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Compound Detail

CHEMBL2043325

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COc1cc(N2C(=O)N(c3ccc(-c4ccc(C(=O)O)cc4C)cc3)C(=O)C23CCN(Cc2ncccc2C)CC3)ncn1

Basic Information

ChEMBL ID CHEMBL2043325
Phase Preclinical
Structure Type MOL
InChI Key KAPZNJYOKZDXPF-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
4
PK Parameters
10
Publications
0
Known Names

Molecular Properties

592.7
MW (Da)
4.87
ALogP
8
HBA
1
HBD
129.1
PSA (Ų)
0.30
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H32N6O5
MW 592.66
Aromatic Rings 4
Heavy Atoms 44
NP-Likeness -1.03

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 8.72 8.72 1.9 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.89 4.89 13000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 11.9 mL.min-1.kg-1 Rattus norvegicus
Cmax 570.0 nM Rattus norvegicus
F 64.0 % Rattus norvegicus
T1/2 4.1 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 Plasma 4
22364528 10.1021/jm201542d Mus musculus 3
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