Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL1684070

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
Cn1c(=O)c(F)c(Nc2ccc(I)cc2F)c2c(=O)n(C[C@H](O)CO)cnc21

Basic Information

ChEMBL ID CHEMBL1684070
Phase Preclinical
Structure Type MOL
InChI Key RCLQNICOARASSR-VIFPVBQESA-N
3
Targets
3
Activities
2
Assay Types
2
PK Parameters
4
Publications
0
Known Names

Molecular Properties

504.2
MW (Da)
1.07
ALogP
8
HBA
3
HBD
109.4
PSA (Ų)
0.45
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H15F2IN4O4
MW 504.23
Aromatic Rings 3
Heavy Atoms 28
NP-Likeness -1.33

Activity Summary

EC50 2 meas. best 8.59
IC50 1 meas. best 8.49

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
COLO 205
CHEMBL614561
EC50 8.59 8.59 2.6 1
A-375
CHEMBL613859
EC50 8.52 8.52 3.0 1
Dual specificity mitogen-activated protein kinase kinase 1
CHEMBL3587
IC50 8.49 8.49 3.2 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 3.05 hr Homo sapiens
T1/2 1.517 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
21310613 10.1016/j.bmcl.2011.01.071 Liver microsomes 2
21310613 10.1016/j.bmcl.2011.01.071 Dual specificity mitogen-activated protein kinase kinase 1 1
21310613 10.1016/j.bmcl.2011.01.071 A-375 1
21310613 10.1016/j.bmcl.2011.01.071 COLO 205 1

Data from ChEMBL 36 via Core Engine