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Compound Detail

CHEMBL387402

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O=C(O)c1ccccc1C(=O)Nc1cc2c(=O)n(O)c(=O)[nH]c2cc1Cl

Basic Information

ChEMBL ID CHEMBL387402
Phase Preclinical
Structure Type MOL
InChI Key JUDLYNLYWMFTBG-UHFFFAOYSA-N
4
Targets
5
Activities
2
Assay Types
0
PK Parameters
10
Publications
0
Known Names

Molecular Properties

375.7
MW (Da)
1.53
ALogP
6
HBA
4
HBD
141.5
PSA (Ų)
0.51
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H10ClN3O6
MW 375.72
Aromatic Rings 3
Heavy Atoms 26
NP-Likeness -1.00

Activity Summary

Ki 3 meas. best 8.09
IC50 2 meas. best 6.21

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Carbonic anhydrase 9
CHEMBL3594
Ki 8.09 8.09 8.1 1
Carbonic anhydrase 12
CHEMBL3242
Ki 8.06 8.06 8.7 1
Unchecked
CHEMBL612545
IC50 6.21 6.005 620.0 2
Glutamate receptor ionotropic, AMPA
CHEMBL2093871
Ki 4.78 4.78 16500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
17004715 10.1021/jm0604880 Mus musculus 9
22704999 10.1016/j.ejmech.2012.05.036 Hippocampus 4
22704999 10.1016/j.ejmech.2012.05.036 Unchecked 3
17004715 10.1021/jm0604880 Unchecked 2
17004715 10.1021/jm0604880 Glutamate receptor ionotropic, AMPA 1
17004715 10.1021/jm0604880 Glutamate NMDA receptor 1
28658574 10.1021/acs.jmedchem.7b00766 Carbonic anhydrase 9 1
28658574 10.1021/acs.jmedchem.7b00766 Carbonic anhydrase 12 1
28658574 10.1021/acs.jmedchem.7b00766 Carbonic anhydrase 1 1
28658574 10.1021/acs.jmedchem.7b00766 Carbonic anhydrase 2 1

Data from ChEMBL 36 via Core Engine