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Compound Detail

CHEMBL2040897

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Cc1nc(C)c(-c2ccc(N3C(=O)N(c4cc(O)ncn4)C4(CCN(Cc5ncccc5C)CC4)C3=O)cc2)s1

Basic Information

ChEMBL ID CHEMBL2040897
Phase Preclinical
Structure Type MOL
InChI Key MRDYEAJRUPFRFX-UHFFFAOYSA-N
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

555.7
MW (Da)
4.63
ALogP
9
HBA
1
HBD
115.7
PSA (Ų)
0.35
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 C29H29N7O3S
MW 555.66
Aromatic Rings 4
Heavy Atoms 40
NP-Likeness -1.28

Activity Summary

IC50 4 meas. best 9.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Prolyl hydroxylase EGLN2
CHEMBL3028
IC50 9.4 9.4 0.4 1
Egl nine homolog 1
CHEMBL5697
IC50 9.05 9.05 0.9 1
Prolyl hydroxylase EGLN3
CHEMBL5705
IC50 8.23 8.23 5.9 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.02 6.02 950.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
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