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Compound Detail

CHEMBL397785

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O=C(O)c1cc(-c2ccccc2)n[nH]1

Basic Information

ChEMBL ID CHEMBL397785
Phase Preclinical
Structure Type MOL
InChI Key QBPUOAJBMXXBNU-UHFFFAOYSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

188.2
MW (Da)
1.77
ALogP
2
HBA
2
HBD
66.0
PSA (Ų)
0.75
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C10H8N2O2
MW 188.19
Aromatic Rings 2
Heavy Atoms 14
NP-Likeness -1.32

Activity Summary

IC50 1 meas. best 3.89
Ki 1 meas.

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 3.89 3.89 130000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 130000.0 nM 3.89 Inhibition of Thermotoga maritima membrane bound pyrophosphatase at 100 uM using... 32292570

Literature References

PubMed DOI Target Context # Activities
12930155 10.1021/jm030888c Hydroxycarboxylic acid receptor 2 1
17588745 10.1016/j.bmcl.2007.06.028 Hydroxycarboxylic acid receptor 2 1
32292570 10.1021/acsmedchemlett.9b00537 Unchecked 1
32435387 10.1021/acsmedchemlett.9b00617 Human immunodeficiency virus type 1 reverse transcriptase 1

Data from ChEMBL 36 via Core Engine