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Compound Detail

CHEMBL2041191

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Cc1cc(C(=O)O)ccc1-c1ccc(N2C(=O)N(c3cnccn3)C3(CCN(Cc4ncccc4C)CC3)C2=O)cn1

Basic Information

ChEMBL ID CHEMBL2041191
Phase Preclinical
Structure Type MOL
InChI Key SSVPMKGPRCBPJY-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
9
Publications
0
Known Names

Molecular Properties

563.6
MW (Da)
4.26
ALogP
8
HBA
1
HBD
132.7
PSA (Ų)
0.34
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 C31H29N7O4
MW 563.62
Aromatic Rings 4
Heavy Atoms 42
NP-Likeness -1.17

Activity Summary

IC50 4 meas. best 9.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Prolyl hydroxylase EGLN2
CHEMBL3028
IC50 9.0 9.0 1.0 1
Egl nine homolog 1
CHEMBL5697
IC50 9.0 9.0 1.0 1
Prolyl hydroxylase EGLN3
CHEMBL5705
IC50 7.37 7.37 43.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.6 5.6 2500.0 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 2
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