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Compound Detail

CHEMBL126988

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O=C(O)COc1cccc(-c2ocnc2-c2nc(-c3ccccc3)c(-c3ccccc3)[nH]2)c1

Basic Information

ChEMBL ID CHEMBL126988
Phase Preclinical
Structure Type MOL
InChI Key NSEKSHQWPKYIBH-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

437.4
MW (Da)
5.53
ALogP
5
HBA
2
HBD
101.2
PSA (Ų)
0.35
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H19N3O4
MW 437.45
Aromatic Rings 5
Heavy Atoms 33
NP-Likeness -0.63

Activity Summary

IC50 1 meas. best 7.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Homo sapiens
CHEMBL372
IC50 7.52 7.52 30.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Homo sapiens IC50 = 30.0 nM 7.52 In vitro inhibition of 5.86 uM ADP-induced human platelet aggregation in platele... 7504734

Literature References

PubMed DOI Target Context # Activities
7504734 10.1021/jm00076a018 Homo sapiens 1

Data from ChEMBL 36 via Core Engine