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Compound Detail

CHEMBL2043327

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Cc1cccnc1CN1CCC2(CC1)C(=O)N(c1ccc(C3CCCCC3)cc1)C(=O)N2c1cc(O)ncn1

Basic Information

ChEMBL ID CHEMBL2043327
Phase Preclinical
Structure Type MOL
InChI Key ZREIKOVBKPAVMW-UHFFFAOYSA-N
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

526.6
MW (Da)
4.94
ALogP
7
HBA
1
HBD
102.8
PSA (Ų)
0.47
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H34N6O3
MW 526.64
Aromatic Rings 3
Heavy Atoms 39
NP-Likeness -0.91

Activity Summary

IC50 5 meas. best 8.72

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Prolyl hydroxylase EGLN2
CHEMBL3028
IC50 8.72 8.72 1.9 1
Egl nine homolog 1
CHEMBL5697
IC50 8.3 8.3 5.0 1
Prolyl hydroxylase EGLN3
CHEMBL5705
IC50 6.92 6.92 120.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.0 6.0 1000.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 4.4 4.4 40000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
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 Mus musculus 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