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Compound Detail

CHEMBL25348

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CO[C@]1(c2cnc(Sc3ccc(/C(C)=N/O)cc3)s2)CCO[C@@H](C)C1

Basic Information

ChEMBL ID CHEMBL25348
Phase Preclinical
Structure Type MOL
InChI Key DTKCJVWJVZZTNV-HXPZODFTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

378.5
MW (Da)
4.53
ALogP
7
HBA
1
HBD
63.9
PSA (Ų)
0.47
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C18H22N2O3S2
MW 378.52
Aromatic Rings 2
Heavy Atoms 25
NP-Likeness -0.32

Activity Summary

IC50 1 meas. best 7.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Homo sapiens
CHEMBL372
IC50 7.4 7.4 40.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Homo sapiens IC50 = 40.0 nM 7.4 In vitro inhibitory activity against LTB4 synthesis in A-23187 stimulated human ... -

Literature References

PubMed DOI Target Context # Activities
- 10.1016/0960-894X(95)00578-H Homo sapiens 1
- 10.1016/0960-894X(95)00578-H Rattus norvegicus 1

Data from ChEMBL 36 via Core Engine