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Compound Detail

CHEMBL4632935

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C=CC(=O)N1CCN(c2nc(OC[C@@H]3CCCN3C)nc3c2CCN(c2cccc4cccc(C)c24)C3)C[C@@H]1CC#N

Basic Information

ChEMBL ID CHEMBL4632935
Phase Preclinical
Structure Type MOL
InChI Key YRYQLVCTQFBRLD-UIOOFZCWSA-N
1
Targets
1
Activities
1
Assay Types
12
PK Parameters
4
Publications
0
Known Names

Molecular Properties

565.7
MW (Da)
4.09
ALogP
8
HBA
0
HBD
88.8
PSA (Ų)
0.40
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C33H39N7O2
MW 565.72
Aromatic Rings 3
Heavy Atoms 42
NP-Likeness -0.57

Activity Summary

IC50 1 meas. best 9.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
GTPase KRas
CHEMBL2189121
IC50 9.0 9.0 1.0 1

Pharmacokinetic Data

Parameter Value Units Species
AUC 4910.0 ng.hr.mL-1 Mus musculus
AUC 39.5 ng.hr.mL-1 Canis lupus familiaris
CL 31.6 mL.min-1.kg-1 Mus musculus
CL 151.0 mL.min-1.kg-1 Canis lupus familiaris
Cmax 2934.31 nM Mus musculus
Cmax 31.46 nM Canis lupus familiaris
F 31.1 % Mus musculus
F 3.67 % Canis lupus familiaris
T1/2 1.33 hr Mus musculus
T1/2 0.966 hr Canis lupus familiaris
Tmax 0.5 hr Mus musculus
Tmax 1.17 hr Canis lupus familiaris

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
GTPase KRas IC50 = 1.0 nM 9.0 Inhibition of KRAS G12C mutant in human NCI-H358 cells assessed as reduction in ... 32250617

Literature References

PubMed DOI Target Context # Activities
32250617 10.1021/acs.jmedchem.9b02052 ADMET 14
32250617 10.1021/acs.jmedchem.9b02052 GTPase KRas 4
32250617 10.1021/acs.jmedchem.9b02052 MIA PaCa-2 2
32250617 10.1021/acs.jmedchem.9b02052 Glutathione S-transferase P 1

Data from ChEMBL 36 via Core Engine