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Compound Detail

CHEMBL295716

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O=C1OCCc2c1[nH]cc1nc3ccccc3c2-1

Basic Information

ChEMBL ID CHEMBL295716
Phase Preclinical
Structure Type MOL
InChI Key OQXPLGJWSJSOEH-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

238.2
MW (Da)
2.38
ALogP
3
HBA
1
HBD
55.0
PSA (Ų)
0.61
QED
0
Ro5 Violations
0
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C14H10N2O2
MW 238.25
Aromatic Rings 1
Heavy Atoms 18
NP-Likeness 0.18

Activity Summary

IC50 1 meas. best 7.38

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 7.38 7.38 42.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 42.0 nM 7.38 In vitro inhibition of [3H]flunitrazepam binding to GABA-A receptor of rat cereb... 2547070

Literature References

PubMed DOI Target Context # Activities
2547070 10.1021/jm00128a023 Unchecked 1

Data from ChEMBL 36 via Core Engine