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Compound Detail

CHEMBL200407

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O=C(NC1CCC1)[C@H]1S[C@@H](n2cnc3c(NCc4cccc(I)c4)nc(Cl)nc32)[C@H](O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL200407
Phase Preclinical
Structure Type MOL
InChI Key YUOKEETUCXPRGI-KSVNGYGVSA-N
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

600.9
MW (Da)
2.70
ALogP
9
HBA
4
HBD
125.2
PSA (Ų)
0.25
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 C21H22ClIN6O3S
MW 600.87
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness -0.90

Activity Summary

Ki 3 meas. best 7.74

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Adenosine receptor A3
CHEMBL256
Ki 7.74 7.74 18.2 1
Adenosine receptor A1
CHEMBL226
Ki 6.9 6.9 126.0 1
Adenosine receptor A2a
CHEMBL251
Ki 6.26 6.26 549.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
16392812 10.1021/jm050595e Adenosine receptor A3 2
16392812 10.1021/jm050595e Adenosine receptor A1 1
16392812 10.1021/jm050595e Adenosine receptor A2a 1

Data from ChEMBL 36 via Core Engine