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Compound Detail

CHEMBL2419485

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CCOC(=O)c1cc(C#N)c(N2CC(C(=O)NS(=O)(=O)Cc3ccc(Cl)cc3)C2)nc1C

Basic Information

ChEMBL ID CHEMBL2419485
Phase Preclinical
Structure Type MOL
InChI Key FZGNWTQJSVKAPD-UHFFFAOYSA-N
3
Targets
5
Activities
1
Assay Types
1
PK Parameters
6
Publications
0
Known Names

Molecular Properties

476.9
MW (Da)
2.17
ALogP
8
HBA
1
HBD
129.5
PSA (Ų)
0.60
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H21ClN4O5S
MW 476.94
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -1.61

Activity Summary

IC50 5 meas. best 8.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
P2Y purinoceptor 12
CHEMBL2001
IC50 8.0 7.0633 10.0 3
Cytochrome P450 3A4
CHEMBL340
IC50 5.48 5.48 3300.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 5.15 5.15 7100.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 26.0 mL.min-1.g-1 Canis lupus familiaris

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
23899349 10.1021/jm400820m P2Y purinoceptor 12 3
23899349 10.1021/jm400820m No relevant target 2
23899349 10.1021/jm400820m Cytochrome P450 3A4 1
23899349 10.1021/jm400820m Cytochrome P450 2C9 1
23899349 10.1021/jm400820m Liver 1
23899349 10.1021/jm400820m Caco-2 1

Data from ChEMBL 36 via Core Engine