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Compound Detail

CHEMBL229845

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Cc1ccc2c(c1)n1ncc(Cl)c1n[n+]2[O-]

Basic Information

ChEMBL ID CHEMBL229845
Phase Preclinical
Structure Type MOL
InChI Key HAQKDTSRYFEZHG-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

234.7
MW (Da)
1.48
ALogP
4
HBA
0
HBD
57.1
PSA (Ų)
0.44
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 C10H7ClN4O
MW 234.65
Aromatic Rings 3
Heavy Atoms 16
NP-Likeness -1.42

Activity Summary

Ki 1 meas. best 6.71

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 6.71 6.71 196.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 196.0 nM 6.71 Displacement of [3H]flumazenil from bovine brain cortex GABAA/Bz receptor 17306981

Literature References

PubMed DOI Target Context # Activities
17306981 10.1016/j.bmc.2007.01.053 Unchecked 1

Data from ChEMBL 36 via Core Engine