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Compound Detail

CHEMBL2031562

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Nc1cc(C(=O)Nc2cccc(-c3nnn[nH]3)c2)cc(C(F)(F)F)c1

Basic Information

ChEMBL ID CHEMBL2031562
Phase Preclinical
Structure Type MOL
InChI Key LHVITJKAAOBDHR-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
3
Publications
0
Known Names

Molecular Properties

348.3
MW (Da)
2.72
ALogP
5
HBA
3
HBD
109.6
PSA (Ų)
0.63
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 C15H11F3N6O
MW 348.29
Aromatic Rings 3
Heavy Atoms 25
NP-Likeness -2.18

Activity Summary

Ki 1 meas. best 6.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 6.0 6.0 1000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 23.44 uL.min-1.(10^6cells)-1 Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Ki = 1000.0 nM 6.0 Inhibition of beta-lactamase CTX-M using nitrocefin as substrate 22296601

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL3301361 ADMET 2
22296601 10.1021/jm2014138 Unchecked 1
- 10.6019/CHEMBL3301361 No relevant target 1

Data from ChEMBL 36 via Core Engine