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Compound Detail

CHEMBL2031556

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O=C(Nc1cccc(-c2nnn[nH]2)c1)c1cccc2[nH]cnc12

Basic Information

ChEMBL ID CHEMBL2031556
Phase Preclinical
Structure Type MOL
InChI Key OUXPKPPPOPWHCW-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
1
PK Parameters
3
Publications
0
Known Names

Molecular Properties

305.3
MW (Da)
2.00
ALogP
5
HBA
3
HBD
112.2
PSA (Ų)
0.54
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 C15H11N7O
MW 305.30
Aromatic Rings 4
Heavy Atoms 23
NP-Likeness -2.07

Activity Summary

Ki 1 meas. best 5.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Ki 5.89 5.89 1300.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 44.67 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 = 1300.0 nM 5.89 Inhibition of beta-lactamase CTX-M using nitrocefin as substrate 22296601

Literature References

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

Data from ChEMBL 36 via Core Engine