosine receptor A2a
CHEMBL251
Ki 7.62 7.62 24.0 1
Adenosine receptor A2a
CHEMBL251
EC50 7.42 7.42 38.0 1
Adenosine receptor A3
CHEMBL256
Ki 7.41 7.41 39.0 1
Adenosine receptor A2b
CHEMBL255
EC50 6.06 6.06 866.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
25780876 10.1021/acs.jmedchem.5b00215 Adenosine receptor A2a 2
25780876 10.1021/acs.jmedchem.5b00215 Adenosine receptor A1 1
25780876 10.1021/acs.jmedchem.5b00215 Adenosine receptor A2b 1
25780876 10.1021/acs.jmedchem.5b00215 Adenosine receptor A3 1

Data from ChEMBL 36 via Core Engine