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Compound Detail

CHEMBL2041192

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Cc1cccnc1CN1CCC2(CC1)C(=O)N(c1ccc(-c3ccc(C(=O)O)cc3)cc1)C(=O)N2c1ccncn1

Basic Information

ChEMBL ID CHEMBL2041192
Phase Preclinical
Structure Type MOL
InChI Key ROQKQYJTPICBKQ-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
4
PK Parameters
10
Publications
0
Known Names

Molecular Properties

548.6
MW (Da)
4.55
ALogP
7
HBA
1
HBD
119.8
PSA (Ų)
0.35
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H28N6O4
MW 548.60
Aromatic Rings 4
Heavy Atoms 41
NP-Likeness -0.97

Activity Summary

IC50 4 meas. best 9.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Egl nine homolog 1
CHEMBL5697
IC50 9.7 9.7 0.2 1
Prolyl hydroxylase EGLN2
CHEMBL3028
IC50 9.52 9.52 0.3 1
Prolyl hydroxylase EGLN3
CHEMBL5705
IC50 8.68 8.68 2.1 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.51 4.51 31000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 16.0 mL.min-1.kg-1 Rattus norvegicus
Cmax 580.0 nM Rattus norvegicus
F 8.0 % Rattus norvegicus
T1/2 2.2 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22364528 10.1021/jm201542d Rattus norvegicus 5
22364528 10.1021/jm201542d Mus musculus 4
22364528 10.1021/jm201542d Plasma 4
22364528 10.1021/jm201542d Egl nine homolog 1 1
22364528 10.1021/jm201542d Prolyl hydroxylase EGLN2 1
22364528 10.1021/jm201542d Prolyl hydroxylase EGLN3 1
22364528 10.1021/jm201542d Voltage-gated inwardly rectifying potassium channel KCNH2 1
22364528 10.1021/jm201542d Cytochrome P450 3A4 1
22364528 10.1021/jm201542d Cytochrome P450 2C9 1
22364528 10.1021/jm201542d Cytochrome P450 2D6 1

Data from ChEMBL 36 via Core Engine