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Compound Detail

CHEMBL5090910

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CN1CCC[C@H]1COc1nc(N2CCNCC2)c2cnc(-c3cc(O)cc4ccccc34)c(F)c2n1
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL5090910
Phase Preclinical
Structure Type MOL
InChI Key CAUBBKORANNIKG-SFHVURJKSA-N
1
Targets
2
Activities
2
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

488.6
MW (Da)
3.57
ALogP
8
HBA
2
HBD
86.6
PSA (Ų)
0.44
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H29FN6O2
MW 488.57
Aromatic Rings 4
Heavy Atoms 36
NP-Likeness -0.33

Activity Summary

IC50 1 meas. best 6.01
Kd 1 meas. best 6.72

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
 Kd 6.72 6.72 190.0 1
Unchecked
CHEMBL612545
 IC50 6.01 6.01 980.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Kd = 190.0 nM 6.72 Binding affinity to human AviTEV6His-tagged KRAS isoform 4B G12D mutant (1 to 16... 34889605
Unchecked IC50 = 980.0 nM 6.01 Inhibition of human C-terminal Avi biotinylated tagged KRAS isoform 4B G12D muta... 34889605

Literature References

PubMed DOI Target Context # Activities
34889605 10.1021/acs.jmedchem.1c01688 Unchecked 2

Data from ChEMBL 36 via Core Engine