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

CHEMBL5592276

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
O=C([C@@H]1CCN1S(=O)(=O)c1ccc(N2CCC(F)(F)C2)c(-c2cc3ccccc3[nH]2)c1)N1CCOCC1

Basic Information

ChEMBL ID CHEMBL5592276
Phase Preclinical
Structure Type MOL
InChI Key NVQXXKKPIRCCIU-DEOSSOPVSA-N
1
Targets
1
Activities
1
Assay Types
2
PK Parameters
4
Publications
0
Known Names

Molecular Properties

530.6
MW (Da)
3.30
ALogP
5
HBA
1
HBD
86.0
PSA (Ų)
0.55
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H28F2N4O4S
MW 530.60
Aromatic Rings 3
Heavy Atoms 37
NP-Likeness -1.27

Activity Summary

EC50 1 meas. best 8.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
EC50 8.3 8.3 5.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 2851.0 mL.min-1.kg-1 Homo sapiens
CL 4854.0 mL.min-1.kg-1 Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked EC50 = 5.0 nM 8.3 Inhibition of STT3A/STT3B mediated N-linked glycosylation in human H1-HeLa cells... 39136957

Literature References

PubMed DOI Target Context # Activities
39136957 10.1021/acs.jmedchem.4c01402 ADMET 3
39136957 10.1021/acs.jmedchem.4c01402 Unchecked 1
39136957 10.1021/acs.jmedchem.4c01402 Hepatocyte 1
39136957 10.1021/acs.jmedchem.4c01402 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine