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Compound Detail

CHEMBL2041182

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Cc1cc(N2C(=O)N(c3ccc(-c4ccc(C(=O)O)cc4C)cc3)C(=O)C23CCN(Cc2ncccc2C)CC3)ncn1

Basic Information

ChEMBL ID CHEMBL2041182
Phase Preclinical
Structure Type MOL
InChI Key AEFKPNYWNAAZGP-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

576.7
MW (Da)
5.17
ALogP
7
HBA
1
HBD
119.8
PSA (Ų)
0.31
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H32N6O4
MW 576.66
Aromatic Rings 4
Heavy Atoms 43
NP-Likeness -0.99

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 8.49 8.49 3.2 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.42 4.42 38000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22364528 10.1021/jm201542d Mus musculus 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