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Compound Detail

CHEMBL5566946

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CC(C)n1c(=O)n(C)c2cnc3cc(F)c(-c4ccc(OCCCN(C)C)nc4)cc3c21

Basic Information

ChEMBL ID CHEMBL5566946
Phase Preclinical
Structure Type MOL
InChI Key WJGVVHLQSBDKMS-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
9
PK Parameters
7
Publications
0
Known Names

Molecular Properties

437.5
MW (Da)
4.00
ALogP
7
HBA
0
HBD
65.2
PSA (Ų)
0.41
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H28FN5O2
MW 437.52
Aromatic Rings 4
Heavy Atoms 32
NP-Likeness -1.41

Activity Summary

IC50 2 meas. best 8.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Serine-protein kinase ATM
CHEMBL3797
IC50 8.8 8.8 1.6 1
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
CHEMBL4005
IC50 4.8 4.8 15848.9 1

Pharmacokinetic Data

Parameter Value Units Species
CL 25.0 mL.min-1.kg-1 Rattus norvegicus
CL 53.0 mL.min-1.kg-1 Canis lupus familiaris
F 48.0 % Rattus norvegicus
F 31.0 % Canis lupus familiaris
Fu 0.17 - Rattus norvegicus
Fu 0.42 - Canis lupus familiaris
Fu 0.32 - Homo sapiens
T1/2 3.2 hr Rattus norvegicus
T1/2 6.4 hr Canis lupus familiaris

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
38306388 10.1021/acs.jmedchem.3c02277 ADMET 17
38306388 10.1021/acs.jmedchem.3c02277 No relevant target 2
38306388 10.1021/acs.jmedchem.3c02277 Serine-protein kinase ATM 1
38306388 10.1021/acs.jmedchem.3c02277 Serine/threonine-protein kinase ATR 1
38306388 10.1021/acs.jmedchem.3c02277 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform 1
38306388 10.1021/acs.jmedchem.3c02277 Serine/threonine-protein kinase mTOR 1
38306388 10.1021/acs.jmedchem.3c02277 DNA-dependent protein kinase catalytic subunit 1

Data from ChEMBL 36 via Core Engine