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Compound Detail

CHEMBL2041170

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Cc1cccnc1CN1CCC2(CC1)C(=O)N(c1ccc(-c3ccc(N4CCOCC4)cc3)cc1)C(=O)N2c1cc(O)ncn1

Basic Information

ChEMBL ID CHEMBL2041170
Phase Preclinical
Structure Type MOL
InChI Key WOFLYJYTODVGLV-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
9
Publications
0
Known Names

Molecular Properties

605.7
MW (Da)
4.40
ALogP
9
HBA
1
HBD
115.2
PSA (Ų)
0.32
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 C34H35N7O4
MW 605.70
Aromatic Rings 4
Heavy Atoms 45
NP-Likeness -1.09

Activity Summary

IC50 4 meas. best 9.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Prolyl hydroxylase EGLN2
CHEMBL3028
IC50 9.3 9.3 0.5 1
Egl nine homolog 1
CHEMBL5697
IC50 9.22 9.22 0.6 1
Prolyl hydroxylase EGLN3
CHEMBL5705
IC50 8.01 8.01 9.8 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.89 4.89 13000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
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