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Compound Detail

CHEMBL3098241

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CCCSc1nc(N[C@@H]2C[C@H]2c2ccc(F)c(F)c2)c2nnn([C@H]3[C@H](O)[C@H](O)[C@@H](O)[C@H]3F)c2n1

Basic Information

ChEMBL ID CHEMBL3098241
Phase Preclinical
Structure Type MOL
InChI Key JLYCDVDEIUIVQR-VQGFLVHSSA-N
3
Targets
3
Activities
1
Assay Types
6
PK Parameters
6
Publications
0
Known Names

Molecular Properties

496.5
MW (Da)
1.95
ALogP
10
HBA
4
HBD
129.2
PSA (Ų)
0.29
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 C21H23F3N6O3S
MW 496.52
Aromatic Rings 3
Heavy Atoms 34
NP-Likeness -1.22

Activity Summary

IC50 3 meas. best 6.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
P2Y purinoceptor 12
CHEMBL2001
IC50 6.66 6.66 220.0 1
P2Y purinoceptor 12
CHEMBL2188
IC50 6.54 6.54 290.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 5.05 5.05 8820.0 1

Pharmacokinetic Data

Parameter Value Units Species
AUC 469.0 ng.hr.mL-1 Canis lupus familiaris
AUC 1204.0 ng.hr.mL-1 Rattus norvegicus
Cmax 221.54 nM Canis lupus familiaris
Cmax 610.25 nM Rattus norvegicus
T1/2 1.94 hr Canis lupus familiaris
T1/2 3.56 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
24332627 10.1016/j.bmcl.2013.11.055 Rattus norvegicus 16
24332627 10.1016/j.bmcl.2013.11.055 Canis familiaris 5
24332627 10.1016/j.bmcl.2013.11.055 P2Y purinoceptor 12 2
24332627 10.1016/j.bmcl.2013.11.055 Cytochrome P450 2C9 1
24332627 10.1016/j.bmcl.2013.11.055 ADMET 1
24332627 10.1016/j.bmcl.2013.11.055 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine