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Compound Detail

CHEMBL141264

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[O-][S+](Cc1cc(OCc2cc(C(F)(F)F)cc(C(F)(F)F)c2)ccn1)c1nc2cscc2[nH]1

Basic Information

ChEMBL ID CHEMBL141264
Phase Preclinical
Structure Type MOL
InChI Key NETSEFWQEMFBOV-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

505.5
MW (Da)
5.94
ALogP
5
HBA
1
HBD
73.9
PSA (Ų)
0.26
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H13F6N3O2S2
MW 505.47
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -0.90

Activity Summary

IC50 1 meas. best 5.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Oryctolagus cuniculus
CHEMBL374
IC50 5.96 5.96 1100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Oryctolagus cuniculus IC50 = 1100.0 nM 5.96 In vitro inhibition of 14C amino-pyrine uptake was determined in isolated rabbit... 1310742

Literature References

PubMed DOI Target Context # Activities
1310742 10.1021/jm00081a004 Oryctolagus cuniculus 1
1310742 10.1021/jm00081a004 Potassium-transporting ATPase 1
1310742 10.1021/jm00081a004 Rattus norvegicus 1
1310742 10.1021/jm00081a004 Canis familiaris 1

Data from ChEMBL 36 via Core Engine