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Compound Detail

CHEMBL2448536

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CC[S+]([O-])(=NC)c1ccc(Nc2ncc(C(F)(F)F)c(N[C@@H]3CCC[C@H]3N(C)C)n2)cc1

Basic Information

ChEMBL ID CHEMBL2448536
Phase Preclinical
Structure Type MOL
InChI Key MIZGEGJKPOLHOH-XZQBWAKSSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

470.6
MW (Da)
4.61
ALogP
7
HBA
2
HBD
88.5
PSA (Ų)
0.57
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 C21H29F3N6OS
MW 470.57
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -0.88

Activity Summary

IC50 2 meas. best 7.68

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protein-tyrosine kinase 2-beta
CHEMBL5469
IC50 7.68 7.65 21.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19428251 10.1016/j.bmcl.2009.04.093 Protein-tyrosine kinase 2-beta 2
19428251 10.1016/j.bmcl.2009.04.093 Focal adhesion kinase 1 1
19428251 10.1016/j.bmcl.2009.04.093 Liver microsomes 1
19428251 10.1016/j.bmcl.2009.04.093 MDCK 1
19428251 10.1016/j.bmcl.2009.04.093 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine