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Compound Detail

CHEMBL2041190

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Cc1cc(C(=O)O)ccc1-c1ccc(N2C(=O)N(c3cnccn3)C3(CCN(Cc4ncccc4C)CC3)C2=O)cc1

Basic Information

ChEMBL ID CHEMBL2041190
Phase Preclinical
Structure Type MOL
InChI Key YEMQCJMGXORROI-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
4
PK Parameters
12
Publications
0
Known Names

Molecular Properties

562.6
MW (Da)
4.86
ALogP
7
HBA
1
HBD
119.8
PSA (Ų)
0.33
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 C32H30N6O4
MW 562.63
Aromatic Rings 4
Heavy Atoms 42
NP-Likeness -1.06

Activity Summary

IC50 4 meas. best 9.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Prolyl hydroxylase EGLN2
CHEMBL3028
IC50 9.7 9.7 0.2 1
Egl nine homolog 1
CHEMBL5697
IC50 9.7 9.7 0.2 1
Prolyl hydroxylase EGLN3
CHEMBL5705
IC50 9.1 9.1 0.8 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.14 5.14 7200.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 22.0 mL.min-1.kg-1 Rattus norvegicus
Cmax 390.0 nM Rattus norvegicus
F 29.0 % Rattus norvegicus
T1/2 1.5 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
22364528 10.1021/jm201542d Voltage-dependent L-type calcium channel subunit alpha-1C 1
22364528 10.1021/jm201542d Nuclear receptor subfamily 1 group I member 2 1

Data from ChEMBL 36 via Core Engine